WorldWideScience

Sample records for controlled crystal chirality

  1. Generation of Absolute Controlled Crystal Chirality by the Removal of Crystal Water from Achiral Crystal of Nucleobase Cytosine

    OpenAIRE

    Kawasaki, Tsuneomi; Hakoda, Yuko; Mineki, Hiroko; Suzuki, Kenta; Soai, Kenso

    2010-01-01

    The enantioselective formation of chiral crystal of achiral nucleobase cytosine was achieved mediated by the crystal direction selective dehydration of crystal water in the achiral crystal of cytosine monohydrate (P21/c). Heat transfer from the enantiotopic face of the single crystal of cytosine monohydrate afforded the enantiomorphous crystal of anhydrous cytosine.

  2. Polarization control of quantum dot emission by chiral photonic crystal slabs.

    Science.gov (United States)

    Lobanov, Sergey V; Weiss, Thomas; Gippius, Nikolay A; Tikhodeev, Sergei G; Kulakovskii, Vladimir D; Konishi, Kuniaki; Kuwata-Gonokami, Makoto

    2015-04-01

    We investigate theoretically the polarization properties of the quantum dot's (QDs) optical emission from chiral photonic crystal structures made of achiral materials in the absence of external magnetic field at room temperature. The mirror symmetry of the local electromagnetic field is broken in this system due to the decreased symmetry of the chiral modulated layer. As a result, the radiation of randomly polarized QDs normal to the structure becomes partially circularly polarized. The sign and degree of circular polarization are determined by the geometry of the chiral modulated structure and depend on the radiation frequency. A degree of circular polarization up to 99% can be achieved for randomly distributed QDs, and can be close to 100% for some single QDs.

  3. Controlling circular polarization of light emitted by quantum dots using chiral photonic crystal slab

    CERN Document Server

    Lobanov, S V; Gippius, N A; Maksimov, A A; Filatov, E V; Tartakovskii, I I; Kulakovskii, V D; Weiss, T; Schneider, C; Geßler, J; Kamp, M; Höfling, S

    2015-01-01

    Polarization properties of the emission have been investigated for quantum dots embedded in chiral photonic crystal structures made of achiral planar GaAs waveguides. A modification of the electromagnetic mode structure due to the chiral grating fabricated by partial etching of the waveguide layer has been shown to result in a high circular polarization degree $\\rho_c$ of the quantum dot emission in the absence of external magnetic field. The physical nature of the phenomenon can be understood in terms of the reciprocity principle taking into account the structural symmetry. At the resonance wavelength, the magnitude of $|\\rho_c|$ is predicted to exceed 98%. The experimentally achieved value of $|\\rho_c|=81$% is smaller, which is due to the contribution of unpolarized light scattered by grating defects, thus breaking its periodicity. The achieved polarization degree estimated removing the unpolarized nonresonant background from the emission spectra can be estimated to be as high as 96%, close to the theoretic...

  4. Planar optics with patterned chiral liquid crystals

    Science.gov (United States)

    Kobashi, Junji; Yoshida, Hiroyuki; Ozaki, Masanori

    2016-06-01

    Reflective metasurfaces based on metallic and dielectric nanoscatterers have attracted interest owing to their ability to control the phase of light. However, because such nanoscatterers require subwavelength features, the fabrication of elements that operate in the visible range is challenging. Here, we show that chiral liquid crystals with a self-organized helical structure enable metasurface-like, non-specular reflection in the visible region. The phase of light that is Bragg-reflected off the helical structure can be controlled over 0-2π depending on the spatial phase of the helical structure; thus planar elements with arbitrary reflected wavefronts can be created via orientation control. The circular polarization selectivity and external field tunability of Bragg reflection open a wide variety of potential applications for this family of functional devices, from optical isolators to wearable displays.

  5. Viscoelastic modes in chiral liquid crystals

    Indian Academy of Sciences (India)

    K A Suresh

    2003-08-01

    Viscoelastic properties of liquid crystals are very important for applications like display technology. However, there are not many direct techniques to study them. In this review, we describe our studies on the viscoelastic modes of some chiral liquid crystals using dynamic light scattering. We discuss viscoelastic modes corresponding to the C director fluctuations in the chiral smectic C phase and the behaviour of the Goldstone-mode near the chiral smectic C–smectic A phase transition. In cholesteric liquid crystals, we consider the director fluctuations in a wavevector range comparable to the inverse pitch of the cholesteric. Here, the study of the scattered light in the vicinity of the Bragg reflection using a novel geometry will be presented.

  6. Single chirality through crystal grinding

    NARCIS (Netherlands)

    Noorduin, W.L.

    2010-01-01

    The properties of chiral molecules in living organisms can be different for left- and right-handed molecules. Therefore, ways to produce molecules of single handedness are of paramount importance, especially for economical, high yielding processes to synthesize pharmaceutical compounds that must be

  7. Chiral Liquid Crystals: Structures, Phases, Effects

    Directory of Open Access Journals (Sweden)

    Ingo Dierking

    2014-06-01

    Full Text Available The introduction of chirality, i.e., the lack of mirror symmetry, has a profound effect on liquid crystals, not only on the molecular scale but also on the supermolecular scale and phase. I review these effects, which are related to the formation of supermolecular helicity, the occurrence of novel thermodynamic phases, as well as electro-optic effects which can only be observed in chiral liquid crystalline materials. In particular, I will discuss the formation of helical superstructures in cholesteric, Twist Grain Boundary and ferroelectric phases. As examples for the occurrence of novel phases the Blue Phases and Twist Grain Boundary phases are introduced. Chirality related effects are demonstrated through the occurrence of ferroelectricity in both thermotropic as well as lyotropic liquid crystals. Lack of mirror symmetry is also discussed briefly for some biopolymers such as cellulose and DNA, together with its influence on liquid crystalline behavior.

  8. Nanoconfinement-Induced Structures in Chiral Liquid Crystals

    OpenAIRE

    2013-01-01

    We employ Monte Carlo simulations in a specialized isothermal-isobaric and in the grand canonical ensemble to study structure formation in chiral liquid crystals as a function of molecular chirality. Our model potential consists of a simple Lennard-Jones potential, where the attractive contribution has been modified to represent the orientation dependence of the interaction between a pair of chiral liquid-crystal molecules. The liquid crystal is confined between a pair of planar and atomicall...

  9. Reconfigurable self-assembly through chiral control of interfacial tension.

    Science.gov (United States)

    Gibaud, Thomas; Barry, Edward; Zakhary, Mark J; Henglin, Mir; Ward, Andrew; Yang, Yasheng; Berciu, Cristina; Oldenbourg, Rudolf; Hagan, Michael F; Nicastro, Daniela; Meyer, Robert B; Dogic, Zvonimir

    2012-01-04

    From determining the optical properties of simple molecular crystals to establishing the preferred handedness in highly complex vertebrates, molecular chirality profoundly influences the structural, mechanical and optical properties of both synthetic and biological matter on macroscopic length scales. In soft materials such as amphiphilic lipids and liquid crystals, the competition between local chiral interactions and global constraints imposed by the geometry of the self-assembled structures leads to frustration and the assembly of unique materials. An example of particular interest is smectic liquid crystals, where the two-dimensional layered geometry cannot support twist and chirality is consequently expelled to the edges in a manner analogous to the expulsion of a magnetic field from superconductors. Here we demonstrate a consequence of this geometric frustration that leads to a new design principle for the assembly of chiral molecules. Using a model system of colloidal membranes, we show that molecular chirality can control the interfacial tension, an important property of multi-component mixtures. This suggests an analogy between chiral twist, which is expelled to the edges of two-dimensional membranes, and amphiphilic surfactants, which are expelled to oil-water interfaces. As with surfactants, chiral control of interfacial tension drives the formation of many polymorphic assemblages such as twisted ribbons with linear and circular topologies, starfish membranes, and double and triple helices. Tuning molecular chirality in situ allows dynamical control of line tension, which powers polymorphic transitions between various chiral structures. These findings outline a general strategy for the assembly of reconfigurable chiral materials that can easily be moved, stretched, attached to one another and transformed between multiple conformational states, thus allowing precise assembly and nanosculpting of highly dynamical and designable materials with complex

  10. Perpetually self-propelling chiral single crystals.

    Science.gov (United States)

    Panda, Manas K; Runčevski, Tomče; Husain, Ahmad; Dinnebier, Robert E; Naumov, Panče

    2015-02-11

    When heated, single crystals of enantiomerically pure D- and L-pyroglutamic acid (PGA) are capable of recurring self-actuation due to rapid release of latent strain during a structural phase transition, while the racemate is mechanically inactive. Contrary to other thermosalient materials, where the effect is accompanied by crystal explosion due to ejection of debris or splintering, the chiral PGA crystals respond to internal strain with unprecedented robustness and can be actuated repeatedly without deterioration. It is demonstrated that this superelasticity is attained due to the low-dimensional hydrogen-bonding network which effectively accrues internal strain to elicit propulsion solely by elastic deformation without disintegration. One of the two polymorphs (β) associated with the thermosalient phase transition undergoes biaxial negative thermal expansion (αa = -54.8(8) × 10(-6) K(-1), αc = -3.62(8) × 10(-6) K(-1)) and exceptionally large uniaxial thermal expansion (αb = 303(1) × 10(-6) K(-1)). This second example of a thermosalient solid with anomalous expansion indicates that the thermosalient effect can be expected for first-order phase transitions in soft crystals devoid of an extended 3D hydrogen-bonding network that undergo strongly anisotropic thermal expansion around the phase transition.

  11. Synthesis of a Chiral Crystal Form of MOF-5, CMOF-5, by Chiral Induction.

    Science.gov (United States)

    Zhang, Shi-Yuan; Li, Dan; Guo, Dong; Zhang, Hui; Shi, Wei; Cheng, Peng; Wojtas, Lukasz; Zaworotko, Michael J

    2015-12-16

    Chiral variants of the prototypal metal-organic framework MOF-5, Λ-CMOF-5 and Δ-CMOF-5, have been synthesized by preparing MOF-5 in the presence of L-proline or D-proline, respectively. CMOF-5 crystallizes in chiral space group P213 instead of Fm3̅m as exhibited by MOF-5. The phase purity of CMOF-5 was validated by single-crystal and powder X-ray diffraction, infrared spectroscopy, thermogravimetric analysis, N2 adsorption, microanalysis, and solid-state vibrational circular dichroism. CMOF-5 undergoes a reversible single crystal-to-single crystal phase change to MOF-5 when immersed in a variety of organic solvents, although N-methyl-2-pyrrolidone (NMP) does not induce loss of chirality. Indeed, MOF-5 undergoes chiral induction when immersed in NMP, affording racemic CMOF-5.

  12. Spatial control of chirality in supramolecular aggregates

    Science.gov (United States)

    Castriciano, Maria A.; Gentili, Denis; Romeo, Andrea; Cavallini, Massimiliano; Scolaro, Luigi Monsù

    2017-01-01

    Chirality is one of the most intriguing properties of matter related to a molecule’s lack of mirror symmetry. The transmission of chirality from the molecular level up to the macroscopic scale has major implications in life sciences but it is also relevant for many chemical applications ranging from catalysis to spintronic. These technological applications require an accurate control of morphology, homogeneity and chiral handedness of thin films and nanostructures. We demonstrate a simple approach to specifically transfer chirality to the model supramolecular system of J aggregates of the protonated form of tetrakis(4-sulfonatophenyl)-porphyrin by utilizing a soft lithography technique. This approach successfully allows the fabrication of an ordered distribution of sub-micrometric structures in precise and controllable positions with programmed chirality, providing a fundamental breakthrough toward the exploitation of chiral supramolecular aggregates in technological applications, such as sensors, non-linear optics and spintronic. PMID:28275239

  13. Spatial control of chirality in supramolecular aggregates.

    Science.gov (United States)

    Castriciano, Maria A; Gentili, Denis; Romeo, Andrea; Cavallini, Massimiliano; Scolaro, Luigi Monsù

    2017-03-09

    Chirality is one of the most intriguing properties of matter related to a molecule's lack of mirror symmetry. The transmission of chirality from the molecular level up to the macroscopic scale has major implications in life sciences but it is also relevant for many chemical applications ranging from catalysis to spintronic. These technological applications require an accurate control of morphology, homogeneity and chiral handedness of thin films and nanostructures. We demonstrate a simple approach to specifically transfer chirality to the model supramolecular system of J aggregates of the protonated form of tetrakis(4-sulfonatophenyl)-porphyrin by utilizing a soft lithography technique. This approach successfully allows the fabrication of an ordered distribution of sub-micrometric structures in precise and controllable positions with programmed chirality, providing a fundamental breakthrough toward the exploitation of chiral supramolecular aggregates in technological applications, such as sensors, non-linear optics and spintronic.

  14. Supramolecular tilt chirality in crystals of steroids and alkaloids.

    Science.gov (United States)

    Hisaki, Ichiro; Tohnai, Norimitsu; Miyata, Mikiji

    2008-03-01

    The concept of supramolecular chirality has assumed increasing importance in association with the development of supramolecular chemistry over the last two decades. In chiral crystals, 2 1 helical molecular assemblies are frequently observed as key motifs. Helical handedness of the 2 1 assemblies, however, has not been determined from the mathematical or crystallographical viewpoints. In this context, we have proposed two new concepts, three-axial chirality and tilt chirality. On the basis of the concepts, we describe supramolecular chirality and determine the handedness of 2 1 assemblies that are composed of relatively complicated molecules with multiple stereogenic centers such as brucine, bile acids, and cinchona alkaloids as well as those of simple molecules.

  15. Theory of ion-chirality relation in ferroelectric liquid crystals

    Science.gov (United States)

    Lahiri, T.; Pal Majumder, T.

    2012-04-01

    The presence of impurity ions in ferroelectric liquid crystals (FLC) could produce a significant impact on the chirality of the medium with a possible modification in the polarization profile of the system. We theoretically observed these possibilities by considering an in-plane and bulk free energy density for the sample. Based on a suitable chirality transfer formalism, we explained the role of impurity ions in altering the chiral nature of a FLC medium. A continuous transition from modulated phases to uniform phases is also predicted within the framework of this theory. Then, we investigated the possible modification in the polarization profile driven by ionic impurities.

  16. Lateral shift in one-dimensional quasiperiodic chiral photonic crystal

    Energy Technology Data Exchange (ETDEWEB)

    Da, Jian, E-mail: dajian521@sina.com [Department of Information Engineering, Huaian Senior Vocational and Technical School, Feiyao road, Huaian 223005, Jiangsu Province (China); Mo, Qi, E-mail: moqiyueyang@163.com [School of Software, Yunnan University, Cuihu Bai Road, Kunming City, Yunnan Province 650091 (China); Cheng, Yaokun [Department of Information Engineering, Huaian Senior Vocational and Technical School, Feiyao road, Huaian 223005, Jiangsu Province (China); Liu, Taixiang [Taishan Vocational College of Nursing, Shandong Province 271000 (China)

    2015-02-01

    We investigate the lateral shift of a one-dimensional quasiperiodic photonic crystal consisting of chiral and conventional dielectric materials. The effect of structural irregularity on lateral shift is evaluated by stationary-phase approach. Our results show that the lateral shift can be modulated by varying the structural irregularity in quasiperiodic structure. Besides, the position of peak in lateral shift spectrum stays sensitive to the chiral factor of chiral materials. In comparison with that of periodic structure, quasiperiodic structure provides an extra degree of freedom to manipulate the lateral shift.

  17. Nanoconfinement-induced structures in chiral liquid crystals.

    Science.gov (United States)

    Melle, Michael; Theile, Madlona; Hall, Carol K; Schoen, Martin

    2013-08-28

    We employ Monte Carlo simulations in a specialized isothermal-isobaric and in the grand canonical ensemble to study structure formation in chiral liquid crystals as a function of molecular chirality. Our model potential consists of a simple Lennard-Jones potential, where the attractive contribution has been modified to represent the orientation dependence of the interaction between a pair of chiral liquid-crystal molecules. The liquid crystal is confined between a pair of planar and atomically smooth substrates onto which molecules are anchored in a hybrid fashion. Hybrid anchoring allows for the formation of helical structures in the direction perpendicular to the substrate plane without exposing the helix to spurious strains. At low chirality, we observe a cholesteric phase, which is transformed into a blue phase at higher chirality. More specifically, by studying the unit cell and the spatial arrangement of disclination lines, this blue phase can be established as blue phase II. If the distance between the confining substrates and molecular chirality are chosen properly, we see a third structure, which may be thought of as a hybrid, exhibiting mixed features of a cholesteric and a blue phase.

  18. Nanoconfinement-Induced Structures in Chiral Liquid Crystals

    Directory of Open Access Journals (Sweden)

    Carol K. Hall

    2013-08-01

    Full Text Available We employ Monte Carlo simulations in a specialized isothermal-isobaric and in the grand canonical ensemble to study structure formation in chiral liquid crystals as a function of molecular chirality. Our model potential consists of a simple Lennard-Jones potential, where the attractive contribution has been modified to represent the orientation dependence of the interaction between a pair of chiral liquid-crystal molecules. The liquid crystal is confined between a pair of planar and atomically smooth substrates onto which molecules are anchored in a hybrid fashion. Hybrid anchoring allows for the formation of helical structures in the direction perpendicular to the substrate plane without exposing the helix to spurious strains. At low chirality, we observe a cholesteric phase, which is transformed into a blue phase at higher chirality. More specifically, by studying the unit cell and the spatial arrangement of disclination lines, this blue phase can be established as blue phase II. If the distance between the confining substrates and molecular chirality are chosen properly, we see a third structure, which may be thought of as a hybrid, exhibiting mixed features of a cholesteric and a blue phase.

  19. Criteria of backscattering in chiral one-way photonic crystals

    Science.gov (United States)

    Cheng, Pi-Ju; Chang, Shu-Wei

    2016-03-01

    Optical isolators are important devices in photonic circuits. To reduce the unwanted reflection in a robust manner, several setups have been realized using nonreciprocal schemes. In this study, we show that the propagating modes in a strongly-guided chiral photonic crystal (no breaking of the reciprocity) are not backscattering-immune even though they are indeed insensitive to many types of scatters. Without the protection from the nonreciprocity, the backscattering occurs under certain circumstances. We present a perturbative method to calculate the backscattering of chiral photonic crystals in the presence of chiral/achiral scatters. The model is, essentially, a simplified analogy to the first-order Born approximation. Under reasonable assumptions based on the behaviors of chiral photonic modes, we obtained the expression of reflection coefficients which provides criteria for the prominent backscattering in such chiral structures. Numerical examinations using the finite-element method were also performed and the results agree well with the theoretical prediction. From both our theory and numerical calculations, we find that the amount of backscattering critically depends on the symmetry of scatter cross sections. Strong reflection takes place when the azimuthal Fourier components of scatter cross sections have an order l of 2. Chiral scatters without these Fourier components would not efficiently reflect the chiral photonic modes. In addition, for these chiral propagating modes, disturbances at the most significant parts of field profiles do not necessarily result in the most effective backscattering. The observation also reveals what types of scatters or defects should be avoided in one-way applications of chiral structures in order to minimize the backscattering.

  20. Molecular modeling study of chiral drug crystals: lattice energy calculations.

    Science.gov (United States)

    Li, Z J; Ojala, W H; Grant, D J

    2001-10-01

    The lattice energies of a number of chiral drugs with known crystal structures were calculated using Dreiding II force field. The lattice energies, including van der Waals, Coulombic, and hydrogen-bonding energies, of homochiral and racemic crystals of some ephedrine derivatives and of several other chiral drugs, are compared. The calculated energies are correlated with experimental data to probe the underlying intermolecular forces responsible for the formation of racemic species, racemic conglomerates, or racemic compounds, termed chiral discrimination. Comparison of the calculated energies among ephedrine derivatives reveals that a greater Coulombic energy corresponds to a higher melting temperature, while a greater van der Waals energy corresponds to a larger enthalpy of fusion. For seven pairs of homochiral and racemic compounds, correlation of the differences between the two forms in the calculated energies and experimental enthalpy of fusion suggests that the van der Waals interactions play a key role in the chiral discrimination in the crystalline state. For salts of the chiral drugs, the counter ions diminish chiral discrimination by increasing the Coulombic interactions. This result may explain why salt forms favor the formation of racemic conglomerates, thereby facilitating the resolution of racemates.

  1. Microwave modulation characteristics of twisted liquid crystals with chiral dopant

    Directory of Open Access Journals (Sweden)

    Rui Yuan

    2017-01-01

    Full Text Available Adding a chiral dopant in twisted nematic (TN liquid crystal cell can stabilize the orientation of liquid crystal molecules, particularly in high TN (HTN or super TN (STN liquid crystal cells. The difference in pitches in liquid crystal is induced by the chiral dopant, and these different pitches affect the orientation of liquid crystal director under an external applied voltage and influence the characteristics of microwave modulation. To illustrate this point, the microwave phase shift per unit length (MPSL versus voltage is calculated on the basis of the elastic theory of liquid crystal and the finite-difference iterative method. Enhancing the pitch induced by the chiral dopant in liquid crystal increases the MPSLs, but the stability of the twisted structures is decreased. Thus, appropriate pitches of 100d, 4d, and 2d can be applied in TN, HTN, and STN cells with cell gap d to enhance the characteristics of microwave modulation and stabilize the structures in twisted cell. This method can improve the characteristics of liquid crystal microwave modulators such that the operating voltage and the size of such phase shifters can be decreased.

  2. Chirality Amplification in Tactoids of Lyotropic Chromonic Liquid Crystals

    Science.gov (United States)

    Peng, Chenhui; Lavrentovich, Oleg

    2014-03-01

    We demonstrate an effective chirality amplification based on the long-range forces, extending over the scales of tens of micrometers, much larger than the single molecule (nanometer) scale. The mechanism is rooted in the long-range elastic nature of orientational order in lyotropic chromonic liquid crystals (LCLCs) that represent water solutions of achiral disc-like molecules. Minute quantities of chiral molecules such as amino acid L-alanine and limonene added to the droplets of LCLC lead to chiral amplification characterized by an increase of optical activity by a factor of 103 - 104. This effect allows one to discriminate and detect the absolute configuration of chiral molecules in an aqueous system, thus opening new possibilities in biosensing and other biological applications.

  3. Defect topologies in chiral liquid crystals confined to mesoscopic channels.

    Science.gov (United States)

    Schlotthauer, Sergej; Skutnik, Robert A; Stieger, Tillmann; Schoen, Martin

    2015-05-21

    We present Monte Carlo simulations in the grand canonical and canonical ensembles of a chiral liquid crystal confined to mesochannels of variable sizes and geometries. The mesochannels are taken to be quasi-infinite in one dimension but finite in the two other directions. Under thermodynamic conditions chosen and for a selected value of the chirality coupling constant, the bulk liquid crystal exhibits structural characteristics of a blue phase II. This is established through the tetrahedral symmetry of disclination lines and the characteristic simple-cubic arrangement of double-twist helices formed by the liquid-crystal molecules along all three axes of a Cartesian coordinate system. If the blue phase II is then exposed to confinement, the interplay between its helical structure, various anchoring conditions at the walls of the mesochannels, and the shape of the mesochannels gives rise to a broad variety of novel, qualitative disclination-line structures that are reported here for the first time.

  4. Chirality controlled responsive self-assembled nanotubes in water

    NARCIS (Netherlands)

    van Dijken, D. J.; Stacko, P.; Stuart, M. C. A.; Browne, W. R.; Feringa, B. L.

    2017-01-01

    The concept of using chirality to dictate dimensions and to store chiral information in self-assembled nanotubes in a fully controlled manner is presented. We report a photoresponsive amphiphile that co-assembles with its chiral counterpart to form nanotubes and demonstrate how chirality can be used

  5. Detecting, visualizing, and measuring gold nanoparticle chirality using helical pitch measurements in nematic liquid crystal phases.

    Science.gov (United States)

    Sharma, Anshul; Mori, Taizo; Lee, Huey-Charn; Worden, Matthew; Bidwell, Eric; Hegmann, Torsten

    2014-12-23

    Chirality at the nanoscale, or more precisely, the chirality or chiroptical effects of chiral ligand-capped metal nanoparticles (NPs) is an intriguing and rapidly evolving field in nanomaterial research with promising applications in catalysis, metamaterials, and chiral sensing. The aim of this work was to seek out a system that not only allows the detection and understanding of NP chirality but also permits visualization of the extent of chirality transfer to a surrounding medium. The nematic liquid crystal phase is an ideal candidate, displaying characteristic defect texture changes upon doping with chiral additives. To test this, we synthesized chiral cholesterol-capped gold NPs and prepared well-dispersed mixtures in two nematic liquid crystal hosts. Induced circular dichroism spectropolarimetry and polarized light optical microscopy revealed that all three gold NPs induce chiral nematic phases, and that those synthesized in the presence of a chiral bias (disulfide) are more powerful chiral inducers than those where the NP was formed in the absence of a chiral bias (prepared by conjugation of a chiral silane to preformed NPs). Helical pitch data here visually show a clear dependence on the NP size and the number of chiral ligands bound to the NP surface, thereby supporting earlier experimental and theoretical data that smaller metal NPs made in the presence of a chiral bias are stronger chiral inducers.

  6. Mirror Symmetry Breaking by Chirality Synchronisation in Liquids and Liquid Crystals of Achiral Molecules.

    Science.gov (United States)

    Tschierske, Carsten; Ungar, Goran

    2016-01-04

    Spontaneous mirror symmetry breaking is an efficient way to obtain homogeneously chiral agents, pharmaceutical ingredients and materials. It is also in the focus of the discussion around the emergence of uniform chirality in biological systems. Tremendous progress has been made by symmetry breaking during crystallisation from supercooled melts or supersaturates solutions and by self-assembly on solid surfaces and in other highly ordered structures. However, recent observations of spontaneous mirror symmetry breaking in liquids and liquid crystals indicate that it is not limited to the well-ordered solid state. Herein, progress in the understanding of a new dynamic mode of symmetry breaking, based on chirality synchronisation of transiently chiral molecules in isotropic liquids and in bicontinuous cubic, columnar, smectic and nematic liquid crystalline phases is discussed. This process leads to spontaneous deracemisation in the liquid state under thermodynamic control, giving rise to long-term stable symmetry-broken fluids, even at high temperatures. These fluids form conglomerates that are capable of extraordinary strong chirality amplification, eventually leading to homochirality and providing a new view on the discussion of emergence of uniform chirality in prebiotic systems.

  7. A computational investigation of attrition-enhanced chiral symmetry breaking in conglomerate crystals

    Science.gov (United States)

    Ricci, Francesco; Stillinger, Frank H.; Debenedetti, Pablo G.

    2013-11-01

    Attrition-enhanced chiral symmetry breaking in crystals, also known as Viedma ripening, is a remarkable phenomenon from a variety of perspectives. By providing a direct route to solid-phase homochirality in a controllable manner, it is of inherent interest to those who study chiral symmetry-breaking/amplification mechanisms. When applied to intrinsically chiral molecules, Viedma ripening may have implications for the origin of biological homochirality, as well as applications in chiral drug resolution. Despite an abundance of research, the mechanistic details underlying this phenomenon have not been unambiguously elucidated. We employ a Monte Carlo algorithm to study this driven system, in order to gain further insights into the mechanisms capable of reproducing key experimental signatures. We provide a comprehensive numerical investigation of how the model parameters (attrition rate, liquid-phase racemization kinetics, and the relative rates of growth and dissolution kinetics) impact the system's overall behavior. It is shown that size-dependent crystal solubility alone is insufficient to reproduce most of the experimental signatures of Viedma ripening, and that some form of a solid-phase chiral feedback mechanism must be invoked in order to reproduce experimentally observed behavior. In this work, such feedback mechanisms can take the form of agglomeration, or of artificial modification of the size dependent growth kinetics.

  8. Chiral heteropoly blues and controllable switching of achiral polyoxometalate clusters.

    Science.gov (United States)

    Wang, Yizhan; Li, Haolong; Wu, Che; Yang, Yang; Shi, Lei; Wu, Lixin

    2013-04-22

    Managing the blues: Chiral heteropoly blues of achiral polyoxometalate clusters were created through an intermolecular interaction with a chiral organic compound. Controllable chiroptical switching of the cluster complexes was possible through reversible photochromism of the polyoxometalates (see picture).

  9. The Effect of the Chirality on the Fluctuation of Liquid Crystal

    Science.gov (United States)

    Fatriansyah, Jaka Fajar; Yusuf, Yusril

    2016-10-01

    We investigate the dynamical properties of normal fluctuation modes in chiral phase liquid crystal on the basis of hydrodynamics Ericksen-Leslie theory. We examine the effect of chiral coefficient on dynamic relaxation eigenfrequencies and the scattering intensity. We find that the chiral coefficient only affects slow fluctuation modes, while it does not affect the fast fluctuation modes. This effect of chirality depends on the magnitude of the wave number vector components.

  10. Transformation of Dipeptide-Based Organogels into Chiral Crystals by Cryogenic Treatment.

    Science.gov (United States)

    Liu, Xingcen; Fei, Jinbo; Wang, Anhe; Cui, Wei; Zhu, Pengli; Li, Junbai

    2017-03-01

    Controlled molecular assembly is an important approach for the synthesis of single-component materials with diverse functions. Unlike traditional heat treatment or solvent modulation, cryogenic treatment at 77 K enabled the tunable transition of a self-assembled diphenylalanine organogel into a hexagonal crystal. Under these conditions, the assembled molecules undergo an internal rearrangement in the solid state to form a well-defined chiral crystal structure. Moreover, these assemblies exhibit enhanced emission. This strategy for the synthesis of single-component supramolecular assemblies can create new functions by manipulating phase transitions. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Synthesis and optical activity of isosorbide chiral derivative containing fluorocarbon group as chiral dopant in liquid crystal materials

    Institute of Scientific and Technical Information of China (English)

    Kong Liang Xie; Yin He Su; Chun Xiang Zhang

    2011-01-01

    Novel isosorbide derivative containing perfluorocarbon group, bi(perfluorooctanesulfonyl)isosorbide ester as chiral dopant in liquid crystal, was synthesized. Chemical structure was characterized by elemental analysis, FT-IR, 1H NMR and 19F NMR. The optical texture of the mixture was observed by polarized optical microscopy (POM). Novel chiral dopant containing perfluorocarbon group had excellent optical activity. Its specific rotation and molar rotation were noticeable higher than those of bi(4-chloromethylbenzenecarbonic)isosorbide ester. The fluorocarbon group improved the molar rotation of chiral compound and did not affect optical rotation direction. The texture of the mixture added isosorbide derivative with fluorocarbon group showed the oily streak texture.

  12. Vortexlike topological defects in nematic colloids: chiral colloidal dimers and 2D crystals.

    Science.gov (United States)

    Tkalec, U; Ravnik, M; Zumer, S; Musevic, I

    2009-09-18

    We show that chiral ordering of the underlying complex fluid strongly influences defect formation and colloidal interactions. Nonsingular defect loops with a topological charge -2 are observed, with a cross section identical to hyperbolic vortices in magnetic systems. These loops are binding spontaneously formed pairs of colloidal particles and dimers, which are chiral objects. Chiral dimer-dimer interaction weakly depends on the chirality of dimers and leads to the assembly of 2D nematic colloidal crystals of pure or "mixed" chirality, intercalated with a lattice of nonsingular vortexlike defects.

  13. Planar anchoring strength and pitch measurements in achiral and chiral chromonic liquid crystals using 90-degree twist cells

    Science.gov (United States)

    McGinn, Christine K.; Laderman, Laura I.; Zimmermann, Natalie; Kitzerow, Heinz-S.; Collings, Peter J.

    2013-12-01

    Chromonic liquid crystals are formed by molecules that spontaneously assemble into anisotropic structures in water. The ordering unit is therefore a molecular assembly instead of a molecule as in thermotropic liquid crystals. Although it has been known for a long time that certain dyes, drugs, and nucleic acids form chromonic liquid crystals, only recently has enough knowledge been gained on how to control their alignment so that studies of their fundamental liquid crystal properties can be performed. In this article, a simple method for producing planar alignment of the nematic phase in chromonic liquid crystals is described, and this in turn is used to create twisted nematic structures of both achiral and chiral chromonic liquid crystals. The optics of 90-degree twist cells allows the anchoring strength to be measured in achiral systems, which for this alignment technique is quite weak, about 3×10-7 J/m2 for both disodium cromoglycate and Sunset Yellow FCF. The addition of a chiral amino acid to the system causes the chiral nematic phase to form, and similar optical measurements in 90-degree twist cells produce a measurement of the intrinsic pitch of the chiral nematic phase. From these measurements, the helical twisting power for L-alanine is found to be (1.1±0.4)×10-2 μm-1 wt%-1 for 15 wt% disodium cromoglycate.

  14. Chiral multichromic single crystals for optical devices (LDRD 99406).

    Energy Technology Data Exchange (ETDEWEB)

    Kemp, Richard Alan; Felix, Ana M. (University of New Mexico, Albuquerque, NM)

    2006-12-01

    This report summarizes our findings during the study of a novel system that yields multi-colored materials as products. This system is quite unusual as it leads to multi-chromic behavior in single crystals, where one would expect that only a single color would exist. We have speculated that these novel solids might play a role in materials applications such as non-linear optics, liquid crystal displays, piezoelectric devices, and other similar applications. The system examined consisted of a main-group alkyl compound (a p block element such as gallium or aluminum) complexed with various organic di-imines. The di-imines had substituents of two types--either alkyl or aromatic groups attached to the nitrogen atoms. We observed that single crystals, characterized by X-ray crystallography, were obtained in most cases. Our research during January-July, 2006, was geared towards understanding the factors leading to the multi-chromic nature of the complexes. The main possibilities put forth initially considered (a) the chiral nature of the main group metal, (b) possible reduction of the metal to a lower-valent, radical state, (c) the nature of the ligand(s) attached to the main group metal, and (d) possible degradation products of the ligand leading to highly-colored products. The work carried out indicates that the most likely explanation considered involves degradation of the aromatic ligands (a combination of (c) and (d)), as the experiments performed can clearly rule out (a) and (b).

  15. Evidence of Broken Reciprocity in Chiral Liquid Crystals

    Science.gov (United States)

    Moreira, Michele; Venkataraman, Nithya; Taheri, Bahman; Palffy-Muhoray, Peter

    2008-03-01

    Reciprocity in light scattering is predicated on bounded scattering media with symmetric and linear permittivity, conductivity and permeability. Due to their anisotropy and chirality, cholesteric liquid crystal form periodic dielectric structures. If the periodicity is comparable to the wavelength of light, these phases are self-assembled photonic band gap structures. There appear in the permittivity odd powers of the wave vector resulting from nonlocality and broken inversion symmetry. Evidence of non-reciprocity has been found in optically active crystals by Bennett [1] and in stacks of cholesteric and nematic liquid crystal cells by Takezoe [2]. We present experimental data showing broken reciprocity in transmittance and reflectance in cholesteric cells with different pitches having overlapping but distinct reflection bands. We explain our results in terms of simple analytic descriptions of material properties and propagating modes. [1] P.J. Bennett, S. Dhanjal, Yu. P. Svirko and N. I. Zheludev, Opt. Lett. 21, 1955 (1996) [2] J. Hwang; M.H. Song; B. Park; S. Nishimura; T. Toyooka; J.W. Wu; Y. Takanishi; K. Ishikawa; H. Takezoe, Nat. Mat. 4, 383 (2005).

  16. Visualizing Molecular Chirality in the Organic Chemistry Laboratory Using Cholesteric Liquid Crystals

    Science.gov (United States)

    Popova, Maia; Bretz, Stacey Lowery; Hartley, C. Scott

    2016-01-01

    Although stereochemistry is an important topic in second-year undergraduate organic chemistry, there are limited options for laboratory activities that allow direct visualization of macroscopic chiral phenomena. A novel, guided-inquiry experiment was developed that allows students to explore chirality in the context of cholesteric liquid crystals.…

  17. Enantioselectively controlled release of chiral drug (metoprolol) using chiral mesoporous silica materials

    Science.gov (United States)

    Guo, Zhen; Du, Yu; Liu, Xianbin; Ng, Siu-Choon; Chen, Yuan; Yang, Yanhui

    2010-04-01

    Chiral porous materials have attracted burgeoning attention on account of their potential applications in many areas, such as enantioseparation, chiral catalysis, chemical sensors and drug delivery. In this report, chiral mesoporous silica (CMS) materials with various pore sizes and structures were prepared using conventional achiral templates (other than chiral surfactant) and a chiral cobalt complex as co-template. The synthesized CMS materials were characterized by x-ray diffraction, nitrogen physisorption, scanning electron microscope and transmission electron microscope. These CMS materials, as carriers, were demonstrated to be able to control the enantioselective release of a representative chiral drug (metoprolol). The release kinetics, as modeled by the power law equation, suggested that the release profiles of metoprolol were remarkably dependent on the pore diameter and pore structure of CMS materials. More importantly, R- and S-enantiomers of metoprolol exhibited different release kinetics on CMS compared to the corresponding achiral mesoporous silica (ACMS), attributable to the existence of local chirality on the pore wall surface of CMS materials. The chirality of CMS materials on a molecular level was further substantiated by vibrational circular dichroism measurements.

  18. Enantioselectively controlled release of chiral drug (metoprolol) using chiral mesoporous silica materials

    Energy Technology Data Exchange (ETDEWEB)

    Guo Zhen; Liu Xianbin; Ng, Siu-Choon; Chen Yuan; Yang Yanhui [School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore 637459 (Singapore); Du Yu, E-mail: du_yu@jlu.edu.cn, E-mail: yhyang@ntu.edu.sg [College of Electronic Science and Engineering, Jilin University, Changchun 130012 (China)

    2010-04-23

    Chiral porous materials have attracted burgeoning attention on account of their potential applications in many areas, such as enantioseparation, chiral catalysis, chemical sensors and drug delivery. In this report, chiral mesoporous silica (CMS) materials with various pore sizes and structures were prepared using conventional achiral templates (other than chiral surfactant) and a chiral cobalt complex as co-template. The synthesized CMS materials were characterized by x-ray diffraction, nitrogen physisorption, scanning electron microscope and transmission electron microscope. These CMS materials, as carriers, were demonstrated to be able to control the enantioselective release of a representative chiral drug (metoprolol). The release kinetics, as modeled by the power law equation, suggested that the release profiles of metoprolol were remarkably dependent on the pore diameter and pore structure of CMS materials. More importantly, R- and S-enantiomers of metoprolol exhibited different release kinetics on CMS compared to the corresponding achiral mesoporous silica (ACMS), attributable to the existence of local chirality on the pore wall surface of CMS materials. The chirality of CMS materials on a molecular level was further substantiated by vibrational circular dichroism measurements.

  19. Electrolyte effects on the chiral induction and on its temperature dependence in a chiral nematic lyotropic liquid crystal.

    Science.gov (United States)

    Dawin, Ute C; Osipov, Mikhail A; Giesselmann, Frank

    2010-08-19

    We present a study on the effect of added CsCl and of temperature variation on the chiral induction in a chiral nematic lyotropic liquid crystal (LC) composed of the surfactant cesium perfluorooctanoate (CsPFO), water, and the chiral dopant d-Leucine (d-Leu). The chiral induction was measured as the helical pitch P. The role of the additives CsCl and d-Leu on the phase behavior is investigated and discussed. The thermal stabilization effect of CsCl is shown to lead to an apparent salt effect on the pitch when the pitch is compared at a constant temperature. This apparent effect is removed by comparing the pitch measured for different salt concentrations at a temperature relative to the phase-transition temperatures; thus, the real salt effect on the pitch is described. High salt concentrations are shown to increase the pitch, that is, hinder the chiral induction. The effect is discussed in terms of a decreased solubilization of the amphiphilic chiral solute d-Leu in the micelles due to the salt-induced screening of the surfactant head groups and the consequential denser packing of the surfactants. The temperature variation of the pitch is investigated for all CsCl concentrations and is found to be essentially independent of the salt concentration. The temperature variation is analyzed and discussed in the context of a theoretical model taking into account specific properties of lyotropic liquid crystals. A hyperbolic decrease of the pitch is found with increasing temperature, which is known, from thermotropic liquid crystals, to stem from pretransitional critical fluctuations close to the lamellar phase. However, the experimental data confirmed the theoretical prediction that, at high temperature, that is, far away from the transition into the lamellar phase, the pitch is characterized by a linear temperature dependence which is determined by a combination of steric and dispersion chiral interactions. The parameters of the theoretical expression for the pitch have

  20. Enantiopure Ferrocene-Based Planar-Chiral Iridacycles: Stereospecific Control of Iridium-Centred Chirality.

    Science.gov (United States)

    Arthurs, Ross A; Ismail, Muhammad; Prior, Christopher C; Oganesyan, Vasily S; Horton, Peter N; Coles, Simon J; Richards, Christopher J

    2016-02-24

    Reaction of [IrCp*Cl2 ]2 with ferrocenylimines (Fc=NAr, Ar=Ph, p-MeOC6 H4 ) results in ferrocene C-H activation and the diastereoselective synthesis of half-sandwich iridacycles of relative configuration Sp *,RIr *. Extension to (S)-2-ferrocenyl-4-(1-methylethyl)oxazoline gave highly diastereoselective control over the new elements of planar chirality and metal-based pseudo-tetrahedral chirality, to give both neutral and cationic half-sandwich iridacycles of absolute configuration Sc ,Sp ,RIr . Substitution reactions proceed with retention of configuration, with the planar chirality controlling the metal-centred chirality through an iron-iridium interaction in the coordinatively unsaturated cationic intermediate.

  1. Controlling the amplification of chirality in hydrogen-bonded assemblies

    NARCIS (Netherlands)

    Mateos-Timoneda, Miguel A.; Crego-Calama, Mercedes; Reinhoudt, David N.

    2005-01-01

    The amplification of chirality (a high enantiomeric or diastereomeric excess induced by a small initial amount of chiral bias) on hydrogen-bonded assemblies has been studied using “sergeants-and-soldiers” experiments under thermodynamically controlled conditions. Here it is shown that different subs

  2. Dynamic control of chirality in phosphine ligands for enantioselective catalysis

    NARCIS (Netherlands)

    Zhao, Depeng; Neubauer, Thomas M; Feringa, Ben L

    2015-01-01

    Chirality plays a fundamental role in biology and chemistry and the precise control of chirality in a catalytic conversion is a key to modern synthesis most prominently seen in the production of pharmaceuticals. In enantioselective metal-based catalysis, access to each product enantiomer is commonly

  3. Reversal of helicoidal twist handedness near point defects of confined chiral liquid crystals

    Science.gov (United States)

    Ackerman, Paul J.; Smalyukh, Ivan I.

    2016-05-01

    Handedness of the director twist in cholesteric liquid crystals is commonly assumed to be the same throughout the medium, determined solely by the chirality of constituent molecules or chiral additives, albeit distortions of the ground-state helicoidal configuration often arise due to the effects of confinement and external fields. We directly probe the twist directionality of liquid crystal director structures through experimental three-dimensional imaging and numerical minimization of the elastic free energy and show that spatially localized regions of handedness opposite to that of the chiral liquid crystal ground state can arise in the proximity of twisted-soliton-bound topological point defects. In chiral nematic liquid crystal confined to a film that has a thickness less than the cholesteric pitch and perpendicular surface boundary conditions, twisted solitonic structures embedded in a uniform unwound far-field background with chirality-matched handedness locally relieve confinement-imposed frustration and tend to be accompanied by point defects and smaller geometry-required, energetically costly regions of opposite twist handedness. We also describe a spatially localized structure, dubbed a "twistion," in which a twisted solitonic three-dimensional director configuration is accompanied by four point defects. We discuss how our findings may impinge on the stability of localized particlelike director field configurations in chiral and nonchiral liquid crystals.

  4. Exotic skyrmion crystals in chiral magnets with compass anisotropy

    Science.gov (United States)

    Chen, J. P.; Zhang, Dan-Wei; Liu, J.-M.

    2016-07-01

    The compass-type anisotropy appears naturally in diverse physical contexts with strong spin-orbit coupling (SOC) such as transition metal oxides and cold atomic gases etc, and it has been receiving substantial attention. Motivated by recent studies and particularly recent experimental observations on helimagnet MnGe, we investigate the critical roles of this compass-type anisotropy in modulating various spin textures of chiral magnets with strong SOC, by Monte Carlo simulations based on a classical Heisenberg spin model with Dzyaloshinsky-Moriya interaction and compass anisotropy. A phase diagram with emergent spin orders in the space of compass anisotropy and out-of-plane magnetic field is presented. In this phase diagram, we propose that a hybrid super-crystal structure consisting of alternating half-skyrmion and half-anti-skyrmion is the possible zero-field ground state of MnGe. The simulated evolution of the spin structure driven by magnetic field is in good accordance with experimental observations on MnGe. Therefore, this Heisenberg spin model successfully captures the main physics responsible for the magnetic structures in MnGe, and the present work may also be instructive to research on the magnetic states in other systems with strong SOC.

  5. Cofactor-Controlled Chirality of Tropoisomeric Ligand

    NARCIS (Netherlands)

    Théveau, L.; Bellini, R.; Dydio, P.; Szabo, Z.; van der Werf, A.; Sander, R.A.; Reek, J.N.H.; Moberg, C.

    2016-01-01

    A new tropos ligand with an integrated anion receptor receptor site has been prepared. Chiral carboxylate and phosphate anions that bind in the anion receptor unit proved capable of stabilizing chiral conformations of the achiral flexible bidentate biaryl phosphite ligand, as shown by variable

  6. Liquid Crystal Phases of Molecular Bananas: Polarity and Chirality as Broken Symmetries

    Science.gov (United States)

    Clark, Noel

    2006-03-01

    The study of the interplay of chirality and polarity has been a particularly rich theme of soft matter science since Meyer's seminal discovery that tilted smectics of chiral molecules are macroscopically polar. This event, and the subsequent realization of polar domains and high-speed electro-optic switching in chiral smectics, engaged the liquid crystal community in a worldwide pursuit of novel smectics for applications, featured by the synthesis of more than 50,000 new liquid crystal compounds, and by a consequent broad diversification of the palette of liquid crystal phases and possibilities for supermolecular ordering. A current important activity in this scenario is the study of polar order in synthetically achiral molecules, for example, in molecular bananas, which, as their shape suggests, might be expected to organize in a polar way. Indeed they do, but beyond this, almost everything learned about them has been surprising, including their persistent tendency to exhibit chirality as a spontaneously broken symmetry. I will discuss some of these new phases and phenomena, including the discovery of fluid conglomerates (Pasteur's experiment in a fluid), triclinic fluid order, chiral twist grain boundary phases of achiral molecules, chirality flipping and field-induced deracemization, ferroelectric and antiferroelectric phases with supermolecular- scale polarization modulation, and chiral thermotropic sponge phases.

  7. Multiple chiral topological states in liquid crystals from unstructured light beams

    Energy Technology Data Exchange (ETDEWEB)

    Loussert, Charles; Brasselet, Etienne, E-mail: e.brasselet@loma.u-bordeaux1.fr [Laboratoire Ondes et Matière d' Aquitaine, Univ. Bordeaux, CNRS, UMR 5798, F-33400 Talence (France)

    2014-02-03

    It is shown experimentally that unstructured light beams can generate a wealth of distinct metastable defect structures in thin films of chiral liquid crystals. Various kinds of individual chiral topological states are obtained as well as dimers and trimers, which correspond to the entanglement of several topological unit cells. Self-assembled nested assemblies of several metastable particle-like topological states can also be formed. Finally, we propose and experimentally demonstrate an opto-electrical approach to generate tailor-made architectures.

  8. Enhancing and reducing chirality by opposite circularly-polarized light irradiation on crystalline chiral domains consisting of nonchiral photoresponsive W-shaped liquid crystal molecules.

    Science.gov (United States)

    Choi, Suk-Won; Takezoe, Hideo

    2016-09-28

    We found possible chirality enhancement and reduction in chiral domains formed by photoresponsive W-shaped molecules by irradiation with circularly polarized light (CPL). The W-shaped molecules exhibit a unique smectic phase with spontaneously segregated chiral domains, although the molecules are nonchiral. The chirality control was generated in the crystalline phase, which shows chiral segregation as in the upper smectic phase, and the result appeared to be as follows: for a certain chiral domain, right-CPL stimuli enhanced the chirality, while left-CPL stimuli reduced the chirality, and vice versa for another chiral domain. Interestingly, no domain-size change could be observed after CPL irradiation, suggesting some changes in the causes of chirality. In this way, the present system can recognize the handedness of the applied chiral stimuli. In other words, the present material can be used as a sensitive chiral-stimuli-recognizing material and should find invaluable applications, including in chiroptical switches, sensors, and memories as well as in chiral recognition.

  9. Chirality and its spontaneous symmetry breaking in two liquid crystal systems

    Science.gov (United States)

    Kang, Louis

    Chirality, or handedness, is a key concept spanning all fields of natural science, from biology to mathematics. Chiral structures can arise from achiral building blocks that lack a handedness if their assembly is unstable to chiral deformations, a phenomenon called spontaneous symmetry breaking. We theoretically study the role of chirality in two systems composed of liquid crystals dissolved or suspended in water, and our results match those obtained experimentally by our collaborators. In the first system, we study achiral liquid crystals whose Frank twist modulus is much lower than their splay and bend Frank moduli and which are confined in capillaries. Under homeotropic anchoring, their ground state configuration undergoes spontaneous chiral symmetry breaking when the twist modulus decreases enough relative to the splay and bend moduli. Under degenerate planar anchoring, a small twist-to-saddle-splay ratio of elastic moduli leads to degenerate twisted configurations even though an undeformed configuration is possible. Measuring the twist profile of an experimental system produces a value for the saddle-splay constant, which has been difficult to achieve previously. Under either boundary condition, domain walls and point defects, whose topological charges depend on chirality, separate domains with different degenerate configurations, and certain ones are energetically preferred over others. In the second system, we study filamentous viruses acting as colloidal liquid crystals under the influence of depletion, which promotes condensation of the viruses into 2D colloidal monolayers. These membranes have tunable chirality and show a rich array of emergent behaviors, including a transition from a circular shape to a striking starfish shape upon changing the chirality of constituent viruses, partial coalescence via domain walls through which the viruses twist by 180 degrees, and phase-separated rafts of a particular size when two virus species with different lengths

  10. Chiral Asymmetric Structures in Aspartic Acid and Valine Crystals Assessed by Atomic Force Microscopy.

    Science.gov (United States)

    Teschke, Omar; Soares, David Mendez

    2016-03-29

    Structures of crystallized deposits formed by the molecular self-assembly of aspartic acid and valine on silicon substrates were imaged by atomic force microscopy. Images of d- and l-aspartic acid crystal surfaces showing extended molecularly flat sheets or regions separated by single molecule thick steps are presented. Distinct orientation surfaces were imaged, which, combined with the single molecule step size, defines the geometry of the crystal. However, single molecule step growth also reveals the crystal chirality, i.e., growth orientations. The imaged ordered lattice of aspartic acid (asp) and valine (val) mostly revealed periodicities corresponding to bulk terminations, but a previously unreported molecular hexagonal lattice configuration was observed for both l-asp and l-val but not for d-asp or d-val. Atomic force microscopy can then be used to identify the different chiral forms of aspartic acid and valine crystals.

  11. Molecular engineering of chiral colloidal liquid crystals using DNA origami

    Science.gov (United States)

    Siavashpouri, Mahsa; Wachauf, Christian H.; Zakhary, Mark J.; Praetorius, Florian; Dietz, Hendrik; Dogic, Zvonimir

    2017-08-01

    Establishing precise control over the shape and the interactions of the microscopic building blocks is essential for design of macroscopic soft materials with novel structural, optical and mechanical properties. Here, we demonstrate robust assembly of DNA origami filaments into cholesteric liquid crystals, one-dimensional supramolecular twisted ribbons and two-dimensional colloidal membranes. The exquisite control afforded by the DNA origami technology establishes a quantitative relationship between the microscopic filament structure and the macroscopic cholesteric pitch. Furthermore, it also enables robust assembly of one-dimensional twisted ribbons, which behave as effective supramolecular polymers whose structure and elastic properties can be precisely tuned by controlling the geometry of the elemental building blocks. Our results demonstrate the potential synergy between DNA origami technology and colloidal science, in which the former allows for rapid and robust synthesis of complex particles, and the latter can be used to assemble such particles into bulk materials.

  12. Dynamic Chirality Control of tropos DPCB-digold Skeleton by Chiral Binaphthyldicarboxylate.

    Science.gov (United States)

    Ito, Shigekazu; Nanko, Masaki; Shinozaki, Tomokazu; Kojima, Masafumi; Aikawa, Kohsuke; Mikami, Koichi

    2016-03-18

    The planar 3,4-diphosphinidenecyclobutene (DPCB) can be remarkably twisted into a C2 -type helical structure by dual coordination of a AuCl moiety. A prompt chirality control of the twisted DPCB skeleton ligated by the digold units affords the enantiopure structure by exchanging the chloride ligands for chiral [1,1'-binaphthalene]-2,2'-dicarboxylate. The chirality of the diaurated 2,2'-bis(diphenylphosphanyl)-1,1'-biphenyl (BIPHEP) system can be controlled prior to that of DPCB. Mixing of a DPCB-bis(chlorogold) complex with the chiral silver salt dynamically leads to a single diastereomer, which was characterized by the (31) P NMR spectrum and the CD couplet patterns in the visible (DPCB) area. The absolute configuration of the singly induced helical structure was assigned by the theoretical CD spectra determined by TD-DFT calculations. Intramolecular alkoxycyclization of hexa-4,5-dien-1-ol catalyzed by the asymmetric DPCB-digold structure were also attempted. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. Microsecond-range optical shutter for unpolarized light with chiral nematic liquid crystal

    Energy Technology Data Exchange (ETDEWEB)

    Mohammadimasoudi, Mohammad, E-mail: Mohammad.Mohammadimasoudi@elis.ugent.be; Neyts, Kristiaan; Beeckman, Jeroen [Electronics and Information Systems Department, Ghent University, St. Pietersnieuwstraat 41, 9000 Gent (Belgium); Center for Nano- and Bio-photonics, Ghent University, St. Pietersnieuwstraat 41, 9000 Gent (Belgium); Shin, Jungsoon; Lee, Keechang [Samsung Advanced Institute of Technology, 130 Samsung-ro, Yeongtong-gu, Suwon-si, Gyeonggi-do, 443-803 (Korea, Republic of)

    2015-04-15

    A fast electro-optic shutter is fabricated and demonstrated. The device works independently of the polarization state of the incoming light beam. Modulation between 3% transmission and 60% transmission is obtained within a wavelength range of 50 nm with a response time of 20 μs. The device consists of two partly polymerized chiral nematic liquid crystal layers separated by a half wave plate. The transmission modulation is due to a 50 nm wavelength shift of the photonic band gap of the chiral liquid crystal realized by applying an electric field over a mixture of photo-polymerized LC and non-reactive nematic LC containing a chiral dopant. The shutter features high reflectivity in the photonic band gap. We investigate the influence of the amplitude of the applied voltage on the width and the depth of the reflection band.

  14. Microsecond-range optical shutter for unpolarized light with chiral nematic liquid crystal

    Directory of Open Access Journals (Sweden)

    Mohammad Mohammadimasoudi

    2015-04-01

    Full Text Available A fast electro-optic shutter is fabricated and demonstrated. The device works independently of the polarization state of the incoming light beam. Modulation between 3% transmission and 60% transmission is obtained within a wavelength range of 50 nm with a response time of 20 μs. The device consists of two partly polymerized chiral nematic liquid crystal layers separated by a half wave plate. The transmission modulation is due to a 50 nm wavelength shift of the photonic band gap of the chiral liquid crystal realized by applying an electric field over a mixture of photo-polymerized LC and non-reactive nematic LC containing a chiral dopant. The shutter features high reflectivity in the photonic band gap. We investigate the influence of the amplitude of the applied voltage on the width and the depth of the reflection band.

  15. Engineering chiral light--matter interaction in photonic crystal waveguides with slow light

    CERN Document Server

    Mahmoodian, Sahand; Söllner, Immo; Stobbe, Søren; Lodahl, Peter

    2016-01-01

    We design photonic crystal waveguides with efficient chiral light--matter interfaces that can be integrated with solid-state quantum emitters. By using glide-plane-symmetric waveguides, we show that chiral light-matter interaction can exist even in the presence of slow light with slow-down factors of up to $100$ and therefore the light--matter interaction exhibits both strong Purcell enhancement and chirality. This allows for near-unity directional $\\beta$-factors for a range of emitter positions and frequencies. Additionally, we design an efficient mode adapter to couple light from a standard nanobeam waveguide to the glide-plane symmetric photonic crystal waveguide. Our work sets the stage for performing future experiments on a solid-state platform.

  16. Photoresponsive rolling and bending of thin crystals of chiral diarylethenes

    NARCIS (Netherlands)

    Uchida, Kingo; Sukata, Shin-ichiro; Matsuzawa, Yuji; Akazawa, Masako; de Jong, Jaap J. D.; Katsonis, Nathalie; Kojima, Yuko; Nakamura, Shinichiro; Areephong, Jetsuda; Meetsma, Auke; Feringa, Ben L.

    2008-01-01

    Dithienylhexafluorocyclopentene with (R)- or (S)-N-phenylethylamide substituents formed rod-like and 0.2-1.0 mu m-thick plate-like crystals by sublimation; upon UV irradiation, the crystals bent concavely to the incident light and finally rolled crystals were obtained; the bent crystals were reconve

  17. Photoresponsive rolling and bending of thin crystals of chiral diarylethenes

    NARCIS (Netherlands)

    Uchida, Kingo; Sukata, Shin-ichiro; Matsuzawa, Yuji; Akazawa, Masako; de Jong, Jaap J. D.; Katsonis, Nathalie; Kojima, Yuko; Nakamura, Shinichiro; Areephong, Jetsuda; Meetsma, Auke; Feringa, Ben L.

    2008-01-01

    Dithienylhexafluorocyclopentene with (R)- or (S)-N-phenylethylamide substituents formed rod-like and 0.2-1.0 mu m-thick plate-like crystals by sublimation; upon UV irradiation, the crystals bent concavely to the incident light and finally rolled crystals were obtained; the bent crystals were

  18. Quiralidade em moléculas e cristais Chirality at molecules and crystals

    Directory of Open Access Journals (Sweden)

    Ayres Guimarães Dias

    2009-01-01

    Full Text Available The present contribution describes some concepts of stereochemistry and chirality in molecules and crystals. This paper also reports on the development of a simple and fast experiment to prepare and recognize conglomerate and true racemate of tartaric acid produced by mechanic mixture of commercial enantiomers and recristalization. Optical activity and melting point of mixtures are also used in the analysis.

  19. Photoinduced Reorganization of Motor-Doped Chiral Liquid Crystals : Bridging Molecular Isomerization and Texture Rotation

    NARCIS (Netherlands)

    Bosco, Alessandro; Jongejan, Mahthild G. M.; Eelkema, Rienk; Katsonis, Nathalie; Lacaze, Ernmanuelle; Ferrarini, Alberta; Feringa, Ben L.; Lacaze, Emmanuelle

    2008-01-01

    We recently reported that the photoisomerization of molecular motors used as chiral dopants in a cholesteric liquid crystal film induces a rotational reorganization which can be observed by optical microscopy and produces the motion of microscopic objects placed on top of the film (Feringa, B. L.;

  20. Active control of chirality in nonlinear metamaterials

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Yu; Chai, Zhen; Yang, Hong [State Key Laboratory for Mesoscopic Physics and Department of Physics, Peking University, Beijing 100871 (China); Hu, Xiaoyong, E-mail: xiaoyonghu@pku.edu.cn; Gong, Qihuang [State Key Laboratory for Mesoscopic Physics and Department of Physics, Peking University, Beijing 100871 (China); Collaborative Innovation Center of Quantum Matter, Beijing 100871 (China)

    2015-03-02

    An all-optical tunabe chirality is realized in a photonic metamaterial, the metamolecule of which consists of a nonlinear nano-Au:polycrystalline indium-tin oxide layer sandwiched between two L-shaped gold nano-antennas twisted 90° with each other. The maximum circular dichroism reached 30%. Under excitation of a 40 kW/cm{sup 2} weak pump light, the peak in the circular dichroism shifts 45 nm in the short-wavelength direction. An ultrafast response time of 35 ps is maintained. This work not only opens up the possibility for the realization of ultralow-power and ultrafast all-optical tunable chirality but also offers a way to construct ultrahigh-speed on-chip biochemical sensors.

  1. Longitudinal and transverse pyroelectric effects in a chiral ferroelectric liquid crystal

    Energy Technology Data Exchange (ETDEWEB)

    Yablonskii, S. V., E-mail: yablonskii2005@yandex.ru; Bondarchuk, V. V. [Russian Academy of Sciences, Shubnikov Institute of Crystallography (Russian Federation); Soto-Bustamante, E. A.; Romero-Hasler, P. N. [Universidad de Chile (Chile); Ozaki, M. [Osaka University, Department of Electronic Engineering, Faculty of Engineering (Japan); Yoshino, K. [Shimane Institute for Industrial Technology (Japan)

    2015-04-15

    In this study, we compare the results of experimental investigations of longitudinal and transverse pyroelectric effects in a chiral ferroelectric crystal. In a transverse geometry, we studied freely suspended liquid-crystal films. In both geometries, samples exhibited bistability, demonstrating stable pyroelectric signals of different polarities at zero voltage. It is shown that a bistable cell based on a freely suspended film requires 40 times less energy expenditures as compared to the conventional sandwich-type cell.

  2. Temperature-tunable lasing in negative dielectric chiral nematic liquid crystal

    Science.gov (United States)

    Wu, Ri-Na; Wu, Jie; Wu, Xiao-Jiao; Dai, Qin

    2015-05-01

    In this work, negative dielectric nematic liquid crystal SLC12V620-400, chiral dopant S811, and laser dye DCM are used to prepare dye-doped chiral nematic liquid crystal laser sample. In order to investigate temperature-tunable lasing in negative dielectric chiral nematic liquid crystal, we measure the transmission and lasing spectrum of this sample. The photonic band gap (PBG) is observed to red shift with its width reducing from 71.2 nm to 40.2 nm, and its short-wavelength band edge moves 55.3 nm while the long-wavelength band edge only moves 24.9 nm. The wavelength of output laser is found to red shift from 614.4 nm at 20 °C to 662.8 nm at 67 °C, which is very different from the previous experimental phenomena. The refractive indices, parallel and perpendicular to the director in chiral nematic liquid crystal have different dependencies on temperature. The experiment shows that the pitch of this chiral nematic liquid crystal increases with the increase of temperature. The decrease in the PBG width, different shifts of band edges, and the red shift of laser wavelength are the results of refractive indices change and pitch thermal elongation. Project supported by the National Natural Science Foundation of China (Grant No. 61378042), the Outstanding Young Scholars Growth Plans of Colleges and Universities in Liaoning Province, China (Grant No. LJQ2013022), the Science and Technology Research of Liaoning Province, China (Grant No. L2010465), the Open Funds of Liaoning Province Key Laboratory of Laser and Optical Information of Shenyang Ligong University, China.

  3. Tuning the helical twisting power of nematic liquid crystals induced by chiral 1,2-propanediol derivatives using varied substituents

    Institute of Scientific and Technical Information of China (English)

    Hai Quan Zhang; An Lei Qin

    2012-01-01

    In this study,a novel series of chiral 1,2-propanediol derivatives with different electron-donating and electron-withdrawing groups were synthesized and characterized by FT-IR and 1H NMR.The helical twisting properties of all the chiral dopants were investigated by doping the chiral dopants into a nematic liquid crystal host (SLC- 1717).The results indicate that the donor-acceptor electron effect have a prominent influence on helical twisting property of the chiral nematic phase induced by the chiral dopants.Introducing electron-withdrawing groups into the terminal ends of chiral 1,2-propanediol can decrease the absolute values of the helical twisting power.In addition,the helix inversion temperatures of the induced chiral nematic phase are variational with the change of terminal groups.

  4. Berry Phase of Light under Bragg Reflection by Chiral Liquid-Crystal Media

    Science.gov (United States)

    Barboza, Raouf; Bortolozzo, Umberto; Clerc, Marcel G.; Residori, Stefania

    2016-07-01

    A Berry phase is revealed for circularly polarized light when it is Bragg reflected by a chiral liquid-crystal medium of the same handedness. By using a chiral nematic layer we demonstrate that if the input plane of the layer is rotated with respect to a fixed reference frame, a geometric phase effect occurs for the circularly polarized light reflected by the periodic helical structure of the medium. Theory and numerical simulations are supported by an experimental observation, disclosing novel applications in the field of optical manipulation and fundamental optical phenomena.

  5. Berry phase of light Bragg-reflected by chiral liquid crystal media

    CERN Document Server

    Barboza, Raouf; Residori, Stefania; Clerc, Marcel G

    2016-01-01

    Berry phase is revealed for circularly polarized light when it is Bragg-reflected by a chiral liquid crystal medium of the same handedness. By using a chiral nematic layer we demonstrate that if the input plane of the layer is rotated with respect to a fixed reference frame, then, a geometric phase effect occurs for the circularly polarized light reflected by the periodic helical structure of the medium. Theory and numerical simulations are supported by an experimental observation, disclosing novel applications in the field of optical manipulation and fundamental optical phenomena.

  6. Light amplification by photorefractive ferroelectric liquid crystal blends containing quarter-thiophene photoconductive chiral dopant

    Science.gov (United States)

    Sasaki, T.; Hara, T.; Yamamoto, Y.; Naka, Y.; Le, K. V.

    2017-05-01

    The photorefractive effect is a phenomenon that forms a rewritable hologram in a material. This phenomenon can be utilized in devices including 3D displays, optical tomography, novelty filters, phase conjugate wave generators, and optical amplification. Ferroelectric liquid crystal blends composed of a smectic liquid crystalline mixture, a photoconductive chiral dopant, and an electron trap reagent exhibit significant photorefractivity together with rapid responses. As such, they allow the dynamic amplification of moving optical signals. The photoconductive chiral dopants used in the previous study are ter-thiphene derivatives so that the photorefractive effect was examined at 488 nm. In the present work, chiral dopants possessing quarter-thiphene chromophore were synthesized and the photorefractive effect of the FLC blends at longer wavelength was demonstrated.

  7. Liquid crystal behavior induced assembling fabrication of conductive chiral MWCNTs@NCC nanopaper

    Science.gov (United States)

    Ren, Yumei; Wang, Tianjiao; Chen, Zhimin; Li, Jing; Tian, Qiuge; Yang, Hongxia; Xu, Qun

    2016-11-01

    The conductive chiral MWCNTs@NCC nanopapers obtained by the assembly of nanocrystalline cellulose liquid crystals (NCC LCs) host matrix along with one-dimensional (1-D) multi-walled carbon nanotubes (MWCNTs) have been studied in this work. Circular dichroism (CD) studies show strong signals stemming from the chiral nematic structure. Notably, the introduction of the MWCNTs has a pronounced effect on the chiral structure of the as-prepared nanopaper. Our experimental results indicate the multiple weak molecular interactions existing between MWCNTs and NCC are responsible for the effective dispersion and stabilization of MWCNTs. Moreover it also confirms the resulting nanopaper has an increased conductivity of 4.2 S/m at 1.96 wt% MWCNTs. So the co-assembly of the nanocomposite herein opens a gateway for preparing functional materials combining the photonic properties of the NCC LCs matrix with other building blocks that can supply other advantageous functions.

  8. Hybrid Polyaniline Systems under Chiral and Redox Control

    Institute of Scientific and Technical Information of China (English)

    Toshikazu Hirao; Toshiyuki Moriuchi; Xiuliang Shen; Kenji Morita

    2005-01-01

    @@ 1Introduction Polyanilines are one of the promising electrically conducting π-conjugated polymers with chemical stability. In recent year, there has been increased interest in chiral induction of polyanilines because of their potential use in diverse areas. Chiral polyaniline has been reported to be formed only by the chiral acid dopant[1]. In our previous papers, complexation of polyanilines or their oligomers with transition metals modulates the redox properties of the quinonediimine unit, which is related to the catalytic function in the oxidation reaction[2].The controlled complexation with palladium(Ⅱ) compounds has been achieved to afford the cross-linked network conjugated complexes, in which the quinonediimine moieties serve as bridging coordination sites[3].Another hybrid system consisting of π-conjugated polymer and transition metal is also described.

  9. Molecular dynamics studies and quantification of the effect of chirality on the formation of liquid crystal mesophases

    Energy Technology Data Exchange (ETDEWEB)

    Solymosi, Miklos

    2002-07-01

    Results are presented from theoretical studies and from a series of molecular dynamics simulations undertaken to quantify the effect of chirality on the formation of liquid crystal mesophases. In the theoretical studies we have proposed a scaled chiral index with a formulation which allows comparison to be made between molecules comprising different numbers of atoms. We have undertaken chirality calculations utilizing the proposed scaled chiral index, G{sub 0S}, for one optimized static molecular geometry for a range of liquid crystal chiral dopants and ferroelectric liquid crystal molecules. The scaled chiral index, G{sub 0S}, allows a rapid calculation to be made of a pseudoscalar quantity which shows a good correlation with the helical twisting power of liquid crystal chiral dopants in a nematic liquid crystal solvent. This could prove a powerful aid in the design of novel dopant molecules where the dopant is rigid and the helical twisting is predominantly a steric effect. The same scaled chirality index, G{sub 0S}, calculation for ferroelectric liquid crystal molecules hints at an inverse correlation with spontaneous polarization agreeing with some experimental results. The scaled chiral index is a chemically useful index that can also be decomposed into atomic or functional group contributions, thereby creating a new measure of the asymmetric potential of functional groups and their different possible substitution positions. In the molecular dynamics simulation studies we have investigated two three-site Gay-Berne models, one chiral and the other achiral, each with a rotated central site forming a zigzag shape. In the chiral model one of the end site was additionally rotated out of the plane of the other two sites by a chiral angle {theta}{sub c}. Results from the achiral phase simulations support the theory that steric molecular shape can be associated with a driving force that leads to the smectic A - smectic C phase transition since such a transition was

  10. Liquid crystal behavior induced assembling fabrication of conductive chiral MWCNTs@NCC nanopaper

    Energy Technology Data Exchange (ETDEWEB)

    Ren, Yumei; Wang, Tianjiao; Chen, Zhimin; Li, Jing; Tian, Qiuge; Yang, Hongxia; Xu, Qun, E-mail: qunxu@zzu.edu.cn

    2016-11-01

    Highlights: • In this study conductive chiral MWCNTs@NCC nanopapers were prepared. • The introduction of the MWCNTs has a pronounced effect on the chiral structure of the as-prepared nanopaper. • The multiple weak molecular interactions existing between MWCNTs and NCC are responsible for the effective dispersion and stabilization of MWCNTs. • The resulting nanopaper has an increased conductivity. - Abstract: The conductive chiral MWCNTs@NCC nanopapers obtained by the assembly of nanocrystalline cellulose liquid crystals (NCC LCs) host matrix along with one-dimensional (1-D) multi-walled carbon nanotubes (MWCNTs) have been studied in this work. Circular dichroism (CD) studies show strong signals stemming from the chiral nematic structure. Notably, the introduction of the MWCNTs has a pronounced effect on the chiral structure of the as-prepared nanopaper. Our experimental results indicate the multiple weak molecular interactions existing between MWCNTs and NCC are responsible for the effective dispersion and stabilization of MWCNTs. Moreover it also confirms the resulting nanopaper has an increased conductivity of 4.2 S/m at 1.96 wt% MWCNTs. So the co-assembly of the nanocomposite herein opens a gateway for preparing functional materials combining the photonic properties of the NCC LCs matrix with other building blocks that can supply other advantageous functions.

  11. Dual chirality control of palladium(II) complexes bearing tropos biphenyl diamine ligands.

    Science.gov (United States)

    Aikawa, Kohsuke; Mikami, Koichi

    2005-12-14

    Axial and center chirality of Pd complexes with tropos biphenyl secondary diamine ligands is shown to be controlled by chiral amide (R)-DABNTf, which can efficiently discriminate between two enantiomeric Pd complexes.

  12. Chirality-Controlled Synthesis and Applications of Single-Wall Carbon Nanotubes.

    Science.gov (United States)

    Liu, Bilu; Wu, Fanqi; Gui, Hui; Zheng, Ming; Zhou, Chongwu

    2017-01-24

    Preparation of chirality-defined single-wall carbon nanotubes (SWCNTs) is the top challenge in the nanotube field. In recent years, great progress has been made toward preparing single-chirality SWCNTs through both direct controlled synthesis and postsynthesis separation approaches. Accordingly, the uses of single-chirality-dominated SWCNTs for various applications have emerged as a new front in nanotube research. In this Review, we review recent progress made in the chirality-controlled synthesis of SWCNTs, including metal-catalyst-free SWCNT cloning by vapor-phase epitaxy elongation of purified single-chirality nanotube seeds, chirality-specific growth of SWCNTs on bimetallic solid alloy catalysts, chirality-controlled synthesis of SWCNTs using bottom-up synthetic strategy from carbonaceous molecular end-cap precursors, etc. Recent major progresses in postsynthesis separation of single-chirality SWCNT species, as well as methods for chirality characterization of SWCNTs, are also highlighted. Moreover, we discuss some examples where single-chirality SWCNTs have shown clear advantages over SWCNTs with broad chirality distributions. We hope this review could inspire more research on the chirality-controlled preparation of SWCNTs and equally important inspire the use of single-chirality SWCNT samples for more fundamental studies and practical applications.

  13. Chiral-induced self-assembly sphere phase liquid crystal with fast switching time

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Ji-Liang; Ni, Shui-Bin; Ping Chen, Chao; Lu, Jian-Gang, E-mail: lujg@sjtu.edu.cn; Su, Yikai [National Engineering Lab for TFT-LCD Materials and Technologies, Department of Electronic Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China); Wu, Dong-Qing [College of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China); Song, Xiao-Long; Chen, Chao-Yuan [The Jiangsu Hecheng Display Technology Co., Ltd., Nanjing 211300 (China); Shieh, Han-Ping D. [National Engineering Lab for TFT-LCD Materials and Technologies, Department of Electronic Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China); Department of Photonics and Display Institute, National Chiao Tung University, Hsinchu 300, Taiwan (China)

    2014-03-03

    A fluid self-assembly sphere phase (SP) of liquid crystal induced by chiral dopant is observed in a narrow temperature range between isotropic and blue phase or between isotropic and chiral nematic phase. The SP consists of three-dimensional twist spheres (3-DTSs) and disclinations among 3-DTSs. The temperature range of the SP has been broadened to more than 85 °C by stabilizing the disclinations with amorphous polymer chains. The electro-optical switching time of the polymer-stabilized SP is demonstrated in sub-millisecond with a low switching electric field of 4.4 V μm{sup −1}, which is of promising applications in displays, 3-D tunable photonic crystals, and phase modulators.

  14. Application of computational chemistry methods to the prediction of chirality and helical twisting power in liquid crystal systems

    Science.gov (United States)

    Noto, Anthony G.; Marshall, Kenneth L.

    2005-08-01

    Until recently, it has not been possible to determine, with any real certainty, a complete picture of "chirality" (absolute configuration, optical rotation direction, and helical twisting power) for new chiral compounds without first synthesizing, purifying, characterizing, and testing every new material. Recent advances in computational chemistry now allow the prediction of certain key chiral molecular properties prior to synthesis, which opens the possibility of predetermining the "chiroptical" properties of new liquid crystal dopants and mixtures for advanced optical and photonics applications. A key element to this activity was the development of both the chirality index (G0) by Osipov et al., and the scaled chirality index (G0S) by Solymosi et al., that can be used as a "figure of merit" for molecular chirality. Promising correlations between G0S and both circular dichroism (CD) and the helical twisting power (HTP) of a chiral dopant in a liquid crystal host have been shown by Neal et al., Osipov, and Kuball. Our work improves the predictive capabilities of G0S by taking into account the actual mass of each atom in the molecule in the calculations; in previous studies the mass of each atom was assumed to be equal. This "weighted" scaled chirality index (G0SW) was calculated and correlated to existing experimental HTP data for each member of a series of existing, well-known chiral compounds. The computed HTP using G0SW for these model systems correlated to the experimental data with remarkable accuracy. Weighted, scaled chiral indices were also calculated for the first time for a series of novel chiral transition metal dithiolene dyes for near-IR liquid crystal device applications.

  15. Orbital angular momentum in electron diffraction and its use to determine chiral crystal symmetries

    Science.gov (United States)

    Juchtmans, Roeland; Verbeeck, Jo

    2015-10-01

    In this work we present an alternative way to look at electron diffraction in a transmission electron microscope. Instead of writing the scattering amplitude in Fourier space as a set of plane waves, we use the cylindrical Fourier transform to describe the scattering amplitude in a basis of orbital angular momentum (OAM) eigenstates. We show how working in this framework can be very convenient when investigating, e.g., rotation and screw-axis symmetries. For the latter we find selection rules on the OAM coefficients that unambiguously reveal the handedness of the screw axis. Detecting the OAM coefficients of the scattering amplitude thus offers the possibility to detect the handedness of crystals without the need for dynamical simulations, the thickness of the sample, nor the exact crystal structure. We propose an experimental setup to measure the OAM components where an image of the crystal is taken after inserting a spiral phase plate in the diffraction plane and perform multislice simulations on α quartz to demonstrate how the method indeed reveals the chirality. The experimental feasibility of the technique is discussed together with its main advantages with respect to chirality determination of screw axes. The method shows how the use of a spiral phase plate can be extended from a simple phase imaging technique to a tool to measure the local OAM decomposition of an electron wave, widening the field of interest well beyond chiral space group determination.

  16. Vortex Crystals with Chiral Stripes in Itinerant Magnets

    Science.gov (United States)

    Ozawa, Ryo; Hayami, Satoru; Barros, Kipton; Chern, Gia-Wei; Motome, Yukitoshi; Batista, Cristian D.

    2016-10-01

    We study noncoplanar magnetic ordering in frustrated itinerant magnets. For a family of Kondo square lattice models with classical local moments, we find that a double-Q noncoplanar vortex crystal has lower energy than the single-Q helical order expected from the Ruderman-Kittel-Kasuya-Yosida interaction when the lattice symmetry dictates four global maxima in the bare magnetic susceptibility. By expanding in the small Kondo exchange and the degree of noncoplanarity, we demonstrate that this noncoplanar state arises from a Fermi surface instability occurring in independent sections connected by two ordering wave vectors.

  17. Photoswitching of ferroelectric liquid crystals using chiral thioindigo dopants: The development of a photochemical switch hitter.

    Science.gov (United States)

    Lemieux, Robert P

    2004-01-01

    By virtue of its spontaneous polarization (PS), a ferroelectric SmC* liquid crystal can be switched between two states corresponding to opposite molecular tilt orientations using an electric field, thus producing an ON-OFF light shutter between crossed polarizers. Considerable efforts have been made over the past decade to develop photonic FLC light shutters because of their potential uses in dynamic holography and optical data storage. The ON-OFF switching of a FLC light shutter can be triggered by light via a photoinversion of PS using a photochromic dopant. The spontaneous polarization is a chiral bulk property that can be left-handed (negative) or right-handed (positive), depending on the absolute configuration of the chiral component of the SmC* phase. In the approach described herein, the magnitude of PS is modulated via the photoisomerization of a chiral thioindigo dopant that undergoes a large increase in transverse dipole moment upon trans-cis photoisomerization. The sign of PS is photoinverted using an "ambidextrous" thioindigo dopant containing a chiral 2-octyloxy side chain that is coupled to the thioindigo core and induces a positive PS, and a chiral 2,3-difluorooctyloxy side chain that is decoupled from the core and induces a negative PS. In the trans form, the 2,3-difluorooctyloxy side chain predominates and the net PS induced by the dopant is negative. However, upon trans-cis-photoisomerization, the increase in transverse dipole moment of the 2-octyloxy/thioindigo unit raises its induced PS over that of the decoupled 2,3-difluorooctyloxy side chain, and thus inverts the net sign of PS induced by the dopant from negative to positive.

  18. Low symmetry tetrahedral nematic liquid crystal phases: Ambidextrous chirality and ambidextrous helicity.

    Science.gov (United States)

    Pleiner, Harald; Brand, Helmut R

    2014-02-01

    We discuss the symmetry properties as well as the dynamic behavior of various non-polar nematic liquid crystal phases with tetrahedral order. We concentrate on systems that show biaxial nematic order coexisting with octupolar (tetrahedral) order. Non-polar examples are phases with D2 and S4 symmetries, which can be characterized as biaxial nematics lacking inversion symmetry. It is this combination that allows for new features in the statics and dynamics of these phases. The D2-symmetric phase is chiral, even for achiral molecules, and shows ambidextrous chirality in all three preferred directions. The achiral S4-symmetric phase allows for ambidextrous helicity, similar to the higher-symmetric D2d-symmetric phase. Such phases are candidates for nematic phases made from banana-shaped molecules.

  19. Controlling third harmonic generation with gammadion-shaped chiral metamaterials

    Directory of Open Access Journals (Sweden)

    Chi Zhang

    2016-12-01

    Full Text Available We theoretically investigated third harmonic generation (THG from planar chiral metamaterials consisting of a square array of gammadion-shaped metal-insulator-metal multilayered nanostructures. We show that there exists strong circular dichroism (CD for THG on the proposed chiral metamaterials. We also demonstrate that geometrically mirroring the gammadion -shaped meta-atoms can result in reversal of the THG-CD effect. Based on these CD effects in the optical nonlinear regime, we propose a design of a Fresnel zone plate (FZP for intense focusing of the THG signals, in which adjacent zones of the FZP consist of gammadions with mirror symmetry and generate circularly polarized THG with opposite handedness. Furthermore, we demonstrate that the relative phase of the THG can be continuously changed by rotating the gammadion around its rotational axis, which could be used in the FZP to control the polarization of the output THG signals.

  20. On Chiral Space Groups and Chiral Molecules

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    This note explains the relationship (as well as the absence of a relationship) between chiral space groups and chiral molecules (which have absolute configurations). For a chiral molecule, which must crystallize in a chiral space group, the outcome of the absolute configuration determination must be linked to some other properties of the chiral crystal such as its optical activity for the observation to the relevant.

  1. On Chiral Space Groups and Chiral Molecules

    Institute of Scientific and Technical Information of China (English)

    NgSeikWng; HUSheng-Zhi

    2003-01-01

    This note explains the relationship (as well as the absence of a relationship) between chiral space groups and chiral molecules (which have absolute configurations).For a chiral molecule,which must crystallize in a chiral space group,the outcome of the absolute configuration determination must be linked to some other properties of the chiral crystal such as its optical activity for the observation to the relevant.

  2. Geometric triangular chiral hexagon crystal-like complexes organization in pathological tissues biological collision order.

    Science.gov (United States)

    Díaz, Jairo A; Jaramillo, Natalia A; Murillo, Mauricio F

    2007-12-12

    The present study describes and documents self-assembly of geometric triangular chiral hexagon crystal like complex organizations (GTCHC) in human pathological tissues. The authors have found this architectural geometric expression at macroscopic and microscopic levels mainly in cancer processes. This study is based essentially on macroscopic and histopathologic analyses of 3000 surgical specimens: 2600 inflammatory lesions and 400 malignant tumours. Geometric complexes identified photographically at macroscopic level were located in the gross surgical specimen, and these areas were carefully dissected. Samples were taken to carry out histologic analysis. Based on the hypothesis of a collision genesis mechanism and because it is difficult to carry out an appropriate methodological observation in biological systems, the authors designed a model base on other dynamic systems to obtain indirect information in which a strong white flash wave light discharge, generated by an electronic device, hits over the lines of electrical conductance structured in helicoidal pattern. In their experimental model, the authors were able to reproduce and to predict polarity, chirality, helicoid geometry, triangular and hexagonal clusters through electromagnetic sequential collisions. They determined that similar events among constituents of extracelular matrix which drive and produce piezoelectric activity are responsible for the genesis of GTCHC complexes in pathological tissues. This research suggests that molecular crystals represented by triangular chiral hexagons derived from a collision-attraction event against collagen type I fibrils emerge at microscopic and macroscopic scales presenting a lateral assembly of each side of hypertrophy helicoid fibers, that represent energy flow in cooperative hierarchically chiral electromagnetic interaction in pathological tissues and arises as a geometry of the equilibrium in perturbed biological systems. Further interdisciplinary studies must

  3. Geometric triangular chiral hexagon crystal-like complexes organization in pathological tissues biological collision order.

    Directory of Open Access Journals (Sweden)

    Jairo A Díaz

    Full Text Available The present study describes and documents self-assembly of geometric triangular chiral hexagon crystal like complex organizations (GTCHC in human pathological tissues. The authors have found this architectural geometric expression at macroscopic and microscopic levels mainly in cancer processes. This study is based essentially on macroscopic and histopathologic analyses of 3000 surgical specimens: 2600 inflammatory lesions and 400 malignant tumours. Geometric complexes identified photographically at macroscopic level were located in the gross surgical specimen, and these areas were carefully dissected. Samples were taken to carry out histologic analysis. Based on the hypothesis of a collision genesis mechanism and because it is difficult to carry out an appropriate methodological observation in biological systems, the authors designed a model base on other dynamic systems to obtain indirect information in which a strong white flash wave light discharge, generated by an electronic device, hits over the lines of electrical conductance structured in helicoidal pattern. In their experimental model, the authors were able to reproduce and to predict polarity, chirality, helicoid geometry, triangular and hexagonal clusters through electromagnetic sequential collisions. They determined that similar events among constituents of extracelular matrix which drive and produce piezoelectric activity are responsible for the genesis of GTCHC complexes in pathological tissues. This research suggests that molecular crystals represented by triangular chiral hexagons derived from a collision-attraction event against collagen type I fibrils emerge at microscopic and macroscopic scales presenting a lateral assembly of each side of hypertrophy helicoid fibers, that represent energy flow in cooperative hierarchically chiral electromagnetic interaction in pathological tissues and arises as a geometry of the equilibrium in perturbed biological systems. Further

  4. Chiral Symmetry Breaking During Growing Process of NaClO3 Crystal under Direct-Current Electric Field

    Institute of Scientific and Technical Information of China (English)

    CHEN Wan-Chun; CHEN Xiao-Long

    2007-01-01

    @@ We investigate the influence of dc electric field on chiral symmetry breaking during the growing process of NaClO3 crystal. Nucleation and growth of NaClO3 are completed from an aqueous solution by a fast cooling temperature technology. A pair of polarization microscopes are used to identify a distribution of chiral crystals. Experimental results indicate that the dc electric field has an effect on distribution of chirality, but the direction of the dc electric field is not sensitive to the chiral autocatalysis and selectivity, i.e. the nature convection driving by the gravity does not play an important role on a thin layer of NaClO3 solution. The experimental phenomena may be elucidated by the ECSN mechanism.

  5. Modeling Textural Processes during Self-Assembly of Plant-Based Chiral-Nematic Liquid Crystals

    Directory of Open Access Journals (Sweden)

    Yogesh K. Murugesan

    2010-12-01

    Full Text Available Biological liquid crystalline polymers are found in cellulosic, chitin, and DNA based natural materials. Chiral nematic liquid crystalline orientational order is observed frozen-in in the solid state in plant cell walls and is known as a liquid crystal analogue characterized by a helicoidal plywood architecture. The emergence of the plywood architecture by directed chiral nematic liquid crystalline self assembly has been postulated as the mechanism that leads to optimal cellulose fibril organization. In natural systems, tissue growth and development takes place in the presence of inclusions and secondary phases leaving behind characteristic defects and textures, which provide a unique testing ground for the validity of the liquid crystal self-assembly postulate. In this work, a mathematical model, based on the Landau-de Gennes theory of liquid crystals, is used to simulate defect textures arising in the domain of self assembly, due to presence of secondary phases representing plant cells, lumens and pit canals. It is shown that the obtained defect patterns observed in some plant cell walls are those expected from a truly liquid crystalline phase. The analysis reveals the nature and magnitude of the viscoelastic material parameters that lead to observed patterns in plant-based helicoids through directed self-assembly. In addition, the results provide new guidance to develop biomimetic plywoods for structural and functional applications.

  6. Continuously rotating chiral liquid crystal droplets in a linearly polarized laser trap.

    Science.gov (United States)

    Yang, Y; Brimicombe, P D; Roberts, N W; Dickinson, M R; Osipov, M; Gleeson, H F

    2008-05-12

    The transfer of optical angular momentum to birefringent particles via circularly polarized light is common. We report here on the unexpected, continuous rotation of chiral nematic liquid crystal droplets in a linearly polarized optical trap. The rotation is non-uniform, occurs over a timescale of seconds, and is observed only for very specific droplet sizes. Synchronized vertical motion of the droplet occurs during the rotation. The motion is the result of photo-induced molecular reorganization, providing a micron sized opto-mechanical transducer that twists and translates.

  7. Wave propagation in photonic crystals and metamaterials: Surface waves, nonlinearity and chirality

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Bingnan [Iowa State Univ., Ames, IA (United States)

    2009-01-01

    Photonic crystals and metamaterials, both composed of artificial structures, are two interesting areas in electromagnetism and optics. New phenomena in photonic crystals and metamaterials are being discovered, including some not found in natural materials. This thesis presents my research work in the two areas. Photonic crystals are periodically arranged artificial structures, mostly made from dielectric materials, with period on the same order of the wavelength of the working electromagnetic wave. The wave propagation in photonic crystals is determined by the Bragg scattering of the periodic structure. Photonic band-gaps can be present for a properly designed photonic crystal. Electromagnetic waves with frequency within the range of the band-gap are suppressed from propagating in the photonic crystal. With surface defects, a photonic crystal could support surface modes that are localized on the surface of the crystal, with mode frequencies within the band-gap. With line defects, a photonic crystal could allow the propagation of electromagnetic waves along the channels. The study of surface modes and waveguiding properties of a 2D photonic crystal will be presented in Chapter 1. Metamaterials are generally composed of artificial structures with sizes one order smaller than the wavelength and can be approximated as effective media. Effective macroscopic parameters such as electric permittivity ϵ, magnetic permeability μ are used to characterize the wave propagation in metamaterials. The fundamental structures of the metamaterials affect strongly their macroscopic properties. By designing the fundamental structures of the metamaterials, the effective parameters can be tuned and different electromagnetic properties can be achieved. One important aspect of metamaterial research is to get artificial magnetism. Metallic split-ring resonators (SRRs) and variants are widely used to build magnetic metamaterials with effective μ < 1 or even μ < 0. Varactor based

  8. Absolute configuration and crystal packing for three chiral drugs prone to spontaneous resolution: Guaifenesin, methocarbamol and mephenesin

    Science.gov (United States)

    Bredikhin, Alexander A.; Gubaidullin, Aidar T.; Bredikhina, Zemfira A.; Krivolapov, Dmitry B.; Pashagin, Alexander V.; Litvinov, Igor A.

    2009-02-01

    Popular chiral drugs, guaifenesin, methocarbamol, and mephenesin were investigated by single-crystal X-ray analysis both for enantiopure and racemic samples. The absolute configurations for all substances were established through Flack parameter method. The conglomerate-forming nature for the compounds was confirmed by equivalence of crystal characteristics of enantiopure and racemic samples. The molecular structures and crystal packing details were evaluated and compared with one another for all three investigated substances.

  9. Localised polymer networks in chiral nematic liquid crystals for high speed photonic switching

    Energy Technology Data Exchange (ETDEWEB)

    Tartan, Chloe C., E-mail: chloe.tartan@eng.ox.ac.uk, E-mail: steve.elston@eng.ox.ac.uk; Salter, Patrick S.; Booth, Martin J.; Morris, Stephen M.; Elston, Steve J., E-mail: chloe.tartan@eng.ox.ac.uk, E-mail: steve.elston@eng.ox.ac.uk [Department of Engineering Science, University of Oxford, Parks Road, Oxford OX1 3PJ (United Kingdom)

    2016-05-14

    Self-assembled periodic structures based upon chiral liquid crystalline materials have significant potential in the field of photonics ranging from fast-switching optoelectronic devices to low-threshold lasers. The flexoelectro-optic effect, which is observed in chiral nematic liquid crystals (LCs) when an electric field is applied perpendicular to the helical axis, has significant potential as it exhibits analogue switching in 10–100 μs. However, the major technological barrier that prohibits the commercial realisation of this electro-optic effect is the requirement of a uniform, in-plane alignment of the helix axis between glass substrates. Here, it is shown that periodic polymer structures engineered in the nematic phase of a chiral nematic LC device using direct laser writing can result in the spontaneous formation of the necessary uniform lying helix (ULH) state. Specifically, two-photon polymerization is used in conjunction with a spatial light modulator so as to correct for aberrations introduced by the bounding glass substrates enabling the polymer structures to be fabricated directly into the device. The ULH state appears to be stable in the absence of an externally applied electric field, and the optimum contrast between the bright and dark states is obtained using polymer structures that have periodicities of the order of the device thickness.

  10. Localised polymer networks in chiral nematic liquid crystals for high speed photonic switching

    Science.gov (United States)

    Tartan, Chloe C.; Salter, Patrick S.; Booth, Martin J.; Morris, Stephen M.; Elston, Steve J.

    2016-05-01

    Self-assembled periodic structures based upon chiral liquid crystalline materials have significant potential in the field of photonics ranging from fast-switching optoelectronic devices to low-threshold lasers. The flexoelectro-optic effect, which is observed in chiral nematic liquid crystals (LCs) when an electric field is applied perpendicular to the helical axis, has significant potential as it exhibits analogue switching in 10-100 μs. However, the major technological barrier that prohibits the commercial realisation of this electro-optic effect is the requirement of a uniform, in-plane alignment of the helix axis between glass substrates. Here, it is shown that periodic polymer structures engineered in the nematic phase of a chiral nematic LC device using direct laser writing can result in the spontaneous formation of the necessary uniform lying helix (ULH) state. Specifically, two-photon polymerization is used in conjunction with a spatial light modulator so as to correct for aberrations introduced by the bounding glass substrates enabling the polymer structures to be fabricated directly into the device. The ULH state appears to be stable in the absence of an externally applied electric field, and the optimum contrast between the bright and dark states is obtained using polymer structures that have periodicities of the order of the device thickness.

  11. Bacterial Ice Crystal Controlling Proteins

    Directory of Open Access Journals (Sweden)

    Janet S. H. Lorv

    2014-01-01

    Full Text Available Across the world, many ice active bacteria utilize ice crystal controlling proteins for aid in freezing tolerance at subzero temperatures. Ice crystal controlling proteins include both antifreeze and ice nucleation proteins. Antifreeze proteins minimize freezing damage by inhibiting growth of large ice crystals, while ice nucleation proteins induce formation of embryonic ice crystals. Although both protein classes have differing functions, these proteins use the same ice binding mechanisms. Rather than direct binding, it is probable that these protein classes create an ice surface prior to ice crystal surface adsorption. Function is differentiated by molecular size of the protein. This paper reviews the similar and different aspects of bacterial antifreeze and ice nucleation proteins, the role of these proteins in freezing tolerance, prevalence of these proteins in psychrophiles, and current mechanisms of protein-ice interactions.

  12. The origins of nanotube chirality: Is the edge-catalyst in control?

    Science.gov (United States)

    Penev, Evgeni; Liu, Yuanyue; Yakobson, Boris

    2011-03-01

    The chance for a nanotube of a chiral angle c to emerge from the ``primordial soup'' of carbon atoms on the catalyst is determined by their relative energies. Massive computations allow one to evaluate the ``elastic'' energies of the caps, and the energies of their edges, G(c+C), which appears to be dominating. Importantly, the latter contains a ``chemical phase shift'' C, so that the probability of different chiralities is determined by the chemical conditions at the edge. Preference for specific chirality can be achieved by tuning chemical potential of edge terminating chemical. This offers a rational way to control the tube chiral symmetry, a tantalizing yet so far elusive goal.

  13. Flexoelectro-optic properties of chiral nematic liquid crystals in the uniform standing helix configuration.

    Science.gov (United States)

    Castles, F; Morris, S M; Coles, H J

    2009-09-01

    The flexoelectro-optic effect describes the rotation of the optic axis of a short-pitch chiral nematic liquid crystal under the application of an electric field. We investigate the effect in the uniform standing helix, or "Grandjean" configuration. An in-plane electric field is applied. The director profile is determined numerically using a static one-dimensional continuum model with strong surface anchoring. The Berreman method is used to solve for plane-wave solutions to Maxwell's equations, and predict the optical properties of the resulting structure in general cases. By using a chiral nematic with short pitch between crossed polarizers an optical switch may be generated. With no applied field the configuration is nontransmissive at normal incidence, but becomes transmissive with an applied field. For this case, numerical results using the Berreman method are supplemented with an analytic theory and found to be in good agreement. The transmitted intensity as a function of tilt, the contrast ratio, and the tilt required for full intensity modulation are presented. The angular dependence of the transmission is calculated and the isocontrast curves are plotted. For typical material and cell parameters a switching speed of 0.017 ms and contrast ratio of 1500:1 at normal incidence are predicted, at a switch-on tilt of 41.5 degrees. Experimental verification of the analytic and numerical models is provided.

  14. Generalized Liquid Crystals: Giant Fluctuations and the Vestigial Chiral Order of I , O , and T Matter

    Science.gov (United States)

    Liu, Ke; Nissinen, Jaakko; Slager, Robert-Jan; Wu, Kai; Zaanen, Jan

    2016-10-01

    The physics of nematic liquid crystals has been the subject of intensive research since the late 19th century. However, the focus of this pursuit has been centered around uniaxial and biaxial nematics associated with constituents bearing a D∞ h or D2 h symmetry, respectively. In view of general symmetries, however, these are singularly special since nematic order can in principle involve any point-group symmetry. Given the progress in tailoring nanoparticles with particular shapes and interactions, this vast family of "generalized nematics" might become accessible in the laboratory. Little is known because the order parameter theories associated with the highly symmetric point groups are remarkably complicated, involving tensor order parameters of high rank. Here, we show that the generic features of the statistical physics of such systems can be studied in a highly flexible and efficient fashion using a mathematical tool borrowed from high-energy physics: discrete non-Abelian gauge theory. Explicitly, we construct a family of lattice gauge models encapsulating nematic ordering of general three-dimensional point-group symmetries. We find that the most symmetrical generalized nematics are subjected to thermal fluctuations of unprecedented severity. As a result, novel forms of fluctuation phenomena become possible. In particular, we demonstrate that a vestigial phase carrying no more than chiral order becomes ubiquitous departing from high point-group symmetry chiral building blocks, such as I , O , and T symmetric matter.

  15. Crystal structure of (2R-1-[(methylsulfonyloxy]propan-2-aminium chloride: a chiral molecular salt

    Directory of Open Access Journals (Sweden)

    H. R. Rajegowda

    2015-10-01

    Full Text Available In the title chiral molecular salt, C4H12NO3S+·Cl−, the cation is protonated at the N atom, producing [RNH3]+, where R is CH3SO2OCH2C(HCH3. The N atom in the cation is sp3-hybridized. In the crystal, cations and anions are connected by strong N—H...Cl hydrogen bonds to generate edge-shared 12-membered rings of the form {...Cl...HNH}3. This pattern of hydrogen bonding gives rise to zigzag supramolecular layers in the ab plane. The layers are connected into a three-dimensional architecture by C—H...O hydrogen bonds. The structure was refined as an inversion twin.

  16. Circular dichroism in a three-dimensional semiconductor chiral photonic crystal

    CERN Document Server

    Takahashi, S; Ota, Y; Tatebayashi, J; Iwamoto, S; Arakawa, Y

    2014-01-01

    Circular dichroism covering the telecommunication band is experimentally demonstrated in a semiconductor-based three-dimensional chiral photonic crystal (PhC). We design a rotationally-stacked woodpile PhC structure where neighboring layers are rotated by 60 degrees and three layers construct a single helical unit. The mirror-asymmetric PhC made from GaAs with sub-micron periodicity is fabricated by a micro-manipulation technique. Due to the large contrast of refractive indices between GaAs and air, the experimentally obtained circular dichroism extends over a wide wavelength range, with the transmittance of right-handed circularly polarized incident light being 85% and that of left-handed light being 15% at a wavelength of 1300 nm. The obtained results show good agreement with numerical simulations.

  17. Synthesis, crystal growth and characterization of a chiral compound (triphenylphosphine oxide cadmium iodide): A new semiorganic nonlinear optical material

    Science.gov (United States)

    Santhakumari, R.; Ramamurthi, K.; Stoeckli-Evans, Helen; Hema, R.; Nirmala, W.

    2011-05-01

    Synthesis of semiorganic material, triphenylphosphine oxide cadmium iodide (TPPOCdI), is reported for the first time. Employing the temperature reduction method, a crystal of size 16×7×6 mm 3 was grown from dimethyl sulfoxide (DMSO) solution. Three dimensional crystal structure of the grown crystal was determined by single crystal X-ray diffraction study. The complex crystallizes in the chiral orthorhombic space group P2 12 12 1. FTIR study was carried out in order to confirm the presence of the functional groups. UV-vis-NIR spectral studies show that the crystal is transparent in the wavelength range of 290-1100 nm. The microhardness test was carried out, and the load hardness was measured. Thermogravimetric and differential thermal analyses reveal the thermal stability of the crystal. Second harmonic generation efficiency of the powdered TPPOCdI, tested using Nd: YAG laser, is ∼0.65 times that of potassium dihydrogen orthophosphate.

  18. Quantum optical circulator controlled by a single chirally coupled atom

    Science.gov (United States)

    Scheucher, Michael; Hilico, Adèle; Will, Elisa; Volz, Jürgen; Rauschenbeutel, Arno

    2016-12-01

    Integrated nonreciprocal optical components, which have an inherent asymmetry between their forward and backward propagation direction, are key for routing signals in photonic circuits. Here, we demonstrate a fiber-integrated quantum optical circulator operated by a single atom. Its nonreciprocal behavior arises from the chiral interaction between the atom and the transversally confined light. We demonstrate that the internal quantum state of the atom controls the operation direction of the circulator and that it features a strongly nonlinear response at the single-photon level. This enables, for example, photon number–dependent routing and novel quantum simulation protocols. Furthermore, such a circulator can in principle be prepared in a coherent superposition of its operational states and may become a key element for quantum information processing in scalable integrated optical circuits.

  19. Robert Boyle's chiral crystal chemistry: computational re-evaluation of enantioselective adsorption on quartz.

    Science.gov (United States)

    Kahr, Bart; Chittenden, Brianne; Rohl, Andrew

    2006-02-01

    While searching for early examples of interactions of organic chromophores with minerals in the context of a systematic study of the process of dyeing crystals, we came across Robert Boyle's description of an experiment that may have been evidence of the enantioselective adsorption of a natural product, carminic acid (7-beta-D-glucopyranosyl-9,10-dihydro-3,5,6,8-tetrahydroxy-1-methyl-9,10-dioxo-2-anthracenecarboxylic acid), to the chiral surfaces of alpha-quartz, three centuries before such interactions became the subject of active chemical investigations. In order to determine whether Boyle did indeed observe enantioselective adsorption--albeit unbeknownst to him--we attempted to dye quartz with carminic acid according to his recipe. Quartz adsorbs carminic acid only because on heating it develops a network of microfissures that adsorb dye. This process depends on capillarity, not on specific non-covalent interactions; there is no evidence of enantioselectivity adsorption to heated crystals or enantioselective epitaxy to unheated crystals. These failures changed the focus of our inquiry: Why have almost all attempts to demonstrate the enantioselective adsorption of additives to quartz crystal surfaces been generally confounding and equivocal? In order to answer this question, we complement our experimental historical re-investigation with contemporary computational techniques for modeling crystal surface structure and the adsorption of additives. Minimizations of the energies associated with the adsorption of carminic acid to relaxed, hydrated d- and l-quartz {10(-)0} surfaces are analyzed in light of quartz's abysmal record as an enantioselective stationary phase.

  20. Central-to-axial chirality transfer revealed by liquid crystals: a combined experimental and computational approach for the determination of absolute configuration of carboxylic acids with an α chirality centre.

    Science.gov (United States)

    Ferrarini, Alberta; Ferroni, Fiammetta; Pieraccini, Silvia; Rosini, Carlo; Superchi, Stefano; Spada, Gian Piero

    2011-10-01

    The conversion into 6,7-dihydro-5H-dibenz[c,e]azepine (DAZ) N-protected amides is a viable route for the determination of the absolute configuration of chiral 2-substituted carboxylic acids. The biphenyl moiety of DAZ, besides being a probe of chirality for the electronic circular dichroism (ECD) spectroscopy, makes these systems suitable for configuration assignment by exploiting the chirality amplification which occurs in nematic liquid crystals. To assess the reliability of the liquid crystal method in detecting the absolute stereochemistry of chiral amides bound to a biphenyl group, we measured the helical twisting power of a series of DAZ-N-protected amides and compared these data with the results obtained from ECD measurements. We will show that the liquid crystal method, corroborated by HTP predictions, is trustworthy with our biphenyl derivatives, even when ECD spectra are ambiguous for the presence of aryl moieties displaying strong UV absorptions in the same range of the biphenyl chromophore.

  1. Solvent-induced chirality control in the enantioseparation of 1-phenylethylamine via diastereomeric salt formation.

    Science.gov (United States)

    Kodama, Koichi; Kimura, Yuria; Shitara, Hiroaki; Yasutake, Mikio; Sakurai, Rumiko; Hirose, Takuji

    2011-04-01

    Solvent-induced chirality control in the enantioseparation of 1-phenylethylamine 1 by N-(p-toluenesulfonyl)-(S)-phenylalanine 2 via diastereomeric salt formation was studied. (S)-1·(S)-2 was preferentially crystallized as a less-soluble salt from aqueous alcohol, while (R)-1·(S)-2 salt was mainly obtained by addition of solvents with a six-membered ring such as dioxane, cyclohexane, tetrahydropyran, and cyclohexene to 2-propanol. Further investigations were carried out from the viewpoints of molecular structures, optical rotation measurement, and X-ray crystallographic analyses. Crystallographic analyses have revealed that incorporation of the six-membered ring solvent molecule in (R)-1·(S)-2 without hydrogen bonds changed the molecular conformation of (S)-2 to stabilize the salt, which changed the selectivity of 1 in the enantioseparation.

  2. Solubility and some crystallization properties of conglomerate forming chiral drug guaifenesin in water.

    Science.gov (United States)

    Fayzullin, Robert R; Lorenz, Heike; Bredikhina, Zemfira A; Bredikhin, Alexander A; Seidel-Morgenstern, Andreas

    2014-10-01

    The solubility of 3-(2-methoxyphenoxy)-propane-1,2-diol, the well-known chiral drug guaifenesin 1, in water has been investigated by means of polythermal and isothermal approaches. It was found that the solubilities of racemic and enantiomeric diols rac- and (R)-1 depend strongly on temperature. The ternary phase diagram of the guaifenesin enantiomers in water in the temperature range between 10°C and 40°C was constructed. Clear evidence was obtained that rac-1 crystallizes as a stable conglomerate. The Meyerhoffer coefficient for the guaifenesin-water system is more than two and strongly depends on temperature. Neither crystalline hydrates nor polymorphs were detected within the range of conditions covered. Metastable zone width data with regard to primary nucleation were also collected for rac-1 and (R)-1. On the basis of the knowledge acquired, the resolution of racemic guaifenesin by preferential crystallization from solution could be realized successfully. © 2014 Wiley Periodicals, Inc. and the American Pharmacists Association.

  3. Chiral crystal of a C2v-symmetric 1,3-diazaaulene derivative showing efficient optical second harmonic generation

    KAUST Repository

    Ma, Xiaohua

    2011-03-01

    Achiral nonlinear optical (NLO) chromophores 1,3-diazaazulene derivatives, 2-(4â€-aminophenyl)-6-nitro-1,3-diazaazulene (APNA) and 2-(4â€-N,N-diphenylaminophenyl)-6-nitro-1,3-diazaazulene (DPAPNA), were synthesized with high yield. Despite the moderate static first hyperpolarizabilities (β0) for both APNA [(136 ± 5) à - 10-30 esu] and DPAPNA [(263 ± 20) à - 10-30 esu], only APNA crystal shows a powder efficiency of second harmonic generation (SHG) of 23 times that of urea. It is shown that the APNA crystallization driven cooperatively by the strong H-bonding network and the dipolar electrostatic interactions falls into the noncentrosymmetric P2 12121 space group, and that the helical supramolecular assembly is solely responsible for the efficient SHG response. To the contrary, the DPAPNA crystal with centrosymmetric P-1 space group is packed with antiparalleling dimmers, and is therefore completely SHG-inactive. 1,3-Diazaazulene derivatives are suggested to be potent building blocks for SHG-active chiral crystals, which are advantageous in high thermal stability, excellent near-infrared transparency and high degree of designing flexibility. © 2011 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2011 Optical crystals based on 1,3-diazaazulene derivatives are reported as the first example of organic nonlinear optical crystal whose second harmonic generation activity is found to originate solely from the chirality of their helical supramolecular orientation. The strong H-bond network forming between adjacent choromophores is found to act cooperatively with dipolar electrostatic interactions in driving the chiral crystallization of this material. Copyright © 2011 Wiley Periodicals, Inc.

  4. Polarization Control by Using Anisotropic 3D Chiral Structures

    CERN Document Server

    Chen, Menglin L N; Sha, Wei E I; Choy, Wallace C H; Itoh, Tatsuo

    2016-01-01

    Due to the mirror symmetry breaking, chiral structures show fantastic electromagnetic (EM) properties involving negative refraction, giant optical activity, and asymmetric transmission. Aligned electric and magnetic dipoles excited in chiral structures contribute to extraordinary properties. However, the chiral structures that exhibit n-fold rotational symmetry show limited tuning capability. In this paper, we proposed a compact, light, and highly tunable anisotropic chiral structure to overcome this limitation and realize a linear-to-circular polarization conversion. The anisotropy is due to simultaneous excitations of two different pairs of aligned electric and magnetic dipoles. The 3D omega-like structure, etched on two sides of one PCB board and connected by metallic vias, achieves 60% of linearto- circular conversion (transmission) efficiency at the operating frequency of 9.2 GHz. The desired 90-degree phase shift between the two orthogonal linear polarization components is not only from the finite-thick...

  5. Matched elastic constants for a perfect helical planar state and a fast switching time in chiral nematic liquid crystals.

    Science.gov (United States)

    Yu, Meina; Zhou, Xiaochen; Jiang, Jinghua; Yang, Huai; Yang, Deng-Ke

    2016-05-11

    Chiral nematic liquid crystals possess a self-assembled helical structure and exhibit unique selective reflection in visible and infrared light regions. Their optical properties can be electrically tuned. The tuning involves the unwinding and restoring of the helical structure. We carried out an experimental study on the mechanism of the restoration of the helical structure. We constructed chiral nematic liquid crystals with variable elastic constants by doping bent-dimers and studied their impact on the restoration. With matched twist and bend elastic constants, the helical structure can be restored dramatically fast from the field-induced homeotropic state. Furthermore, defects can be eliminated to produce a perfect planar state which exhibits high selective reflection.

  6. Chiral photochemistry

    CERN Document Server

    Inoue, Yoshihisa

    2004-01-01

    Direct Asymmetric Photochemistry with Circularly Polarized Light, H. RauCoherent Laser Control of the Handedness of Chiral Molecules, P. Brumer and M. ShapiroMagnetochiral Anisotropy in Asymmetric Photochemistry, G.L.J.A.RikkenEnantiodifferentiating Photosensitized Reactions, Y. InoueDiastereodifferentiating Photoreactions, N. Hoffmann and J.-P. PeteChirality in Photochromism, Y. Yokoyama and M. SaitoChiral Photochemistry with Transition Metal Complexes, S. Sakaki and T. HamadaTemplate-Induced Enantioselective Photochemical Reactions in S

  7. Disclination lines at homogeneous and heterogeneous colloids immersed in a chiral liquid crystal.

    Science.gov (United States)

    Melle, Michael; Schlotthauer, Sergej; Hall, Carol K; Diaz-Herrera, Enrique; Schoen, Martin

    2014-08-14

    In the present work we perform Monte Carlo simulations in the isothermal-isobaric ensemble to study defect topologies formed in a cholesteric liquid crystal due to the presence of a spherical colloidal particle. Topological defects arise because of the competition between anchoring at the colloidal surface and the local director. We consider homogeneous colloids with either local homeotropic or planar anchoring to validate our model by comparison with earlier lattice Boltzmann studies. Furthermore, we perform simulations of a colloid in a twisted nematic cell and discuss the difference between induced and intrinsic chirality on the formation of topological defects. We present a simple geometrical argument capable of describing the complex three-dimensional topology of disclination lines evolving near the surface of the colloid. The presence of a Janus colloid in a cholesteric host fluid reveals a rich variety of defect structures. Using the Frank free energy we analyze these defects quantitatively indicating a preferred orientation of the Janus colloid relative to the cholesteric helix.

  8. Chirality control by electric field in periodically poled MgO-doped lithium niobate

    CERN Document Server

    Shi, Lei; Chen, Xianfeng

    2012-01-01

    We study the chirality of periodically poled MgO-doped lithium niobate (MgO:PPLN) by electro-optic (EO) effect. It shows that optical propagation is reciprocal in MgO:PPLN when quasi-phase-matched (QPM) condition is satisfied, which is similar to natural optical active medium like quartz. We also demonstrate that the chirality of MgO:PPLN can be controlled by external electric field.

  9. Preparation of optical active polydiacetylene through gelating and the control of supramolecular chirality

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Achiral diacetylene 10,12-pentacosadinoic acid (PCDA) and a chiral low-molecular-weight organogelator could form co-gel in organic solvent and it could be polymerized in the presence of Zn(II) ion or in the corresponding xerogel under UV-irradiation. Optically active polydiacetylene (PDA) were subsequently obtained. Supramolecular chirality of PDA could be controlled by the chirality of gelators. Left-handed and right-handed helical fibers were obtained by using Land D-gelators in xerogels respectively, and CD spectra exhibited mirror-image circular dichroism. The PDA in xerogel exhibited typical blue-to-red transition responsive to the temperature and pH, while the supramolecular chirality of PDA showed a corresponding change.

  10. Absolute Asymmetric Synthesis : The Origin, Control, and Amplification of Chirality

    NARCIS (Netherlands)

    Feringa, Ben L.; van Delden, Richard A.

    1999-01-01

    One of the fundamental and intriguing aspects of life is the homochirality of the essential molecules. From the early days of stereochemistry, the origin of chirality in biological systems has been a challenge to the chemical sciences and numerous theories and experiments have been reported. Despite

  11. Crystalline and spin chiralities in multiferroics with langasite-type structure and Fe{sub 1–x}Co{sub x}Si crystals

    Energy Technology Data Exchange (ETDEWEB)

    Pikin, S. A., E-mail: pikin@ns.crys.ras.ru; Lyubutin, I. S.; Dudka, A. P. [Russian Academy of Sciences, Shubnikov Institute of Crystallography (Russian Federation)

    2015-09-15

    It is shown that, when magnetic ordering occurs in layered iron-containing langasites (sp. gr. P321), one of the reasons for spin chiralities of different signs is the presence of structural chirality (the existence of inversion twins), which, in turn, is due to the nonsymmetricity of these crystals. Spin helicoids arise in these multiferroics at split sites of Fe{sup 3+} ions below the Néel point. The direction of electric polarization vectors coincides with the direction of the magnetic helicoid axes because of the piezoelectric properties of these materials. Due to the magnetostriction effects, structural chirality wave vector k{sub z} exceeds the magnetic helicoid wave vector by a factor of 2: k{sub z} = 2q{sub z}. The temperatures of transitions to the chiral structural and chiral magnetic states may differ. In particular, if the structural transition initial temperature exceeds the magnetic transition temperature (Τ{sub U}> Τ{sub M}), structural displacements may arise in the absence of magnetism at Τ{sub M} < Τ < Τ{sub U}. In noncentrosymmetric Fe{sub 1–x}Co{sub x}Si crystals (sp. gr. P2{sub 1}3), which are not multiferroics, magnetic chirality is due to the Dzyaloshinski–Moriya interaction. The dependence of the moduli of incommensurate wave number of the corresponding helicoid on the atomic composition of the crystals under consideration is nonmonotonic.

  12. Chirality-controlled synthesis and macro-electronic applications of carbon nanotubes

    Science.gov (United States)

    Zhou, Chongwu

    Carbon nanotubes (CNTs) are promising materials for electronic applications due to their interesting properties. Chirality and electronic property controlled preparation are key challenges which need to be solved for practical use of CNTs in electronics. In this talk, I will first introduce our research on chirality-controlled synthesis of CNTs using metal-free carbon seeds. I will talk about chirality-controlled growth of SWCNTs using chirality-sorted nanotube seeds via a vapour phase epitaxy (VPE) cloning approach. Observations on the chirality-dependent growth rate and active lifetime of the nanotube seeds in the VPE process will be presented. Later, I will talk about selective growth of small diameter semiconducting CNTs using organic chemistry synthesized molecular seeds. In the second part, I will talk about the use of pre-separated, semiconducting-enriched CNTs for macro-electronics, printed electronics, and integrated circuits. Our work on the use of CNTs for thin-film transistors, CNT-IGZO hybrid CMOS circuits, and flexible, bendable, and transparent CNT devices and circuits will be presented. These works demonstrate the great potential of CNTs as advanced electronic materials.

  13. Chiral symmetry breaking by spatial confinement in tactoidal droplets of lyotropic chromonic liquid crystals.

    Science.gov (United States)

    Tortora, Luana; Lavrentovich, Oleg D

    2011-03-29

    In many colloidal systems, an orientationally ordered nematic (N) phase emerges from the isotropic (I) melt in the form of spindle-like birefringent tactoids. In cases studied so far, the tactoids always reveal a mirror-symmetric nonchiral structure, sometimes even when the building units are chiral. We report on chiral symmetry breaking in the nematic tactoids formed in molecularly nonchiral polymer-crowded aqueous solutions of low-molecular weight disodium cromoglycate. The parity is broken by twisted packing of self-assembled molecular aggregates within the tactoids as manifested by the observed optical activity. Fluorescent confocal microscopy reveals that the chiral N tactoids are located at the boundaries of cells. We explain the chirality induction as a replacement of energetically costly splay packing of the aggregates within the curved bipolar tactoidal shape with twisted packing. The effect represents a simple pathway of macroscopic chirality induction in an organic system with no molecular chirality, as the only requirements are orientational order and curved shape of confinement.

  14. Chiral symmetry breaking by spatial confinement in tactoidal droplets of lyotropic chromonic liquid crystals

    Science.gov (United States)

    Tortora, Luana; Lavrentovich, Oleg D.

    2011-01-01

    In many colloidal systems, an orientationally ordered nematic (N) phase emerges from the isotropic (I) melt in the form of spindle-like birefringent tactoids. In cases studied so far, the tactoids always reveal a mirror-symmetric nonchiral structure, sometimes even when the building units are chiral. We report on chiral symmetry breaking in the nematic tactoids formed in molecularly nonchiral polymer-crowded aqueous solutions of low-molecular weight disodium cromoglycate. The parity is broken by twisted packing of self-assembled molecular aggregates within the tactoids as manifested by the observed optical activity. Fluorescent confocal microscopy reveals that the chiral N tactoids are located at the boundaries of cells. We explain the chirality induction as a replacement of energetically costly splay packing of the aggregates within the curved bipolar tactoidal shape with twisted packing. The effect represents a simple pathway of macroscopic chirality induction in an organic system with no molecular chirality, as the only requirements are orientational order and curved shape of confinement. PMID:21402929

  15. Molecular chirality at surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Ernst, Karl-Heinz [Empa, Swiss Federal Laboratories for Materials Science and Technology, Ueberlandstrasse 129, 8600 Duebendorf (Switzerland); Organic Chemistry Institute, University Zurich, 8057 Zuerich (Switzerland)

    2012-11-15

    With the adsorption of larger molecules being increasingly tackled by surface scientists, the aspect of chirality often plays a role. This paper gives a topical review of molecular chirality at surfaces and gives a phenomenological overview of different aspects of adsorption and self-assembly of chiral and prochiral molecules and the principles of mirror-symmetry breaking at a surface. After a brief introduction into the history of molecular chirality and the important role it played for understanding the spatial structure of molecules, definitions of chirality are presented. Topics treated here are principle ways to create single chiral adsorbates, chiral ensembles, and monolayers by achiral molecules, adsorption of intrinsically chiral molecules at achiral and chiral surfaces, long-range symmetry breaking in two-dimensional (2D) crystals due to additional chiral bias, chiral restructuring of solid surfaces under the influence of chiral molecules, switching the handedness of adsorbates, and chirality at the liquid/air interface. An outlook onto further potential research directions and recommendations for further reading, including nonsurface-related sources of chiral topics completes this paper. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  16. Crystal structure of 2-{(R-[1-(4-bromophenylethyl]iminomethyl}-4-(phenyldiazenylphenol, a chiral photochromic Schiff base

    Directory of Open Access Journals (Sweden)

    Ryoji Moriwaki

    2015-11-01

    Full Text Available The title chiral photochromic Schiff base compound, C21H18BrN3O, was synthesized from (R-(+-1-(4-bromophenylethylamine and the salicylaldehyde of an azobenzene derivative. The molecule corresponds to the phenol–imine tautomer, the C=N and N—C bond distances being 1.285 (3 and 1.470 (3 Å, respectively. The diazenyl group adopts a trans form, with an N=N distance of 1.256 (3 Å. The hydroxy group is involved in intramolecular O—H...N hydrogen bonding. In the crystal, C—H...π interactions consolidate the crystal packing of one-dimensional chains, which exhibits short intermolecular Br...C contacts of 3.400 (3 Å.

  17. Recent Advances in Substrate-Controlled Asymmetric Induction Derived from Chiral Pool α-Amino Acids for Natural Product Synthesis.

    Science.gov (United States)

    Paek, Seung-Mann; Jeong, Myeonggyo; Jo, Jeyun; Heo, Yu Mi; Han, Young Taek; Yun, Hwayoung

    2016-07-21

    Chiral pool α-amino acids have been used as powerful tools for the total synthesis of structurally diverse natural products. Some common naturally occurring α-amino acids are readily available in both enantiomerically pure forms. The applications of the chiral pool in asymmetric synthesis can be categorized prudently as chiral sources, devices, and inducers. This review specifically examines recent advances in substrate-controlled asymmetric reactions induced by the chirality of α-amino acid templates in natural product synthesis research and related areas.

  18. Electric-field-induced transport of microspheres in the isotropic and chiral nematic phase of liquid crystals

    Science.gov (United States)

    Oh, Jiyoung; Gleeson, Helen F.; Dierking, Ingo

    2017-02-01

    The application of an electric field to microspheres suspended in a liquid crystal causes particle translation in a plane perpendicular to the applied field direction. Depending on applied electric field amplitude and frequency, a wealth of different motion modes may be observed above a threshold, which can lead to linear, circular, or random particle trajectories. We present the stability diagram for these different translational modes of particles suspended in the isotropic and the chiral nematic phase of a liquid crystal and investigate the angular velocity, circular diameter, and linear velocity as a function of electric field amplitude and frequency. In the isotropic phase a narrow field amplitude-frequency regime is observed to exhibit circular particle motion whose angular velocity increases with applied electric field amplitude but is independent of applied frequency. The diameter of the circular trajectory decreases with field amplitude as well as frequency. In the cholesteric phase linear as well as circular particle motion is observed. The former exhibits an increasing velocity with field amplitude, while decreasing with frequency. For the latter, the angular velocity exhibits an increase with field amplitude and frequency. The rotational sense of the particles on a circular trajectory in the chiral nematic phase is independent of the helicity of the liquid crystalline structure, as is demonstrated by employing a cholesteric twist inversion compound.

  19. Modified High Frequency Radial Spin Wave Mode Spectrum in a Chirality-Controlled Nanopillar

    Science.gov (United States)

    Kolthammer, J. E.; Rudge, J.; Choi, B. C.; Hong, Y. K.

    2016-09-01

    Circular magnetic spin valve nanopillars in a dual vortex configuration have dynamic characteristics strongly dependent on the interlayer dipole coupling. We report here on frequency domain properties of such nanopillars obtained by micromagnetic simulations. After the free layer is chirality switched with spin transfer torque, a radial spin wave eigenmode spectrum forms in the free layer with unusually large edge amplitude. The structure of these modes indicate a departure from the magnetostatic processes typically observed experimentally and treated analytically in low aspect ratio isolated disks. Our findings give new details of dynamic chirality control and relxation in nanopillars and raise potential signatures for experiments.

  20. Synthesis, multiphase characterization, and helicity control in chiral DACH-linked oligothiophenes.

    Science.gov (United States)

    Melucci, Manuela; Barbarella, Giovanna; Gazzano, Massimo; Cavallini, Massimiliano; Biscarini, Fabio; Bongini, Alessandro; Piccinelli, Fabio; Monari, Magda; Bandini, Marco; Umani-Ronchi, Achille; Biscarini, Paolo

    2006-09-25

    A new class of chiral oligothiophenes is described. Mono-, bi-, ter-, and quarterthiophenes have been linked to enantiopure trans-1,2-cyclohexanediamine (DACH) via diamino or diimino moieties. The stereochemistry of DACH, the type of linker, and oligothiophene size determine the conformational flexibility of these molecules and consequently their molecular and supramolecular helicity in solution and in the solid state. The case of diaminobis(bithiophene), which inverts helicity and shows chiral amplification in the transition from solution to film, is described in detail. Based on the combined use of circular dichroism in solution and in the solid state, single-crystal/thin-film X-ray diffraction, and polarized optical microscopy, a working mechanism has been proposed to explain this unexpected behavior.

  1. Dynamic control and amplification of molecular chirality by circular polarized light

    NARCIS (Netherlands)

    Huck, N.P.M.; Jager, W.F.; de Lange, B.; Feringa, B.L.

    1996-01-01

    The enantiomers of a racemic photoresponsive material represent two distinct states that can be modulated with irradiation at a single wavelength by changing the handedness of the light, Dynamic control over molecular chirality was obtained by the interconversion of enantiomers of helically shaped m

  2. Dynamic control and amplification of molecular chirality by circular polarized light

    NARCIS (Netherlands)

    Huck, N.P.M.; Jager, W.F.; de Lange, B.; Feringa, B.L.

    1996-01-01

    The enantiomers of a racemic photoresponsive material represent two distinct states that can be modulated with irradiation at a single wavelength by changing the handedness of the light, Dynamic control over molecular chirality was obtained by the interconversion of enantiomers of helically shaped

  3. Chiral induction in phenanthroline-derived oligoamide foldamers: an acid- and base-controllable switch in helical molecular strands.

    Science.gov (United States)

    Hu, Hai-Yu; Xiang, Jun-Feng; Yang, Yong; Chen, Chuan-Feng

    2008-03-20

    A series of phenanthroline-derived oligoamides bearing a chiral (R)-phenethylamino end group were synthesized that displayed chiral helical induction and subsequently formed one-hand helical foldamers in solution. Moreover, an acid- and base-controllable switch in the helical molecular strands was observed, which has been demonstrated by NMR, UV-vis, and circular dichroism spectroscopy.

  4. Model predictive control of MSMPR crystallizers

    Science.gov (United States)

    Moldoványi, Nóra; Lakatos, Béla G.; Szeifert, Ferenc

    2005-02-01

    A multi-input-multi-output (MIMO) control problem of isothermal continuous crystallizers is addressed in order to create an adequate model-based control system. The moment equation model of mixed suspension, mixed product removal (MSMPR) crystallizers that forms a dynamical system is used, the state of which is represented by the vector of six variables: the first four leading moments of the crystal size, solute concentration and solvent concentration. Hence, the time evolution of the system occurs in a bounded region of the six-dimensional phase space. The controlled variables are the mean size of the grain; the crystal size-distribution and the manipulated variables are the input concentration of the solute and the flow rate. The controllability and observability as well as the coupling between the inputs and the outputs was analyzed by simulation using the linearized model. It is shown that the crystallizer is a nonlinear MIMO system with strong coupling between the state variables. Considering the possibilities of the model reduction, a third-order model was found quite adequate for the model estimation in model predictive control (MPC). The mean crystal size and the variance of the size distribution can be nearly separately controlled by the residence time and the inlet solute concentration, respectively. By seeding, the controllability of the crystallizer increases significantly, and the overshoots and the oscillations become smaller. The results of the controlling study have shown that the linear MPC is an adaptable and feasible controller of continuous crystallizers.

  5. Dynamic control of chirality and self-assembly of double-stranded helicates with light.

    Science.gov (United States)

    Zhao, Depeng; van Leeuwen, Thomas; Cheng, Jinling; Feringa, Ben L

    2017-03-01

    Helicity switching in biological and artificial systems is a fundamental process that allows for the dynamic control of structures and their functions. In contrast to chemical approaches to responsive behaviour in helicates, the use of light as an external stimulus offers unique opportunities to invert the chirality of helical structures in a non-invasive manner with high spatiotemporal precision. Here, we report that unidirectional rotary motors with connecting oligobipyridyl ligands, which can dynamically change their chirality upon irradiation, assemble into metal helicates that are responsive to light. The motor function controls the self-assembly process as well as the helical chirality, allowing switching between oligomers and double-stranded helicates with distinct handedness. The unidirectionality of the light-induced motion governs the sequence of programmable steps, enabling the highly regulated self-assembly of fully responsive helical structures. This discovery paves the way for the future development of new chirality-dependent photoresponsive systems including smart materials, enantioselective catalysts and light-driven molecular machines.

  6. Dynamic control of chirality and self-assembly of double-stranded helicates with light

    Science.gov (United States)

    Zhao, Depeng; van Leeuwen, Thomas; Cheng, Jinling; Feringa, Ben L.

    2016-11-01

    Helicity switching in biological and artificial systems is a fundamental process that allows for the dynamic control of structures and their functions. In contrast to chemical approaches to responsive behaviour in helicates, the use of light as an external stimulus offers unique opportunities to invert the chirality of helical structures in a non-invasive manner with high spatiotemporal precision. Here, we report that unidirectional rotary motors with connecting oligobipyridyl ligands, which can dynamically change their chirality upon irradiation, assemble into metal helicates that are responsive to light. The motor function controls the self-assembly process as well as the helical chirality, allowing switching between oligomers and double-stranded helicates with distinct handedness. The unidirectionality of the light-induced motion governs the sequence of programmable steps, enabling the highly regulated self-assembly of fully responsive helical structures. This discovery paves the way for the future development of new chirality-dependent photoresponsive systems including smart materials, enantioselective catalysts and light-driven molecular machines.

  7. Shells and heart: are human laterality and chirality of snails controlled by the same maternal genes?

    Science.gov (United States)

    Oliverio, Marco; Digilio, Maria Cristina; Versacci, Paolo; Dallapiccola, Bruno; Marino, Bruno

    2010-10-01

    The body of most animals display left-right asymmetry of internal organs. Alteration of such asymmetry results in severe congenital defects particularly affecting the cardiovascular system. The earliest known genes involved in asymmetry, the Nodal signalling cascade, are expressed asymmetrically during embryonic development. Nodal was discovered in the mouse, but orthologs (also involved in left-right specification) were reported in ascidians, sea-urchins, and snails. Mutations in Nodal-pathway genes cause alteration of several aspects of chirality, but not entirely mirror phenotypes of the body. Other factors upstream of nodal must be involved in the generation of left-right asymmetry. In snails, breeding experiments have demonstrated that chirality is controlled by a nuclear gene with maternal effect. Given the available evidence, we propose that an evolutionarily conserved genetic basis of chirality (the same that controls left-right asymmetry in snails) is a major synapomorphy of the Bilateria. This hypothesis fits with the observation that: (a) the proportion of patients with heterotaxy and a detected mutation in a gene of the Nodal cascade is actually low, and (b) horizontal recurrence of laterality defects is remarkably more frequent than vertical recurrence, and includes a notable number of affected sibs and/or repeated abortions from unaffected mothers. Identification of the maternal gene(s) involved will allow for the identification of homozygous females at risk of having affected children and spontaneous abortions, and would provide a general medical framework for understanding the genetics of most alterations of chirality.

  8. Molecular model for chirality phenomena.

    Science.gov (United States)

    Latinwo, Folarin; Stillinger, Frank H; Debenedetti, Pablo G

    2016-10-21

    Chirality is a hallmark feature for molecular recognition in biology and chemical physics. We present a three-dimensional continuum model for studying chirality phenomena in condensed phases using molecular simulations. Our model system is based upon a simple four-site molecule and incorporates non-trivial kinetic behavior, including the ability to switch chirality or racemize, as well as thermodynamics arising from an energetic preference for specific chiral interactions. In particular, we introduce a chiral renormalization parameter that can locally favor either homochiral or heterochiral configurations. Using this model, we explore a range of chirality-specific phenomena, including the kinetics of chiral inversion, the mechanism of spontaneous chiral symmetry breaking in the liquid, chirally driven liquid-liquid phase separation, and chiral crystal structures.

  9. Biomimetic synthesized chiral mesoporous silica: Structures and controlled release functions as drug carrier

    Energy Technology Data Exchange (ETDEWEB)

    Li, Jing; Xu, Lu, E-mail: xl2013109@163.com; Yang, Baixue; Bao, Zhihong; Pan, Weisan; Li, Sanming, E-mail: li_sanming2013@163.com

    2015-10-01

    This work initially illustrated the formation mechanism of chiral mesoporous silica (CMS) in a brand new insight named biomimetic synthesis. Three kinds of biomimetic synthesized CMS (B-CMS, including B-CMS1, B-CMS2 and B-CMS3) were prepared using different pH or stirring rate condition, and their characteristics were tested with transmission electron microscope and small angle X-ray diffraction. The model drug indomethacin was loaded into B-CMS and drug loading content was measured using ultraviolet spectroscopy. The result suggested that pH condition influenced energetics of self-assembly process, mainly packing energetics of the surfactant, while stirring rate was the more dominant factor to determine particle length. In application, indomethacin loading content was measured to be 35.3%, 34.8% and 35.1% for indomethacin loaded B-CMS1, indomethacin loaded B-CMS2 and indomethacin loaded B-CMS3. After loading indomethacin into B-CMS carriers, surface area, pore volume and pore diameter of B-CMS carriers were reduced. B-CMS converted crystalline state of indomethacin to amorphous state, leading to the improved indomethacin dissolution. B-CMS1 controlled drug release without burst-release, while B-CMS2 and B-CMS3 released indomethacin faster than B-CMS1, demonstrating that the particle length, the ordered lever of multiple helixes, the curvature degree of helical channels and pore diameter greatly contributed to the release behavior of indomethacin loaded B-CMS. - Highlights: • Chiral mesoporous silica was synthesized using biomimetic method. • pH influenced energetics of self-assembly process of chiral mesoporous silica. • Stirring rate determined the particle length of chiral mesoporous silica. • Controlled release behaviors of chiral mesoporous silica varied based on structures.

  10. Controlling THz and far-IR waves with chiral and bianisotropic metamaterials

    Directory of Open Access Journals (Sweden)

    Kenanakis George

    2015-01-01

    Full Text Available Chiral and bianisotropic metamaterials, where coupling of magnetic and electric phenomena plays an important role, offer advanced possibilities for the control and manipulation of electromagnetic waves. Such a control is particularly useful in the THz and far-IR region where natural materials do not show strong response and thus they are not offered as components for a direct realization of electromagnetic wave manipulation. Among the most useful and important capabilities of chiral and bianisotropic metamaterials is the advanced control of the wave polarization that they offer, including giant polarization rotation, conversion, filtering, absorption, etc. In this paper we review our recent work demonstrating some of those capabilities, in a variety of structures, both planar and 3D-bulk ones. The structures presented show, among others, large optical activity, tunable/switchable wave ellipticity, and polarization-dependent asymmetric transmission.

  11. Dynamic control of asymmetric electromagnetic wave transmission by active chiral metamaterial

    Science.gov (United States)

    Chen, Ke; Feng, Yijun; Cui, Li; Zhao, Junming; Jiang, Tian; Zhu, Bo

    2017-02-01

    The asymmetric transmission of electromagnetic (EM) wave can be fully manipulated by chiral metamaterials, but little can achieve real-time and high efficient tunability due to challenges in practically deployable solutions. Here, we proposed a new scheme for flexibly and dynamically controlling the asymmetric EM wave transmission at microwave frequencies using planar metamaterial of deep subwavelength thickness incorporated with active components of PIN diodes. The asymmetric transmission of linearly polarized EM wave exhibits a high efficiency and a pronounced real-time continuous tunability controlled by the external stimulation of voltage biasing. In addition, the asymmetric transmission effect can be well preserved at large oblique incident angle up to ±70°. The design principle and EM performance are validated by both full wave simulations and experimental measurements. Such dynamically controllable chiral metamaterial may provide robust and flexible approach to manipulate EM wave propagation, as well as to facilitate EM device integration to create diverse functionalities.

  12. Dynamic control of asymmetric electromagnetic wave transmission by active chiral metamaterial

    Science.gov (United States)

    Chen, Ke; Feng, Yijun; Cui, Li; Zhao, Junming; Jiang, Tian; Zhu, Bo

    2017-01-01

    The asymmetric transmission of electromagnetic (EM) wave can be fully manipulated by chiral metamaterials, but little can achieve real-time and high efficient tunability due to challenges in practically deployable solutions. Here, we proposed a new scheme for flexibly and dynamically controlling the asymmetric EM wave transmission at microwave frequencies using planar metamaterial of deep subwavelength thickness incorporated with active components of PIN diodes. The asymmetric transmission of linearly polarized EM wave exhibits a high efficiency and a pronounced real-time continuous tunability controlled by the external stimulation of voltage biasing. In addition, the asymmetric transmission effect can be well preserved at large oblique incident angle up to ±70°. The design principle and EM performance are validated by both full wave simulations and experimental measurements. Such dynamically controllable chiral metamaterial may provide robust and flexible approach to manipulate EM wave propagation, as well as to facilitate EM device integration to create diverse functionalities. PMID:28202903

  13. Dynamic control of asymmetric electromagnetic wave transmission by active chiral metamaterial.

    Science.gov (United States)

    Chen, Ke; Feng, Yijun; Cui, Li; Zhao, Junming; Jiang, Tian; Zhu, Bo

    2017-02-16

    The asymmetric transmission of electromagnetic (EM) wave can be fully manipulated by chiral metamaterials, but little can achieve real-time and high efficient tunability due to challenges in practically deployable solutions. Here, we proposed a new scheme for flexibly and dynamically controlling the asymmetric EM wave transmission at microwave frequencies using planar metamaterial of deep subwavelength thickness incorporated with active components of PIN diodes. The asymmetric transmission of linearly polarized EM wave exhibits a high efficiency and a pronounced real-time continuous tunability controlled by the external stimulation of voltage biasing. In addition, the asymmetric transmission effect can be well preserved at large oblique incident angle up to ±70°. The design principle and EM performance are validated by both full wave simulations and experimental measurements. Such dynamically controllable chiral metamaterial may provide robust and flexible approach to manipulate EM wave propagation, as well as to facilitate EM device integration to create diverse functionalities.

  14. Chirality and helicity of poly-benzyl-L-glutamate in liquid crystals and a wave structure that mimics collagen helicity in crimp

    Directory of Open Access Journals (Sweden)

    Vidal Benedicto de Campos

    2001-01-01

    Full Text Available Ideal biocompatible polymers must show a mimetic superstructure with biological supra-organization. Collagen-rich structures like tendons and ligaments are materials with various levels of order, from molecules to bundles of fibers, which affect their biomechanical properties and cellular interactions. Poly-benzyl-L-glutamate (PBLG displaying helicity was used here to test the development of wave-like structures as those occurring in collagen fibers. Birefringence of PBLG under various crystallization conditions was studied with a lambda/4 compensator according to Sénarmont. Qualitative observations were plainly sufficient to conclude that the PBLG fibrils were supra-organized helically as a chiral object. During crystallization stretched PBLG formed a helical superstructure with characteristic striation resembling waves (crimp. Supported by optical anisotropy findings, a twisted grain boundary liquid crystal type is proposed as a transition phase in the formation of the PBLG chiral object. A similarity with the wavy organization (crimp of collagen bundles is proposed.

  15. Catalyst self-adaptation in conjugate addition to nitroalkenes and nitroacrylates: instant chirality control in diphenylmethane-based phosphoramidite ligands.

    Science.gov (United States)

    Wakabayashi, Kazuki; Aikawa, Kohsuke; Kawauchi, Susumu; Mikami, Koichi

    2008-04-16

    The tropos diphenylmethane-based phosphoramidite ligand (A) provides high catalytic activity and enantioselectivity in the Cu catalysis of conjugate addition to nitroalkenes and nitroacrylate, by virtue of instant chirality control in A.

  16. Chiral THz metamaterial with tunable optical activity

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Jiangfeng [Los Alamos National Laboratory; Taylor, Antoinette [Los Alamos National Laboratory; O' Hara, John [Los Alamos National Laboratory; Chowdhury, Roy [Los Alamos National Laboratory; Zhao, Rongkuo [IOWA STATE UNIV; Soukoullis, Costas M [IOWA STATE UNIV

    2010-01-01

    Optical activity in chiral metamaterials is demonstrated in simulation and shows actively tunable giant polarization rotation at THz frequencies. Electric current distributions show that pure chirality is achieved by our bi-Iayer chiral metamaterial design. The chirality can be optically controlled by illumination with near-infrared light. Optical activity, occurring in chiral materials such as DNA, sugar and many other bio-molecules, is a phenomenon of great importance to many areas of science including molecular biology, analytical chemistry, optoelectronics and display applications. This phenomenon is well understood at an effective medium level as a magnetic/electric moment excited by the electric/magnetic field of the incident electromagnetic (EM) wave. Usually, natural chiral materials exhibit very weak optical activity e.g. a gyrotropic quartz crystal. The optical activity of chiral metamaterials, however, can be five orders of magnitude stronger. Chiral metamaterials are made of sub-wavelength resonators lacking symmetry planes. The asymmetry allows magnetic moments to be excited by the electric field of the incident EM wave and vice versa. Recently, chiral metamaterials have been demonstrated and lead to prospects in giant optical activity, circular dichroism, negative refraction and reversing the Casmir force. These fascinating optical properties require strong chirality, which may be designed through the microscopic structure of chiral metamaterials. However, these metamaterials have a fixed response function, defined by the geometric structuring, which limits their ability to manipulate EM waves. Active metamaterials realize dynamic control of response functions and have produced many influential applications such as ultra-fast switching devices, frequency and phase modulation and memory devices. Introducing active designs to chiral metamaterials will give additional freedom in controlling the optical activity, and therefore enable dynamic manipulation

  17. Crystallization and solid-state reaction as a route to asymmetric synthesis from achiral starting materials.

    Science.gov (United States)

    Green, B S; Lahav, M

    1975-10-29

    Many molecules which are achiral can crystallize in chiral (enantiomorphic) crystals and, under suitable conditions, crystals of only one chirality may be obtained. The formation of right- or left-handed crystals in excess is equally probable. Lattice-controlled (topochemical) photochemical or thermal solid-state reactions may then afford stable, optically active products. In the presence of the chiral products, achiral reactants may preferentially produce crystals of one chirality, leading to a feedback mechanism for the generation and amplification of optical activity. Amplification of optical activity can also be achieved by solid-state reactions. The optical synthesis of biologically relevant compounds by such routes may be envisaged.

  18. Remote Control of the Planar Chirality in Peptide-Bound Metallomacrocycles and Dynamic-to-Static Planar Chirality Control Triggered by Solvent-Induced 3(10)-to-α-Helix Transitions.

    Science.gov (United States)

    Mamiya, Fumihiko; Ousaka, Naoki; Yashima, Eiji

    2015-11-23

    The dynamic planar chirality in a peptide-bound Ni(II)-salphen-based macrocycle can be remotely controlled. First, a right-handed (P)-3(10)-helix is induced in the dynamic helical oligopeptides by a chiral amino acid residue far from the macrocyclic framework. The induced planar chirality remains dynamic in chloroform and acetonitrile, but is almost completely locked in fluoroalcohols as a result of the solvent-induced transition of the peptide chains from a 3(10)-helix to a wider α-helix, which freezes the rotation of the pendant peptide units around the macrocycle.

  19. Metal Complexes:Novel Chiral Dopants with High Helical Twisting Power in Liquid Crystals

    Institute of Scientific and Technical Information of China (English)

    Manfred; Braun; R.Fleischer; A.Hahn; M.Engelmann; S.Schlecht

    2007-01-01

    1 Introduction A particularly efficient and elegant route to chiral mesophases is based on the addition of small amounts of an enantiomerically pure dopant to a nematic phase so that the latter is converted into a cholesteric phase(See Fig.1).Fig.1 A nematic phase is converted into a cholesteric phase Fig.2 Bis-chelated imine-alkoxy-titanium complexes2 ExperimetalBis-chelated imine-alkoxy-titanium complexes like 1 and 2 (Fig.2) have been synthesizedstarting from triphenyl-substituted aminoethanols, T...

  20. Studies on lithium L-ascorbate dihydrate: An interesting chiral nonlinear optical crystal

    Energy Technology Data Exchange (ETDEWEB)

    Raghavendra Rao, K., E-mail: krrao@physics.iisc.ernet.in [Department of Physics, Indian Institute of Science, Bangalore 560012 (India); Bhat, H.L. [Department of Physics, Indian Institute of Science, Bangalore 560012 (India); Centre for Soft Matter Research, Jalahalli, Bangalore 560013 (India); Elizabeth, Suja [Department of Physics, Indian Institute of Science, Bangalore 560012 (India)

    2013-01-15

    Lithium L-Ascorbate dihydrate (LLA) is a new metal organic nonlinear optical crystal belonging to the saccharide family. Single crystals of LLA were grown from aqueous solution. Solubility of the crystal has a positive temperature coefficient facilitating growth by slow cooling. Rietveld refinement was used to confirm the phase formation. The crystal has prismatic habit with (010), (001) and (10-1) prominent faces. Thermal analysis shows that the crystal is stable up to 102 Degree-Sign C. Transmission spectrum of the crystal extends from 302 nm to 1600 nm. Dielectric spectroscopic analysis revealed Cole-Cole behaviour and prominent piezoelectric resonance peaks were observed in the range of 100-200 kHz. Second harmonic generation (SHG) conversion efficiency of up to 2.56 times that of a phase matched KDP crystal was achieved when the (010) plate of LLA single crystal was rotated about the +ve c axis, by 9.4 Degree-Sign in the clockwise direction. We also observed SHG conical sections which were attributed to noncollinear phase matching. The observation of the third conical section suggests very high birefringence and large nonlinear coefficients. A detailed study of surface laser damage showed that the crystal has high multiple damage thresholds of 9.7 GW cm{sup -2} and 4.2 GW cm{sup -2} at 1064 nm and 532 nm radiation respectively. Highlights: Black-Right-Pointing-Pointer Large nonlinear optical lithium L-ascorbate dihydrate crystals. Black-Right-Pointing-Pointer Crystals exhibit dielectric Cole-Cole behaviour and piezoelectric resonance. Black-Right-Pointing-Pointer Intense collinear and noncollinear second harmonic generation is observed. Black-Right-Pointing-Pointer Crystals possess high surface laser damage thresholds.

  1. Deracemization of Axially Chiral Nicotinamides by Dynamic Salt Formation with Enantiopure Dibenzoyltartaric Acid (DBTA

    Directory of Open Access Journals (Sweden)

    Fumitoshi Yagishita

    2013-11-01

    Full Text Available Dynamic atroposelective resolution of chiral salts derived from oily racemic nicotinamides and enantiopure dibenzoyltartaric acid (DBTA was achieved by crystallization. The absolute structures of the axial chiral nicotinamides were determined by X-ray structural analysis. The chirality could be controlled by the selection of enantiopure DBTA as a chiral auxiliary. The axial chirality generated by dynamic salt formation was retained for a long period after dissolving the chiral salt in solution even after removal of the chiral acid. The rate of racemization of nicotinamides could be controlled based on the temperature and solvent properties, and that of the salts was prolonged compared to free nicotinamides, as the molecular structure of the pyridinium ion in the salts was different from that of acid-free nicotinamides.

  2. The helical phase of chiral nematic liquid crystals as the Bianchi VII(0) group manifold

    CERN Document Server

    Gibbons, G W

    2011-01-01

    We show that the optical structure of the helical phase of a chiral nematic is naturally associated with the Bianchi VII(0) group manifold. The Joets-Ribotta metric governing propagation of the extraordinary rays is invariant under the simply transitive action of the universal cover of the three dimensional Euclidean group of two dimensions. Thus extraordinary light rays are geodesics of a left-invariant metric on this Bianchi type VII(0) group. We are able to solve by separation of variables both the wave equation and the Hamilton-Jacobi equation for this metric. The former reduces to Mathieu's equation and the later to the quadrantal pendulum equation. We further discuss Maxwell's equations for uniaxial optical materials where the configuration is invariant under a group action. The material is not assumed to be impedance matched, thus going beyond the usual scope of transformation optics. We show that for a chiral nematic in its helical phase Maxwell's equations reduce to a generalised Mathieu equation. Ou...

  3. Chirality versus dichroism: Competition and role in conical diffraction displayed from the Nd:Bi2ZnOB2O6 acentric biaxial laser crystal

    Science.gov (United States)

    Brenier, A.; Majchrowski, A.; Michalski, E.

    2017-10-01

    We have grown acentric chiral Nd-doped BZBO single crystals by the Kyropoulos method, cut perpendicular to the optical axis. With a focused beam at wavelengths in the spectral domain of transparency with various polarizations, the conoscopy patterns revealed the specific role of chirality: disappearance of the optical axis replaced by two C-directions, linear polarization rotation and spiral patterns. The specific rotatory power was measured. The output near field exhibits the influence of chirality on the conical diffraction. Going to wavelengths in the spectral domain of absorption corresponding to the 4I9/2 → 4F5/2 Nd3+ transition, we first studied the chirality/dichroism competition from propagation along the C-directions, characterizing the circular and elliptic eigen-modes. We exhibited the wavelengths at which the ellipse degenerates linearly, signature of the chirality/dichroism balancing. The second aspect is the existence of the optical axis which can be restored if the dichroism is high enough. In this case a singular Voigt wave can propagate. From the experimental determination of the optical parameters, a theoretical description has been proposed, leading to quite well agreement in the far field (conoscopy) and in the near field (conical diffraction).

  4. Regulating the modulus of a chiral liquid crystal polymer network by light.

    Science.gov (United States)

    Kumar, Kamlesh; Schenning, Albertus P H J; Broer, Dirk J; Liu, Danqing

    2016-04-01

    We report a novel way to modulate the elastic modulus of azobenzene containing liquid crystal networks (LCNs) by exposure to light. The elastic modulus can cycle between different levels by controlling the illumination conditions. Exposing the polymer network to UV light near the trans absorption band of azobenzene gives a small reduction of the glass transition temperature thereby lowering the modulus. The addition of blue light addressing the cis absorption band surprisingly amplifies this effect. The continuous oscillatory effects of the trans-to-cis isomerization of the azobenzene overrule the overall net cis conversion. The influence on the chain dynamics of the network is demonstrated by dynamic mechanical thermal analysis which shows a large shift of the glass transition temperature and a modulus decrease by more than two orders of magnitude. The initial high modulus and the glassy state are recovered within a minute in the dark by switching off the light sources, despite the observation that azobenzene is still predominantly in its cis state. Based on these new findings, we are able to create a shape memory polymer LCN film at room temperature using light.

  5. A Nodal-independent and tissue-intrinsic mechanism controls heart-looping chirality

    Science.gov (United States)

    Noël, Emily S.; Verhoeven, Manon; Lagendijk, Anne Karine; Tessadori, Federico; Smith, Kelly; Choorapoikayil, Suma; den Hertog, Jeroen; Bakkers, Jeroen

    2013-11-01

    Breaking left-right symmetry in bilateria is a major event during embryo development that is required for asymmetric organ position, directional organ looping and lateralized organ function in the adult. Asymmetric expression of Nodal-related genes is hypothesized to be the driving force behind regulation of organ laterality. Here we identify a Nodal-independent mechanism that drives asymmetric heart looping in zebrafish embryos. In a unique mutant defective for the Nodal-related southpaw gene, preferential dextral looping in the heart is maintained, whereas gut and brain asymmetries are randomized. As genetic and pharmacological inhibition of Nodal signalling does not abolish heart asymmetry, a yet undiscovered mechanism controls heart chirality. This mechanism is tissue intrinsic, as explanted hearts maintain ex vivo retain chiral looping behaviour and require actin polymerization and myosin II activity. We find that Nodal signalling regulates actin gene expression, supporting a model in which Nodal signalling amplifies this tissue-intrinsic mechanism of heart looping.

  6. 3D spirals with controlled chirality fabricated using metal-assisted chemical etching of silicon.

    Science.gov (United States)

    Hildreth, Owen J; Fedorov, Andrei G; Wong, Ching Ping

    2012-11-27

    The ability to fabricate 3D spiraling structures using metal-assisted chemical etching (MaCE) is one of the unique advantages of MaCE over traditional etching methods. However, control over the chirality of the spiraling structures has not been established. In this work, a systematic parametric study was undertaken for MaCE of star-shaped catalysts, examining the influence of arm shape, arm length, number of arms, center core diameter, and catalyst thickness on the rotation direction. This data was used to identify a set of geometric parameters that reliably induce rotation in a predefined direction such that large arrays of 3D spiraling structures can be fabricated with the same chirality. Electroless deposition into the MaCE template was used to examine the full etch path of the catalyst and an experimental fit was established to control rotation angle by adjusting the catalyst's center core diameter. The ability to fabricate large arrays of 3D spiraling structures with predefined chirality could have important applications in photonics and optoelectronics.

  7. Controlled growth of semiconductor crystals

    Science.gov (United States)

    Bourret-Courchesne, Edith D.

    1992-01-01

    A method for growth of III-V, II-VI and related semiconductor single crystals that suppresses random nucleation and sticking of the semiconductor melt at the crucible walls. Small pieces of an oxide of boron B.sub.x O.sub.y are dispersed throughout the comminuted solid semiconductor charge in the crucible, with the oxide of boron preferably having water content of at least 600 ppm. The crucible temperature is first raised to a temperature greater than the melt temperature T.sub.m1 of the oxide of boron (T.sub.m1 =723.degree. K. for boron oxide B.sub.2 O.sub.3), and the oxide of boron is allowed to melt and form a reasonably uniform liquid layer between the crucible walls and bottom surfaces and the still-solid semiconductor charge. The temperature is then raised to approximately the melt temperature T.sub.m2 of the semiconductor charge material, and crystal growth proceeds by a liquid encapsulated, vertical gradient freeze process. About half of the crystals grown have a dislocation density of less than 1000/cm.sup.2. If the oxide of boron has water content less than 600 ppm, the crucible material should include boron nitride, a layer of the inner surface of the crucible should be oxidized before the oxide of boron in the crucible charge is melted, and the sum of thicknesses of the solid boron oxide layer and liquid boron oxide layer should be at least 50 .mu.m.

  8. Electric-field-controlled suppression of Walker breakdown and chirality switching in magnetic domain wall motion

    Science.gov (United States)

    Chen, Hong-Bo; Li, You-Quan

    2016-07-01

    We theoretically study the dynamics of a magnetic domain wall controlled by an electric field in the presence of the spin flexoelectric interaction. We reveal that this interaction generates an effective spin torque and results in significant changes in the current-driven domain wall motion. In particular, the electric field can stabilize the domain wall motion, leading to strong suppression of the current-induced Walker breakdown and thus allowing a higher maximum wall velocity. We can furthermore use this electric-field control to efficiently switch the chirality of a moving domain wall in the steady regime.

  9. Magnetic Control of Convection during Protein Crystallization

    Science.gov (United States)

    Ramachandran, N.; Leslie, F. W.

    2004-01-01

    An important component in biotechnology, particularly in the area of protein engineering and rational drug design is the knowledge of the precise three-dimensional molecular structure of proteins. The quality of structural information obtained from X-ray diffraction methods is directly dependent on the degree of perfection of the protein crystals. As a consequence, the growth of high quality macromolecular Crystals for diffraction analyses has been the central focus for bio-chemists, biologists, and bioengineers. Macromolecular crystals are obtained from solutions that contain the crystallizing species in equilibrium with higher aggregates, ions, precipitants, other possible phases of the protein, foreign particles, the walls of container, and a likely host of other impurities. By changing transport modes in general, i.e., reduction of convection and Sedimentation as is achieved in "microgravity", we have been able to dramatically affect the movement and distribution of macromolecules in the fluid, and thus their transport, f o d o n of crystal nuclei, and adsorption to the crystal surface. While a limited number of high quality crystals from space flights have been obtained, as the recent National Research Council (NRC) review of the NASA microgravity crystallization program pointed out, the scientific approach and research in crystallization of proteins has been mainly empirical yielding inconclusive results. We postulate that we can reduce convection in ground-based experiments and we can understand the different aspects of convection control through the use of strong magnetic fields and field gradients. We postulate that limited convection in a magnetic field will provide the environment for the growth of high quality crystals. The approach exploits the variation of fluid magnetic susceptibility with counteracts on for this purpose and the convective damping is realized by appropriately positioning the crystal growth cell so that the magnetic susceptibility

  10. BRIEF REPORT OF ACTIVE CONTROLLED AND OBSERVABLE PROTEIN CRYSTALLIZATION FACILITY

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    @@ There are two tendency of development on space protein crystal growth facility.Increase the number of samples, for commercial purpose, or observe and control the crystallization process, for study of crystallization process.

  11. Molecular chirality and chiral capsule-type dimer formation of cyclic triamides via hydrogen-bonding interactions.

    Science.gov (United States)

    Fujimoto, Noriko; Matsumura, Mio; Azumaya, Isao; Nishiyama, Shizuka; Masu, Hyuma; Kagechika, Hiroyuki; Tanatani, Aya

    2012-05-18

    Chiral properties of bowl-shaped cyclic triamides bearing functional groups with hydrogen-bonding ability were examined. Chiral induction of cyclic triamide 3a was observed by addition of chiral amine in solution, and chiral separation was achieved by simple crystallization to afford chiral capsule-type dimer structure of 4a.

  12. Light-Directed Dynamic Chirality Inversion in Functional Self-Organized Helical Superstructures.

    Science.gov (United States)

    Bisoyi, Hari Krishna; Li, Quan

    2016-02-24

    Helical superstructures are widely observed in nature, in synthetic polymers, and in supramolecular assemblies. Controlling the chirality (the handedness) of dynamic helical superstructures of molecular and macromolecular systems by external stimuli is a challenging task, but is of great fundamental significance with appealing morphology-dependent applications. Light-driven chirality inversion in self-organized helical superstructures (i.e. cholesteric, chiral nematic liquid crystals) is currently in the limelight because inversion of the handedness alters the chirality of the circularly polarized light that they selectively reflect, which has wide potential for application. Here we discuss the recent developments toward inversion of the handedness of cholesteric liquid crystals enabled by photoisomerizable chiral molecular switches or motors. Different classes of chiral photoresponsive dopants (guests) capable of conferring light-driven reversible chirality inversion of helical superstructures fabricated from different nematic hosts are discussed. Rational molecular designs of chiral molecular switches toward endowing handedness inversion to the induced helical superstructures of cholesteric liquid crystals are highlighted. This Review is concluded by throwing light on the challenges and opportunities in this emerging frontier, and it is expected to provide useful guidelines toward the development of self-organized soft materials with stimuli-directed chirality inversion capability and multifunctional host-guest systems.

  13. Orbital angular momentum in electron diffraction and its use to determine chiral crystal symmetries

    CERN Document Server

    Juchtmans, Roeland

    2015-01-01

    In this work we present an alternative way to look at electron diffraction in a transmission electron microscope. In stead of writing the scattering amplitude in Fourier space as a set of plane waves, we use the cylindrical Fourier transform to describe the scattering amplitude in a basis of orbital angular momentum (OAM) eigenstates. We show how working in this framework can be very convenient when investigating e.g. rotation and screw axis symmetries. For the latter we find selection rules on the OAM-coefficients that unambiguously reveal the handedness of the screw axis. Detecting the OAM-coefficients of the scattering amplitude thus offers the possibility to detect the handedness of crystals without the need for dynamical simulations, the thickness of the sample nor the exact crystal structure. We propose an experimental setup to measure the OAM-components where an image of the crystal is taken after inserting a spiral phase plate in the diffraction plane and perform mulsti-slice simulations on $\\alpha$-q...

  14. Couette-Taylor crystallizer: Effective control of crystal size distribution and recovery of L-lysine in cooling crystallization

    Science.gov (United States)

    Nguyen, Anh-Tuan; Yu, Taekyung; Kim, Woo-Sik

    2017-07-01

    A Couette-Taylor crystallizer is developed to enhance the L-Lysine crystal size distribution and recovery in the case of continuous cooling crystallization. When using the proposed Couette-Taylor (CT) crystallizer, the size distribution and crystal product recovery were much narrower and higher, respectively, than those from a conventional stirred tank (ST) crystallizer. Here, the coefficient of the size distribution for the crystal product from the CT crystallizer was only 0.45, while it was 0.78 in the case of the conventional ST crystallizer at an agitation speed of 700 rpm, mean residence time of 20 min, and feed concentration of 900 (g/L). Furthermore, when using the CT crystallizer, the crystal product recovery was remarkably enhanced up to 100%wt with a mean residence time of only 20 min, while it required a mean residence time of at least 60 min when using the conventional ST crystallizer. This result indicates that the CT crystallizer was much more effective than the conventional ST crystallizer in terms of controlling a narrower size distribution and achieving a 100%wt L-lysine crystal product recovery from continuous cooling crystallization. The advantage of the CT crystallizer over the conventional ST crystallizer was explained based on the higher energy dissipation of the Taylor vortex flow and larger surface area for heat transfer of the CT crystallizer. Here, the energy dissipation of the Taylor vortex flow in the CT crystallizer was 13.6 times higher than that of the random fluid motion in the conventional ST crystallizer, while the surface area per unit volume for heat transfer of the CT crystallizer was 8.0 times higher than that of the conventional ST crystallizer. As a result, the mixing condition and heat transfer of the CT crystallizer were much more effective than those of the conventional ST crystallizer for the cooling crystallization of L-lysine, thereby enhancing the L-lysine crystal size distribution and product recovery.

  15. Fixation of chiral smectic liquid crystal (S)-(+)-4-(2-methyl-1-butyloyloxy)phenyl 4-[1-(propenoyloxy) butiloxy] benzoate using UV curing techniques

    Energy Technology Data Exchange (ETDEWEB)

    Afrizal,, E-mail: rizalunj04@yahoo.com; Nurdelima,; Umeir [Faculty of Mathemathics and Natural Science, University of State Jakarta, Jakarta (Indonesia); Hikam, Muhammad; Soegiyono, Bambang [Department of Materials Science, University of Indonesia, Depok (Indonesia); Riswoko, Asep [Center for Material Technology, BPPT, Jl. MH.Thamrin 8 Jakarta (Indonesia)

    2014-03-24

    Chiral Smectic Liquid Crystal (S)-(+)-4-(2-methyl-1-butyloyloxy)phenyl 4-[1-(propenoyloxy) butiloxy] benzoate has been synthesized using method of steglich esterification at room temperature. The mesomorphic behavior of chiral smectic at 55°C that showed schlieren texture in POM analysis. Fixation of structure chiral smectic liquid crystal by means of photopolymerization of monomer (S)-(+)-4-(2-methyl-1-butyloyloxy)phenyl 4-[1-(propenoyloxy) butiloxy] benzoate under UV irradiation which called UV curing techniques. The curing process using UV 3 lamps 100 volt at 60°C for an hour. The product of photopolymerization could be seen by analysis of FTIR spectra both monomer and polymer. FTIR spectra of monomer, two peaks for ester carbonyl and C-C double bond groups appeared at 1729.09 cm-1and 3123.46 cm{sup −1}. After UV curing process, peak for the carbonyl group at 1729.09 cm{sup −1} decreased and a new peak at 1160.21 cm{sup −1} appeared due to the carbonyl group attached to a C-C bond group and then peak at 3123.46 cm{sup −1} for C-C double bond group was disappeared.

  16. Tuning the Cavity Size and Chirality of Self-Assembling 3D DNA Crystals

    Energy Technology Data Exchange (ETDEWEB)

    Simmons, Chad R.; Zhang, Fei; MacCulloch, Tara; Fahmi, Noureddine; Stephanopoulos, Nicholas; Liu, Yan; Seeman, Nadrian C. [Department; Yan, Hao

    2017-08-02

    The foundational goal of structural DNA nanotechnology—the field that uses oligonucleotides as a molecular building block for the programmable self-assembly of nanostructured systems—was to use DNA to construct three-dimensional (3D) lattices for solving macromolecular structures. The programmable nature of DNA makes it an ideal system for rationally constructing self-assembled crystals and immobilizing guest molecules in a repeating 3D array through their specific stereospatial interactions with the scaffold. In this work, we have extended a previously described motif (4 × 5) by expanding the structure to a system that links four double-helical layers; we use a central weaving oligonucleotide containing a sequence of four six-base repeats (4 × 6), forming a matrix of layers that are organized and dictated by a series of Holliday junctions. In addition, we have assembled mirror image crystals (l-DNA) with the identical sequence that are completely resistant to nucleases. Bromine and selenium derivatives were obtained for the l- and d-DNA forms, respectively, allowing phase determination for both forms and solution of the resulting structures to 3.0 and 3.05 Å resolution. Both right- and left-handed forms crystallized in the trigonal space groups with mirror image 3-fold helical screw axes P32 and P31 for each motif, respectively. The structures reveal a highly organized array of discrete and well-defined cavities that are suitable for hosting guest molecules and allow us to dictate a priori the assembly of guest–DNA conjugates with a specified crystalline hand.

  17. Progressive Transformation between Two Magnetic Ground States for One Crystal Structure of a Chiral Molecular Magnet.

    Science.gov (United States)

    Li, Li; Nishihara, Sadafumi; Inoue, Katsuya; Kurmoo, Mohamedally

    2016-03-21

    We report the exceptional observation of two different magnetic ground states (MGS), spin glass (SG, T(B) = 7 K) and ferrimagnet (FI, T(C) = 18 K), for one crystal structure of [{Mn(II)(D/L-NH2ala)}3{Mn(III)(CN)6}]·3H2O obtained from [Mn(CN)6](3-) and D/L-aminoalanine, in contrast to one MGS for [{Mn(II)(L-NH2ala)}3{Cr(III)(CN)6}]·3H2O. They consist of three Mn(NH2ala) helical chains bridged by M(III)(CN)6 to give the framework with disordered water molecules in channels and between the M(III)(CN)6. Both MGS are characterized by a negative Weiss constant, bifurcation in ZFC-FC magnetizations, blocking of the moments, both components of the ac susceptibilities, and hysteresis. They differ in the critical temperatures, absolute magnetization for 5 Oe FC (lack of spontaneous magnetization for the SG), and the shapes of the hysteresis and coercive fields. While isotropic pressure increases both T(crit) and the magnetizations linearly and reversibly in each case, dehydration progressively transforms the FI into the SG as followed by concerted in situ magnetic measurements and single-crystal diffraction. The relative strengths of the two moderate Mn(III)-CN-Mn(II) antiferromagnetic (J1 and J2), the weak Mn(II)-OCO-Mn(II) (J3), and Dzyaloshinkii-Moriya antisymmetric (DM) interactions generate the two sets of characters. Examination of the bond lengths and angles for several crystals and their corresponding magnetic properties reveals a correlation between the distortion of Mn(III)(CN)6 and the MGS. SG is favored by higher magnetic anisotropy by less distorted Mn(III)(CN)6 in good accordance with the Mn-Cr system. This conclusion is also born out of the magnetization measurements on orientated single crystals with fields parallel and perpendicular to the unique c axis of the hexagonal space group.

  18. Observation of blue phase in chiral nematic liquid crystal and its stabilization by silica nanoparticles

    Science.gov (United States)

    Singh, Arshdeep; Malik, Praveen; Jayoti, Divya

    2016-01-01

    In the present work, we report the blue phase (BP) in a binary mixture of cholesteryl nonanoate (CN) and N-(4-ethoxybenzylidene)-4-butylaniline (EBBA). The mixture exhibits BP over a temperature range of 2.3 K at optimum composition (50:50) of liquid crystals (LCs). The effect of silica nanoparticles (SNPs) doping on thermal stability of BPs has also been demonstrated and nearly 6 K wide BP temperature range was achieved at 0.5 wt.% of SNPs. A porous type texture was also observed during the BP formation process in the doped samples.

  19. Spectral signatures of chirality

    DEFF Research Database (Denmark)

    Pedersen, Jesper Goor; Mortensen, Asger

    2009-01-01

    We present a new way of measuring chirality, via the spectral shift of photonic band gaps in one-dimensional structures. We derive an explicit mapping of the problem of oblique incidence of circularly polarized light on a chiral one-dimensional photonic crystal with negligible index contrast...... to the formally equivalent problem of linearly polarized light incident on-axis on a non-chiral structure with index contrast. We derive analytical expressions for the first-order shifts of the band gaps for negligible index contrast. These are modified to give good approximations to the band gap shifts also...

  20. Crystallization-induced properties from morphology-controlled organic crystals.

    Science.gov (United States)

    Park, Chibeom; Park, Ji Eun; Choi, Hee Cheul

    2014-08-19

    During the past two decades, many materials chemists have focused on the development of organic molecules that can serve as the basis of cost-effective and flexible electronic, optical, and energy conversion devices. Among the potential candidate molecules, metal-free or metal-containing conjugated organic molecules offer high-order electronic conjugation levels that can directly support fast charge carrier transport, rapid optoelectric responses, and reliable exciton manipulation. Early studies of these molecules focused on the design and synthesis of organic unit molecules that exhibit active electrical and optical properties when produced in the form of thin film devices. Since then, researchers have worked to enhance the properties upon crystallization of the unit molecules as single crystals provide higher carrier mobilities and exciton recombination yields. Most recently, researchers have conducted in-depth studies to understand how crystallization induces property changes, especially those that depend on specific crystal surfaces. The different properties that depend on the crystal facets have been of particular interest. Most unit molecules have anisotropic structures, and therefore produce crystals with several unique crystal facets with dissimilar molecular arrangements. These structural differences would also lead to diverse electrical conductance, optical absorption/emission, and even chemical interaction properties depending on the crystal facet investigated. To study the effects of crystallization and crystal facet-dependent property changes, researchers must grow or synthesize crystals of highly conjugated molecules that have both a variety of morphologies and high crystallinity. Morphologically well-defined organic crystals, that form structures such as wires, rods, disks, and cubes, provide objects that researchers can use to evaluate these material properties. Such structures typically occur as single crystals with well-developed facets with

  1. New Tests of Chiral Perturbation Theory in η Decays Using the Crystal Ball

    Science.gov (United States)

    Nefkens, B. M. K.; Prakhov, S.; Berger, E.; Clajus, M.; Marušić, A.; McDonald, S.; Nefkens, B. M. K.; Phaisangittisakul, N.; Prakhov, S.; Pulver, M.; Starostin, A.; Tippens, W. B.; Isenhower, D.; Sadler, M.; Allgower, C.; Spinka, H.; Comfort, J.; Craig, K.; Ramirez, T.; Kycia, T.; Peterson, J.; Briscoe, W.; Shafi, A.; Staudenmaier, H. M.; Manley, D. M.; Olmsted, J.; Peaslee, D.; Bekrenev, V.; Koulbardis, A.; Kozlenko, N.; Kruglov, S.; Lopatin, I.; Huber, G. M.; Knecht, N.; Lolos, G. J.; Papandreou, Z.; Slaus, I.; Supek, I.; Grosnick, D.; Koetke, D.; Manweiler, R.; Stanislaus, S.

    2001-12-01

    The G-parity violating η → 3π0 decay occurs primarily as a consequence of the up-down quark mass difference, mu - md. In the standard notation 1 A(η → 3π0) (mu - md)(1 + αz) and Γ(η → 3π0) (mu - md)2(1 + 2αz), where α is the quadratic slope parameter, z = (ρ /ρ max } )2 \\ ∑ {(Ei{π o } - mη /3)2 } , ρ is the distance from the center of the Dalitz plot. Thus far χPTh has not succeeded in accounting fully for the experimental η → 3π decay rate. The expanded {O}(p4 ) calculation which includes pion-pion rescattering to all orders 2 is still too low by (34 ± 10)%. It has been suggested 3 that this might be due to dynamical effects with terms {O}(p6 ) such as {L}6 \\ Fπ 2 trmDμ UDμ U\\dag trDν UDν U\\dag . This possibility may be explored by a precise measurement of the quadratic slope parameter α in η → 3π0 decay. The existing data are inconclusive. GAMS-2000 4 obtained α = -(22±23) × 10-3. The Crystal Barrel 5 has reported α = -(52±15±10) × 10-3. The theoretical prediction 2 is α = -(14 to 7) × 10-3 ...

  2. Chiral atomically thin films

    Science.gov (United States)

    Kim, Cheol-Joo; Sánchez-Castillo, A.; Ziegler, Zack; Ogawa, Yui; Noguez, Cecilia; Park, Jiwoong

    2016-06-01

    Chiral materials possess left- and right-handed counterparts linked by mirror symmetry. These materials are useful for advanced applications in polarization optics, stereochemistry and spintronics. In particular, the realization of spatially uniform chiral films with atomic-scale control of their handedness could provide a powerful means for developing nanodevices with novel chiral properties. However, previous approaches based on natural or grown films, or arrays of fabricated building blocks, could not offer a direct means to program intrinsic chiral properties of the film on the atomic scale. Here, we report a chiral stacking approach, where two-dimensional materials are positioned layer-by-layer with precise control of the interlayer rotation (θ) and polarity, resulting in tunable chiral properties of the final stack. Using this method, we produce left- and right-handed bilayer graphene, that is, a two-atom-thick chiral film. The film displays one of the highest intrinsic ellipticity values (6.5 deg μm-1) ever reported, and a remarkably strong circular dichroism (CD) with the peak energy and sign tuned by θ and polarity. We show that these chiral properties originate from the large in-plane magnetic moment associated with the interlayer optical transition. Furthermore, we show that we can program the chiral properties of atomically thin films layer-by-layer by producing three-layer graphene films with structurally controlled CD spectra.

  3. Chirality in thiolate-protected gold clusters.

    Science.gov (United States)

    Knoppe, Stefan; Bürgi, Thomas

    2014-04-15

    Over recent years, research on thiolate-protected gold clusters Au(m)(SR)n has gained significant interest. Milestones were the successful determination of a series of crystal structures (Au102(SR)44, Au25(SR)18, Au38(SR)24, Au36(SR)24, and Au28(SR)20). For Au102(SR)44, Au38(SR)24, and Au28(SR)20, intrinsic chirality was found. Strong Cotton effects (circular dichroism, CD) of gold clusters protected by chiral ligands have been reported a long time ago, indicating the transfer of chiral information from the ligand into the cluster core. Our lab has done extensive studies on chiral thiolate-protected gold clusters, including those protected with chiral ligands. We demonstrated that vibrational circular dichroism can serve as a useful tool for the determination of conformation of the ligand on the surface of the cluster. The first reports on crystal structures of Au102(SR)44 and Au38(SR)24 revealed the intrinsic chirality of these clusters. Their chirality mainly arises from the arrangement of the ligands on the surface of the cluster cores. As achiral ligands are used to stabilize the clusters, racemic mixtures are obtained. However, the separation of the enantiomers by HPLC was demonstrated which enabled the measurement of their CD spectra. Thermally induced inversion allows determination of the activation parameters for their racemization. The inversion demonstrates that the gold-thiolate interface is anything but fixed; in contrast, it is rather flexible. This result is of fundamental interest and needs to be considered in future applications. A second line of our research is the selective introduction of chiral, bidentate ligands into the ligand layer of intrinsically chiral gold clusters. The ligand exchange reaction is highly diastereoselective. The bidentate ligand connects two of the protecting units on the cluster surface and thus effectively stabilizes the cluster against thermally induced inversion. A minor (but significant) influence of chiral ligands to

  4. Chirality Switching by Martensitic Transformation in Protein Cylindrical Crystals: Application to Bacterial Flagella

    Science.gov (United States)

    Komai, Ricardo Kiyohiro

    Martensitic transformations provide unique engineering properties that, when designed properly, become important parts of new technology. Martensitic transformations have been studied for many years in traditional alloys (iron, steel, titanium, etc.), however there is still much to be learned in regards to these transformations in biological materials. Olson and Hartman showed in 1982 that these transformations are also observed in bacterial flagella and T4 bacteriophage viral sheaths, allowing for propulsion of bacteria in a fluid environment and, for the virus, is responsible for the infection mechanism. This work demonstrates, using the bacterial flagella as an example, that these transformations can be modelled using thermodynamic methods that are also used to model the transformations in alloys. This thesis work attempts to explain the transformations that occur in bacterial flagella, which are capable of small strain, highly reversible martensitic transformations. The first stress/temperature phase diagrams of these flagella were created by adding the mechanical energy of the transformation of the flagella to limited chemical thermodynamics information of the transformation. Mechanical energy is critical to the transformation process because the bacterial body applies a torque to the radius of the flagella. Finally, work has begun and will be completed in regards to understanding the kinetics of the transformation of the flagella. The motion of the transformation interface can be predicted by using a Landau-Ginzburg model. The crystallography of the transformation in bacterial flagella is also being computed to determine the invariant lines of transformation that occur within this cylindrical crystal. This work has shown that it is possible to treat proteins in a similar manner that alloys are treated when using thermodynamic modelling. Much can be learned from translating what is known regarding phase transformations in hard material systems to soft, organic

  5. Mechanism of chirality conversion by periodic change of temperature: Role of chiral clusters

    Science.gov (United States)

    Katsuno, Hiroyasu; Uwaha, Makio

    2016-01-01

    By grinding crystals in a solution, the chirality of crystal structure (and the molecular chirality for the case of chiral molecules as well) can be converted, and the cause of the phenomenon is attributed to crystal growth with chiral clusters. We show that the recently found chirality conversion with a periodic change of temperature can also be explained by crystal growth with chiral clusters. With the use of a generalized Becker-Döring model, which includes enantio-selective incorporation of small chiral clusters to large solid clusters, the change of cluster distribution and the mass flow between clusters are studied. The chiral clusters act as a reservoir to pump out the minority species to the majority, and the exponential amplification of the enantiomeric excess found in the experiment is reproduced in the numerical calculation.

  6. 47 CFR 95.651 - Crystal control required.

    Science.gov (United States)

    2010-10-01

    ... 47 Telecommunication 5 2010-10-01 2010-10-01 false Crystal control required. 95.651 Section 95.651... SERVICES Technical Regulations Certification Requirements § 95.651 Crystal control required. All transmitters used in the Personal Radio Services must be crystal controlled, except an R/C station that...

  7. Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)2XF6 (X = P, As, Sb).

    Science.gov (United States)

    Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis

    2016-10-13

    Control of the structural type in metallic enantiopure and racemic radical cation salts is achieved through hydrogen bonding interactions between the chiral donor DM-EDT-TTF and the XF6 anions (X = P, As, Sb), determined by the anion size and the chiral information.

  8. Identifying microwave magnetic resonance in chiral elements for creation of controlled matched absorbing metastructures

    Science.gov (United States)

    Kraftmakher, G. A.; Butylkin, V. S.; Kazantsev, Yu. N.; Mal'tsev, V. P.; Temirov, Yu. Sh.

    2017-01-01

    It has been suggested a method for identifying and separating magnetic and electric microwave resonance responses of conductive chiral and bianisotropic elements by reflection of electromagnetic waves in the standing and traveling-wave modes. It has been observed experimentally (in waveguide) and confirmed numerically (in free space) that magnetic resonance, which is excited by microwave magnetic field h, and electric resonances, excited by electric field E, show drastically different resonance curves of reflection. These distinctions allow to identifying the magnetic resonance response and using magnetically excited elements for broadband matching of absorbers instead of traditional quarter-wavelength layer. We have fabricated and investigated matched absorbing metastructures which are controlled by voltage as well by light of remote laser pointer.

  9. Spectroscopy of f -f transitions, crystal-field calculations, and magnetic and quadrupole helix chirality in DyF e3(BO3) 4

    Science.gov (United States)

    Popova, M. N.; Chukalina, E. P.; Boldyrev, K. N.; Stanislavchuk, T. N.; Malkin, B. Z.; Gudim, I. A.

    2017-03-01

    We present the results of temperature- and polarization-dependent high-resolution optical spectroscopy studies of DyF e3(BO3) 4 performed in spectral ranges 40 -300 c m-1 and 3000 -23 000 c m-1 . The crystal-field (CF) parameters for the D y3 + ions in the P 3121 (P 3221 ) phase of DyF e3(BO3) 4 are obtained from calculations based on the analysis of the measured f-f transitions. Recently, quadrupole helix chirality and its domain structure was observed in resonant x-ray diffraction experiments on DyF e3(BO3) 4 using circularly polarized x rays [T. Usui, Y. Tanaka, H. Nakajima, M. Taguchi, A. Chainani, M. Oura, S. Shin, N. Katayama, H. Sawa, Y. Wakabayashi, and T. Kimura, Nat. Mater. 13, 611 (2014), 10.1038/nmat3942]. Using the obtained set of the CF parameters, we calculate temperature dependencies of the electronic quadrupole moments of the D y3 + ions induced by the low-symmetry (C2) CF component and show that the quadrupole helix chirality can be explained quantitatively. We also consider the temperature dependencies of the bulk magnetic dc-susceptibility and the helix chirality of the single-site magnetic susceptibility tensors of the D y3 + ions in the paramagnetic P 3121 (P 3221 ) phase and suggest the neutron and resonant x-ray diffraction experiments in a magnetic field to reveal the helix chirality of field-induced magnetic moments.

  10. Biological control of crystal texture: A widespread strategy for adapting crystal properties to function

    Energy Technology Data Exchange (ETDEWEB)

    Berman, A.; Leiserowitz, L.; Weiner, S.; Addadi, L. (Weizmann Inst. of Science, Rehovot (Israel)); Hanson, J.; Koetzle, T.F. (Brookhaven National Lab., Upton, NY (United States))

    1993-02-05

    Textures of calcite crystals from a variety of mineralized tissues belong to organisms from four phyla were examined with high-resolution synchrotron x-ray radiation. Significant differences in coherence length and angular spread were observed between taxonomic groups. Crystals from polycrystalline skeletal ensembles were more perfect than those that function as single-crystal elements. Different anistropic effects on crystal texture were observed for sea urchin and mollusk calcite crystals, whereas none was found for the foraminifer, Patellina, and the control calcite crystals. These results show that the manipulation of crystal texture in different organisms is under biological control and that crystal textures in some tissues are adapted to function. A better understanding of this apparently widespread biological phenomenon may provide new insights for improving synthetic crystal-containing materials. 18 refs., 3 figs., 1 tab.

  11. Chiral Ligands Derived from Carbohydrates. 21.Crystal Structure of Methyl-4,6-O-benzylidene-3-deoxy-3-(salicylideneamino)-α-D-altropyranoside

    Institute of Scientific and Technical Information of China (English)

    LIU Pei; JIA Li; TONG Qing-Song; MENG Xiang-Hua; FENG Yan-Fang; SHI Ji-Cheng

    2008-01-01

    A new chiral Schiff base derived from carbohydrate, methyl-4,6-O-benzylidene-3- deoxy-3-(salicylideneamino)-α-D-altropyranoside, has been synthesized by reacting methyl 3-ami- no-4,6-O-benzylidene-3-deoxy-α-D-altropyranoside with salicylaldehyde in methanol and charac- terized by IR, 1H NMR, 13C NMR, MS, elemental analysis, and X-ray crystal structure analysis.The crystal belongs to orthorhombic, space group P212121 with a = 8.0856(16), b = 10.786(2), c = 22.690(5) -, V = 1978.8(7) -3, Z = 4, Mr = 385.40, Dc = 1.294 g/cm3, μ = 0.095 mm-1, F(000) = 816, the final R = 0.0379 and wR = 0.0811 for 2597 independent reflections.In the title compound, the pyrano-ring adopts a twisted 1C4 chair conformation.

  12. Crystal structure of 2-{(R)-[1-(4-bromo-phen-yl)eth-yl]imino-meth-yl}-4-(phenyl-diazen-yl)phenol, a chiral photochromic Schiff base.

    Science.gov (United States)

    Moriwaki, Ryoji; Akitsu, Takashiro

    2015-11-01

    The title chiral photochromic Schiff base compound, C21H18BrN3O, was synthesized from (R)-(+)-1-(4-bromo-phen-yl)ethyl-amine and the salicyl-aldehyde of an azo-benzene derivative. The mol-ecule corresponds to the phenol-imine tautomer, the C=N and N-C bond distances being 1.285 (3) and 1.470 (3) Å, respectively. The diazenyl group adopts a trans form, with an N=N distance of 1.256 (3) Å. The hy-droxy group is involved in intra-molecular O-H⋯N hydrogen bonding. In the crystal, C-H⋯π inter-actions consolidate the crystal packing of one-dimensional chains, which exhibits short inter-molecular Br⋯C contacts of 3.400 (3) Å.

  13. Voltage-controlled nanoscale reconfigurable magnonic crystal

    Science.gov (United States)

    Wang, Qi; Chumak, Andrii V.; Jin, Lichuan; Zhang, Huaiwu; Hillebrands, Burkard; Zhong, Zhiyong

    2017-04-01

    A nanoscale reconfigurable magnonic crystal is designed using voltage-controlled perpendicular magnetic anisotropy (PMA) in ferromagnetic-dielectric heterostructures. A periodic array of gate metallic strips is placed on top of a MgO/Co structure in order to apply a periodic electric field and to modify the PMA in Co. It is numerically demonstrated that the introduction of PMA, which can be realized experimentally via applying a voltage, modifies the spin-wave propagation and leads to the formation of band gaps in the spin-wave spectrum. The band gaps can be controlled, i.e., it is possible to switch band gaps on and off within a few tens of nanoseconds. The width and the center frequency of the band gaps are defined by the applied voltage. Finally, it is shown that the introduction of PMA to selected, rather than to all gate strips allows for a predefined modification of the band-gap spectra. The proposed voltage-controlled reconfigurable magnonic crystal opens a way to low power consumption magnonic applications.

  14. Preparation and crystallization control of nanoparticle hydroxyapatite

    Institute of Scientific and Technical Information of China (English)

    Lianfeng Guo; Wenguang Zhang; Chengtao Wang

    2004-01-01

    Nanoparticle hydroxyapatite was prepared by a wet chemical precipitation method. The effects of different synthesis conditions, I.e. Contents of reagents (0.2, 0.5 and 0.8 mol/L), reaction temperatures (20, 37, 55 and 75℃) and reaction time (0-24 h),were studied based on crystallization process analysis and the effects of washing methods (with water or alcohol) were also studied.Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), electron diffraction (ED) and inductively coupled plasma spectroscopy (ICP) were used to characterize the powders. Chemical analysis shows that the purity of the precipitated hydroxyapatite largely depends on reaction time. X-ray diffraction and TEM micrographs results show that reaction temperature is a key factor affecting crystallinity, morphology and particle size. Degree of supersaturation and stirring also affects the crystallization. Particles are in a shape of short rod and have a size of 20-40 nm in length at 20℃ and 37℃,but acicular morphology and a size of 150-170 nm in length at 75C. Particles are monocrystalline at 20℃ and 37℃, and are polycrystalline at 55℃ and 75℃. The results show that stoichiometry hydroxyapatite with controlled particle size, morphology and crystallinity can be obtained by carefully controlling the reaction conditions.

  15. Chiral nematic stained glass: controlling the optical properties of nanocrystalline cellulose-templated materials.

    Science.gov (United States)

    Kelly, Joel A; Shopsowitz, Kevin E; Ahn, Jun Myun; Hamad, Wadood Y; MacLachlan, Mark J

    2012-12-18

    Chiral nematic mesoporous materials decorated with metal nanoparticles have been prepared using the templated self-assembly of nanocrystalline cellulose (NCC). By adding small quantities of ionic compounds to aqueous dispersions of NCC and tetramethoxysilane (TMOS), the helical pitch of the chiral nematic structure could be manipulated in a manner complementary to the ratio of NCC/TMOS previously demonstrated by our group. We have studied the transformation of these ion-loaded composites into high surface area mesoporous silica and carbon films decorated with metal nanoparticles through calcination and carbonization, respectively. This general and straightforward approach to prepare chiral nematic metal nanoparticle assemblies may be useful in a variety of applications, particularly for their chiral optical properties.

  16. Crystal Structure of Chiral Acetato-bridged Binuclear Cyclopalladated complex[Pd(μ-O2CM3)(S-C6H4CHMeNH2)]2

    Institute of Scientific and Technical Information of China (English)

    杨帆; 李一平; 聂娟; 汤杰; 何鸣元

    2003-01-01

    Reaction of (S)-α-methylbenzylamine with Pd(OAc)2 in anhydrous HOAc produced the chiral complex[Pd(μ-O2CMe)(S-C6H4CHMeNH2)]2.(1).The complex was characterized by 1H NMR spectroscopy,elemental analysis and a single-crystal Xray analysis.The X-ray crystal structure analysis revealed that complex 1 has four isomers:two outer and two inner isomers.

  17. Syntheses and Crystal Structures of Chiral BINOL Derivatives and Their Applications in Enantioselective Lewis Acid Catalyzed Addition of Diethylzinc to Aldehydes

    Institute of Scientific and Technical Information of China (English)

    LIU Guo-Hua; YU Han; Yang Liang-Zhun; YAO Mei; FANG Hai-Bin; XUE Yun-Ning

    2007-01-01

    Two novel chiral BINOL derivatives with bis(benzylamine) groups at the 3,3' positions have been synthesized through the condensation reaction between 2,2'-bis(methoxy- methyleneoxy)-1,1'-binaphthyl-3,3'-dicarboxylic acid and benzylamine or N-phenyl benzylamine in the presence of triethylamine. Suitable single crystal of (R)-N,N'-dibenzyl-2,2'-dihydroxy-1,1'-binaphthly-3,3'-diformamide (R)-3 for X-ray diffraction was obtained by recrystallization at room temperature from the mixture solvents. Crystallographic data of (R)-3: C40H36N2O6, Mr=640.71, monoclinic, space group P21, a=6.746(3), b=21.883(9), c=11.723(5) (A), β=104.605(7)°, Z=2, V=1674.7(12) (A)3, Dc=1.271 g/cm3, F(000)=676, R=0.0729, Wr=0.1687 and μ(MoKα)=0.086 mm-1. Two chiral BINOL ligands were found to be effective in the enantioselective addition of diethylzinc to aldehydes and much different enantioselectivity was observed both in the presence and absence of Ti(OiPr)4. In the former case, (R)-3 showed moderate enantioselectivity, which was lower than that of (R)-BINOL's; and in the latter case, (R)-4 gave the highest enantioselectivity up to 93.3% ee.*

  18. Three-dimensional chiral microstructures fabricated by structured optical vortices in isotropic material

    CERN Document Server

    Ni, Jincheng; Zhang, Chenchu; Hu, Yanlei; Yang, Liang; Lao, Zhaoxin; Xu, Bing; Li, Jiawen; Wu, Dong; Chu, Jiaru

    2016-01-01

    Optical vortices, as a kind of structured beam with helical phase wavefronts and doughnut shape intensity distribution, have been used for fabricating chiral structures in metal and spiral patterns in anisotropic polarization-dependent azobenzene polymer. However, in isotropic polymer, the fabricated microstructures are typically confined to non-chiral cylindrical geometry due to two-dimensional doughnut intensity profile of optical vortices. Here we develop a powerful strategy for realizing chiral microstructures in isotropic material by coaxial interference of a vortex beam and a plane wave, which produces three-dimensional (3D) spiral optical fields. This coaxial interference beams are creatively produced by designing the contrivable holograms consisting of azimuthal phase and equiphase loaded on liquid-crystal spatial light modulator. Then, in isotropic polymer, 3D chiral microstructures are achieved under illumination of the coaxial interference femtosecond laser beams with their chirality controlled by ...

  19. Group Theory of Circular-Polarization Effects in Chiral Photonic Crystals with Four-Fold Rotation Axes, Applied to the Eight-Fold Intergrowth of Gyroid Nets

    CERN Document Server

    Saba, Matthias; Mecke, Klaus; Gu, Min; Schröder-Turk, Gerd E

    2013-01-01

    We use group or representation theory and scattering matrix calculations to derive analytical results for the band structure topology and the scattering parameters, applicable to any chiral photonic crystal with body-centered cubic symmetry I432 for circularly-polarised incident light. We demonstrate in particular that all bands along the cubic [100] direction can be identi?ed with the irreducible representations E+/-,A and B of the C4 point group. E+ and E- modes represent the only transmission channels for plane waves with wave vector along the ? line, and can be identi?ed as non-interacting transmission channels for right- (E-) and left-circularly polarised light (E+), respectively. Scattering matrix calculations provide explicit relationships for the transmission and reflectance amplitudes through a ?nite slab which guarantee equal transmission rates for both polarisations and vanishing ellipticity below a critical frequency, yet allowing for ?nite rotation of the polarisation plane. All results are veri?...

  20. Optically Biaxial, Re-entrant and Frustrated Mesophases in Chiral, Non-symmetric Liquid Crystal Dimers and Binary Mixtures.

    Science.gov (United States)

    Padmini, Vediappen; Babu, Palakurthy Nani; Nair, Geetha G; Rao, D S Shankar; Yelamaggad, Channabasaveshwar V

    2016-10-20

    Sixteen optically active, non-symmetric dimers, in which cyanobiphenyl and salicylaldimine mesogens are interlinked by a flexible spacer, were synthesized and characterized. While the terminal chiral tail, in the form of either (R)-2-octyloxy or (S)-2-octyloxy chain attached to salicylaldimine core, was held constant, the number of methylene units in the spacer was varied from 3 to 10 affording eight pairs of (R & S) enantiomers. They were probed for their thermal properties with the aid of orthoscopy, conoscopy, differential scanning calorimetry and X-ray powder diffraction. In addition, the binary mixture study was carried out using chiral and achiral dimers with the intensions of stabilizing optically biaxial phase/s, re-entrant phases and important phase sequences. Notably, one of the chiral dimers as well as some mixtures exhibited a biaxial smectic A (SmAb ) phase appearing between a uniaxial SmA and a re-entrant uniaxial SmA phases. The mesophases such as chiral nematic (N*) and frustrated phases viz., blue phases (BPs) and twist grain boundary (TGB) phases, were also found to occur in most of the dimers and mixtures. X-ray diffraction studies revealed that the dimers possessing oxybutoxy and oxypentoxy spacers show interdigitated (SmAd ) phase where smectic periodicity is over 1.4 times the molecular length; whereas in the intercalated SmA (SmAc ) phase formed by a dimer having oxydecoxy spacer the periodicity was found to be approximately half the molecular length. The handedness of the helical structure of the N* phases formed by two enantiomers was examined with the aid of CD measurements; as expected, these enantiomers showed optical activities of equal magnitudes but with opposite signs. Overall, it appears that the chiral dimers and mixtures presented herein may serve as model systems in design and developing novel materials exhibiting the apolar SmAb phase possessing D2h symmetry and nematic-type biaxiality. © 2016 Wiley-VCH Verlag GmbH & Co. KGa

  1. Fabrication of Metarodielectric Photonic Crystals for Microwave Control

    Energy Technology Data Exchange (ETDEWEB)

    Takinami, Yohei; Kirihara, Soshu, E-mail: y-takinami@jwri.osaka-u.ac.jp [Smart Processing Reserch Center, Joining and Welding Reserch Institute, Osaka University (Japan)

    2011-05-15

    Photonic crystals have inspired a great deal of interests as key platforms for effective control of electromagnetic wave. They can suppress incident waves at a certain frequency by Bragg diffraction and exhibit photonic band gap. Photonic band gap structures can be applied for effective and compact wave control equipments. In this investigation, metal photonic crystals were fabricated by stereolithography and heat treatment process. Furthermore, metal-dielectric crystal was created through impregnation process of dielectric media. This concept of metal-dielectric photonic crystal is expected to contribute for not only the downsizing of electromagnetic wave devices, but also thermal flow control.

  2. Crystal structures of three mercury(II complexes [HgCl2L] where L is a bidentate chiral imine ligand

    Directory of Open Access Journals (Sweden)

    Guadalupe Hernández

    2015-12-01

    Full Text Available The crystal structures of three complexes [HgCl2L] were determined, namely, (S-(+-dichlorido[1-phenyl-N-(pyridin-2-ylmethylideneethylamine-κ2N,N′]mercury(II, [HgCl2(C14H14N2], (S-(+-dichlorido[1-(4-methylphenyl-N-(pyridin-2-ylmethylideneethylamine-κ2N,N′]mercury(II, [HgCl2(C15H16N2], and (1S,2S,3S,5R-(+-dichlorido[N-(pyridin-2-ylmethylideneisopinocampheylamine-κ2N,N′]mercury(II, [HgCl2(C16H22N2]. The complexes consist of a bidentate chiral imine ligand coordinating to HgCl2 and crystallize with four independent molecules in the first complex and two independent molecules in the other two. The coordination geometry of mercury is tetrahedral, with strong distortion towards a disphenoidal geometry, as a consequence of the imine bite angle being close to 70°. The Cl—Hg—Cl angles span a large range, 116.0 (2–138.3 (3°, which is related to the aggregation state in the crystals. For small Cl—Hg—Cl angles, complexes have a tendency to form dimers, via intermolecular Hg...Cl contacts. These contacts become less significant in the third complex, which features the largest intramolecular Cl—Hg—Cl angles.

  3. Crystallization of lysozyme with (R)-, (S)- and (RS)-2-methyl-2, 4-pentanediol

    Energy Technology Data Exchange (ETDEWEB)

    Stauber, Mark [Yeshiva University, 2495 Amsterdam Avenue, New York, NY 10033-3312 (United States); Yeshiva University, 2495 Amsterdam Avenue, New York, NY 10033-3312 (United States); Jakoncic, Jean [Brookhaven National Laboratory, Building 725D, Upton, NY 11973-5000 (United States); Berger, Jacob; Karp, Jerome M.; Axelbaum, Ariel; Sastow, Dahniel [Yeshiva University, 2495 Amsterdam Avenue, New York, NY 10033-3312 (United States); Yeshiva University, 2495 Amsterdam Avenue, New York, NY 10033-3312 (United States); Buldyrev, Sergey V. [Yeshiva University, 2495 Amsterdam Avenue, New York, NY 10033-3312 (United States); Hrnjez, Bruce J. [Collegiate School, 260 West 78th Street, New York, NY 10024-6559 (United States); Asherie, Neer, E-mail: asherie@yu.edu [Yeshiva University, 2495 Amsterdam Avenue, New York, NY 10033-3312 (United States); Yeshiva University, 2495 Amsterdam Avenue, New York, NY 10033-3312 (United States)

    2015-03-01

    Crystallization of lysozyme with (R)-2-methyl-2, 4-pentanediol produces more ordered crystals and a higher resolution protein structure than crystallization with (S)-2-methyl-2, 4-pentanediol. The results suggest that chiral interactions with chiral additives are important in protein crystal formation. Chiral control of crystallization has ample precedent in the small-molecule world, but relatively little is known about the role of chirality in protein crystallization. In this study, lysozyme was crystallized in the presence of the chiral additive 2-methyl-2, 4-pentanediol (MPD) separately using the R and S enantiomers as well as with a racemic RS mixture. Crystals grown with (R)-MPD had the most order and produced the highest resolution protein structures. This result is consistent with the observation that in the crystals grown with (R)-MPD and (RS)-MPD the crystal contacts are made by (R)-MPD, demonstrating that there is preferential interaction between lysozyme and this enantiomer. These findings suggest that chiral interactions are important in protein crystallization.

  4. Controlling electric, magnetic, and chiral dipolar emission with PT-symmetric potentials

    CERN Document Server

    Alaeian, Hadiseh

    2014-01-01

    We investigate the effect of parity-time (PT)-symmetric optical potentials on the radiation of achiral and chiral emitters. Mode coalescence and the appearance of exceptional points lead to orders-of-magnitude enhancements in the emitted dipole power. Further, the emitter can be tuned to behave as a strong optical source or absorber based on the non-Hermiticity parameter. Chiral enantiomers radiating near PT metamaterials exhibit a 4.5-fold difference in their decay rate. The results of this work could enable new atom-cavity interactions for quantum optics, as well as all- optical enantio-specific separation.

  5. STUDY ON MAGNETIC FIELD-INDUCED ORIENTATION OF A CHIRAL SIDE-CHAIN LIQUID CRYSTAL POLYACRYLATE USING INFRARED DICHROISM

    Institute of Scientific and Technical Information of China (English)

    HE Liu; JIN Shunzi; ZHANG Shufan; QI Zongneng; WANG Fosong

    1996-01-01

    Magnetic field-induced orientation of a chiral side chain liquid crystalline polyacrylate (P-11) was studied by using IR dichroism. For the investigated P-11, it has been shown that the magnetic alignment takes place over the entire temperature range between its melting point and clearing point and the orientation level is strongly temperature-dependent, the development with time of the magnetic orientation follows an exponential-type relation,and the smectic phase state influences the thermal relaxation process in the absence of the magnetic field.

  6. Controlling spontaneous emission of light by photonic crystals

    DEFF Research Database (Denmark)

    Lodahl, Peter

    2005-01-01

    Photonic bandgap crystals were proposed almost two decades ago as a unique tool for controlling propagation and emission of light. Since then the research field of photonic crystals has exploded and many beautiful demonstrations of the use of photonic crystals and fibers for molding light...... propagation have appeared that hold great promises for integrated optics. These major achievements solidly demonstrate the ability to control propagation of light. In contrast, an experimental demonstration of the use of photonic crystals for timing the emission of light has so far lacked. In a recent...

  7. Chiral algebras

    CERN Document Server

    Beilinson, Alexander

    2004-01-01

    Chiral algebras form the primary algebraic structure of modern conformal field theory. Each chiral algebra lives on an algebraic curve, and in the special case where this curve is the affine line, chiral algebras invariant under translations are the same as well-known and widely used vertex algebras. The exposition of this book covers the following topics: the "classical" counterpart of the theory, which is an algebraic theory of non-linear differential equations and their symmetries; the local aspects of the theory of chiral algebras, including the study of some basic examples, such as the ch

  8. Synthesis of SAPO-56 with controlled crystal size

    Science.gov (United States)

    Wu, Ting; Feng, Xuhui; Carreon, Maria L.; Carreon, Moises A.

    2017-03-01

    Herein, we present the hydrothermal synthesis of SAPO-56 crystals with relatively controlled crystal/particle size. The effects of water content, aluminum source, gel composition, stirring, crystallization temperature and time, as well as the incorporation of crystal growth inhibitors during synthesis were systematically investigated. The synthesized SAPO-56 crystals displayed BET surface areas as high as ˜630 m2 g-1 with relative narrow size distribution in the ˜5-60 μm range. Nitrogen BET surface areas in the 451 to 631 m2 g-1 range were observed. Decreasing the crystallization temperature from 220 to 210 °C helped to decrease the average SAPO-56 crystal size. Diluted gel compositions promoted the formation of smaller crystals. Crystal growth inhibitors were found to be helpful in reducing crystal size and narrow the size distribution. Specifically, ˜5 μm SAPO-56 crystals displaying narrow size distribution were synthesized employing aluminum-tri-sec-butoxide as Al source, high water content, and high stirring rates.

  9. Control and femtosecond time-resolved imaging of torsion in a chiral molecule

    DEFF Research Database (Denmark)

    Hansen, Jonas Lerche; Nielsen, Jens Hedegaard; Madsen, Christian Bruun;

    2012-01-01

    We study how the combination of long and short laser pulses can be used to induce torsion in an axially chiral biphenyl derivative (3,5-difluoro-3′,5′-dibromo-4′-cyanobiphenyl). A long, with respect to the molecular rotational periods, elliptically polarized laser pulse produces 3D alignment of t...

  10. Control and femtosecond time-resolved imaging of torsion in a chiral molecule

    DEFF Research Database (Denmark)

    Hansen, Jonas Lerche; Nielsen, Jens Hedegaard; Madsen, Christian Bruun

    2012-01-01

    We study how the combination of long and short laser pulses can be used to induce torsion in an axially chiral biphenyl derivative (3,5-difluoro-3′,5′-dibromo-4′-cyanobiphenyl). A long, with respect to the molecular rotational periods, elliptically polarized laser pulse produces 3D alignment of t...

  11. Optical Anisotropy and Four Possible Orientations of a Nematic Liquid Crystal on the Same Film of a Photochromic Chiral Smectic Polymer

    Science.gov (United States)

    Blinov, Lev M.; Barberi, Riccardo; Kozlovsky, Mikhail V.; Lazarev, Vladimir V.; de Santo, Maria P.

    Spin coated films of a chiral comb-like liquid crystalline copolymer containing azobenzene chromophores in its side chains are optically isotropic in their twisted smectic-like glassy state. In contact with a nematic liquid crystal (5CB, E7, MBBA) they provide a degenerate planar orientation. When irradiated by unpolarized UV light, they orient the same nematics homeotropically. Treated with linearly polarized UV light they orient nematics homogeneously with the director along the electric vector of the exciting light. After a combined irradiation first with unpolarized UV light and then with linearly polarized visible light, the films again provide a homogeneous liquid crystal orientation, this time with the director perpendicular to the visible light electric vector. The phenomena observed are related to the light induced optical anisotropy. Two main processes are responsible for the anisotropy (1) a UV light depletion of trans-isomers of the azobenzene chromophores from the chosen direction and (2) a reorientation of the chromophores by polarized visible light.

  12. Controlling spontaneous emission of light by photonic crystals

    DEFF Research Database (Denmark)

    Lodahl, Peter

    2005-01-01

    Photonic bandgap crystals were proposed almost two decades ago as a unique tool for controlling propagation and emission of light. Since then the research field of photonic crystals has exploded and many beautiful demonstrations of the use of photonic crystals and fibers for molding light...... propagation have appeared that hold great promises for integrated optics. These major achievements solidly demonstrate the ability to control propagation of light. In contrast, an experimental demonstration of the use of photonic crystals for timing the emission of light has so far lacked. In a recent...... publication in Nature, we have demonstrated experimentally that both the direction and time of spontaneous emission can be controlled, thereby confirming the original proposal by Eli Yablonovich that founded the field of photonic crystals. We believe that this work opens new opportunities for solid...

  13. Liquid-crystal intraocular adaptive lens with wireless control

    NARCIS (Netherlands)

    Simonov, A.N.; Vdovine, G.V.; Loktev, M.

    2007-01-01

    We present a prototype of an adaptive intraocular lens based on a modal liquid-crystal spatial phase modulator with wireless control. The modal corrector consists of a nematic liquid-crystal layer sandwiched between two glass substrates with transparent low- and high-ohmic electrodes, respectively.

  14. Liquid-crystal intraocular adaptive lens with wireless control

    NARCIS (Netherlands)

    Simonov, A.N.; Vdovine, G.V.; Loktev, M.

    2007-01-01

    We present a prototype of an adaptive intraocular lens based on a modal liquid-crystal spatial phase modulator with wireless control. The modal corrector consists of a nematic liquid-crystal layer sandwiched between two glass substrates with transparent low- and high-ohmic electrodes, respectively.

  15. Control of exceptional points in photonic crystal slabs

    DEFF Research Database (Denmark)

    Kaminski, Piotr Marek; Taghizadeh, Alireza; Breinbjerg, Olav

    2017-01-01

    Various ways of controlling the extent of the ring of exceptional points in photonic crystal slabs are investigated. The extent of the ring in photonic crystal slabs is found to vary with the thickness of the slab. This enables recovery of Dirac cones in open, non-Hermitian systems......, such as a photonic crystal slab. In this case, all three bands exhibit a bound state in the continuum in close proximity of the Γ point. These results may lead to new designs of small photonic-crystal-based lasers exhibiting high-quality factors....

  16. Chiral superconductors.

    Science.gov (United States)

    Kallin, Catherine; Berlinsky, John

    2016-05-01

    Chiral superconductivity is a striking quantum phenomenon in which an unconventional superconductor spontaneously develops an angular momentum and lowers its free energy by eliminating nodes in the gap. It is a topologically non-trivial state and, as such, exhibits distinctive topological modes at surfaces and defects. In this paper we discuss the current theory and experimental results on chiral superconductors, focusing on two of the best-studied systems, Sr2RuO4, which is thought to be a chiral triplet p-wave superconductor, and UPt3, which has two low-temperature superconducting phases (in zero magnetic field), the lower of which is believed to be chiral triplet f-wave. Other systems that may exhibit chiral superconductivity are also discussed. Key signatures of chiral superconductivity are surface currents and chiral Majorana modes, Majorana states in vortex cores, and the possibility of half-flux quantum vortices in the case of triplet pairing. Experimental evidence for chiral superconductivity from μSR, NMR, strain, polar Kerr effect and Josephson tunneling experiments are discussed.

  17. Magnetic Control of MOF Crystal Orientation and Alignment.

    Science.gov (United States)

    Cheng, Fei; Marshall, Ellis S; Young, Adam J; Robinson, Peter J; Bouillard, Jean-Sebastien G; Adawi, Ali M; Vermeulen, Nicolaas A; Farha, Omar K; Reithofer, Michael R; Chin, Jia Min

    2017-09-14

    Most MOFs possess anisotropic properties, the full exploitation of which necessitates a general strategy for the controllable orientation of such MOF crystals. Current methods largely rely upon layer-by-layer MOF epitaxy or tuning of MOF crystal growth on appropriate substrates, yielding MOFs with fixed crystal orientations. Here, the dynamic magnetic alignment of different MOF crystals (NH2-MIL-53(Al) and NU-1000) is shown. The MOFs were magnetized by electrostatic adsorption of iron oxide nanoparticles, dispersed in curable polymer resins (Formlabs 1+ clear resin / Sylgard® 184), magnetically oriented and fixed by resin curing. The importance of crystal orientation on MOF functionality was demonstrated whereby magnetically aligned NU-1000/Sylgard® 184 composite was excited with linearly polarized 405 nm light, affording an anisotropic fluorescence response dependent on the polarization angle of the excitation beam relative to NU-1000 crystal orientation. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Nonlinear MIMO Control of a Continuous Cooling Crystallizer

    Directory of Open Access Journals (Sweden)

    Pedro Alberto Quintana-Hernández

    2012-01-01

    Full Text Available In this work, a feedback control algorithm was developed based on geometric control theory. A nonisothermal seeded continuous crystallizer model was used to test the algorithm. The control objectives were the stabilization of the third moment of the crystal size distribution (μ3 and the crystallizer temperature (T; the manipulated variables were the stirring rate and the coolant flow rate. The nonlinear control (NLC was tested at operating conditions established within the metastable zone. Step changes of magnitudes ±0.0015 and ±0.5°C were introduced into the set point values of the third moment and crystallizer temperature, respectively. In addition, a step change of ±1°C was introduced as a disturbance in the feeding temperature. Closed-loop stability was analyzed by calculating the eigenvalues of the internal dynamics. The system presented a stable dynamic behavior when the operation conditions maintain the crystallizer concentration within the metastable zone. Closed-loop simulations with the NLC were compared with simulations that used a classic PID controller. The PID controllers were tuned by minimizing the integral of the absolute value of the error (IAE criterion. The results showed that the NLC provided a suitable option for continuous crystallization control. For all analyzed cases, the IAEs obtained with NLC were smaller than those obtained with the PID controller.

  19. Enzymatically Controlled Vacancies in Nanoparticle Crystals

    Energy Technology Data Exchange (ETDEWEB)

    Barnaby, Stacey N.; Ross, Michael B.; Thaner, Ryan V.; Lee, Byeongdu; Schatz, George C.; Mirkin, Chad A.

    2016-08-01

    In atomic systems, the mixing of metals results in distinct phase behavior that depends on the identity and bonding characteristics of the atoms. In nanoscale systems, the use of oligonucleotides as programmable “bonds” that link nanoparticle “atoms” into superlattices allows for the decoupling of atom identity and bonding. While much research in atomic systems is dedicated to understanding different phase behavior of mixed metals, it is not well understood on the nanoscale how changes in the nanoscale “bond” affect the phase behavior of nanoparticle crystals. In this work, the identity of the atom is kept the same but the chemical nature of the bond is altered, which is not possible in atomic systems, through the use of DNA and RNA bonding elements. These building blocks assemble into single crystal nanoparticle superlattices with mixed DNA and RNA bonding elements throughout. The nanoparticle crystals can be dynamically changed through the selective and enzymatic hydrolysis of the RNA bonding elements, resulting in superlattices that retain their crystalline structure and habit, while incorporating up to 35% random vacancies generated from the nanoparticles removed. Therefore, the bonding elements of nanoparticle crystals can be enzymatically and selectively addressed without affecting the nature of the atom.

  20. Controlling electric, magnetic, and chiral dipolar emission with PT-symmetric potentials

    Energy Technology Data Exchange (ETDEWEB)

    Alaeian, Hadiseh; Dionne, Jennifer A.

    2015-06-01

    We investigate the effect of parity-time (PT) symmetric optical potentials on the radiation of achiral and chiral dipole sources. Two properties unique to PT-symmetric potentials are observed. First, the dipole can be tuned to behave as a strong optical emitter or absorber based on the non-Hermiticity parameter and the dipole location. Second, exceptional points give rise to new system resonances that lead to orders-of-magnitude enhancements in the dipolar emitted or absorbed power. Utilizing these properties, we show that enantiomers of chiral molecules near PT-symmetric metamaterials exhibit a 4.5-fold difference in their emitted power and decay rate. The results of this work could enable new atom-cavity interactions for quantum optics, as well as all-optical enantioselective separation.

  1. Surface control of alkyl chain conformations and 2D chiral amplification.

    Science.gov (United States)

    Hauptmann, Nadine; Scheil, Katharina; Gopakumar, Thiruvancheril G; Otte, Franziska L; Schütt, Christian; Herges, Rainer; Berndt, Richard

    2013-06-19

    Trioctyl-functionalized triazatriangulenium (trioctyl-TATA) deposited on Au(111) and Ag(111) surfaces by electrospray ionization was investigated using low-temperature scanning tunneling microscopy. The molecule surprisingly adsorbs with gauche rather than anti conformations of the octyl groups. We observed chiral amplification in the islands. Only one of the eight possible configurations of the octyl groups was found in homochiral hexagonal networks. Quantum-chemical calculations confirmed and explained the preference for the gauche conformations of adsorbed trioctyl-TATA.

  2. Factors That Control Successful Entropically Driven Chiral Separations in SFC and HPLC.

    Science.gov (United States)

    Stringham, R W; Blackwell, J A

    1997-04-01

    With temperature increases, selectivity of chiral separations decreases until enantiomers coelute at an isoelution temperature. Above this temperature, elution order should reverse and selectivity will increase with temperature. In this region, separation is termed "entropically driven". Entropically driven chiral separations hold the promise of being able to concurrently increase selectivity and column efficiency by means of increased temperature. The ability to achieve such separations is hindered by high isoelution temperatures. The isoelution temperature is determined by a balance of enthalpic and entropic contributions. A variety of mobile phase modifiers are evaluated for their ability to moderate these contributions. Results suggest that more use should be made of non-alcohol modifiers. The major barrier to entropically driven separations was found to be the nonspecific retention increase that is characteristic when the critical temperature is traversed. Use of hexane in place of CO(2) shifts the position of the retention increase away from the temperature range used in this study, and dramatically successful entropically driven chiral separations are obtained.

  3. Stimuli-Directed Helical Chirality Inversion and Bio-Applications

    Directory of Open Access Journals (Sweden)

    Ziyu Lv

    2016-08-01

    Full Text Available Helical structure is a sophisticated ubiquitous motif found in nature, in artificial polymers, and in supramolecular assemblies from microscopic to macroscopic points of view. Significant progress has been made in the synthesis and structural elucidation of helical polymers, nevertheless, a new direction for helical polymeric materials, is how to design smart systems with controllable helical chirality, and further use them to develop chiral functional materials and promote their applications in biology, biochemistry, medicine, and nanotechnology fields. This review summarizes the recent progress in the development of high-performance systems with tunable helical chirality on receiving external stimuli and discusses advances in their applications as drug delivery vesicles, sensors, molecular switches, and liquid crystals. Challenges and opportunities in this emerging area are also presented in the conclusion.

  4. Controllable Optical Bistability in a Crystal of Molecular Magnets System

    Institute of Scientific and Technical Information of China (English)

    LIU Ji-Bing; LU Xin-You; HAO Xiang-Ying; SI Liu-Gang; YANG Xiao-Xue

    2008-01-01

    We investigate the formation of opticai bistability (OB) in a crystal of molecular magnets contained in a unidirectional ring cavity. The crystal is subjected to one de magnetic field and two (probe and coupling) ac resonant magnetic field. The results show that OB can be controlled efficiently by adjusting the intensity of the control field, the detuning of probe magnetic field and the cooperation parameter. Furthermore, within certain parameter range, the optical multistablity (OM) can also be observed in the crystal medium. This investigation can be used for designing new types of nonelectronic devices for realizing switching process.

  5. Controlling Anderson localization in disordered photonic crystal waveguides

    CERN Document Server

    Garcia, P D; Stobbe, S; Lodahl, P

    2010-01-01

    We prove Anderson localization in a disordered photonic crystal waveguide by measuring the ensemble-averaged localization length which is controlled by the dispersion of the photonic crystal waveguide. In such structures, the localization length shows a 10-fold variation between the fast- and the slow-light regime and, in the latter case, it becomes shorter than the sample length thus giving rise to strongly confined modes. The dispersive behavior of the localization length demonstrates the close relation between Anderson localization and the photon density of states in disordered photonic crystals, which opens a promising route to controlling and exploiting Anderson localization for efficient light confinement.

  6. A liquid crystalline chirality balance for vapours

    Science.gov (United States)

    Ohzono, Takuya; Yamamoto, Takahiro; Fukuda, Jun-Ichi

    2014-04-01

    Chiral discrimination of vapours plays an important role in olfactory perception of biological systems and its realization by artificial sensors has been an intriguing challenge. Here, we report a simple method that tangibly visualizes the chirality of a diverse variety of molecules dissolved from vapours with high sensitivity, by making use of a structural change in a periodic microstructure of a nematic liquid crystal confined in open microchannels. This microstructure is accompanied by a topological line defect of a zigzag form with equal lengths of ‘zig’ and ‘zag.’ We find that a tiny amount of vapour of chiral molecules injected onto the liquid crystal induces the imbalance of ‘zig’ and ‘zag’ depending on its enantiomeric excess within a few seconds. Our liquid-crystal-based ‘chirality balance’ offers a simple, quick and versatile chirality-sensing/-screening method for gas-phase analysis (for example, for odours, environmental chemicals or drugs).

  7. Chiral acidic amino acids induce chiral hierarchical structure in calcium carbonate

    Science.gov (United States)

    Jiang, Wenge; Pacella, Michael S.; Athanasiadou, Dimitra; Nelea, Valentin; Vali, Hojatollah; Hazen, Robert M.; Gray, Jeffrey J.; McKee, Marc D.

    2017-04-01

    Chirality is ubiquitous in biology, including in biomineralization, where it is found in many hardened structures of invertebrate marine and terrestrial organisms (for example, spiralling gastropod shells). Here we show that chiral, hierarchically organized architectures for calcium carbonate (vaterite) can be controlled simply by adding chiral acidic amino acids (Asp and Glu). Chiral, vaterite toroidal suprastructure having a `right-handed' (counterclockwise) spiralling morphology is induced by L-enantiomers of Asp and Glu, whereas `left-handed' (clockwise) morphology is induced by D-enantiomers, and sequentially switching between amino-acid enantiomers causes a switch in chirality. Nanoparticle tilting after binding of chiral amino acids is proposed as a chiral growth mechanism, where a `mother' subunit nanoparticle spawns a slightly tilted, consequential `daughter' nanoparticle, which by amplification over various length scales creates oriented mineral platelets and chiral vaterite suprastructures. These findings suggest a molecular mechanism for how biomineralization-related enantiomers might exert hierarchical control to form extended chiral suprastructures.

  8. Frequency doubling crystals

    Science.gov (United States)

    Wang, Francis; Velsko, Stephan P.

    1989-01-01

    A systematic approach to the production of frequency conversion crystals is described in which a chiral molecule has attached to it a "harmonic generating unit" which contributes to the noncentrosymmetry of the molecule. Certain preferred embodiments of such harmonic generating units include carboxylate, guanadyly and imidazolyl units. Certain preferred crystals include L-arginine fluoride, deuterated L-arginine fluoride, L-arginine chloride monohydrate, L-arginine acetate, dithallium tartrate, ammonium N-acetyl valine, N-acetyl tyrosine and N-acetyl hydroxyproline. Chemical modifications of the chiral molecule, such as deuteration, halogenation and controlled counterion substitution are available to adapt the dispersive properties of a crystal in a particular wavelength region.

  9. One more chiral drug prone to spontaneous resolution: Binary phase diagram, absolute configuration, and crystal packing of bevantolol hydrochloride

    Science.gov (United States)

    Bredikhina, Zemfira A.; Zakharychev, Dmitry V.; Gubaidullin, Aidar T.; Bredikhin, Alexander A.

    2009-11-01

    Spontaneous resolution of cardioselective β1-adrenergic blocker bevantolol hydrochloride1·HCl was established by IR spectroscopy, differential scanning calorimetry, and by single crystal X-ray analysis both for enantiopure and racemic samples. The absolute configuration of 1·HCl was evaluated through Flack parameter method. The molecular structure and crystal packing details were evaluated; the symmetry independent fragment of the P1 unit cell consists of two molecules which have almost identical spatial arrangement, but differ sufficiently in the nature of nitrogen atoms: quaternary form in one case and free amine form in the other.

  10. Spontaneous resolution upon crystallization of chiral La(III) and Gd(III) MOFs from achiral dihydroxymalonate.

    Science.gov (United States)

    Gil-Hernández, Beatriz; Höppe, Henning A; Vieth, Jana K; Sanchiz, Joaquin; Janiak, Christoph

    2010-11-21

    The achiral chelating and bridging dihydroxymalonato (mesoxalato) ligand is a new enantiopurity enforcer in extended structures by yielding the Λ/Δ-metal configured homochiral MOFs 2D-[Ln(2)(μ-mesoxalato)(3)(H(2)O)(6)] (Ln = La(III), Gd(III)) through self-resolution during crystal growth.

  11. Controlling elastic waves with small phononic crystals containing rigid inclusions

    KAUST Repository

    Peng, Pai

    2014-05-01

    We show that a two-dimensional elastic phononic crystal comprising rigid cylinders in a solid matrix possesses a large complete band gap below a cut-off frequency. A mechanical model reveals that the band gap is induced by negative effective mass density, which is affirmed by an effective medium theory based on field averaging. We demonstrate, by two examples, that such elastic phononic crystals can be utilized to design small devices to control low-frequency elastic waves. One example is a waveguide made of a two-layer anisotropic elastic phononic crystal, which can guide and bend elastic waves with wavelengths much larger than the size of the waveguide. The other example is the enhanced elastic transmission of a single-layer elastic phononic crystal loaded with solid inclusions. The effective mass density and reciprocal of the modulus of the single-layer elastic phononic crystal are simultaneously near zero. © CopyrightEPLA, 2014.

  12. Controlled Growth of Rubrene Nanowires by Eutectic Melt Crystallization

    Science.gov (United States)

    Chung, Jeyon; Hyon, Jinho; Park, Kyung-Sun; Cho, Boram; Baek, Jangmi; Kim, Jueun; Lee, Sang Uck; Sung, Myung Mo; Kang, Youngjong

    2016-03-01

    Organic semiconductors including rubrene, Alq3, copper phthalocyanine and pentacene are crystallized by the eutectic melt crystallization. Those organic semiconductors form good eutectic systems with the various volatile crystallizable additives such as benzoic acid, salicylic acid, naphthalene and 1,3,5-trichlorobenzene. Due to the formation of the eutectic system, organic semiconductors having originally high melting point (Tm > 300 °C) are melted and crystallized at low temperature (Te = 40.8–133 °C). The volatile crystallizable additives are easily removed by sublimation. For a model system using rubrene, single crystalline rubrene nanowires are prepared by the eutectic melt crystallization and the eutectic-melt-assisted nanoimpinting (EMAN) technique. It is demonstrated that crystal structure and the growth direction of rubrene can be controlled by using different volatile crystallizable additives. The field effect mobility of rubrene nanowires prepared using several different crystallizable additives are measured and compared.

  13. Self-organization ability of chiral Nα-substituted, Nβ-Boc protected α-hydrazino acetamides in the crystal and solution states.

    Science.gov (United States)

    Moussodia, Ralph-Olivier; Romero, Eugenie; Wenger, Emmanuel; Jamart-Grégoire, Brigitte; Acherar, Samir

    2017-08-29

    The limitations of peptides have severely hampered their use in pharmacology, thus prompting the design of new peptidomimetic foldamers. This requires precise knowledge of the secondary structure of new compounds and the ability to predict their self-organization. Conformational studies of the basic units of these foldamers can be of invaluable assistance in designing new bioactive compounds. To this end, we investigated the conformation of three chiral Nα-substituted, Nβ-Boc protected α-hydrazino acetamide model compounds containing various side chains both on the Nα- and Cα- atoms in both the crystal and solution states. On the basis of IR spectroscopy, NMR and X-ray diffraction experiments, we demonstrated that these three models adopt conformational preferences, relying on eight-, six- or five-membered H-bonded pseudocycles (C8, C6 or C5), depending on the steric bulk of both Nα- or Cα- side chains. This study sheds light onto the versatile self-organization ability of the specific class of α-Nα-hydrazinopeptides and emphasizes the key role of the Cα- side chain on the conformational preference of the self-structuration.

  14. Supramolecular Chirality: Solvent Chirality Transfer in Molecular Chemistry and Polymer Chemistry

    Directory of Open Access Journals (Sweden)

    Michiya Fujiki

    2014-08-01

    Full Text Available Controlled mirror symmetry breaking arising from chemical and physical origin is currently one of the hottest issues in the field of supramolecular chirality. The dynamic twisting abilities of solvent molecules are often ignored and unknown, although the targeted molecules and polymers in a fluid solution are surrounded by solvent molecules. We should pay more attention to the facts that mostly all of the chemical and physical properties of these molecules and polymers in the ground and photoexcited states are significantly influenced by the surrounding solvent molecules with much conformational freedom through non-covalent supramolecular interactions between these substances and solvent molecules. This review highlights a series of studies that include: (i historical background, covering chiral NaClO3 crystallization in the presence of d-sugars in the late 19th century; (ii early solvent chirality effects for optically inactive chromophores/fluorophores in the 1960s–1980s; and (iii the recent development of mirror symmetry breaking from the corresponding achiral or optically inactive molecules and polymers with the help of molecular chirality as the solvent use quantity.

  15. Isotopic chirality

    Energy Technology Data Exchange (ETDEWEB)

    Floss, H.G. [Univ. of Washington, Seattle, WA (United States)

    1994-12-01

    This paper deals with compounds that are chiral-at least in part, due to isotope substitution-and their use in tracing the steric course of enzyme reaction in vitro and in vivo. There are other applications of isotopically chiral compounds (for example, in analyzing the steric course of nonenzymatic reactions and in probing the conformation of biomolecules) that are important but they will not be discussed in this context.

  16. Phase behavior and crystal structure of 3-(1-naphthyloxy)- and 3-(4-indolyloxy)-propane-1,2-diol, synthetic precursors of chiral drugs propranolol and pindolol

    Science.gov (United States)

    Bredikhin, Alexander A.; Gubaidullin, Aidar T.; Bredikhina, Zemfira A.; Fayzullin, Robert R.; Samigullina, Aida I.; Zakharychev, Dmitry V.

    2013-08-01

    Valuable precursors of popular chiral drugs propranolol and pindolol, 3-(1-naphthyloxy)-propane-1,2-diol 3 and 3-(4-indolyloxy)-propane-1,2-diol 4 were investigated by IR spectroscopy, DSC, and X-ray diffraction methods. Both compounds, crystallizing from enantiopure feed material, form "guaifenesin-like" crystal packing in which the classic H-bonded bilayers, framed in both sides by hydrophobic fragments of the molecules, acts as the basic crystal-forming motif. Diol 4 prone to spontaneous resolution and conserves its packing pattern crystallizing from racemate. Under the same conditions, diol 3 forms weakly stable solid racemic compound. Some reasons for such a behavior are identified and discussed.

  17. Nematic twist cell: Strong chirality induced at the surfaces

    Science.gov (United States)

    Lin, Tzu-Chieh; Nemitz, Ian R.; Pendery, Joel S.; Schubert, Christopher P. J.; Lemieux, Robert P.; Rosenblatt, Charles

    2013-04-01

    A nematic twist cell having a thickness gradient was filled with a mixture containing a configurationally achiral liquid crystal (LC) and chiral dopant. A chiral-based linear electrooptic effect was observed on application of an ac electric field. This "electroclinic effect" varied monotonically with d, changing sign at d =d0 where the chiral dopant exactly compensated the imposed twist. The results indicate that a significant chiral electrooptic effect always exists near the surfaces of a twist cell containing molecules that can be conformationally deracemized. Additionally, this approach can be used to measure the helical twisting power (HTP) of a chiral dopant in a liquid crystal.

  18. Controlled coupling of photonic crystal cavities using photochromic tuning

    CERN Document Server

    Cai, Tao; Solomon, Glenn S; Waks, Edo

    2013-01-01

    We present a method to control the resonant coupling interaction in a coupled-cavity photonic crystal molecule by using a local and reversible photochromic tuning technique. We demonstrate the ability to tune both a two-cavity and a three-cavity photonic crystal molecule through the resonance condition by selectively tuning the individual cavities. Using this technique, we can quantitatively determine important parameters of the coupled-cavity system such as the photon tunneling rate. This method can be scaled to photonic crystal molecules with larger numbers of cavities, which provides a versatile method for studying strong interactions in coupled resonator arrays.

  19. Nanowire Oriented On-Surface Growth of Chiral Cystine Crystalline Nanosheets.

    Science.gov (United States)

    Zhang, Shenxiang; Zhang, Feng; Qin, Haili; Hu, Liang; Jin, Jian

    2015-08-18

    Exploration of an effective route to achieve the controlled growth of two-dimensional (2D) molecular crystal is of scientific significance yet greatly underdeveloped due to the complexity of weak intermolecular interactions, thus leading to difficulty of inducing anisotropic 2D growth. We report here a facile nanowire oriented on-surface growth strategy for the fabrication of cystine crystalline nanosheets with finely controlled thickness (1.1, 1.9, 2.9, and 4.8 nm which correspond to one layer, two layers, three layers, and five layers of crystal cystine, respectively) and large areas (>100 μm(2)). The cystine crystalline nanosheets display chirality delivered by chiral cysteine monomers, either l-cysteine or d-cysteine. The chiral nanosheets with structural precision and chemical diversity could serve as a novel 2D platform for constructing advanced hybrid materials.

  20. Anion effect on the binary and ternary phase diagrams of chiral medetomidine salts and conglomerate crystal formation.

    Science.gov (United States)

    Choobdari, Ebrahim; Fakhraian, Hossein; Peyrovi, Mohammad Hassan

    2014-03-01

    The binary phase diagrams of hydrogen halides salts of medetomidine (Med.HX, X:Br,I) and hydrogen oxalate salt of medetomidine (Med.Ox) were determined based on thermogravimetric/differential thermal analysis (TGA/DTA) and their crystal structure behavior was confirmed by comparison of the X-ray diffractometry and FT-IR spectroscopy of the racemate and pure enantiomer. All hydrogen halide salts presented racemic compound behavior. Heat of fusion of halides salt of (rac)-medetomidine decreased with ionic radius increase. Eutectic points for Med.HCl (previously reported), Med.HBr, and Med.HI rest were unchanged approximately. The solubility of different enantiomeric mixtures of Med.HBr and Med.HI were measured at 10, 20, and 30°C in 2-propanol showing a solubility increase with ionic radius. A binary phase diagram of Med.Ox shows a racemic conglomerate behavior. The solubility of enantiomeric mixtures of Med.Ox were measured at 10, 20, 30, and 40°C. The ternary phase diagram of Med.Ox in ethanol conforms to a conglomerate crystal forming system, favoring its enantiomeric purification by preferential crystallization.

  1. Controlling Anderson localization in disordered photonic crystal waveguides

    DEFF Research Database (Denmark)

    Garcia-Fernández, David; Smolka, Stephan; Stobbe, Søren

    2010-01-01

    of a disordered photonic crystal waveguide and attributed to Anderson localization. We have tested this hypothesis by measuring the light localization length, ξloc, in a disordered photonic crystal waveguide and checked explicitly the criterion of one dimensional Anderson localization that ξloc is shorter than...... the waveguide length LS. Our measurements demonstrate for the first time the close relation between light localization and density of states, which can be used ultimately for controlling Anderson localized modes....

  2. Controlling Anderson localization in disordered photonic crystal waveguides

    DEFF Research Database (Denmark)

    Garcia-Fernández, David; Smolka, Stephan; Stobbe, Søren;

    2010-01-01

    of a disordered photonic crystal waveguide and attributed to Anderson localization. We have tested this hypothesis by measuring the light localization length, ξloc, in a disordered photonic crystal waveguide and checked explicitly the criterion of one dimensional Anderson localization that ξloc is shorter than...... the waveguide length LS. Our measurements demonstrate for the first time the close relation between light localization and density of states, which can be used ultimately for controlling Anderson localized modes....

  3. A plant tendril mimic soft actuator with phototunable bending and chiral twisting motion modes

    Science.gov (United States)

    Wang, Meng; Lin, Bao-Ping; Yang, Hong

    2016-12-01

    In nature, plant tendrils can produce two fundamental motion modes, bending and chiral twisting (helical curling) distortions, under the stimuli of sunlight, humidity, wetting or other atmospheric conditions. To date, many artificial plant-like mechanical machines have been developed. Although some previously reported materials could realize bending or chiral twisting through tailoring the samples into various ribbons along different orientations, each single ribbon could execute only one deformation mode. The challenging task is how to endow one individual plant tendril mimic material with two different, fully tunable and reversible motion modes (bending and chiral twisting). Here we show a dual-layer, dual-composition polysiloxane-based liquid crystal soft actuator strategy to synthesize a plant tendril mimic material capable of performing two different three-dimensional reversible transformations (bending versus chiral twisting) through modulation of the wavelength band of light stimuli (ultraviolet versus near-infrared). This material has broad application prospects in biomimetic control devices.

  4. Location control of crystal grains in excimer laser crystallization of silicon thin films

    Science.gov (United States)

    Kumomi, Hideya

    2003-07-01

    Location of crystal grains in polycrystalline Si thin films formed by excimer-laser crystallization is controlled by manipulating the superlateral-growth phenomenon. The superlateral growth of a single grain occurs preferentially at an artificial site where nanometer-sized crystallites are embedded in the precursory amorphous thin films. Only a part of the crystallites embedded in the site could survive the melting and grow to serve as the seed crystal in the subsequent recrystallization. Such grain-location control provides a basis for two-dimensional control of the grain-boundary location in low-temperature polycrystalline Si thin films, which is essential to the device-to-device uniformity of high-performance thin-film transistors.

  5. Kinetically controlled synthesis of monoglyceryl esters from chiral and prochiral acids methyl esters catalyzed by immobilized Rhizomucor miehei lipase.

    Science.gov (United States)

    Acosta, Andreina; Filice, Marco; Fernandez-Lorente, Gloria; Palomo, Jose M; Guisan, Jose M

    2011-01-01

    Partial acylation of only one primary hydroxyl group of glycerol generates a chiral center at position 2. Rhizomucor miehei lipase (RML) catalyzes the kinetically controlled transesterification of different aromatic carboxylic acids methyl esters with glycerol. High synthetic yields of glyceryl esters (around 70-80%) were obtained even in the presence of significant concentrations of water (from 5% to 20%). After a long incubation of the reaction mixture in the presence of the biocatalyst only pure free acid was obtained. Other lipases (from Geobacillus thermocatenulatus and from Thermomyces lanuginose) also catalyzed similar kinetically controlled transesterifications although less efficiently. RML immobilized on Sepharose-Q showed a high activity and specificity, compared to the immobilization by other techniques, only producing monoglyceryl esters with all substrates. In particular, monoglyceryl-phenylmalonate product was synthesized in 82% overall yield and >99% diastereomeric excess at pH 7.0 and 37°C and 90% glycerol.

  6. Surface-modified silica colloidal crystals: nanoporous films and membranes with controlled ionic and molecular transport.

    Science.gov (United States)

    Zharov, Ilya; Khabibullin, Amir

    2014-02-18

    Nanoporous membranes are important for the study of the transport of small molecules and macromolecules through confined spaces and in applications ranging from separation of biomacromolecules and pharmaceuticals to sensing and controlled release of drugs. For many of these applications, chemists need to gate the ionic and molecular flux through the nanopores, which in turn depends on the ability to control the nanopore geometry and surface chemistry. Most commonly used nanoporous membrane materials are based on polymers. However, the nanostructure of polymeric membranes is not well-defined, and their surface is hard to modify. Inorganic nanoporous materials are attractive alternatives for polymers in the preparation of nanoporous membranes. In this Account, we describe the preparation and surface modification of inorganic nanoporous films and membranes self-assembled from silica colloidal spheres. These spheres form colloidal crystals with close-packed face centered cubic lattices upon vertical deposition from colloidal solutions. Silica colloidal crystals contain ordered arrays of interconnected three dimensional voids, which function as nanopores. We can prepare silica colloidal crystals as supported thin films on various flat solid surfaces or obtain free-standing silica colloidal membranes by sintering the colloidal crystals above 1000 °C. Unmodified silica colloidal membranes are capable of size-selective separation of macromolecules, and we can surface-modify them in a well-defined and controlled manner with small molecules and polymers. For the surface modification with small molecules, we use silanol chemistry. We grow polymer brushes with narrow molecular weight distribution and controlled length on the colloidal nanopore surface using atom transfer radical polymerization or ring-opening polymerization. We can control the flux in the resulting surface-modified nanoporous films and membranes by pH and ionic strength, temperature, light, and small molecule

  7. The influence of a chiral amino acid on the helical handedness of PNA in solution and in crystals

    DEFF Research Database (Denmark)

    Rasmussen, Hanne B.; Petersson, B; Nielsen, P E;

    2004-01-01

    The X-ray structure of a self-complementary PNA hexamer (H-CGTACG-L-Lys-NH(2)) has been determined to 2.35 A resolution. The introduction of an L-lysine moiety has previously been shown to induce a preferred left-handedness of the PNA double helices in aqueous solution. However, in the crystal...... for the left-handed helix of this hexameric PNA in aqueous solution as expected. The calculations indicate that the difference in the free energy of solvation between the left-handed and the right-handed helix is the determining factor for the preference of the left-handed helix in aqueous solution....

  8. Electro-optical characteristics of a chiral hybrid in-plane switching liquid crystal mode for high brightness.

    Science.gov (United States)

    Gwag, Jin Seog; Sohn, Kyunghwa; Kim, Young-Ki; Kim, Jae-Hoon

    2008-08-04

    We propose a new in-plane switching (IPS) nematic liquid crystal (LC) mode which uses a twist effect with a hybrid LC alignment and interdigitated electrodes as an approach for a high brightness. This is optimized to a normally white mode to minimize loss of transmittance at the electrode compared to the conventional IPS mode. The proposed mode shows an excellent dark state because the bulk LCs are aligned in parallel to the optic axis of the polarizer under low electric fields. Consequently, this proposed mode exhibits a much higher contrast ratio (980:1) than that of the conventional IPS mode (550:1).

  9. Effects of molecular chirality on self-assembly and switching in liquid crystals at the cross-over between rod-like and bent shapes.

    Science.gov (United States)

    Ocak, Hale; Poppe, Marco; Bilgin-Eran, Belkız; Karanlık, Gürkan; Prehm, Marko; Tschierske, Carsten

    2016-09-21

    A bent-core compound derived from a 4-cyanoresorcinol core unit with two terephthalate based rod-like wings and carrying chiral 3,7-dimethyloctyloxy side chains has been synthesized in racemic and enantiomerically pure form and characterized by polarizing microscopy, differential scanning calorimetry, X-ray diffraction and electro-optical investigations to study the influence of molecular chirality on the superstructural chirality and polar order in lamellar liquid crystalline phases. Herein we demonstrate that the coupling of molecular chirality with superstructural layer chirality in SmCsPF domain phases (forming energetically distinct diastereomeric pairs) can fix the tilt direction and thus stabilize synpolar order, leading to bistable ferroelectric switching in the SmC* phases of the (S)-enantiomer, whereas tristable modes determine the switching of the racemate. Moreover, the mechanism of electric field induced molecular reorganization changes from a rotation around the molecular long axis in the racemate to a rotation on the tilt-cone for the (S)-enantiomer. At high temperature the enantiomer behaves like a rod-like molecule with a chirality induced ferroelectric SmC* phase and an electroclinic effect in the SmA'* phase. At reduced temperature sterically induced polarization, due to the bent molecular shape, becomes dominating, leading to much higher polarization values, thus providing access to high polarization ferroelectric materials with weakly bent compounds having only "weakly chiral" stereogenic units. Moreover, the field induced alignment of the SmCsPF(()*()) domains gives rise to a special kind of electroclinic effect appearing even in the absence of molecular chirality. Comparison with related compounds indicates that the strongest effects of chirality appear for weakly bent molecules with a relatively short coherence length of polar order, whereas for smectic phases with long range polar order the effects of the interlayer interfaces can override

  10. Chirality-Controlled Growth of Single-Wall Carbon Nanotubes Using Vapor Phase Epitaxy: Mechanistic Understanding and Scalable Production

    Science.gov (United States)

    2016-09-15

    cloning process is illustrated in Fig. 1a. Firstly, chirality- pure SWCNT seeds obtained from the DNA-based separation were deposited onto the...chiralities of the nanotube seeds are preserved in the extended portion of the nanotubes, and the semiconducting nature of the grown (7, 6) and (6...order to determine whether the original chiralities were preserved during the cloning process , we used micro-Raman to characterize the pristine and

  11. Enantioselective recognition at mesoporous chiral metal surfaces

    Science.gov (United States)

    Wattanakit, Chularat; Côme, Yémima Bon Saint; Lapeyre, Veronique; Bopp, Philippe A.; Heim, Matthias; Yadnum, Sudarat; Nokbin, Somkiat; Warakulwit, Chompunuch; Limtrakul, Jumras; Kuhn, Alexander

    2014-02-01

    Chirality is widespread in natural systems, and artificial reproduction of chiral recognition is a major scientific challenge, especially owing to various potential applications ranging from catalysis to sensing and separation science. In this context, molecular imprinting is a well-known approach for generating materials with enantioselective properties, and it has been successfully employed using polymers. However, it is particularly difficult to synthesize chiral metal matrices by this method. Here we report the fabrication of a chirally imprinted mesoporous metal, obtained by the electrochemical reduction of platinum salts in the presence of a liquid crystal phase and chiral template molecules. The porous platinum retains a chiral character after removal of the template molecules. A matrix obtained in this way exhibits a large active surface area due to its mesoporosity, and also shows a significant discrimination between two enantiomers, when they are probed using such materials as electrodes.

  12. Asymmetric synthesis using chiral-encoded metal

    Science.gov (United States)

    Yutthalekha, Thittaya; Wattanakit, Chularat; Lapeyre, Veronique; Nokbin, Somkiat; Warakulwit, Chompunuch; Limtrakul, Jumras; Kuhn, Alexander

    2016-08-01

    The synthesis of chiral compounds is of crucial importance in many areas of society and science, including medicine, biology, chemistry, biotechnology and agriculture. Thus, there is a fundamental interest in developing new approaches for the selective production of enantiomers. Here we report the use of mesoporous metal structures with encoded geometric chiral information for inducing asymmetry in the electrochemical synthesis of mandelic acid as a model molecule. The chiral-encoded mesoporous metal, obtained by the electrochemical reduction of platinum salts in the presence of a liquid crystal phase and the chiral template molecule, perfectly retains the chiral information after removal of the template. Starting from a prochiral compound we demonstrate enantiomeric excess of the (R)-enantiomer when using (R)-imprinted electrodes and vice versa for the (S)-imprinted ones. Moreover, changing the amount of chiral cavities in the material allows tuning the enantioselectivity.

  13. Electro-optic switching in iron oxide nanoparticle embedded paramagnetic chiral liquid crystal via magneto-electric coupling

    Energy Technology Data Exchange (ETDEWEB)

    Goel, Puja, E-mail: pujagoel@gmail.com [Division of Agricultural Chemicals, Indian Agricultural Research Institute, New Delhi 110012 (India); Arora, Manju; Biradar, Ashok M. [Materials Physics and Engineering Division, CSIR-National Physical Laboratory, Dr. K. S. Krishnan Marg, New Delhi 110012 (India)

    2014-03-28

    The variation in optical texture, electro-optic, and dielectric properties of iron oxide nanoparticles (NPs) embedded ferroelectric liquid crystal (FLC) with respect to change in temperature and electrical bias conditions are demonstrated in the current investigations. Improvement in spontaneous polarization and response time in nanocomposites has been attributed to magneto-electric (ME) coupling resulting from the strong interaction among the ferromagnetic nanoparticle's exchange field (due to unpaired e{sup −}) and the field of liquid crystal molecular director. Electron paramagnetic resonance spectrum of FLC material gives a broad resonance signal with superimposed components indicating the presence of a source of spin. This paramagnetic behavior of host FLC material had been a major factor in strengthening the guest host interaction by giving an additional possibility of (a) spin-spin interaction and (b) interactions between magnetic-dipole and electric-dipole moments (ME effects) in the composite materials. Furthermore, the phenomenon of dielectric and static memory effect in these composites are also observed which yet again confirms the coupling of magnetic NP's field with FLC's director orientation. We therefore believe that such advanced soft materials holding the optical and electrical properties of conventional LCs with the magnetic and electronic properties of ferromagnetic nanoparticles are going to play a key role in the development of futuristic multifunctional optical devices.

  14. Highly diastereoselective dioxetane formation in the photooxygenation of enecarbamates with an oxazolidinone chiral auxiliary: steric control in the [2 + 2] cycloaddition of singlet oxygen through conformational alignment.

    Science.gov (United States)

    Adam, Waldemar; Bosio, Sara G; Turro, Nicholas J

    2002-07-31

    The photooxygenation of oxazolidinone-substituted enecarbamates leads to diastereomerically pure dioxetanes. The high diastereoselectivity is rationalized in terms of effective pi-facial control achieved by shielding one side of the double bond with the chiral auxiliary. The absolute configuration of the dioxetanes is assigned by derivatization to diols.

  15. Chiral Quantum Optics

    CERN Document Server

    Lodahl, Peter; Stobbe, Søren; Schneeweiss, Philipp; Volz, Jürgen; Rauschenbeutel, Arno; Pichler, Hannes; Zoller, Peter

    2016-01-01

    At the most fundamental level, the interaction between light and matter is manifested by the emission and absorption of single photons by single quantum emitters. Controlling light--matter interaction is the basis for diverse applications ranging from light technology to quantum--information processing. Many of these applications are nowadays based on photonic nanostructures strongly benefitting from their scalability and integrability. The confinement of light in such nanostructures imposes an inherent link between the local polarization and propagation direction of light. This leads to {\\em chiral light--matter interaction}, i.e., the emission and absorption of photons depend on the propagation direction and local polarization of light as well as the polarization of the emitter transition. The burgeoning research field of {\\em chiral quantum optics} offers fundamentally new functionalities and applications both for single emitters and ensembles thereof. For instance, a chiral light--matter interface enables...

  16. Control and femtosecond time-resolved imaging of torsion in a chiral molecule

    CERN Document Server

    Hansen, Jonas L; Madsen, Christian Bruun; Lindhardt, Anders Thyboe; Johansson, Mikael P; Skrydstrup, Troels; Madsen, Lars Bojer; Stapelfeldt, Henrik

    2012-01-01

    We study how the combination of long and short laser pulses, can be used to induce torsion in an axially chiral biphenyl derivative (3,5-difluoro-3',5'-dibromo-4'-cyanobiphenyl). A long, with respect to the molecular rotational periods, elliptically polarized laser pulse produces 3D alignment of the molecules, and a linearly polarized short pulse initiates torsion about the stereogenic axis. The torsional motion is monitored in real-time by measuring the dihedral angle using femtosecond time-resolved Coulomb explosion imaging. Within the first 4 picoseconds, torsion occurs with a period of 1.25 picoseconds and an amplitude of 3 degrees in excellent agreement with theoretical calculations. At larger times the quantum states of the molecules describing the torsional motion dephase and an almost isotropic distribution of the dihedral angle is measured. We demonstrate an original application of covariance analysis of two-dimensional ion images to reveal strong correlations between specific ejected ionic fragments...

  17. Compact electrically controlled broadband liquid crystal photonic bandgap fiber polarizer

    DEFF Research Database (Denmark)

    Wei, Lei; Alkeskjold, Thomas Tanggaard; Bjarklev, Anders Overgaard

    2009-01-01

    An electrically controlled liquid crystal photonic-bandgap fiber polarizer is experimentally demonstrated. A maximum 21.3dB electrically tunable polarization extinction ratio is achieved with 45° rotatable transmission axis as well as switched on and off in 1300nm–1600nm.......An electrically controlled liquid crystal photonic-bandgap fiber polarizer is experimentally demonstrated. A maximum 21.3dB electrically tunable polarization extinction ratio is achieved with 45° rotatable transmission axis as well as switched on and off in 1300nm–1600nm....

  18. Chiral liquids

    Directory of Open Access Journals (Sweden)

    Zakharov V.I.

    2015-01-01

    Full Text Available We review briefly properties of chiral liquids, or liquids with massless fermionic constituents. We concentrate on three effects, namely, the low ratio of viscosity η to entropy density s, chiral magnetic and vortical effects. We sketch standard derivations of these effects in the hydrodynamic approximation and then concentrate on possibile unifying approach which is based on consideration of the (anomalously conserved axial current. The point is that the conservation of chirality is specific for the microscopic, field-theoretic description of massless fermions and their interactions. On the macroscopic side, the standard hydrodynamic equations are not consistent, generally speaking, with conservation of a helical macroscopic motion. Imposing extra constraints on the hydrodynamics might resolve this “clash-of-symmetries” paradox.

  19. Chiral Nanoscience and Nanotechnology

    OpenAIRE

    Dibyendu S. Bag; T.C. Shami; K.U. Bhasker Rao

    2008-01-01

    The paper reviews nanoscale science and technology of chiral molecules/macromolecules-under twosubtopics-chiral nanotechnology and nano-chiral technology. Chiral nanotechnology discusses thenanotechnology, where molecular chirality plays a role in the properties of materials, including molecularswitches, molecular motors, and other molecular devices; chiral supramolecules and self-assembled nanotubesand their functions are also highlighted. Nano-chiral technology  describes the nanoscale appr...

  20. Control over colloidal crystallization by shear and electric fields

    NARCIS (Netherlands)

    Wu, Y.L.

    2007-01-01

    We used shear flow and an electric field to control colloidal crystallization. The structures were examined in situ with confocal microscopy. For experiments under shear, a new parallel plate shear cell was designed. It had a zero-velocity plane that was stationary with respect to the microscope. Th

  1. Liquid-crystal intraocular adaptive lens with wireless control.

    Science.gov (United States)

    Simonov, Aleksey N; Vdovin, Gleb; Loktev, Mikhail

    2007-06-11

    We present a prototype of an adaptive intraocular lens based on a modal liquid-crystal spatial phase modulator with wireless control. The modal corrector consists of a nematic liquid-crystal layer sandwiched between two glass substrates with transparent low- and high-ohmic electrodes, respectively. Adaptive correction of ocular aberrations is achieved by changing the amplitude and the frequency of the applied control voltage. The convex-shaped glass substrates provide the required initial focusing power of the lens. A loop antenna mounded on the rim of the lens delivers an amplitude-modulated radio-frequency control signal to the integrated rectifier circuit that drives the liquid-crystal modal corrector. In vitro measurements of a 5-mm clear aperture prototype with an initial focusing power of +12.5 diopter, remotely driven by a radio-frequency control unit at ~6 MHz, were carried out using a Shack-Hartmann wavefront sensor. The lens based on a 40-mum thick liquid-crystal layer allows for an adjustable defocus of 4 waves, i. e. an accommodation of ~2.51 dioptres at a wavelength of 534 nm, and correction of spherical aberration coefficient ranging from -0.8 to 0.67 waves. Frequency-switching technique was employed to increase the response speed and eliminate transient overshoots in aberration coefficients. The full-scale settling time of the adaptive modal corrector was measured to be ~4 s.

  2. Site-controlled quantum dots coupled to photonic crystal waveguides

    DEFF Research Database (Denmark)

    Rigal, B.; de Lasson, Jakob Rosenkrantz; Jarlov, C.;

    2016-01-01

    We demonstrate selective optical coupling of multiple, site controlled semiconductor quantum dots (QDs) to photonic crystal waveguide structures. The impact of the exact position and emission spectrum of the QDs on the coupling efficiency is elucidated. The influence of optical disorder and end...

  3. Nanoscopic Manipulation and Imaging of Liquid Crystals

    Energy Technology Data Exchange (ETDEWEB)

    Rosenblatt, Charles S. [Case Western Reserve Univ., Cleveland, OH (United States)

    2014-02-04

    This is the final project report. The project’s goals centered on nanoscopic imaging and control of liquid crystals and surfaces. We developed and refined techniques to control liquid crystal orientation at surfaces with resolution as small as 25 nm, we developed an optical imaging technique that we call Optical Nanotomography that allows us to obtain images inside liquid crystal films with resolution of 60 x 60 x 1 nm, and we opened new thrust areas related to chirality and to liquid crystal/colloid composites.

  4. Controllable reflection of X-rays on crystals of saccharose

    CERN Document Server

    Navasardyan, M A; Hayrapetyan, K T; Gabrielyan, R T

    2003-01-01

    Multiple (ten times and more) increase in intensities of separate reflections and of lauegram reflections from organic single crystals of saccharose (C sub 1 2H sub 2 2O sub 1 1) was observed under influence of certain temperature gradient. On the base of the present experiment and the data of our previous woks we show that the controllable reflection process has a common nature and the intensity of the diffracted beam under external influences does not depend on the total number of electrons per unit volume of the unit cell of the single crystal.

  5. Wave control through soft microstructural curling: bandgap shifting, reconfigurable anisotropy and switchable chirality

    Science.gov (United States)

    Celli, Paolo; Gonella, Stefano; Tajeddini, Vahid; Muliana, Anastasia; Ahmed, Saad; Ounaies, Zoubeida

    2017-03-01

    In this work, we discuss and numerically validate a strategy to attain reversible macroscopic changes in the wave propagation characteristics of cellular metamaterials with soft microstructures. The proposed cellular architecture is characterized by unit cells featuring auxiliary populations of symmetrically-distributed smart cantilevers stemming from the nodal locations. Through an external stimulus (the application of an electric field), we induce extreme, localized, reversible curling deformation of the cantilevers—a shape modification which does not affect the overall shape, stiffness and load bearing capability of the structure. By carefully engineering the spatial pattern of straight (non activated) and curled (activated) cantilevers, we can induce several profound modifications of the phononic characteristics of the structure: generation and/or shifting of total and partial bandgaps, cell symmetry relaxation (which implies reconfigurable wave beaming), and chirality switching. While in this work we discuss the specific case of composite cantilevers with a PDMS core and active layers of electrostrictive terpolymer P(VDF-TrFE-CTFE), the strategy can be extended to other smart materials (such as dielectric elastomers or shape-memory polymers).

  6. Observation of glycine zipper and unanticipated occurrence of ambidextrous helices in the crystal structure of a chiral undecapeptide

    Directory of Open Access Journals (Sweden)

    Ramagopal Udupi A

    2007-08-01

    Full Text Available Abstract Background The de novo design of peptides and proteins has recently surfaced as an approach for investigating protein structure and function. This approach vitally tests our knowledge of protein folding and function, while also laying the groundwork for the fabrication of proteins with properties not precedented in nature. The success of these studies relies heavily on the ability to design relatively short peptides that can espouse stable secondary structures. To this end, substitution with α, β-dehydroamino acids, especially α, β-dehydrophenylalanine (ΔPhe comes in use for spawning well-defined structural motifs. Introduction of ΔPhe induces β-bends in small and 310-helices in longer peptide sequences. Results The present report is an investigation of the effect of incorporating two glycines in the middle of a ΔPhe containing undecapeptide. A de novo designed undecapeptide, Ac-Gly1-Ala2-ΔPhe3-Leu4-Gly5-ΔPhe6-Leu7-Gly8-ΔPhe9-Ala10-Gly11-NH2, was synthesized and characterized using X-ray diffraction and Circular Dichroism spectroscopic methods. Crystallographic studies suggest that, despite the presence of L-amino acid (L-Ala and L-Leu residues in the middle of the sequence, the peptide adopts a 310-helical conformation of ambidextrous screw sense, one of them a left-handed (A and the other a right-handed (B 310-helix with A and B being antiparallel to each other. However, CD studies reveal that the undecapeptide exclusively adopts a right-handed 310-helical conformation. In the crystal packing, three different interhelical interfaces, Leu-Leu, Gly-Gly and ΔPhe-ΔPhe are observed between the helices A and B. A network of C-H...O hydrogen bonds are observed at ΔPhe-ΔPhe and Gly-Gly interhelical interfaces. An important feature observed is the occurrence of glycine zipper motif at Gly-Gly interface. At this interface, the geometric pattern of interhelical interactions seems to resemble those observed between helices in

  7. Novel Chiral Auxiliaries of BIAZOLs

    Institute of Scientific and Technical Information of China (English)

    CHEN; Arh-Hwang

    2001-01-01

    Asymmetric catalysis is one of the most challenging and formidable endeavor in organic synthesis. The development of chiral auxiliaries is a key in the asymmetric catalysis. Azulenoids, a parent structure of bicyclo[5.3.0]decapentaene with 10 πelectrons, are useful as dye materials, medical treatment of inflammation and hypertension, and the development of liquid crystals. In continuing to investigate synthetic application of azulenoids, we have studied to develop novel chiral auxiliaries of BIAZOLs. The BIAZOLs were synthesized from dicyclopentadiene and characterized using spectroscopies.  ……

  8. Novel Chiral Auxiliaries of BIAZOLs

    Institute of Scientific and Technical Information of China (English)

    CHEN Arh-Hwang; YUAN Shou-Bin; CHIU Shu-Ching

    2001-01-01

    @@ Asymmetric catalysis is one of the most challenging and formidable endeavor in organic synthesis. The development of chiral auxiliaries is a key in the asymmetric catalysis. Azulenoids, a parent structure of bicyclo[5.3.0]decapentaene with 10 πelectrons, are useful as dye materials, medical treatment of inflammation and hypertension, and the development of liquid crystals. In continuing to investigate synthetic application of azulenoids, we have studied to develop novel chiral auxiliaries of BIAZOLs. The BIAZOLs were synthesized from dicyclopentadiene and characterized using spectroscopies.

  9. A new approach to the CZ crystal growth weighing control

    Science.gov (United States)

    Kasimkin, P. V.; Moskovskih, V. A.; Vasiliev, Y. V.; Shlegel, V. N.; Yuferev, V. S.; Vasiliev, M. G.; Zhdankov, V. N.

    2014-03-01

    The aim of a new approach was to improve the robustness of the weighing control of CZ growth especially for semiconductors, for which the “anomalous“ behavior of the apparent weight provokes instability of the servo-loop. In the described method, the periodic reciprocating measuring motion of small amplitude is superposed on the uniform pull-rod movement. The cross-sectional area is determined from the weight sensor responses that are modulated mainly by the forces of hydrostatic pressure. By the example of germanium crystal growth, it is shown that in the control system, based on such a way of the diameter measuring, a simple PI control law provides a good close loop system's stability and dynamics for the materials with the “anomalous” behavior of a weighing signal. The effect of a meniscus on the modulation measuring of a crystal diameter is also discussed.

  10. Chiral Biomarkers in Meteorites

    Science.gov (United States)

    Hoover, Richard B.

    2010-01-01

    The chirality of organic molecules with the asymmetric location of group radicals was discovered in 1848 by Louis Pasteur during his investigations of the rotation of the plane of polarization of light by crystals of sodium ammonium paratartrate. It is well established that the amino acids in proteins are exclusively Levorotary (L-aminos) and the sugars in DNA and RNA are Dextrorotary (D-sugars). This phenomenon of homochirality of biological polymers is a fundamental property of all life known on Earth. Furthermore, abiotic production mechanisms typically yield recemic mixtures (i.e. equal amounts of the two enantiomers). When amino acids were first detected in carbonaceous meteorites, it was concluded that they were racemates. This conclusion was taken as evidence that they were extraterrestrial and produced by abiologically. Subsequent studies by numerous researchers have revealed that many of the amino acids in carbonaceous meteorites exhibit a significant L-excess. The observed chirality is much greater than that produced by any currently known abiotic processes (e.g. Linearly polarized light from neutron stars; Circularly polarized ultraviolet light from faint stars; optically active quartz powders; inclusion polymerization in clay minerals; Vester-Ulbricht hypothesis of parity violations, etc.). This paper compares the measured chirality detected in the amino acids of carbonaceous meteorites with the effect of these diverse abiotic processes. IT is concluded that the levels observed are inconsistent with post-arrival biological contamination or with any of the currently known abiotic production mechanisms. However, they are consistent with ancient biological processes on the meteorite parent body. This paper will consider these chiral biomarkers in view of the detection of possible microfossils found in the Orgueil and Murchison carbonaceous meteorites. Energy dispersive x-ray spectroscopy (EDS) data obtained on these morphological biomarkers will be

  11. Crystallization engineering as a route to epitaxial strain control

    Directory of Open Access Journals (Sweden)

    Andrew R. Akbashev

    2015-10-01

    Full Text Available The controlled synthesis of epitaxial thin films offers opportunities for tuning their functional properties via enabling or suppressing strain relaxation. Examining differences in the epitaxial crystallization of amorphous oxide films, we report on an alternate, low-temperature route for strain engineering. Thin films of amorphous Bi–Fe–O were grown on (001SrTiO3 and (001LaAlO3 substrates via atomic layer deposition. In situ X-ray diffraction and X-ray photoelectron spectroscopy studies of the crystallization of the amorphous films into the epitaxial (001BiFeO3 phase reveal distinct evolution profiles of crystallinity with temperature. While growth on (001SrTiO3 results in a coherently strained film, the same films obtained on (001LaAlO3 showed an unstrained, dislocation-rich interface, with an even lower temperature onset of the perovskite phase crystallization than in the case of (001SrTiO3. Our results demonstrate how the strain control in an epitaxial film can be accomplished via its crystallization from the amorphous state.

  12. Circularly polarized lasing in chiral modulated semiconductor microcavity with GaAs quantum wells

    CERN Document Server

    Demenev, A A; Schneider, C; Brodbeck, S; Kamp, M; Höfling, S; Lobanov, S V; Weiss, T; Gippius, N A; Tikhodeev, S G

    2016-01-01

    We report the elliptically, close to circularly polarized lasing at $\\hbar\\omega = 1.473$ and 1.522 eV from an AlAs/AlGaAs Bragg microcavity with 12 GaAs quantum wells in the active region and chiral-etched upper distributed Bragg refractor under optical pump at room temperature. The advantage of using the chiral photonic crystal with a large contrast of dielectric permittivities is its giant optical activity, allowing to fabricate a very thin half-wave plate, with a thickness of the order of the emitted light wavelength, and to realize the monolithic control of circular polarization.

  13. Stegosaurus chirality

    OpenAIRE

    Cameron, R.P.; Cameron, J. A.; Barnett, S. M.

    2016-01-01

    We explain that Stegosaurus exhibited exterior chirality and observe that the largest plate in particular of USNM 4394, USNM 4714, DMNS 2818 and NHMUK R36730 appears to have tilted to the right rather than to the left in each case. Several instances in which Stegosaurus specimens have been confused with their distinct, hypothetical mirror-image forms are highlighted. We believe our findings to be consistent with the hypothesis that Stegosaurus's plates acted primarily as display structures. A...

  14. Evidence of Chiral Order in the Charge-Ordered Phase of Superconducting La1.875Ba0.125Cuo4 Single Crystals Using Polar Kerr-Effect Measurements

    Science.gov (United States)

    Karapetyan, Hovnatan; Xia, Jing; Hücker, M.; Gu, G. D.; Tranquada, J. M.; Fejer, M. M.; Kapitulnik, A.

    2014-01-01

    High resolution polar Kerr effect measurements were performed on La1.875Ba0.125CuO4 single crystals revealing that a finite Kerr signal is measured below an onset temperature TK that coincides with the charge ordering transition temperature TCO. We further show that the sign of the Kerr signal cannot be trained with the magnetic field, is found to be the same on opposite sides of the same crystal, and is odd with respect to strain in the diagonal direction of the unit cell. These observations are consistent with a chiral "gyrotropic" order above Tc for La1.875Ba0.125CuO4; similarities to other cuprates suggest that it is a universal property in the pseudogap regime.

  15. Synthesis and characterization of a chiral dimeric copper(II) complex: Crystal structure of [Cu2(-Cl)2(HL)2].H2O(H2L = -(-)-2-[(2-hydroxy-1-phenyl-ethylimino)-methyl]-phenol)

    Indian Academy of Sciences (India)

    Chullikkattil P Pradeep; Panthapally S Zacharias; Samar K Das

    2005-03-01

    Synthesis and characterization of an optically active binuclear dichloro-bridged copper(II) complex [Cu2(-Cl)2(HL)2]$\\cdot$H2O 1 (H2L = -(-)-2-[(2-hydroxy-1-phenyl-ethylimino)-methyl]-phenol) of a Schiff-base derived from salicylaldehyde and ()-(+)-2-phenylglycinol are described. Compound 1 crystallizes in the orthorhombic chiral P212121 space group with = 4, = 10.21(2), = 11.574(3), = 25.364(9). Each copper shows square pyramidal geometry with O2NCl2 coordination and the Cu2Cl2 core geometry adopts a butterfly shape. Crystals of 1 were further characterized by elemental analysis, IR, UV-visible and EPR spectroscopy and circular dichroism (CD) studies.

  16. Controlling Anderson localization in disordered photonic crystal waveguides

    DEFF Research Database (Denmark)

    Garcia-Fernández, David; Smolka, Stephan; Stobbe, Søren

    Quantum optics and quantum information technologies require enhancement of light-matter interaction by, for example, confining light in a small volume. A very recently demonstrated route towards light confinement makes use of multiple scattering of light and wave interference in disordered photonic...... structures [1,2]. Originally proposed for electrons by P. W. Anderson [3], only completely random systems without any long-range correlation between the scattering sites have been used so far, meaning that the Anderson-localized modes cannot be controlled. In disordered photonic crystals, these modes...... are predicted to appear at frequencies in or near a band gap [4] providing a possible way to control Anderson-localized modes. We have tested this hypothesis by measuring the light localization length, ξ, in a disordered photonic crystal waveguide (PCW) as a function of the dispersive slowdown factor of light...

  17. Tunable and rotatable polarization controller using photonic crystal fiber filled with liquid crystal

    DEFF Research Database (Denmark)

    Wei, Lei; Alkeskjold, Thomas Tanggaard; Bjarklev, Anders Overgaard

    2010-01-01

    We design and fabricate a compact tunable and rotatable polarization controller using liquid crystal photonic band gap fibers. The electrically and thermally induced phase shift in the Poincaré sphere and corresponding birefringence change are measured. The direction of the electric field...... is managed by connecting four electrodes in different electrode configurations, and the thermal tunability is controlled by on-chip heaters. According to the results, a quarter-wave plate and a half-wave plate working in the wavelength range of 1520–1600 nm are experimentally demonstrated....

  18. Control of Perovskite Crystal Growth by Methylammonium Lead Chloride Templating.

    Science.gov (United States)

    Binek, Andreas; Grill, Irene; Huber, Niklas; Peters, Kristina; Hufnagel, Alexander G; Handloser, Matthias; Docampo, Pablo; Hartschuh, Achim; Bein, Thomas

    2016-04-20

    State-of-the-art solar cells based on methylammonium lead iodide (MAPbI3 ) now reach efficiencies over 20 %. This fast improvement was possible with intensive research in perovskite processing. In particular, chloride-based precursors are known to have a positive influence on the crystallization of the perovskite. Here, we used a combination of in-situ X-ray diffraction and charge-transport measurements to understand the influence of chloride during perovskite crystallization in planar heterojunction solar cells. We show that MAPbCl3 crystallizes directly after the deposition of the starting solution and acts as a template for the formation of MAPbI3 . Additionally, we show that the charge-carrier mobility doubles by extending the time for the template formation. Our results give a deeper understanding of the influence of chloride in the synthesis of MAPbI3 and illustrate the importance of carefully controlling crystallization for reproducible, high-efficiency solar cells.

  19. Authenticity control of essential oils containing citronellal and citral by chiral and stable-isotope gas-chromatographic analysis.

    Science.gov (United States)

    Nhu-Trang, Tran-Thi; Casabianca, Hervé; Grenier-Loustalot, Marie-Florence

    2006-12-01

    Enantioselective capillary GC on a Supelco beta-DEX 225 column (heptakis(2,3-di-O-acetyl-6-O-tert-butyldimethylsilyl)-beta-cyclodextrin SPB 20poly--20% diphenyl, 80% dimethylsiloxane) and isotope-ratio mass spectrometry, coupled online with capillary GC on an HP5 column have been used for origin-specific analysis and authenticity control of essential oils, for example lemon (Citrus limon), lemongrass (Cymbopogon citratus and Cymbopogon flexuosus), citronella (Cymbopogon nardus L.--Ceylon type and Cymbopogon winterianus--Java type), Litsea cubeba, Lippia citriodora, lemon myrtle (Backhousia citriodora), lemon gum (Eucalyptus citriodora), and, especially, precious lemon balm oil (Melissa officinalis L.). Isotope data (delta13C(PDB) and delta2H(V-SMOW)) for citral (neral + geranial) and citronellal from on-line GC-C/Py-IRMS and chiral data for citronellal in these essential oils are reported. The possibility of using these data to determine the origin of these essential oils and to detect adulteration is discussed. Principal-components analysis (PCA) of specific compounds in two essential oils of lemongrass and Litsea cubeba was performed as a practical statistical method for distinguishing between these two types of oil.

  20. A liquid crystalline chirality balance for vapours

    OpenAIRE

    Ohzono, Takuya; Yamamoto, Takahiro; Fukuda, Jun-Ichi

    2014-01-01

    Chiral discrimination of vapours plays an important role in olfactory perception of biological systems and its realization by artificial sensors has been an intriguing challenge. Here, we report a simple method that tangibly visualizes the chirality of a diverse variety of molecules dissolved from vapours with high sensitivity, by making use of a structural change in a periodic microstructure of a nematic liquid crystal confined in open microchannels. This microstructure is accompanied by a t...

  1. Chiral magnetic effect in condensed matter systems

    Science.gov (United States)

    Li, Qiang; Kharzeev, Dmitri E.

    2016-12-01

    The chiral magnetic effect (CME) is the generation of electrical current induced by chirality imbalance in the presence of magnetic field. It is a macroscopic manifestation of the quantum chiral anomaly [S. L. Adler. Axial-vector vertex in spinor electrodynamics. Physical Review, 177, 2426 (1969), J. S. Bell and R. Jackiw. A PCAC puzzle: π 0 γγin the σ-model. Il Nuovo Cimento A, 60, 47-61 (1969)] in systems possessing charged chiral fermions. In quark-gluon plasma containing nearly massless quarks, the chirality imbalance is sourced by the topological transitions. In condensed matter systems, the chiral quasiparticles emerge in gapless semiconductors with two energy bands having pointlike degeneracies opening the path to the study of chiral anomaly [H. B. Nielsen and M. Ninomiya. The Adler-Bell-Jackiw anomaly and Weyl fermions in a crystal. Physics Letters B, 130, 389-396 (1983)]. Recently, these novel materials - so-called Dirac and Weyl semimetals have been discovered experimentally, are suitable for the investigation of the CME in condensed matter experiments. Here we report on the first experimental observation of the CME in a 3D Dirac semimetal ZrTe5 [Q. Li, D. E. Kharzeev, C. Zhang, Y. Huang, I. Pletikosić, A. V. Fedorov, R. D. Zhong, J. A. Schneeloch, G. D. Gu, and T. Valla. Chiral magnetic effect in ZrTe5. Nature Physics (2016) doi:10.1038/nphys3648].

  2. Crystal Phase Quantum Well Emission with Digital Control.

    Science.gov (United States)

    Assali, S; Lähnemann, J; Vu, T T T; Jöns, K D; Gagliano, L; Verheijen, M A; Akopian, N; Bakkers, E P A M; Haverkort, J E M

    2017-09-18

    One of the major challenges in the growth of quantum well and quantum dot heterostructures is the realization of atomically sharp interfaces. Nanowires provide a new opportunity to engineer the band structure as they facilitate the controlled switching of the crystal structure between the zinc-blende (ZB) and wurtzite (WZ) phases. Such a crystal phase switching results in the formation of crystal phase quantum wells (CPQWs) and quantum dots (CPQDs). For GaP CPQWs, the inherent electric fields due to the discontinuity of the spontaneous polarization at the WZ/ZB junctions lead to the confinement of both types of charge carriers at the opposite interfaces of the WZ/ZB/WZ structure. This confinement leads to a novel type of transition across a ZB flat plate barrier. Here, we show digital tuning of the visible emission of WZ/ZB/WZ CPQWs in a GaP nanowire by changing the thickness of the ZB barrier. The energy spacing between the sharp emission lines is uniform and is defined by the addition of single ZB monolayers. The controlled growth of identical quantum wells with atomically flat interfaces at predefined positions featuring digitally tunable discrete emission energies may provide a new route to further advance entangled photons in solid state quantum systems.

  3. Chiral morphology of calcite through selective binding of amino acids

    Science.gov (United States)

    Orme, Christine

    2002-03-01

    Many living organisms contain biominerals and composites with finely tuned properties, reflecting a remarkable level of control over the nucleation, growth and shape of the constituent crystals. Peptides and proteins play an important role in achieving this control. Using in situ AFM we find that site-specific binding of amino acid residues to surface steps changes the step-edge free energies, giving rise to direction-specific binding energies unique to individual amino acid enantiomers and leading to chiral modifications that propagate from atomic length scales to macroscopic length scales. Molecular modeling studies support an energetic basis for the differences in binding. Our results emphasize that the mechanism under-lying crystal modification through organic molecules is best understood by considering both stereochemical recognition as well as the effects of binding on the interfacial energies of the growing crystal.

  4. Controlling protein crystal growth rate by means of temperature

    Energy Technology Data Exchange (ETDEWEB)

    SantamarIa-Holek, I; Gadomski, A [Institute of Mathematics and Physics, University of Technology and Life Sciences, PL-85796 Bydgoszcz (Poland); RubI, J M, E-mail: isholek.fc@gmail.com, E-mail: agad@utp.edu.pl, E-mail: mrubi@ub.edu [Departament de Fisica Fonamental, University of Barcelona, Av. Diagonal 647, E-08028 Barcelona (Spain)

    2011-06-15

    We have proposed a model to analyze the growth kinetics of lysozyme crystals/aggregates under non-isothermal conditions. The model was formulated through an analysis of the entropy production of the growth process which was obtained by taking into account the explicit dependence of the free energy on the temperature. We found that the growth process is coupled with temperature variations, resulting in a novel Soret-type effect. We identified the surface entropy of the crystal/aggregate as a decisive ingredient controlling the behavior of the average growth rate as a function of temperature. The behavior of the Gibbs free energy as a function of temperature is also analyzed. The agreement between theory and experiments is very good in the range of temperatures considered.

  5. Controlling protein crystal growth rate by means of temperature.

    Science.gov (United States)

    Sanamaría-Holek, I; Gadomski, A; Rubí, J M

    2011-06-15

    We have proposed a model to analyze the growth kinetics of lysozyme crystals/aggregates under non-isothermal conditions. The model was formulated through an analysis of the entropy production of the growth process which was obtained by taking into account the explicit dependence of the free energy on the temperature. We found that the growth process is coupled with temperature variations, resulting in a novel Soret-type effect. We identified the surface entropy of the crystal/aggregate as a decisive ingredient controlling the behavior of the average growth rate as a function of temperature. The behavior of the Gibbs free energy as a function of temperature is also analyzed. The agreement between theory and experiments is very good in the range of temperatures considered.

  6. Co-crystallization as a separation technology: controlling product concentrations by co-crystals

    NARCIS (Netherlands)

    Urbanus, J.; Roelands, C.P.M.; Verdoes, D.; Jansens, P.J.; Horst, J.H. ter

    2010-01-01

    Co-crystallization is known as a product formulation technology, but it can also be used as a tool to solve crystallization problems. Product removal by co-crystallization in fermentations is used as a showcase to demonstrate the potential of co-crystallization as a separation technique. In

  7. Co-crystallization as a separation technology: controlling product concentrations by co-crystals

    NARCIS (Netherlands)

    Urbanus, J.; Roelands, C.P.M.; Verdoes, D.; Jansens, P.J.; Horst, J.H. ter

    2010-01-01

    Co-crystallization is known as a product formulation technology, but it can also be used as a tool to solve crystallization problems. Product removal by co-crystallization in fermentations is used as a showcase to demonstrate the potential of co-crystallization as a separation technique. In fermenta

  8. Chiral Nanoscience and Nanotechnology

    Directory of Open Access Journals (Sweden)

    Dibyendu S. Bag

    2008-09-01

    Full Text Available The paper reviews nanoscale science and technology of chiral molecules/macromolecules-under twosubtopics-chiral nanotechnology and nano-chiral technology. Chiral nanotechnology discusses thenanotechnology, where molecular chirality plays a role in the properties of materials, including molecularswitches, molecular motors, and other molecular devices; chiral supramolecules and self-assembled nanotubesand their functions are also highlighted. Nano-chiral technology  describes the nanoscale approaches to chiraltechnology such as asymmetric synthesis and catalysis, chiral separation and detection, and enantiomericanalysis. Chiral sensors have also been included. The state-of-the-art chiral research at DMSRDE,Kanpur isalso presented.Defence Science Journal, 2008, 58(5, pp.626-635, DOI:http://dx.doi.org/10.14429/dsj.58.1685

  9. Experimental implementation of automatic 'cycle to cycle' control to a nonlinear chiral simulated moving bed separation.

    Science.gov (United States)

    Grossmann, Cristian; Langel, Christian; Mazzotti, Marco; Morari, Manfred; Morbidelli, Massimo

    2010-03-26

    In order to better exploit the economic potential of the simulated moving bed chromatography a 'cycle to cycle' controller which only requires the information about the linear adsorption behavior and the overall average porosity of the columns has been proposed. Recently, an automated on-line HPLC monitoring system which determines the concentrations in the two product streams averaged over one cycle, and returns them as feedback information to the controller was implemented. The new system allows for an accurate determination of the average concentration of the product streams even if the plant is operated at high concentrations. This paper presents the experimental implementation of the 'cycle to cycle' control concept to the separation of guaifenesin enantiomers under nonlinear chromatographic conditions, i.e. at high feed concentrations. Different case studies have been carried out to challenge the controller under realistic operation conditions, e.g. introducing pump disturbances and changing the feed concentration during the operation. The experimental results clearly demonstrate that the controller can indeed deliver the specified purities and improve the process performance.

  10. Controlled, bio-inspired self-assembly of cellulose-based chiral reflectors

    NARCIS (Netherlands)

    Dumanli, Ahu Gumrah; Kamita, Gen; Landman, Jasper; van der Kooij, Hanne; Glover, Beverley J.; Baumberg, Jeremy J.; Steiner, Ullrich; Vignolini, Silvia

    2014-01-01

    The self-assembly process of photonic structures made of cellulose nanocrystals is studied in detail by locally monitoring and controlling water evaporation. Three different stages during the evaporation process are identified. Spectroscopy quantifies the amount of disorder in the fabricated samples

  11. Enantioselective Biotransformation of Chiral Persistent Organic Pollutants.

    Science.gov (United States)

    Zhang, Ying; Ye, Jing; Liu, Min

    2017-01-01

    Enantiomers of chiral compounds commonly undergo enantioselective transformation in most biologically mediated processes. As chiral persistent organic pollutants (POPs) are extensively distributed in the environment, differences between enantiomers in biotransformation should be carefully considered to obtain exact enrichment and specific health risks. This review provides an overview of in vivo biotransformation of chiral POPs currently indicated in the Stockholm Convention and their chiral metabolites. Peer-reviewed journal articles focused on the research question were thoroughly searched. A set of inclusion and exclusion criteria were developed to identify relevant studies. We mainly compared the results from different animal models under controlled laboratory conditions to show the difference between enantiomers in terms of distinct transformation potential. Interactions with enzymes involved in enantioselective biotransformation, especially cytochrome P450 (CYP), were discussed. Further research areas regarding this issue were proposed. Limited evidence for a few POPs has been found in 30 studies. Enantioselective biotransformation of α-hexachlorocyclohexane (α-HCH), chlordane, dichlorodiphenyltrichloroethane (DDT), heptachlor, hexabromocyclododecane (HBCD), polychlorinated biphenyls (PCBs), and toxaphene, has been investigated using laboratory mammal, fish, bird, and worm models. Tissue and excreta distributions, as well as bioaccumulation and elimination kinetics after administration of racemate and pure enantiomers, have been analyzed in these studies. Changes in enantiomeric fractions have been considered as an indicator of enantioselective biotransformation of chiral POPs in most studies. Results of different laboratory animal models revealed that chiral POP biotransformation is seriously affected by chirality. Pronounced results of species-, tissue-, gender-, and individual-dependent differences are observed in in vivo biotransformation of chiral POPs

  12. Morphological control and polarization switching in polymer dispersed liquid crystal materials and devices

    Indian Academy of Sciences (India)

    K K Raina; Pankaj Kumar; Praveen Malik

    2006-11-01

    Liquid crystals dispersed in polymer systems constitute novel class of optical materials. The precise control of the liquid crystal droplet morphology in the polymer matrix is essentially required to meet the prerequisites of display device. Experiments have been carried out to investigate and identify the material properties and processing conditions required for the precise control of the droplet morphology of the dispersed liquid crystal systems. Polarization switching has been studied. Aligned liquid crystal dispersed systems showed higher polarization over unaligned ones.

  13. Chiral mirrors

    Energy Technology Data Exchange (ETDEWEB)

    Plum, Eric, E-mail: erp@orc.soton.ac.uk [Optoelectronics Research Centre and Centre for Photonic Metamaterials, University of Southampton, Highfield, Southampton SO17 1BJ (United Kingdom); Zheludev, Nikolay I., E-mail: niz@orc.soton.ac.uk [Optoelectronics Research Centre and Centre for Photonic Metamaterials, University of Southampton, Highfield, Southampton SO17 1BJ (United Kingdom); The Photonics Institute and Centre for Disruptive Photonic Technologies, Nanyang Technological University, Singapore 637378 (Singapore)

    2015-06-01

    Mirrors are used in telescopes, microscopes, photo cameras, lasers, satellite dishes, and everywhere else, where redirection of electromagnetic radiation is required making them arguably the most important optical component. While conventional isotropic mirrors will reflect linear polarizations without change, the handedness of circularly polarized waves is reversed upon reflection. Here, we demonstrate a type of mirror reflecting one circular polarization without changing its handedness, while absorbing the other. The polarization-preserving mirror consists of a planar metasurface with a subwavelength pattern that cannot be superimposed with its mirror image without being lifted out of its plane, and a conventional mirror spaced by a fraction of the wavelength from the metasurface. Such mirrors enable circularly polarized lasers and Fabry-Pérot cavities with enhanced tunability, gyroscopic applications, polarization-sensitive detectors of electromagnetic waves, and can be used to enhance spectroscopies of chiral media.

  14. Controlling Anderson localization in disordered photonic crystal waveguides

    DEFF Research Database (Denmark)

    Garcia-Fernández, David; Smolka, Stephan; Stobbe, Søren

    structures [1,2]. Originally proposed for electrons by P. W. Anderson [3], only completely random systems without any long-range correlation between the scattering sites have been used so far, meaning that the Anderson-localized modes cannot be controlled. In disordered photonic crystals, these modes...... denoted by ng. By coupling light into a PCW with a tapered fiber (Fig. 1a), we have measured the ensemble-averaged exponential decay of the light distribution in the range 885 nm ... of the waveguide. Our measurements demonstrate for the first time the close relation between light localization and density of states [5], which can be used ultimately for controlling the extension and spectral position of Anderson-localized modes....

  15. Controlled crystallization of hydroxyapatite under hexadecylamine self-assembled monolayer

    Institute of Scientific and Technical Information of China (English)

    黄苏萍; 周科朝; 刘咏; 黄伯云

    2003-01-01

    The role of self-assembled monolayer in inducing the crystal growth was investigated by X-ray diffractions (XRD), and scanning electron microscopy (SEM). Results show that crystallization in the absence of monolayer results in a mixture of poorly crystallized calcium phosphates, including hydroxyapatite (HAP) and octacalcium phosphate (OCP), while the presence of self-assembled monolayer gives rise to oriented and well crystallized HAP crystals. Moreover, the HAP crystal grows very quickly under the self-assembled monolayer, whereas very little calcium phosphate crystals grow without the monolayer. It is rationalized that the hexadecylamine monolayer with high polarity and charged density leads to increase supersaturation and lower the interfacial energy, which attributes to the HAP crystals nucleation. On the other hand, the positive headgroups construct the ordered "recognized site" with distinct size and topology, which results in the oriented HAP crystals deposit.

  16. Systematic Modelling and Crystal Size Distribution Control for Batch Crystallization Processes

    DEFF Research Database (Denmark)

    Abdul Samad, Noor Asma Fazli; Singh, Ravendra; Sin, Gürkan

    Crystallization processes form an important class of separation methods that are frequently used in the chemical, the pharmaceutical and the food industry. The specifications of the crystal product are usually given in terms of crystal size, shape and purity. In order to predict the desired cryst...

  17. Morphological appearances and photo-controllable coloration of dye-doped cholesteric liquid crystal/polymer coaxial microfibers fabricated by coaxial electrospinning technique.

    Science.gov (United States)

    Lin, Jia-De; Chen, Che-Pei; Chen, Lin-Jer; Chuang, Yu-Chou; Huang, Shuan-Yu; Lee, Chia-Rong

    2016-02-08

    This study systematically investigates the morphological appearance of azo-chiral dye-doped cholesteric liquid crystal (DDCLC)/polymer coaxial microfibers obtained through the coaxial electrospinning technique and examines, for the first time, their photocontrollable reflection characteristics. Experimental results show that the quasi-continuous electrospun microfibers can be successfully fabricated at a high polymer concentration of 17.5 wt% and an optimum ratio of 2 for the feeding rates of sheath to core materials at 25 °C and a high humidity of 50% ± 2% in the spinning chamber. Furthermore, the optical controllability of the reflective features for the electrospun fibers is studied in detail by changing the concentration of the azo-chiral dopant in the core material, the UV irradiation intensity, and the core diameter of the fibers. Relevant mechanisms are addressed to explain the optical-control behaviors of the DDCLC coaxial fibers. Considering the results, optically controllable DDCLC coaxial microfibers present potential applications in UV microsensors and wearable smart textiles or swabs.

  18. Chiral conducting polymers.

    Science.gov (United States)

    Kane-Maguire, Leon A P; Wallace, Gordon G

    2010-07-01

    This critical review describes the preparation and properties of a relatively new class of chiral macromolecules, namely chiral conducting polymers. It focuses in particular on examples based on polypyrrole, polythiophene and polyaniline. They possess remarkable properties, combining not only chirality with electrical conductivity but also the ability to undergo facile redox and pH switching. These unique properties have opened up a range of exciting new potential applications, including as chiral sensors, as novel stationary phases for chiral separations, and as chiral electrodes for electrochemical asymmetric synthesis (153 references).

  19. Progress of Rod-like Chiral Supramolecular Liquid Crystals Based on Intermolecular Hydrogen Bonding%基于分子间氢键的棒状手性液晶的研究进展

    Institute of Scientific and Technical Information of China (English)

    左飞龙; 吴奕环; 时志强; 武长城

    2012-01-01

    Due to its unique optical-electro properties, facile synthesis and stimuli responsiveness to the environment, chiral supramolecular liquid crystals based on intermolecular hydrogen bonding have been becoming one of the hot topics in domain of supramolecular chemistry and been winning more application in functional materials, nonlinear optics and biomedical science, etc. This paper presents a brief review on the rod-like hydrogen-bonding chiral liquid crystals (RHCLC). The molecular structure, chiral group, substituent group, flexible chain, stability of these hydrogen-bonded supramolecular complexes and their relation to the observed liquid crystalline phases are the main topics of this review. Recent research achievements about RHCLC sorted by hydrogen bonds groups such as carboxylic acid and pyridine are introduced. At last the future development of RHCLC is prospected.%分子间氢键棒状手性液晶因其兼具手性液晶奇特的光电性能和氢键液晶的便捷制备以及独特的外界刺激响应性,在功能材料、非线性光学、生物医学等领域具有潜在的应用价值,一直是超分子液晶领域的研究热点.文章按照形成氢键互补基团的不同,将其划分为3种类型,即羧酸-羧酸类、羧酸吡啶类和其他类型氢键,介绍了此三类氢键棒状手性液晶近年来的研究进展.详细归纳了氢键质子给受体的分子结构、氢键稳定性、手性中心位置、取代基、柔性链长度等对液晶性能的影响,并在此基础上,对其未来发展做了展望.

  20. Control of the Diameter and Chiral Angle Distributions during Production of Single-Wall Carbon Nanotubes

    Science.gov (United States)

    Nikolaev, Pavel

    2009-01-01

    Many applications of single wall carbon nanotubes (SWCNT), especially in microelectronics, will benefit from use of certain (n,m) nanotube types (metallic, small gap semiconductor, etc.) Especially fascinating is the possibility of quantum conductors that require metallic armchair nanotubes. However, as produced SWCNT samples are polydisperse, with many (n,m) types present and typical approx.1:2 metal/semiconductor ratio. Nanotube nucleation models predict that armchair nuclei are energetically preferential due to formation of partial triple bonds along the armchair edge. However, nuclei can not reach any meaningful thermal equilibrium in a rapidly expanding and cooling plume of carbon clusters, leading to polydispersity. In the present work, SWCNTs were produced by a pulsed laser vaporization (PLV) technique. The carbon vapor plume cooling rate was either increased by change in the oven temperature (expansion into colder gas), or decreased via "warm-up" with a laser pulse at the moment of nucleation. The effect of oven temperature and "warm-up" on nanotube type population was studied via photoluminescence, UV-Vis-NIR absorption and Raman spectroscopy. It was found that reduced temperatures leads to smaller average diameters, progressively narrower diameter distributions, and some preference toward armchair structures. "Warm-up" shifts nanotube population towards arm-chair structures as well, but the effect is small. Possible improvement of the "warm-up" approach to produce armchair SWCNTs will be discussed. These results demonstrate that PLV production technique can provide at least partial control over the nanotube (n,m) population. In addition, these results have implications for the understanding the nanotube nucleation mechanism in the laser oven.

  1. In situ measurement and dynamic control of the evaporation rate in vapor diffusion crystallization of proteins

    Science.gov (United States)

    Shu, Zhan-Yong; Gong, Hai-Yun; Bi, Ru-Chang

    1998-08-01

    A special device with a weight-sensitive facility was designed for monitoring and controlling the water evaporation in vapor diffusion protein crystallization. The device made it possible to measure the weight of the drop in real time while the crystallization experiment was going on normally. The precise water equilibration curves under different crystallization conditions could be obtained automatically. By monitoring and controlling the evaporation rate, the crystallization of hen egg-white lysozyme and trichosanthin, a plant protein from Chinese herb, was optimized by regulating the reservoir solution dynamically. The experimental results of these two proteins indicate both the feasibility of the device and the usefulness of dynamic control technique. Compared with traditional crystallization experiments, dynamically controlled crystallization can reduce the number of nuclei, increase the crystal size and save experimental time effectively.

  2. Coexistence of both gyroid chiralities in individual butterfly wing scales of Callophrys rubi.

    Science.gov (United States)

    Winter, Benjamin; Butz, Benjamin; Dieker, Christel; Schröder-Turk, Gerd E; Mecke, Klaus; Spiecker, Erdmann

    2015-10-20

    The wing scales of the Green Hairstreak butterfly Callophrys rubi consist of crystalline domains with sizes of a few micrometers, which exhibit a congenitally handed porous chitin microstructure identified as the chiral triply periodic single-gyroid structure. Here, the chirality and crystallographic texture of these domains are investigated by means of electron tomography. The tomograms unambiguously reveal the coexistence of the two enantiomeric forms of opposite handedness: the left- and right-handed gyroids. These two enantiomers appear with nonequal probabilities, implying that molecularly chiral constituents of the biological formation process presumably invoke a chiral symmetry break, resulting in a preferred enantiomeric form of the gyroid structure. Assuming validity of the formation model proposed by Ghiradella H (1989) J Morphol 202(1):69-88 and Saranathan V, et al. (2010) Proc Natl Acad Sci USA 107(26):11676-11681, where the two enantiomeric labyrinthine domains of the gyroid are connected to the extracellular and intra-SER spaces, our findings imply that the structural chirality of the single gyroid is, however, not caused by the molecular chirality of chitin. Furthermore, the wing scales are found to be highly textured, with a substantial fraction of domains exhibiting the directions of the gyroid crystal aligned parallel to the scale surface normal. Both findings are needed to completely understand the photonic purpose of the single gyroid in gyroid-forming butterflies. More importantly, they show the level of control that morphogenesis exerts over secondary features of biological nanostructures, such as chirality or crystallographic texture, providing inspiration for biomimetic replication strategies for synthetic self-assembly mechanisms.

  3. Anion-switchable supramolecular gels for controlling pharmaceutical crystal growth

    Science.gov (United States)

    Foster, Jonathan A.; Piepenbrock, Marc-Oliver M.; Lloyd, Gareth O.; Clarke, Nigel; Howard, Judith A. K.; Steed, Jonathan W.

    2010-12-01

    We describe the use of low-molecular-weight supramolecular gels as media for the growth of molecular crystals. Growth of a range of crystals of organic compounds, including pharmaceuticals, was achieved in bis(urea) gels. Low-molecular-weight supramolecular gelators allow access to an unlimited range of solvent systems, in contrast to conventional aqueous gels such as gelatin and agarose. A detailed study of carbamazepine crystal growth in four different bis(urea) gelators, including a metallogelator, is reported. The crystallization of a range of other drug substances, namely sparfloxacin, piroxicam, theophylline, caffeine, ibuprofen, acetaminophen (paracetamol), sulindac and indomethacin, was also achieved in supramolecular gel media without co-crystal formation. In many cases, crystals can be conveniently recovered from the gels by using supramolecular anion-triggered gel dissolution; however, crystals of substances that themselves bind to anions are dissolved by them. Overall, supramolecular gel-phase crystallization offers an extremely versatile new tool in pharmaceutical polymorph screening.

  4. Chiral Gravitational Waves from Chiral Fermions

    CERN Document Server

    Anber, Mohamed M

    2016-01-01

    We report on a new mechanism that leads to the generation of primordial chiral gravitational waves, and hence, the violation of the parity symmetry in the Universe. We show that nonperturbative production of fermions with a definite helicity is accompanied by the generation of chiral gravitational waves. This is a generic and model-independent phenomenon that can occur during inflation, reheating and radiation eras, and can leave imprints in the cosmic microwave background polarization and may be observed in future ground- and space-based interferometers. We also discuss a specific model where chiral gravitational waves are generated via the production of light chiral fermions during pseudoscalar inflation.

  5. Chiral gravitational waves from chiral fermions

    Science.gov (United States)

    Anber, Mohamed M.; Sabancilar, Eray

    2017-07-01

    We report on a new mechanism that leads to the generation of primordial chiral gravitational waves, and hence, the violation of the parity symmetry in the Universe. We show that nonperturbative production of fermions with a definite helicity is accompanied by the generation of chiral gravitational waves. This is a generic and model-independent phenomenon that can occur during inflation, reheating and radiation eras, and can leave imprints in the cosmic microwave background polarization and may be observed in future ground- and space-based interferometers. We also discuss a specific model where chiral gravitational waves are generated via the production of light chiral fermions during pseudoscalar inflation.

  6. Feedback control of flow alignment in sheared liquid crystals.

    Science.gov (United States)

    Strehober, David A; Schöll, Eckehard; Klapp, Sabine H L

    2013-12-01

    Based on a continuum theory, we investigate the manipulation of the nonequilibrium behavior of a sheared liquid crystal via closed-loop feedback control. Our goal is to stabilize a specific dynamical state, that is, the stationary "flow alignment," under conditions where the uncontrolled system displays oscillatory director dynamics with in-plane symmetry. To this end we employ time-delayed feedback control (TDFC), where the equation of motion for the ith component q(i)(t) of the order parameter tensor is supplemented by a control term involving the difference q(i)(t)-q(i)(t-τ). In this diagonal scheme, τ is the delay time. We demonstrate that the TDFC method successfully stabilizes flow alignment for suitable values of the control strength K and τ; these values are determined by solving an exact eigenvalue equation. Moreover, our results show that only small values of K are needed when the system is sheared from an isotropic equilibrium state, contrary to the case where the equilibrium state is nematic.

  7. Photoswitching of helical twisting power by chiral photochromic diarylethene dopants

    Science.gov (United States)

    Yamaguchi, Tadatsugu; Irie, Masahiro

    2002-12-01

    Two kinds of chiral diarylethene derivatives were synthesized and used as dopants for photoresponsive liquid crystals. Both derivatives underwent thermally irreversible and fatigue resistant photochromic reactions and exhibited reversible circular diochroism (CD) spectral changes. Large photostimulated pitch chances of chiral nematic K-15 liquid crystals were observed by the addition of the derivatives as dopants. The relation between the optical rotation and the twisting power force was discussed.

  8. Liquid-crystal adaptive lenses with modal control.

    Science.gov (United States)

    Naumov, A F; Loktev, M Y; Guralnik, I R; Vdovin, G

    1998-07-01

    We report on a novel approach to the realization of nematic liquid-crystal (LC) phase correctors to form spherical and cylindrical wave fronts. A LC cell with a distributed reactive electrical impedance was driven by an ac voltage applied to the cell boundary to yield the desired spatial distribution of the refractive index. The two-dimensional function of the phase delay introduced into the light beam depends on the frequency of the ac control voltage, the geometry of the boundary electrode surrounding the LC cell, and the electrical parameters of the cell. We realized a cylindrical adaptive lens with a clear aperture of 15 mm x 4mm and a spherical adaptive lens with circular aperture of 6.5 mm. Both devices are capable of focusing collimated light in the range infinity...0.5 m.

  9. Mechanical Response of DNA–Nanoparticle Crystals to Controlled Deformation

    Science.gov (United States)

    2016-01-01

    The self-assembly of DNA-conjugated nanoparticles represents a promising avenue toward the design of engineered hierarchical materials. By using DNA to encode nanoscale interactions, macroscale crystals can be formed with mechanical properties that can, at least in principle, be tuned. Here we present in silico evidence that the mechanical response of these assemblies can indeed be controlled, and that subtle modifications of the linking DNA sequences can change the Young’s modulus from 97 kPa to 2.1 MPa. We rely on a detailed molecular model to quantify the energetics of DNA–nanoparticle assembly and demonstrate that the mechanical response is governed by entropic, rather than enthalpic, contributions and that the response of the entire network can be estimated from the elastic properties of an individual nanoparticle. The results here provide a first step toward the mechanical characterization of DNA–nanoparticle assemblies, and suggest the possibility of mechanical metamaterials constructed using DNA. PMID:27725959

  10. Synthesis of chiral dopants based on carbohydrates.

    Science.gov (United States)

    Tsuruta, Toru; Koyama, Tetsuo; Yasutake, Mikio; Hatano, Ken; Matsuoka, Koji

    2014-07-01

    Chiral dopants based on carbohydrates for nematic liquid crystals were synthesized from D-glucose, and their helical twisting power (HTP) values were evaluated. The chiral dopants induced helices in the host nematic liquid crystals. An acetyl derivative having an ether-type glycosidic linkage between carbohydrate and a mesogenic moiety showed the highest HTP value of 10.4 μm(-1), while an acetyl derivative having an anomeric ester-type linkage did not show any HTP. It was surprising that this molecule had no HTP despite the presence of chirality in the molecule. A relationship between HTP and specific rotation was not observed in this study. Copyright © 2014 Elsevier Ltd. All rights reserved.

  11. Controllable light diffraction in woodpile photonic crystals filled with liquid crystal

    Energy Technology Data Exchange (ETDEWEB)

    Ho, Chih-Hua; Zeng, Hao; Wiersma, Diederik S. [European Laboratory for Non-Linear Spectroscopy (LENS), University of Florence, via Nello Carrara 1, 50019 Sesto Fiorentino (Italy); Cheng, Yu-Chieh; Maigyte, Lina; Trull, Jose; Cojocaru, Crina [Departament de Física i Enginyeria Nuclear, Universitat Politècnica de Catalunya, Colom 11, 08222 Terrassa (Spain); Staliunas, Kestutis [Departament de Física i Enginyeria Nuclear, Universitat Politècnica de Catalunya, Colom 11, 08222 Terrassa (Spain); Institucio Catalana de Reserca i Estudis Avançats (ICREA), passeig Lluis Companys 23, 08010 Barcelona (Spain)

    2015-01-12

    An approach to switching between different patterns of light beams transmitted through the woodpile photonic crystals filled with liquid crystals is proposed. The phase transition between the nematic and isotropic liquid crystal states leads to an observable variation of the spatial pattern transmitted through the photonic structure. The transmission profiles in the nematic phase also show polarization sensibility due to refractive index dependence on the field polarization. The experimental results are consistent with a numerical calculation by Finite Difference Time Domain method.

  12. Directional Control of Plasmon-Exciton interaction with Plexcitonic Crystals

    Science.gov (United States)

    Balci, Sinan; Karademir, Ertugrul; Kocabas, Coskun; Aydinli, Atilla

    2015-03-01

    Plexcitons are strongly coupled plasmon excitons modes. In this work, we developed a platform, consisting of one and two dimensional corrugated surface patterns coated with a thin metal film and a dye solution. This system shows a controlled coupling action based on the excitation direction of SPP modes. Our scheme is based on the control of wavelengths of the forbidden SPP modes. Three kinds of patterns have been tested; a one dimensional uniform, a triangular, and a square lattice type crystals. For all three cases, lowest wavelength of the band gap is observed in Γ to M direction. For triangular and square lattice cases, band gap center oscillates between two finite values for every 60° and 90°s, respectively. We utilized this behavior to control SPP and J-aggregate coupling. We observe directional dependence of Rabi splitting energy varying between 0 meV and 60 meV . Square lattice gives the ability to tune a larger band gap, whereas triangular lattice gives higher number of symmetry points. Simulations show that, an 80 nm deep triangular lattice with 280 nm periodicity can result in omnidirectional decoupling of plexcitons. TUBITAK, Grants 110T790, 110T589, and 112T091.

  13. SSZ-13 Crystallization by Particle Attachment and Deterministic Pathways to Crystal Size Control.

    Science.gov (United States)

    Kumar, Manjesh; Luo, Helen; Román-Leshkov, Yuriy; Rimer, Jeffrey D

    2015-10-14

    Many synthetic and natural crystalline materials are either known or postulated to grow via nonclassical pathways involving the initial self-assembly of precursors that serve as putative growth units for crystallization. Elucidating the pathway(s) by which precursors attach to crystal surfaces and structurally rearrange (postattachment) to incorporate into the underlying crystalline lattice is an active and expanding area of research comprising many unanswered fundamental questions. Here, we examine the crystallization of SSZ-13, which is an aluminosilicate zeolite that possesses exceptional physicochemical properties for applications in separations and catalysis (e.g., methanol upgrading to chemicals and the environmental remediation of NO(x)). We show that SSZ-13 grows by two concerted mechanisms: nonclassical growth involving the attachment of amorphous aluminosilicate particles to crystal surfaces and classical layer-by-layer growth via the incorporation of molecules to advancing steps on the crystal surface. A facile, commercially viable method of tailoring SSZ-13 crystal size and morphology is introduced wherein growth modifiers are used to mediate precursor aggregation and attachment to crystal surfaces. We demonstrate that small quantities of polymers can be used to tune crystal size over 3 orders of magnitude (0.1-20 μm), alter crystal shape, and introduce mesoporosity. Given the ubiquitous presence of amorphous precursors in a wide variety of microporous crystals, insight of the SSZ-13 growth mechanism may prove to be broadly applicable to other materials. Moreover, the ability to selectively tailor the physical properties of SSZ-13 crystals through molecular design offers new routes to optimize their performance in a wide range of commercial applications.

  14. Fabrication and characterization of three-dimensional biomimetic chiral composites.

    Science.gov (United States)

    Turner, Mark D; Schröder-Turk, Gerd E; Gu, Min

    2011-05-09

    Here we show the fabrication and characterization of a novel class of biomimetic photonic chiral composites inspired by a recent finding in butterfly wing-scales. These three-dimensional networks have cubic symmetry, are fully interconnected, have robust mechanical strength and possess chirality which can be controlled through the composition of multiple chiral networks, providing an excellent platform for developing novel chiral materials. Using direct laser writing we have fabricated different types of chiral composites that can be engineered to form novel photonic devices. We experimentally show strong circular dichroism and compare with numerical simulations to illustrate the high quality of these three-dimensional photonic structures.

  15. Highly efficient chiral resolution of DL-arginine by cocrystal formation followed by recrystallization under preferential-enrichment conditions.

    Science.gov (United States)

    Iwama, Sekai; Kuyama, Kazunori; Mori, Yuko; Manoj, Kochunnoonny; Gonnade, Rajesh G; Suzuki, Katsuaki; Hughes, Colan E; Williams, P Andrew; Harris, Kenneth D M; Veesler, Stéphane; Takahashi, Hiroki; Tsue, Hirohito; Tamura, Rui

    2014-08-11

    An excellent chiral symmetry-breaking spontaneous enantiomeric resolution phenomenon, denoted preferential enrichment, was observed on recrystallization of the 1:1 cocrystal of dl-arginine and fumaric acid, which is classified as a racemic compound crystal with a high eutectic ee value (>95 %), under non-equilibrium crystallization conditions. On the basis of temperature-controlled video microscopy and in situ time-resolved solid-state (13) C NMR spectroscopic studies on the crystallization process, a new mechanism of phase transition that can induce preferential enrichment is proposed.

  16. Separation of Chiral Active Pharmaceutical Ingredients

    DEFF Research Database (Denmark)

    Chaaban, Joussef Hussein

    is regarded as a first step towards a fully continuous PC process. The current knowledge of the importance of crystallization processes in the pharmaceutical industry and the complex thermodynamic and kinetic phenomena accompanied with the separation of chiral compounds are addressed. The experimental work...

  17. Tuning flexibility to control selectivity in soft porous crystals

    Science.gov (United States)

    Mahynski, Nathan A.; Shen, Vincent K.

    2017-01-01

    We use flat-histogram Monte Carlo simulations to study how changing the flexibility of soft porous crystals (SPCs) affects their selective adsorption of a binary, size-asymmetric supercritical fluid. Specifically, we consider mesoporous SPCs which have multiple minima in their free energy profiles as a function of pore size such that they are capable of exhibiting polymorphism between a narrow and large pore phase. While specific fluid-pore interactions determine the shape of both pores' selectivity curve as a function of adsorbate pressure, an individual pore tends to selectively adsorb a species based on the size of the adsorbate molecule relative to itself, thereby shifting the pore's selectivity curve relative to its polymorph. By controlling the flexibility of a SPC, the relative thermodynamic stability of the two pore phases may be varied, thereby changing the overall selectivity of the SPC during adsorbate loading. We investigate this for two classes of SPCs: one representative of "gate-opening" materials and another of "breathing" materials. For gate-opening materials, this control is much more salient than in breathing ones. However, for the latter, we illustrate how to tune the free energy profile to create materials which breathe multiple times during adsorption/desorption.

  18. Electro-optical switching by liquid-crystal controlled metasurfaces

    CERN Document Server

    Decker, Manuel; Minovich, Alexander; Staude, Isabelle; Miroshnichenko, Andrey E; Chigrin, Dmitry; Neshev, Dragomir N; Jagadish, Chennupati; Kivshar, Yuri S

    2013-01-01

    We study the optical response of a metamaterial surface created by a lattice of split-ring resonators covered with a nematic liquid crystal and demonstrate millisecond timescale switching between electric and magnetic resonances of the metasurface. This is achieved due to a high sensitivity of liquid-crystal molecular reorientation to the symmetry of the metasurface as well as to the presence of a bias electric field. Our experiments are complemented by numerical simulations of the liquid-crystal reorientation.

  19. The Kinetics of Chirality Assignment in Catalytic Single Walled Carbon Nanotube Growth

    OpenAIRE

    Xu, Ziwei; Yan, Tianying; Ding, Feng

    2014-01-01

    Chirality-selected single-walled carbon nanotubes (SWCNTs) ensure a great potential of building ~1 nm sized electronics. However, the reliable method for chirality-selected SWCNT is still pending. Here we present a theoretical study on the SWCNT's chirality assignment and control during the catalytic growth. This study reveals that the chirality of a SWCNT is determined by the kinetic incorporation of the pentagon formation during SWCNT nucleation. Therefore, chirality is randomly assigned on...

  20. Agglomeration Control during Ultrasonic Crystallization of an Active Pharmaceutical Ingredient

    Directory of Open Access Journals (Sweden)

    Bjorn Gielen

    2017-02-01

    Full Text Available Application of ultrasound during crystallization can efficiently inhibit agglomeration. However, the mechanism is unclear and sonication is usually enabled throughout the entire process, which increases the energy demand. Additionally, improper operation results in significant crystal damage. Therefore, the present work addresses these issues by identifying the stage in which sonication impacts agglomeration without eroding the crystals. This study was performed using a commercially available API that showed a high tendency to agglomerate during seeded crystallization. The crystallization progress was monitored using process analytical tools (PAT, including focus beam reflectance measurements (FBRM to track to crystal size and number and Fourier transform infrared spectroscopy (FTIR to quantify the supersaturation level. These tools provided insight in the mechanism by which ultrasound inhibits agglomeration. A combination of improved micromixing, fast crystal formation which accelerates depletion of the supersaturation and a higher collision frequency prevent crystal cementation to occur. The use of ultrasound as a post-treatment can break some of the agglomerates, but resulted in fractured crystals. Alternatively, sonication during the initial seeding stage could assist in generating nuclei and prevent agglomeration, provided that ultrasound was enabled until complete desupersaturation at the seeding temperature. FTIR and FBRM can be used to determine this end point.

  1. Baryons and Chiral Symmetry

    CERN Document Server

    Liu, Keh-Fei

    2016-01-01

    The relevance of chiral symmetry in baryons is highlighted in three examples in the nucleon spectroscopy and structure. The first one is the importance of chiral dynamics in understanding the Roper resonance. The second one is the role of chiral symmetry in the lattice calculation of $\\pi N \\sigma$ term and strangeness. The third one is the role of chiral $U(1)$ anomaly in the anomalous Ward identity in evaluating the quark spin and the quark orbital angular momentum. Finally, the chiral effective theory for baryons is discussed.

  2. Chiral Rotational Spectroscopy

    CERN Document Server

    Cameron, Robert P; Barnett, Stephen M

    2015-01-01

    We introduce chiral rotational spectroscopy: a new technique that enables the determination of the individual optical activity polarisability components $G_{XX}'$, $G_{YY}'$, $G_{ZZ}'$, $A_{X,YZ}$, $A_{Y,ZX}$ and $A_{Z,XY}$ of chiral molecules, in a manner that reveals the enantiomeric constitution of a sample whilst yielding an incisive signal even for a racemate. Chiral rotational spectroscopy could find particular use in the analysis of molecules that are chiral by virtue of their isotopic constitution and molecules with multiple chiral centres. The principles that underpin chiral rotational spectroscopy can also be exploited in the search for molecular chirality in space, which, if found, may add weight to hypotheses that biological homochirality and indeed life itself are of cosmic origin.

  3. On chiral and non chiral 1D supermultiplets

    Energy Technology Data Exchange (ETDEWEB)

    Toppan, Francesco, E-mail: toppan@cbpf.b [Centro Brasileiro de Pesquisas Fisicas (TEO/CBPF), Rio de Janeiro, RJ (Brazil). Coordenacao de Fisica Teorica

    2011-07-01

    In this talk I discuss and clarify some issues concerning chiral and non chiral properties of the one-dimensional supermultiplets of the N-extended supersymmetry. Quaternionic chirality can be defined for N = 4, 5, 6, 7, 8. Octonionic chirality for N = 8 and beyond. Inequivalent chiralities only arise when considering several copies of N = 4 or N = 8 supermultiplets. (author)

  4. Generation of Supramolecular Chirality around Twofold Rotational or Helical Axes in Crystalline Assemblies of Achiral Components

    Directory of Open Access Journals (Sweden)

    Mikiji Miyata

    2015-10-01

    Full Text Available A multi-point approximation method clarifies supramolecular chirality of twofold rotational or helical assemblies as well as bundles of the one-dimensional (1D assemblies. While one-point approximation of materials claims no chirality generation of such assemblies, multi-point approximations do claim possible generation in the 1D assemblies of bars and plates. Such chirality derives from deformations toward three-axial directions around the helical axes. The chiral columns are bundled in chiral ways through symmetry operations. The preferable right- or left-handed columns are bundled together to yield chiral crystals with right- or left-handedness, respectively, indicating that twofold helix symmetry operations cause chiral crystals composed of achiral components via a three-stepwise and three-directional process.

  5. Chiral symmetry and chiral-symmetry breaking

    Energy Technology Data Exchange (ETDEWEB)

    Peskin, M.E.

    1982-12-01

    These lectures concern the dynamics of fermions in strong interaction with gauge fields. Systems of fermions coupled by gauge forces have a very rich structure of global symmetries, which are called chiral symmetries. These lectures will focus on the realization of chiral symmetries and the causes and consequences of thier spontaneous breaking. A brief introduction to the basic formalism and concepts of chiral symmetry breaking is given, then some explicit calculations of chiral symmetry breaking in gauge theories are given, treating first parity-invariant and then chiral models. These calculations are meant to be illustrative rather than accurate; they make use of unjustified mathematical approximations which serve to make the physics more clear. Some formal constraints on chiral symmetry breaking are discussed which illuminate and extend the results of our more explicit analysis. Finally, a brief review of the phenomenological theory of chiral symmetry breaking is presented, and some applications of this theory to problems in weak-interaction physics are discussed. (WHK)

  6. Cooperative expression of atomic chirality in inorganic nanostructures

    Science.gov (United States)

    Wang, Peng-Peng; Yu, Shang-Jie; Govorov, Alexander O.; Ouyang, Min

    2017-02-01

    Cooperative chirality phenomena extensively exist in biomolecular and organic systems via intra- and inter-molecular interactions, but study of inorganic materials has been lacking. Here we report, experimentally and theoretically, cooperative chirality in colloidal cinnabar mercury sulfide nanocrystals that originates from chirality interplay between the crystallographic lattice and geometric morphology at different length scales. A two-step synthetic scheme is developed to allow control of critical parameters of these two types of handedness, resulting in different chiral interplays expressed as observables through materials engineering. Furthermore, we adopt an electromagnetic model with the finite element method to elucidate cooperative chirality in inorganic systems, showing excellent agreement with experimental results. Our study enables an emerging class of nanostructures with tailored cooperative chirality that is vital for fundamental understanding of nanoscale chirality as well as technology applications based on new chiroptical building blocks.

  7. Enantioselective Nanoporous Carbon Based on Chiral Ionic Liquids.

    Science.gov (United States)

    Fuchs, Ido; Fechler, Nina; Antonietti, Markus; Mastai, Yitzhak

    2016-01-04

    One of the greatest challenges in modern chemical processing is to achieve enantiospecific control in chemical reactions using chiral media such as chiral mesoporous materials. Herein, we describe a novel and effective synthetic pathway for the preparation of enantioselective nanoporous carbon, based on chiral ionic liquids (CILs). CILs of phenylalanine (CIL(Phe)) are used as precursors for the carbonization of chiral mesoporous carbon. We employ circular dichroism spectroscopy, isothermal titration calorimetry (ITC), and chronoamperometry in order to demonstrate the chiral nature of the mesoporous carbon. The approach presented in this paper is highly significant for the development of a new type of chiral porous materials for enantioselective chemistry. In addition, it contributes significantly to our understanding of the structure and nature of chiral nanoporous materials and surfaces. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  8. Kinetic crystallization separation process of the inositol isomers by controlling metastable zones

    Science.gov (United States)

    Konuki, Kaname; Hirasawa, Izumi

    2013-06-01

    D-chiro-inositol (DCI) is prepared by the immobilized enzyme reaction which uses myo-inositol (MI) as the substrate and the conversion rate is about 13%. The aim of this study was to develop a separation method for high purity DCI crystals from a reaction solution including low purity DCI only by the crystallization process. We succeeded in separating DCI crystals of 96% purity by water cooling crystallization, but it was presumed that scale-up was difficult. Although we tried anti-solvent crystallization similar to water cooling crystallization, high purity DCI crystals were not obtained. Therefore, we proposed the crystallization separation process by controlling metastable zones. The purity of a desired compound is controlled by this process, because solid-liquid separation is achieved before crystallization of compound in metastable zone. By the crystallization using this method, the DCI crystals of 97% purity were obtained. Although the yield per batch is about 50%, the actual yield is improved as the last mother liquor returns into the process of the following batch. When this process was repeated, the purity and the yield of DCI were reproduced and the robustness of this process was proved. It is expected that scale-up of this process will be successful, and this purification method could be applicable to similar systems such as separation of isomers and analogs.

  9. Automatic control unit for A neutron diffraction crystal spectrometer

    Energy Technology Data Exchange (ETDEWEB)

    Adib, M.; Abbas, Y.; Mostafa, M.; Hamouda, I.

    1982-01-01

    An automatic transistorized unit has been designed and constructed to control the operation of the double axis crystal spectrometer installed in front of one of the horizontal channels of the ET-RR-1 reactor. The function of the automatic unit is to store the diffracted neutrons at a certain angle with respect to the direction of the incident neutron beam in a selected channel of a 1024-multichannel analyzer for a certain preadjusted time period. AT the end of this time period the unit rotates the spectrometer's arm to another angle, selects the next channel of the MCA and provides the measurement of the diffracted neutron for the same time period. Such a sequence is repeated automatically over all angles required for the neutron diffraction pattern of the sample under investigation. As a result, the stored information at the MCA provides the neutron diffraction pattern as a function of channel number, where each channel corresponds to a certain scattering angle. The stored distribution at MCA can be obtained through the analyzer read out unit. The designed automatic unit has the possibility of providing the neutron diffraction pattern using a 6-digit scaler and a printer.

  10. Extrinsic electromagnetic chirality in metamaterials

    OpenAIRE

    Plum, E.; Fedotov, V. A.; Zheludev, N. I.

    2009-01-01

    Three- and two-dimensional chirality arising from the mutual orientation of non-chiral planar metamaterial structures and the incident electromagnetic wave (extrinsic chirality) lead to pronounced optical activity, circular dichroism and asymmetric transmission indistinguishable from those seen in media consisting of three- and two-dimensionally chiral molecules (intrinsic chirality).

  11. Controlled in meso phase crystallization--a method for the structural investigation of membrane proteins.

    Directory of Open Access Journals (Sweden)

    Jan Kubicek

    Full Text Available We investigated in meso crystallization of membrane proteins to develop a fast screening technology which combines features of the well established classical vapor diffusion experiment with the batch meso phase crystallization, but without premixing of protein and monoolein. It inherits the advantages of both methods, namely (i the stabilization of membrane proteins in the meso phase, (ii the control of hydration level and additive concentration by vapor diffusion. The new technology (iii significantly simplifies in meso crystallization experiments and allows the use of standard liquid handling robots suitable for 96 well formats. CIMP crystallization furthermore allows (iv direct monitoring of phase transformation and crystallization events. Bacteriorhodopsin (BR crystals of high quality and diffraction up to 1.3 Å resolution have been obtained in this approach. CIMP and the developed consumables and protocols have been successfully applied to obtain crystals of sensory rhodopsin II (SRII from Halobacterium salinarum for the first time.

  12. Control of Polishing Machine of Crystal Blank which Used Network Analyzer

    Science.gov (United States)

    Wakamoto, Satoru; Nakazawa, Mitsuo

    Quartz crystal devices have become an essential factor in electronic equipment such as mobile communication equipment or PC. As prices of electronic equipment have lowered, the cost-down of quartz crystal devices has been strongly demanded. To achieve the cost-down of quartz crystal device manufacturing, which uses a complex manufacturing process, the yield of the quartz crystal blank lapping process, which is the preliminary process of the quartz crystal device manufacturing process, must be increased. By introducing the network analyzer to the quartz crystal blank lapping process, we have obtained real time lapping characteristics. By obtaining the new process characteristics in real-time and visualizing them when changing lapping conditions, the network analyzer can now optimize the conditions of the process. In addition, the network analyzer can now measure the optical quartz crystal blank polishing process, which was difficult to measure by using a conventional controller.

  13. Chiral Surface Waves for Enhanced Circular Dichroism

    CERN Document Server

    Pellegrini, Giovanni; Celebrano, Michele; Duò, Lamberto; Biagioni, Paolo

    2016-01-01

    We present a novel chiral sensing platform that combines a one-dimensional photonic crystal design with a birefringent surface defect. The platform sustains simultaneous transverse electric and transverse magnetic surface modes, which are exploited to generate chiral surface waves. The present design provides homogeneous and superchiral fields of both handednesses over arbitrarily large areas in a wide spectral range, resulting in the enhancement of the circular dichroism signal by two orders of magnitude, thus paving the road toward the successful combination of surface-enhanced spectroscopies and electromagnetic superchirality.

  14. Chiral surface waves for enhanced circular dichroism

    Science.gov (United States)

    Pellegrini, Giovanni; Finazzi, Marco; Celebrano, Michele; Duò, Lamberto; Biagioni, Paolo

    2017-06-01

    We present a novel chiral sensing platform that combines a one-dimensional photonic crystal design with a birefringent surface defect. The platform sustains simultaneous transverse electric and transverse magnetic surface modes, which are exploited to generate chiral surface waves. The present design provides homogeneous and superchiral fields of both handednesses over arbitrarily large areas in a wide spectral range, resulting in the enhancement of the circular dichroism signal by more than two orders of magnitude, thus paving the road toward the successful combination of surface-enhanced spectroscopies and electromagnetic superchirality.

  15. Intelligent Chiral Sensing Based on Supramolecular and Interfacial Concepts

    Directory of Open Access Journals (Sweden)

    Hironori Izawa

    2010-07-01

    Full Text Available Of the known intelligently-operating systems, the majority can undoubtedly be classed as being of biological origin. One of the notable differences between biological and artificial systems is the important fact that biological materials consist mostly of chiral molecules. While most biochemical processes routinely discriminate chiral molecules, differentiation between chiral molecules in artificial systems is currently one of the challenging subjects in the field of molecular recognition. Therefore, one of the important challenges for intelligent man-made sensors is to prepare a sensing system that can discriminate chiral molecules. Because intermolecular interactions and detection at surfaces are respectively parts of supramolecular chemistry and interfacial science, chiral sensing based on supramolecular and interfacial concepts is a significant topic. In this review, we briefly summarize recent advances in these fields, including supramolecular hosts for color detection on chiral sensing, indicator-displacement assays, kinetic resolution in supramolecular reactions with analyses by mass spectrometry, use of chiral shape-defined polymers, such as dynamic helical polymers, molecular imprinting, thin films on surfaces of devices such as QCM, functional electrodes, FET, and SPR, the combined technique of magnetic resonance imaging and immunoassay, and chiral detection using scanning tunneling microscopy and cantilever technology. In addition, we will discuss novel concepts in recent research including the use of achiral reagents for chiral sensing with NMR, and mechanical control of chiral sensing. The importance of integration of chiral sensing systems with rapidly developing nanotechnology and nanomaterials is also emphasized.

  16. Gelation induced supramolecular chirality: chirality transfer, amplification and application.

    Science.gov (United States)

    Duan, Pengfei; Cao, Hai; Zhang, Li; Liu, Minghua

    2014-08-14

    Supramolecular chirality defines chirality at the supramolecular level, and is generated from the spatial arrangement of component molecules assembling through non-covalent interactions such as hydrogen bonding, van der Waals interactions, π-π stacking, hydrophobic interactions and so on. During the formation of low molecular weight gels (LMWGs), one kind of fascinating soft material, one frequently encounters the phenomenon of chirality as well as chiral nanostructures, either from chiral gelators or even achiral gelators. A view of gelation-induced supramolecular chirality will be very helpful to understand the self-assembly process of the gelator molecules as well as the chiral structures, the regulation of the chirality in the gels and the development of the "smart" chiral materials such as chiroptical devices, catalysts and chiral sensors. It necessitates fundamental understanding of chirality transfer and amplification in these supramolecular systems. In this review, recent progress in gelation-induced supramolecular chirality is discussed.

  17. A systematic framework for design of process monitoring and control (PAT) systems for crystallization processes

    DEFF Research Database (Denmark)

    Abdul Samad, Noor Asma Fazli Bin; Sin, Gürkan; Gernaey, Krist

    2013-01-01

    for generation of the supersaturation set-point for supersaturation control, as well as a tool for design of a process monitoring and control system (also called Process Analytical Technology (PAT) system). This systematic design allows one to generate the necessary problem-chemical system specific model......A generic computer-aided framework for systematic design of a process monitoring and control system for crystallization processes has been developed to study various aspects of crystallization operations.The systematic design framework contains a generic crystallizer modelling toolbox, a tool......, the necessary supersaturation set-point as well as a PAT system design including implementation of monitoring tools and control strategies in order to produce the desired target product properties notably crystal size distribution (CSD) and shape for a wide range of crystallization processes. Application...

  18. Directing peptide crystallization through curvature control of nanotubes.

    Science.gov (United States)

    Gobeaux, Frédéric; Tarabout, Christophe; Fay, Nicolas; Meriadec, Cristelle; Ligeti, Melinda; Buisson, David-Alexandre; Cintrat, Jean-Christophe; Artzner, Franck; Paternostre, Maïté

    2014-07-01

    In the absence of efficient crystallization methods, the molecular structures of fibrous assemblies have so far remained rather elusive. In this paper, we present a rational method to crystallize the lanreotide octapeptide by modification of a residue involved in a close contact. Indeed, we show that it is possible to modify the curvature of the lanreotide nanotubes and hence their diameter. This fine tuning leads to crystallization because the radius of curvature of the initially bidimensional peptide wall can be increased up to a point where the wall is essentially flat and a crystal is allowed to grow along a third dimension. By comparing X-ray diffraction data and Fourier transform Raman spectra, we show that the nanotubes and the crystals share similar cell parameters and molecular conformations, proving that there is indeed a structural continuum between these two morphologies. These results illustrate a novel approach to crystallization and represent the first step towards the acquisition of an Å-resolution structure of the lanreotide nanotubes β-sheet assembly.

  19. Chiral rotational spectroscopy

    Science.gov (United States)

    Cameron, Robert P.; Götte, Jörg B.; Barnett, Stephen M.

    2016-09-01

    We introduce chiral rotational spectroscopy, a technique that enables the determination of the orientated optical activity pseudotensor components BX X, BY Y, and BZ Z of chiral molecules, in a manner that reveals the enantiomeric constitution of a sample and provides an incisive signal even for a racemate. Chiral rotational spectroscopy could find particular use in the analysis of molecules that are chiral solely by virtue of their isotopic constitution and molecules with multiple chiral centers. A basic design for a chiral rotational spectrometer together with a model of its functionality is given. Our proposed technique offers the more familiar polarizability components αX X, αY Y, and αZ Z as by-products, which could see it find use even for achiral molecules.

  20. Chiral Superfluidity for QCD

    CERN Document Server

    Kalaydzhyan, Tigran

    2014-01-01

    We argue that the strongly coupled quark-gluon plasma formed at LHC and RHIC can be considered as a chiral superfluid. The "normal" component of the fluid is the thermalized matter in common sense, while the "superfluid" part consists of long wavelength (chiral) fermionic states moving independently. We use the bosonization procedure with a finite cut-off and obtain a dynamical axion-like field out of the chiral fermionic modes. Then we use relativistic hydrodynamics for macroscopic description of the effective theory obtained after the bosonization. Finally, solving the hydrodynamic equations in gradient expansion, we find that in the presence of external electromagnetic fields or rotation the motion of the "superfluid" component gives rise to the chiral magnetic, chiral vortical, chiral electric and dipole wave effects. Latter two effects are specific for a two-component fluid, which provides us with crucial experimental tests of the model.

  1. Emerging chirality in nanoscience.

    Science.gov (United States)

    Wang, Yong; Xu, Jun; Wang, Yawen; Chen, Hongyu

    2013-04-07

    Chirality in nanoscience may offer new opportunities for applications beyond the traditional fields of chirality, such as the asymmetric catalysts in the molecular world and the chiral propellers in the macroscopic world. In the last two decades, there has been an amazing array of chiral nanostructures reported in the literature. This review aims to explore and categorize the common mechanisms underlying these systems. We start by analyzing the origin of chirality in simple systems such as the helical spring and hair vortex. Then, the chiral nanostructures in the literature were categorized according to their material composition and underlying mechanism. Special attention is paid to highlight systems with original discoveries, exceptional structural characteristics, or unique mechanisms.

  2. Mechanical separation of chiral dipoles by chiral light

    CERN Document Server

    Canaguier-Durand, Antoine; Genet, Cyriaque; Ebbesen, Thomas W

    2013-01-01

    Optical forces take on a specific form when involving chiral light fields interacting with chiral objects. We show that optical chirality density and flow can have mechanical effects through reactive and dissipative components of chiral forces exerted on chiral dipoles. Remarkably, these force components are directly related to standard observables: optical rotation and circular dichroism, respectively. As a consequence, resulting forces and torques are dependent on the enantiomeric form of the chiral dipole. This leads to promising strategies for the mechanical separation of chiral objects using chiral light forces.

  3. A microchip to analyze single crystal growth and size-controllability

    Institute of Scientific and Technical Information of China (English)

    PANG YuanFeng; LIU JiangJiang; LI HaiFang; LIN JinMing

    2009-01-01

    A microfluidic device to control single crystallization on the micron scale has been developed.The salt solution was stored in the nano-volume gaps between the arrays of protrudent circular plots in the microchip.The mixed organic solvent was injected into the chip as the counter diffusion phase for crystallization forming.This device provides a liquid-liquid interface through which only one phase flows while the other stays at the fixed plot.Therefore,it is possible to control the position of crystallization on the fixed plot.We can control the size and the uniformity of single crystals from 5 to 50 μm in length by adjusting the relative factors,such as interface lifetime,breeds of the mix-organic solvents and inject- ing velocities.The longer interface lifetime and lower organic solvent injecting velocities can bring up larger and more asymmetric crystals,which nearly shows the same trend compared with the macroscopic crystallization.Finally,the effect of the surfactant on the crystallization in the micro-device was studied.By adding the surfactant into the liquid-liquid interface,smaller sizes of crystals can be obtained without changing the crystal configuration.

  4. A microchip to analyze single crystal growth and size-controllability

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    A microfluidic device to control single crystallization on the micron scale has been developed. The salt solution was stored in the nano-volume gaps between the arrays of protrudent circular plots in the microchip. The mixed organic solvent was injected into the chip as the counter diffusion phase for crystallization forming. This device provides a liquid-liquid interface through which only one phase flows while the other stays at the fixed plot. Therefore, it is possible to control the position of crystallization on the fixed plot. We can control the size and the uniformity of single crystals from 5 to 50 μm in length by adjusting the relative factors, such as interface lifetime, breeds of the mix-organic solvents and injecting velocities. The longer interface lifetime and lower organic solvent injecting velocities can bring up larger and more asymmetric crystals, which nearly shows the same trend compared with the macroscopic crystallization. Finally, the effect of the surfactant on the crystallization in the microdevice was studied. By adding the surfactant into the liquid-liquid interface, smaller sizes of crystals can be obtained without changing the crystal configuration.

  5. Rational enantioselective design of chiral heterobimetallic single-chain magnets: synthesis, crystal structures and magnetic properties of oxamato-bridged M(II)Cu(II) chains (M=Mn, Co).

    Science.gov (United States)

    Ferrando-Soria, Jesús; Cangussu, Danielle; Eslava, Mercedes; Journaux, Yves; Lescouëzec, Rodrigue; Julve, Miguel; Lloret, Francesc; Pasán, Jorge; Ruiz-Pérez, Catalina; Lhotel, Elsa; Paulsen, Carley; Pardo, Emilio

    2011-10-24

    A new series of neutral oxamato-bridged M(II)Cu(II) chiral chains of general formula [MCuL(x)(S)(m)(H(2)O)(n)]·aS·bH(2)O [L(1)=(M)-1,1'-binaphthalene-2,2'-bis(oxamate) with M=Mn (1a) and Co (1b); L(2)=(P)-1,1'-binaphthalene-2,2'-bis(oxamate) with M=Mn (2a) and Co (2b)] and the analogous racemic chains of formula [MCuL(3)(S)(m)(H(2)O)(n)]·aS·bH(2)O [L(3)=1,1'-binaphthalene-2,2'-bis(oxamate) with M=Mn (3a) and Co (3b)] have been prepared by reaction of the corresponding dianionic oxamatocopper(II) complex [Cu(L(x))](2-) with Mn(2+) or Co(2+) cations in either dimethylformamide (DMF) or dimethyl sulfoxide (DMSO). Solid circular dichroism (CD) spectra of the bimetallic chain compounds were recorded to establish their chiral and enantiomeric nature. They exhibit maximum positive and negative Cotton effects, each pair of enantiomeric chains being non-superimposable mirror images. The crystal structures of the Mn(II)Cu(II) (1a-3a) and the Co(II)Cu(II) (1b and 2b) chain compounds were solved by single-crystal X-ray diffraction methods. Our attempts to obtain X-ray quality crystals of 3b were unsuccessful. The values of the shortest interchain Mn···Mn and Co···Co distances are indicative of a good isolation of neighbouring chains in the crystal lattice, which is caused by the bulky aromatic ligand. Although all the Mn(II)Cu(II) and Co(II)Cu(II) chains exhibit ferrimagnetic behaviour (-J(MnCu)=18.9-26.6 cm(-1) and -J(CoCu)=19.5-32.5 cm(-1)), only the enantiopure Co(II)Cu(II) chains (1b and 2b) show slow magnetic relaxation at low temperatures (T(B)=0.6-1.8 K), which is a characteristic of single-chain magnets (SCMs) and is related to the magnetic anisotropy of the high-spin Co(II) ion. Analysis of the SCM behaviour of 1b and 2b, based on Glauber's theory for an Ising one-dimensional system, shows a thermally activated mechanism for the magnetic relaxation (Arrhenius law dependence). The energy barriers (E(a)) to reverse the magnetisation direction are 8.2 (1b) and

  6. Chiral Shock Waves

    CERN Document Server

    Sen, Srimoyee

    2016-01-01

    We study shock waves in relativistic chiral matter. We argue that the conventional Rankine- Hugoinot relations are modified due to the presence of chiral transport phenomena. We show that the entropy discontinuity in a weak shock wave is linearly proportional to the pressure discontinuity when the effect of chiral transport becomes sufficiently large. We also show that rarefaction shock waves, which do not exist in usual nonchiral fluids, can appear in chiral matter. These features are exemplified by shock propagation in dense neutrino matter in the hydrodynamic regime.

  7. Anomalous chiral superfluidity

    Energy Technology Data Exchange (ETDEWEB)

    Lublinsky, Michael, E-mail: lublinsky@phys.uconn.ed [Department of Physics and Astronomy, Stony Brook University, Stony Brook, NY 11794 (United States); Physics Department, Ben-Gurion University, Beer Sheva 84105 (Israel); Zahed, Ismail [Department of Physics and Astronomy, Stony Brook University, Stony Brook, NY 11794 (United States)

    2010-02-08

    We discuss both the anomalous Cartan currents and the energy-momentum tensor in a left chiral theory with flavor anomalies as an effective theory for flavored chiral phonons in a chiral superfluid with the gauged Wess-Zumino-Witten term. In the mean-field (leading tadpole) approximation the anomalous Cartan currents and the energy-momentum tensor take the form of constitutive currents in the chiral superfluid state. The pertinence of higher order corrections and the Adler-Bardeen theorem is briefly noted.

  8. Control of crystal growth in water purification by directional freeze crystallization

    Science.gov (United States)

    Conlon, William M. (Inventor)

    1996-01-01

    A Directional Freeze Crystallization system employs an indirect contact heat exchanger to freeze a fraction of liquid to be purified. The unfrozen fraction is drained away and the purified frozen fraction is melted. The heat exchanger must be designed in accordance with a Growth Habit Index to achieve efficient separation of contaminants. If gases are dissolved in the liquid, the system must be pressurized.

  9. Transfer of noncovalent chiral information along an optically inactive helical peptide chain: allosteric control of asymmetry of the C-terminal site by external molecule that binds to the N-terminal site.

    Science.gov (United States)

    Ousaka, Naoki; Inai, Yoshihito

    2009-02-20

    This study aims at demonstrating end-to-end transfer of noncovalent chiral information along a peptide chain. The domino-type induction of helical sense is proven by using achiral peptides 1-m of bis-chromophoric sequence with different chain lengths: H-(Aib-Delta(Z)Phe)(m)-(Aib-Delta(Z)Bip)(2)-Aib-OCH(3) [m = 2, 4, and 6; Aib = alpha-aminoisobutyric acid; Delta(Z)Phe = (Z)-alpha,beta-didehydrophenylalanine; Delta(Z)Bip = (Z)-beta-(4,4'-biphenyl)-alpha,beta-didehydroalanine]. They all showed the tendency to adopt a 3(10)-helix. Whereas peptide 1-m originally shows no circular dichroism (CD) signals, marked CD signals were induced at around 270-320 nm based on both the beta-aryl didehydroresidues by chiral Boc-proline (Boc = tert-butoxycarbonyl). The observed CD spectra were interpreted on the basis of the exciton chirality method and theoretical CD simulation of several helical conformations that were energy-minimized. The experimental and theoretical CD analysis reveals that Boc-l-proline induces the preference for a right-handed helicity in the whole chain of 1-m. Such noncovalent chiral induction was not observed in the corresponding N-terminally protected 1-m. Obviously, helicity induction in 1-m originates from the binding of Boc-proline to the N-terminal site. In the 17-mer (1-6), the information of helix sense reaches the 16th residue from the N-terminus. We have monitored precise transfer of noncovalent chiral stimulus along a helical peptide chain. The present study also proposes a primitive allosteric model of a single protein-mimicking backbone. Here chiral molecule binding the N-terminal site of 1-6 controls the chiroptical signals and helical sense of the C-terminal site about 30 A away.

  10. Doped Chiral Polymer Metamaterials Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Doped Chiral Polymer Metamaterials (DCPM) with tunable resonance frequencies have been developed by adding plasmonic inclusions into chiral polymers with variable...

  11. An automatic device for the quality control of large-scale crystal's production

    CERN Document Server

    Baccaro, S; Castellani, M; Cecilia, A; Dafinei, I; Diemoz, M; Guerra, S; Longo, E; Montecchi, M; Organtini, G; Pellegrini, F

    2001-01-01

    In 1999, the construction of the electromagnetic calorimeter of the Compact Muon Solenoid (CMS) experiment started. Half of the barrel calorimeter made of 61200 lead tungstate (PWO) crystals will be assembled and tested in the Regional Centre of INFN-ENEA in Rome, Italy. Before assembling, all 30600 PWO crystals will be qualified for scintillation and radiation hardness characteristics by a specially built Automatic Crystal Control System. The measuring techniques for crystal qualification and performances of the automatic system will be discussed in this work. (11 refs).

  12. Reducible chiral metamaterials

    CERN Document Server

    Ciattoni, Alessandro; Rizza, Carlo

    2016-01-01

    We introduce the concept of 3D reducible metamaterials whose constituent permittivity can be modelled by a factorized profile. The separated cartesian coordinates dependence, easily achieved in all-optical reconfigurable materials, allows to physically regard a reducible metamaterial as a superposition of three fictitious 1D generating media. We prove that, in the long-wavelength limit, the electromagnetic response of reducible metamaterials can be reconstructed from the properties of the 1D generating media whose interplay provides large freedom to control the electromagnetic chirality. Our approach introduces an unprecedented decomposition strategy in metamaterial science which allows the full ab-initio and flexible design of a complex 3D bianisotropic response by using 1D metamaterials as basic building blocks.

  13. Crystal structure analysis and chiral recognition study of Delta-[Ru(bpy)2(py)2][(+)-O,O'-dibenzoylD-tartrate].12H2O and Lambda-[Ru(bpy)2(py)2][(-)-O,O'-dibenzoyl-L-tartrate].12H2O.

    Science.gov (United States)

    Kolp, B; Viebrock, H; von Zelewsky, A; Abeln, D

    2001-03-12

    The molecular structure and crystal-packing mode of the enantiopure chiral building blocks Delta-[Ru(bpy)(2)(py)(2)][(+)-O,O'-dibenzoyl-D-tartrate].12H(2)O (I) and Lambda-[Ru(bpy)(2)(py)(2)][(-)-O,O'-dibenzoyl-L-tartrate].12H(2)O (II) have been determined by single-crystal X-ray diffraction data. This study proposes a model of how the L- and D-dibenzoyltartrate anions recognize the chirality of the hydrophobic [Ru(bpy)(2)(py)(2)](2+) complex. The monoclinic unit cell contains four complex cations, four tartrate anions, and 48 water molecules. Since there are no possibilities to form hydrogen bonds between the cations and anions, chiral recognition is due to crystal packing. Two benzoyl rings of two different tartrate anions are gripping the two bpy-planes of the Ru-complex. Further a third benzoyl ring from a tartrate anion is packed between the two pyridine rings, favoring one enantiomeric form to crystallize from aqueous solution. Crystal structure data for I at 153 K: a = 15.342(3) A, b = 19.200(4) A, c = 18.872(4) A, beta = 104.841(3) degrees, monoclinic space group C(2), R(1)= 0.0239 (I > 2sigma(I)), R(2) = 0.0606, Flack parameter = 0.0115 (with esd 0.0166). For II at 293 K: a = 15.376(4) A, b = 19.388(11) A, c = 19.085(7) A, beta = 105.11(2) degrees, monoclinic space group C121, R(1)= 0.0686 (I > 2sigma(I)), R(2) = 0.1819, Flack parameter = -0.0100 (with esd 0.0521).

  14. Controllable liquid crystal gratings for an adaptive 2D/3D auto-stereoscopic display

    Science.gov (United States)

    Zhang, Y. A.; Jin, T.; He, L. C.; Chu, Z. H.; Guo, T. L.; Zhou, X. T.; Lin, Z. X.

    2017-02-01

    2D/3D switchable, viewpoint controllable and 2D/3D localizable auto-stereoscopic displays based on controllable liquid crystal gratings are proposed in this work. Using the dual-layer staggered structure on the top substrate and bottom substrate as driven electrodes within a liquid crystal cell, the ratio between transmitting region and shielding region can be selectively controlled by the corresponding driving circuit, which indicates that 2D/3D switch and 3D video sources with different disparity images can reveal in the same auto-stereoscopic display system. Furthermore, the controlled region in the liquid crystal gratings presents 3D model while other regions maintain 2D model in the same auto-stereoscopic display by the corresponding driving circuit. This work demonstrates that the controllable liquid crystal gratings have potential applications in the field of auto-stereoscopic display.

  15. The electric properties and the current-controlled differential negative resistance of cBN crystal

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The electric properties of nonintentionally doped n-cubic boron nitride(cBN) crystal are investigated.The cBN crystal was transformed from hexagonal-boron nitride(h-BN) under high pressure(HP) and high temperature(HT) using magnesium powder as catalyst.At room temperature,the current-voltage(I-V) characteristics of cBN crystal are measured and found to be nonlinear.When the electric field is in the range of(1―1.5)×105 V/cm,the avalanche breakdown occurs inside the whole cBN crystal.At this same time,the bright blue-violet with the wavelength of 380―400 nm from the cBN crystal is observed.When measuring the I-V curve after breakdown of cBN crystal,the current-controlled differential negative resistance phenomenon is observed.The breakdown is repeatable.

  16. Control of Crystal Morphology for Mold Flux During High-Aluminum AHSS Continuous Casting Process

    Science.gov (United States)

    GUO, Jing; SEO, Myung-Duk; SHI, Cheng-Bin; CHO, Jung-Wook; KIM, Seon-Hyo

    2016-08-01

    In the present manuscript, the efforts to control the crystal morphology are carried out aiming at improving the lubrication of lime-alumina-based mold flux for casting advanced high-strength steel with high aluminum. Jackson α factors for crystals of melt crystallization in multi-component mold fluxes are established and reasonably evaluated by applying thermodynamic databases to understand the crystal morphology control both in lime-alumina-based and lime-silica-based mold fluxes. The results show that Jackson α factor and supercooling are the most critical factors to determine the crystal morphology in a mold flux. Crystals precipitating in mold fluxes appear with different morphologies due to their different Jackson α factors and are likely to be more faceted with higher Jackson α factor. In addition, there is a critical supercooling degree for crystal morphology dendritic transition. When the supercooling over the critical value, the crystals transform from faceted shape to dendritic ones in morphology as the kinetic roughening occurs. Typically, the critical supercooling degrees for cuspidine dendritic transition in the lime-silica-based mold fluxes are evaluated to be between 0.05 and 0.06. Finally, addition of a small amount of Li2O in the mold flux can increase the Jackson α factor and decrease the supercooling for cuspidine precipitation; thus, it is favorable to enhance a faceted cuspidine crystal.

  17. Embarras de richesses – It is not good to be too anomalous: Accurate structure of selenourea, a chiral crystal of planar molecules

    Science.gov (United States)

    Luo, Zhipu

    2017-01-01

    Selenourea, SeC(NH2)2, recently found an application as a derivatization reagent providing a significant anomalous diffraction signal used for phasing macromolecular crystal structures. The crystal structure of selenourea itself was solved about 50 years ago, from data recorded on films and evaluated by eye and refined to R = 0.15 with errors of bond lengths and angles about 0.1 Å and 6°. In the current work this structure is re-evaluated on the basis of synchrotron data and refined to R1 = 0.021 with bond and angle errors about 0.007 Å and 0.5°. The nine planar molecules of selenourea pack either in the P31 or in the P32 unit cell. All unique molecules are connected by a complex network of Se•••H-N hydrogen bonds and Se•••Se contacts. The packing of selenourea molecules is highly pseudosymmetric, approximating either of the P31(2)12, R3, and R32 space groups. Because the overwhelming majority of diffracted X-ray intensity originates form the anomalously scattering selenium atoms, the measurable anomalous Bijvoet differences are diminished and it was not possible to solve this crystal structure based on the anomalous signal alone. PMID:28207770

  18. Optical chirality in gyrotropic media: symmetry approach

    Science.gov (United States)

    Proskurin, Igor; Ovchinnikov, Alexander S.; Nosov, Pavel; Kishine, Jun-ichiro

    2017-06-01

    We discuss optical chirality in different types of gyrotropic media. Our analysis is based on the formalism of nongeometric symmetries of Maxwell’s equations in vacuum generalized to material media with given constituent relations. This approach enables us to directly derive conservation laws related to nongeometric symmetries. For isotropic chiral media, we demonstrate that like a free electromagnetic field, both duality and helicity generators belong to the basis set of nongeometric symmetries that guarantees the conservation of optical chirality. In gyrotropic crystals, which exhibit natural optical activity, the situation is quite different from the case of isotropic media. For light propagating along a certain crystallographic direction, there arises two distinct cases: (1) the duality is broken but the helicity is preserved, or (2) only the duality symmetry survives. We show that the existence of one of these symmetries (duality or helicity) is enough to define optical chirality. In addition, we present examples of low-symmetry media, where optical chirality cannot be defined.

  19. Helical Ordering in Chiral Block Copolymers

    Science.gov (United States)

    Zhao, Wei; Hong, Sung Woo; Chen, Dian; Grason, Gregory; Russell, Thomas

    2012-02-01

    Introducing molecular chirality into the segments of block copolymers can influence the nature of the resultant morphology. Such an effect was found for poly(styrene-b-L-lactide) (PS-b-PLLA) diblock copolymers where hexagonally packed PLLA helical microdomains (H* phase) form in a PS matrix. However, molecular ordering of PLLA within the helical microdomains and the transfer of chirality from the segmental level to the mesoscale is still not well understood. We developed a field theoretic model to describe the interactions between segments of chiral blocks, which have the tendency to form a ``cholesteric'' texture. Based on the model, we calculated the bulk morphologies of chiral AB diblock copolymers using self-consistent field theory (SCFT). Experiments show that the H* phase only forms when microphase separation between PS and PLLA block happens first and crystallization of PLLA block is suppressed or happens within confined microdomain. Hence, crystalline ordering is not necessary for H* phase formation. The SCFT offers the chance to explore the range of thermodynamic stability of helical structures in the phase diagram of chiral block copolymer melts, by tuning parameters not only like the block segregation strength and composition, but also new parameters such as the ratio between preferred helical pitch to the radius of gyration and the Frank elastic constant for inter-segment distortions.

  20. Liquid crystal multi-mode lenses and axicons based on electronic phase shift control.

    Science.gov (United States)

    Kirby, Andrew K; Hands, Philip J; Love, Gordon D

    2007-10-17

    We report on the principle of operation, construction and testing of a liquid crystal lens which is controlled by distributing voltages across the control electrodes, which are in turn controlled by adjusting the phase of the applied voltages. As well as (positive and negative) defocus, then lenses can be used to control tip/tilt, astigmatism, and to create variable axicons.

  1. Self-organized internal architectures of chiral micro-particles

    OpenAIRE

    2014-01-01

    The internal architecture of polymeric self-assembled chiral micro-particles is studied by exploring the effect of the chirality, of the particle sizes, and of the interface/surface properties in the ordering of the helicoidal planes. The experimental investigations, performed by means of different microscopy techniques, show that the polymeric beads, resulting from light induced polymerization of cholesteric liquid crystal droplets, preserve both the spherical shape and the internal self-org...

  2. Regioselective synthesis of chiral dimethyl-bis(ethylenedithiotetrathiafulvalene sulfones

    Directory of Open Access Journals (Sweden)

    Flavia Pop

    2015-07-01

    Full Text Available Enantiopure (R,R and (S,S-dimethyl-bis(ethylenedithiotetrathiafulvalene monosulfones have been synthesized by the aerial oxidation of the chiral dithiolates generated from the propionitrile-protected precursors. Both enantiomers crystallize in the orthorhombic chiral space group P212121. They show a boat-type conformation of the TTF moiety, a rather rigid dithiin sulfone ring and the methyl groups in a bisequatorial conformation. Cyclic voltammetry measurements indicate fully reversible oxidation in radical cation and dication species.

  3. Orthoconic liquid crystals--a case study.

    Science.gov (United States)

    Lagerwall, Sven T

    2014-06-01

    Since the early investigations on liquid crystals it was realized how the confining surfaces often determine the textures and even properties of the material. This influence is particularly complex and important for chiral materials. When we come to chiral smectics the surfaces may have dramatic effects. These are illustrated on the ferroelectric liquid crystals; they then again increase in importance for the antiferroelectric liquid crystals where the most recent example is given by the orthoconic liquid crystals.

  4. Demonstration of Optically Controlled re-Routing in a Photonic Crystal Three-Port Switch

    DEFF Research Database (Denmark)

    Combrié, S.; Heuck, Mikkel; Xavier, S.

    2012-01-01

    We present an experimental demonstration of optically controlled re-routing of a signal in a photonic crystal cavity-waveguide structure with 3 ports. This represents a key functionality of integrated all-optical signal processing circuits....

  5. Applications of chiral symmetry

    CERN Document Server

    Pisarski, R D

    1995-01-01

    I discuss several topics in the applications of chiral symmetry at nonzero temperature, including: where the rho goes, disoriented chiral condensates, and the phase diagram for QCD with 2+1 flavors. (Based upon talks presented at the "Workshop on Finite Temperature QCD", Wuhan, P.R.C., April, 1994.)

  6. Morphological control of zinc tricarbohydrazide perchlorate crystals:Theoretical and experimental study

    Institute of Scientific and Technical Information of China (English)

    LIU Rui; QI ShuYuan; ZHANG TongLai; ZHOU ZunNing; YANG Li; ZHANG JianGuo

    2013-01-01

    The theoretical crystal-morphology of zinc tricarbohydrazide perchlorate (ZnCP) was studied using the morphology simulation software.The growth trends and surface characteristics were calculated using the Bravais-Friedel-Donnay-Harker (BFDH),Growth Morphology,and Equilibrium Morphology methods; these provide theoretical guidance for the choice of crystal-control reagents.On the basis of the simulations,experiments were carried out to study the effects of five different crystal-control reagents,including carboxymethylcellulose (A),polyacrylamide (B),dextrin (C),Tween 40 (D),and Tween 60 (E),in the control of the crystal-morphology of ZnCP.Mixtures of two reagents and higher temperatures were used to further optimize the ZnCP crystals.The results show that ZnCP crystals are well dispersed,and have a large apparent density and regular crystal-morphology under the control of a mixture of reagents A and E in a mass ratio of 1 ∶ 4 at 80℃.

  7. Voltage-controlled narrowband and wide, variable-range four-segment quartz crystal oscillator.

    Science.gov (United States)

    Ruslan, Ruzaini; Satoh, Tomio; Akitsu, Tetsuya

    2012-03-01

    In this work, our goal is to develop a voltage-controlled variable-frequency quartz crystal oscillator with narrowband response, wide, variable frequency range and the capacity to oscillate across the series resonance frequency using a four-segment configuration of a quartz crystal oscillator. In conventional quartz oscillators, the quartz resonator is inserted in the feedback loop between the input and the output of the active circuit, providing sufficient gain and the phase relation. In the oscillator developed here, the quartz crystal resonator is inserted between the loop circuit and the ground potential. The performance of the voltage-controlled variable-frequency oscillator is demonstrated across the series resonance frequency.

  8. Manipulating the Lorentz force via the chirality of nanoparticles

    Science.gov (United States)

    Wang, Maoyan; Li, Hailong; Dong, Yuliang; Zhang, Xiaochuan; Du, Ming; Wang, Rui; Xu, Tong; Wu, Jian

    2016-12-01

    We demonstrate that a single plane wave pulls a chiral nanoparticle toward the light source. The nanoparticle exhibits optical gain in a particular wavelength region. The equivalence of the generalized and alternative expressions of the Lorentz force density relating to bound charges for chiral media is numerically validated. By considering the two-dimensional electromagnetic problem of incident plane waves normally impinged on active chiral cylinders, it is shown that the gradient force is mainly contributed by the bound electric and magnetic current densities of the cross-polarized waves. We also investigate how the medium parameters and impedance mismatch can be used to manipulate the pulling or pushing Lorentz forces between two chiral cylinders. This finding may provide a recipe to understand the light interaction with multiple chiral nanoparticles of arbitrary shapes (in general) with the aid of the numerical approach. It could be a promising avenue in controlling the optical micromanipulation for chiral nanoparticles with mirroring asymmetry.

  9. Geometrical approach to central molecular chirality: a chirality selection rule

    OpenAIRE

    Capozziello, S.; Lattanzi, A

    2004-01-01

    Chirality is of primary importance in many areas of chemistry and has been extensively investigated since its discovery. We introduce here the description of central chirality for tetrahedral molecules using a geometrical approach based on complex numbers. According to this representation, for a molecule having n chiral centres, it is possible to define an index of chirality. Consequently a chirality selection rule has been derived which allows the characterization of a molecule as achiral, e...

  10. Enantiomer-Specific State Transfer of Chiral Molecules

    CERN Document Server

    Eibenberger, Sandra; Patterson, David

    2016-01-01

    State-selective enantiomeric excess is realized using microwave-driven coherent population transfer. The method selectively promotes either R- or S- molecules to a higher rotational state by phase-controlled microwave pulses that drive electric-dipole allowed rotational transitions. We demonstrate the method using a racemic mixture of 1,2-propanediol. This method of chiral enrichment can be applied to nearly any chiral molecule that can be vaporized and cooled to the point where rotationally resolved spectroscopy is possible, including molecules that rapidly racemize. The rapid chiral switching demonstrated here allows for new applications in high-precision spectroscopic searches for parity violation in chiral molecules.

  11. A Generic Framework for Systematic Design of Process Monitoring and Control System for Crystallization Processes

    DEFF Research Database (Denmark)

    Abdul Samad, Noor Asma Fazli Bin; Meisler, Kresten Troelstrup; Sin, Gürkan

    2012-01-01

    A generic framework for systematic design of a process monitoring and control system for crystallization processes has been developed in order to obtain the desired end-product properties notably the crystal size distribution (CSD). The design framework contains a generic crystallizer modelling...... tool-box, a tool for design of operational policies as well as a tool for design of process monitoring and control systems. Through this framework, it is possible for a wide range of crystallization processes to generate the necessary problem-system specific model, the necessary operational policy...... and a Process Analytical Technology (PAT) system design including implementation of monitoring tools and control strategies in order to produce a desired product with its corresponding target properties. Application of the framework is highlighted through a case study involving the system potassium dihydrogen...

  12. Solution Coating of Superior Large-Area Flexible Perovskite Thin Films with Controlled Crystal Packing

    KAUST Repository

    Li, Jianbo

    2017-05-08

    Solution coating of organohalide lead perovskites offers great potential for achieving low-cost manufacturing of large-area flexible optoelectronics. However, the rapid coating speed needed for industrial-scale production poses challenges to the control of crystal packing. Herein, this study reports using solution shearing to confine crystal nucleation and growth in large-area printed MAPbI3 thin films. Near single-crystalline perovskite microarrays are demonstrated with a high degree of controlled macroscopic alignment and crystal orientation, which exhibit significant improvements in optical and optoelectronic properties comparing with their random counterparts, spherulitic, and nanograined films. In particular, photodetectors based on the confined films showing intense anisotropy in charge transport are fabricated, and the device exhibits significantly improved performance in all aspects by one more orders of magnitude relative to their random counterparts. It is anticipated that perovskite films with controlled crystal packing may find applications in high-performance, large-area printed optoelectronics, and solar cells.

  13. Magneto-optic Crystal Polarization Controller Assisted Mode-Locked Fiber Laser

    Institute of Scientific and Technical Information of China (English)

    ZHAO Guang-Zhen; GUI Li-Li; XIAO Xiao-Sheng; YANG Chang-Xi

    2011-01-01

    We report a passively mode-locked erbium-doped fiber laser based on a compact magneto-optic crystal polarization controller. The length of the polarization controller consisting of four magneto-optic crystal rotators and two quarter wave-plates is only 10cm.Adjusting the polarization controller, central wavelength around 1559nm and repetition rate 21.10 MHz mode-locked pulse are obtained. Pulse duration and 3 dB spectrum width are 598.4fs and 6.24nm respectively. Single pulse energy is about 151.7pJ. Because of its small size, low insertion loss,good controllability and negligible dispersion, the magneto-optic crystal polarization controller could be an ideal polarization controller in fiber lasers.

  14. Stabilizing control of crystal size distribution in continuous crystallization processes; Renzoku shoseki purosesu ni okeru kessho ryukei bunpu no anteika seigyo

    Energy Technology Data Exchange (ETDEWEB)

    Naito, K.; Sotowa, K.; Kano, M.; Hasebe, S.; Hashimoto, I. [Kyoto Univ. (Japan). Faculty of Engineering

    1998-03-01

    The sustained oscillation of the crystal size distribution (CSD) in continuous crystallization process is analyzed by simulation using a detailed model. CSD can not be used as a controlled variable because of its distributed nature. Therefore, the method of selecting representability indices for CSD and the stabilizing control of CSD based on those indices are investigated. A multi-loop scheme is proposed, wherein a system with the third moment of large crystal and the rate of product flow from the continuous crystallizer used as the controlled variable and the operating variable, respectively, is added to the SISO control system which employs microcrystal population density as the controlled variable and the microcrystal flow rate as the operating variable. The controlling performances of the newly proposed multi-loop scheme and the SISO control scheme are compared. It is confirmed that the proposed controlling method is effective when the constrain from the microcrystal flow rate is strict. 6 refs., 14 figs., 2 tabs.

  15. Controlled growth of ultrathin Mo2C superconducting crystals on liquid Cu surface

    Science.gov (United States)

    Geng, Dechao; Zhao, Xiaoxu; Li, Linjun; Song, Peng; Tian, Bingbing; Liu, Wei; Chen, Jianyi; Shi, Dong; Lin, Ming; Zhou, Wu; Loh, Kian Ping

    2017-03-01

    Exhibiting thickness-dependent change in the critical temperature (T c) for the onset of superconductivity, Mo2C has emerged as an important new member in the family of two-dimensional atomic crystals. Controllable growth in terms of morphology and thickness is necessary to elucidate its intrinsic properties at the 2D limit. Here we demonstrate the chemical vapor deposition of ultrathin Mo2C crystals on liquid Cu surface where the morphology of the crystals can be controlled by tuning the carbon supersaturation. A unique staggered carbon vacancy ordering is discovered in Mo2C crystals having particular geometries. Thickness engineering of the crystal can be achieved by controlling the thickness of the Cu catalyst layer, which affords a facile route to grow ultrathin 2D samples. Ultrathin Mo2C crystals so obtained, have been characterized using aberration corrected scanning transmission electron microscopy annular dark field imaging, where the co-existence of both AA and AB stacking modes is observed. The high crystallinity of the Mo2C crystals synthesized in this work is attested by its characteristic sharp superconducting transition.

  16. Synthesis and characterization of chiral thorium(IV) and uranium(IV) benzamidinate complexes

    Energy Technology Data Exchange (ETDEWEB)

    Schoene, Sebastian; Maerz, Juliane; Kaden, Peter; Patzschke, Michael; Ikeda-Ohno, Atsushi [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Chemistry of the F-Elements

    2017-06-01

    Two chiral benzamidinate complexes of tetravalent actinides (Th(IV) and U(IV)) were synthesized using a salt metathesis reaction of the corresponding actinide(IV) tetrachlorides and the potassium salt of the chiral benzamidine (S,S)-N,N-Bis-(1-phenylethyl)-benzamidine ((S)-HPEBA). The structure of the complexes was determined with single crystal X-ray diffraction. These are the first examples of chiral amidinate complexes of actinides.

  17. Large-grained copper indium diselenide crystal growth by computer-controlled high-pressure liquid-encapsulated directional solidification

    Science.gov (United States)

    Schwerdtfeger, C. R.; Ciszek, T. F.

    1992-12-01

    Large-grained copper indium diselenide crystal growth by computer-controlled high-pressure liquid-encapsulated directional solidification is presented. A supply of good quality angle crystals is essential to characterization of the fundamental material properties. [AIP

  18. Applications of chiral symmetry

    Energy Technology Data Exchange (ETDEWEB)

    Pisarski, R.D.

    1995-03-01

    The author discusses several topics in the applications of chiral symmetry at nonzero temperature. First, where does the rho go? The answer: up. The restoration of chiral symmetry at a temperature T{sub {chi}} implies that the {rho} and a{sub 1} vector mesons are degenerate in mass. In a gauged linear sigma model the {rho} mass increases with temperature, m{sub {rho}}(T{sub {chi}}) > m{sub {rho}}(0). The author conjectures that at T{sub {chi}} the thermal {rho} - a{sub 1}, peak is relatively high, at about {approximately}1 GeV, with a width approximately that at zero temperature (up to standard kinematic factors). The {omega} meson also increases in mass, nearly degenerate with the {rho}, but its width grows dramatically with temperature, increasing to at least {approximately}100 MeV by T{sub {chi}}. The author also stresses how utterly remarkable the principle of vector meson dominance is, when viewed from the modern perspective of the renormalization group. Secondly, he discusses the possible appearance of disoriented chiral condensates from {open_quotes}quenched{close_quotes} heavy ion collisions. It appears difficult to obtain large domains of disoriented chiral condensates in the standard two flavor model. This leads to the last topic, which is the phase diagram for QCD with three flavors, and its proximity to the chiral critical point. QCD may be very near this chiral critical point, and one might thereby generated large domains of disoriented chiral condensates.

  19. Molecular-Level Design of Heterogeneous Chiral Catalysis

    Energy Technology Data Exchange (ETDEWEB)

    Francisco Zaera

    2012-03-21

    , and the development of ways to imprint chiral centers on achiral solid surfaces. Chiral catalysis is not only a problem of great importance in its own right, but also the ultimate test of how to control selectivity in catalysis. The time is ripe for fundamental work in heterogeneous chiral catalysis to provide the U.S. with a leadership role in developing the next generation of catalytic processes for medicinal and agrochemical manufacturing. Our team provides the required expertise for a synergistic and comprehensive integration of physical and chemical experimentation with solid state and molecular reactivity theories to solve this problem.

  20. Electrically controllable liquid crystal photonic bandgap fiber with dual-frequency control

    DEFF Research Database (Denmark)

    Scolari, Lara; Alkeskjold, Thomas Tanggaard; Riishede, Jesper

    2005-01-01

    We present an electrically tunable liquid crystal photonic bandgap fiber device based on a dual frequency liquid crystal with pre-tilted molecules that allows the bandgaps to be continuously tuned. The frequency dependent behavior of the liquid crystal enables active shifting of the bandgaps toward...

  1. Magnetic field controlled single crystal growth and surface modification of titanium alloys exposed for biocompatibility

    Science.gov (United States)

    Hermann, Regina; Uhlemann, Margitta; Wendrock, Horst; Gerbeth, Gunter; Büchner, Bernd

    2011-03-01

    The aim of this work is growth and characterisation of Ti55Nb45 (wt%) single crystals by floating-zone single crystal growth of intermetallic compounds using two-phase radio-frequency (RF) electromagnetic heating. Thereby, the process and, in particular, the flow field in the molten zone is influenced by additional magnetic fields. The growth of massive intermetallic single crystals is very often unsuccessful due to an unfavourable solid-liquid interface geometry enclosing concave fringes. It is generally known that the crystallization process stability is enhanced if the crystallization interface is convex. For this, a tailored magnetic two-phase stirrer system has been developed, which enables a controlled influence on the melt ranging from intensive inwards to outwards flows. Since Ti is favourably light, strong and biocompatible, it is one of the few materials that naturally match the requirements for implantation in the human body. Therefore, the magnetic system was applied to crystal growth of Ti alloys. The grown crystals were oriented and cut to cubes with the desired crystallographic orientations [1 0 0] and [1 0 1] normally on a plane. The electron backscatter diffraction (EBSD) technique was applied to clearly determine crystal orientation and to localize grain boundaries. The formation of oxidic nanotubes on Ti surfaces in dependence of the grain orientation was investigated, performed electrochemically by anodic oxidation from fluoride containing electrolyte.

  2. Direction-specific interactions control crystal growth by oriented attachment

    DEFF Research Database (Denmark)

    Li, Dongsheng; Nielsen, Michael H; Lee, Jonathan R.I.

    2012-01-01

    initiated at the contact point. Interface elimination proceeds at a rate consistent with the curvature dependence of the Gibbs free energy. Measured translational and rotational accelerations show that strong, highly direction-specific interactions drive crystal growth via oriented attachment....... using a fluid cell to directly observe oriented attachment of iron oxyhydroxide nanoparticles. The particles undergo continuous rotation and interaction until they find a perfect lattice match. A sudden jump to contact then occurs over less than 1 nanometer, followed by lateral atom-by-atom addition...

  3. Chiral supergravity and anomalies

    CERN Document Server

    Mielke, E W; Macias, Alfredo; Mielke, Eckehard W.

    1999-01-01

    Similarily as in the Ashtekar approach, the translational Chern-Simons term is, as a generating function, instrumental for a chiral reformulation of simple (N=1) supergravity. After applying the algebraic Cartan relation between spin and torsion, the resulting canonical transformation induces not only decomposition of the gravitational fields into selfdual and antiselfdual modes, but also a splitting of the Rarita-Schwinger fields into their chiral parts in a natural way. In some detail, we also analyze the consequences for axial and chiral anomalies.

  4. Effect of ultrasonic irradiation on the number of acetylsalicylic acid crystals produced under the supersaturated condition and the ability of controlling the final crystal size via primary nucleation

    Science.gov (United States)

    Miyasaka, Etsuko; Kato, Yumi; Hagisawa, Minoru; Hirasawa, Izumi

    2006-03-01

    The purposes of this study were to investigate the effects of ultrasound irradiation on the number of crystals formed in an acetylsalicyclic acid crystallization process and to assess the controllability of the final product size via the number of primary nuclei. The number of crystals present after primary nucleation was counted and the relationship between the final product size and the number of crystals was examined. Additionally, the growing ASA crystals were observed, since ultrasound energy not only may control primary nucleation but may also the perfection of the crystal shape. At a high level of ultrasonic energy, ultrasound irradiation increased the average number of crystals, an effect that has been reported often; however, at a low level of ultrasonic energy it decreased the average number of crystals, and moreover, these opposing ultrasonic effects on the number of crystals interchanged at a specific energy threshold. These results reveal two novel phenomena—that there is an energy region where ultrasonic irradiation inhibits primary nucleation, and that a specific amount of ultrasonic energy is needed to activate primary nucleation. On the other hand, the final product size almost depended upon the number of primary nuclei, indicating that the final product size could be controlled via the number of crystals influenced by ultrasound irradiation. According to the photographs of crystals, they were not destroyed by the process. Therefore, it was proposed that ultrasound energy does not destroy the perfection of the crystal shape but only controls primary nucleation under the condition: both short irradiation time and low supersaturated condition.

  5. Automatic Control System for the High Pressure CdTe Crystal Growth Furnace

    OpenAIRE

    Petr Praus; Eduard Belas; Jiri Bok; Roman Fesh; Jan Franc; Pavel Hoschl

    2006-01-01

    CdTe and (CdZn)Te bulk single crystals have been widely used as substrates for MBE and LPE epitaxy of infrared (HgCd)Te as well as gamma- and X-ray detectors. The Cd1-xZnxTe (x = 0.04-0.1) single crystals with diameter up to 100 mm and height at most 40 mm were prepared in our laboratory in a vertical arrangement by gradual cooling of the melt (the Vertical Gradient Freezing method). Achievement of excellent crystal quality required full control of Cd pressure during the growth process and ap...

  6. Controlling crystal phases in GaAs nanowires grown by Au-assisted molecular beam epitaxy.

    Science.gov (United States)

    Dheeraj, D L; Munshi, A M; Scheffler, M; van Helvoort, A T J; Weman, H; Fimland, B O

    2013-01-11

    Control of the crystal phases of GaAs nanowires (NWs) is essential to eliminate the formation of stacking faults which deteriorate the optical and electronic properties of the NWs. In addition, the ability to control the crystal phase of NWs provides an opportunity to engineer the band gap without changing the crystal material. We show that the crystal phase of GaAs NWs grown on GaAs(111)B substrates by molecular beam epitaxy using the Au-assisted vapor-liquid-solid growth mechanism can be tuned between wurtzite (WZ) and zinc blende (ZB) by changing the V/III flux ratio. As an example we demonstrate the realization of WZ GaAs NWs with a ZB GaAs insert that has been grown without changing the substrate temperature.

  7. Catalysis of Dynamical Chiral Symmetry Breaking by Chiral Chemical Potential

    CERN Document Server

    Braguta, V V

    2016-01-01

    In this paper we study the properties of media with chiral imbalance parameterized by chiral chemical potential. It is shown that depending on the strength of interaction between constituents in the media the chiral chemical potential either creates or enhances dynamical chiral symmetry breaking. Thus the chiral chemical potential plays a role of the catalyst of dynamical chiral symmetry breaking. Physically this effect results from the appearance of the Fermi surface and additional fermion states on this surface which take part in dynamical chiral symmetry breaking. An interesting conclusion which can be drawn is that at sufficiently small temperature chiral plasma is unstable with respect to condensation of Cooper pairs and dynamical chiral symmetry breaking even for vanishingly small interactions between constituents.

  8. Locally Enhanced and Tunable Optical Chirality in Helical Metamaterials

    CERN Document Server

    Gutsche, Philipp; Burger, Sven

    2016-01-01

    We report on a numerical study of optical chirality. Intertwined gold helices illuminated with plane waves concentrate right and left circularly polarized electromagnetic field energy to sub-wavelength regions. These spots of enhanced chirality can be smoothly shifted in position and magnitude by varying illumination parameters, allowing for the control of light-matter interactions on a nanometer scale.

  9. Improved chiral SFC screening for analytical method development.

    Science.gov (United States)

    Schafer, Wes; Chandrasekaran, Tilak; Pirzada, Zainab; Zhang, Chaowei; Gong, Xiaoyi; Biba, Mirlinda; Regalado, Erik L; Welch, Christopher J

    2013-11-01

    In this study we describe the evaluation of a recently developed supercritical fluid chromatography (SFC) instrument for automated chiral SFC method development. The greatly improved gradient dwell volume and liquid flow control of the new instrument in combination with the use of shorter columns containing smaller stationary phase particles affords chiral SFC method development that is faster and more universal than previous systems.

  10. Deracemization of bilirubin as the marker of the chirality of micellar aggregates.

    Science.gov (United States)

    Sorrenti, Alessandro; Altieri, Barbara; Ceccacci, Francesca; Di Profio, Pietro; Germani, Raimondo; Giansanti, Luisa; Savelli, Gianfranco; Mancini, Giovanna

    2012-01-01

    The deracemization of bilirubin in micellar aggregates of structurally correlated chiral surfactants was studied by circular dichroism experiments and exploited as the marker of the expression of chirality of the aggregates. The obtained results suggest that the hydrophobic interactions control the transfer of chirality from the monomers to the aggregates, and that different regions of the same aggregate might feature opposite enantiorecognition capabilities.

  11. Automatic Control System for the High Pressure CdTe Crystal Growth Furnace

    Directory of Open Access Journals (Sweden)

    Petr Praus

    2006-08-01

    Full Text Available CdTe and (CdZnTe bulk single crystals have been widely used as substrates for MBE and LPE epitaxy of infrared (HgCdTe as well as gamma- and X-ray detectors. The Cd1-xZnxTe (x = 0.04-0.1 single crystals with diameter up to 100 mm and height at most 40 mm were prepared in our laboratory in a vertical arrangement by gradual cooling of the melt (the Vertical Gradient Freezing method. Achievement of excellent crystal quality required full control of Cd pressure during the growth process and application of high Cd pressures (up to 4 bar at growth temperature. An electronic control system was designed to control both temperature and internal pressure of two zones CZT crystal growth furnace by using two high performance PID controllers/setpoint programmers. Two wire current loop serial communication bus was used for the data exchange and computer control of the furnace electronics setup. Control software was written to supervise the crystal growth process and to collect all important data and parameters.

  12. Controlling stereochemical outcomes of asymmetric processes by catalyst remote molecular functionalizations: chiral diamino-oligothiophenes (DATs) as ligands in asymmetric catalysis.

    Science.gov (United States)

    Albano, Vincenzo Giulio; Bandini, Marco; Barbarella, Giovanna; Melucci, Manuela; Monari, Magda; Piccinelli, Fabio; Tommasi, Simona; Umani-Ronchi, Achille

    2006-01-11

    The synthesis, characterization, and structure-guided application of a new class of highly versatile chiral C(2)-symmetric diamine-oligothiophene ligands in Pd-catalyzed asymmetric transformations are presented. Experimental investigations of the intimate role of pendant pi-conjugate oligothiophenes in determining the catalytic activity of the corresponding chiral Pd complexes are described. Their unusual behavior opens up new routes toward the logical design of finely tuned organometallic catalysts by remote structural functionalizations.

  13. Study of Fluid Flow Control in Protein Crystallization using Strong Magnetic Fields

    Science.gov (United States)

    Ramachandran, Narayanan; Leslie, Fred; Ciszak, Ewa

    2002-01-01

    An important component in biotechnology, particularly in the area of protein engineering and rational drug design is the knowledge of the precise three-dimensional molecular structure of proteins. The quality of structural information obtained from X-ray diffraction methods is directly dependent on the degree of perfection of the protein crystals. As a consequence, the growth of high quality macromolecular crystals for diffraction analyses has been the central focus for biochemists, biologists, and bioengineers. Macromolecular crystals are obtained from solutions that contain the crystallizing species in equilibrium with higher aggregates, ions, precipitants, other possible phases of the protein, foreign particles, the walls of the container, and a likely host of other impurities. By changing transport modes in general, i.e., reduction of convection and sedimentation, as is achieved in "microgravity", researchers have been able to dramatically affect the movement and distribution of macromolecules in the fluid, and thus their transport, formation of crystal nuclei, and adsorption to the crystal surface. While a limited number of high quality crystals from space flights have been obtained, as the recent National Research Council (NRC) review of the NASA microgravity crystallization program pointed out, the scientific approach and research in crystallization of proteins has been mainly empirical yielding inconclusive results. We postulate that we can reduce convection in ground-based experiments and we can understand the different aspects of convection control through the use of strong magnetic fields and field gradients. Whether this limited convection in a magnetic field will provide the environment for the growth of high quality crystals is still a matter of conjecture that our research will address. The approach exploits the variation of fluid magnetic susceptibility with concentration for this purpose and the convective damping is realized by appropriately

  14. Optically probed symmetry breaking in the chiral magnet Cu2OSeO3

    NARCIS (Netherlands)

    Versteeg, R. B.; Vergara, I.; Schaefer, S. D.; Bischoff, D.; Aqeel, A.; Palstra, T. T. M.; Grueninger, M.; van Loosdrecht, P. H. M.

    2016-01-01

    We report on the linear optical properties of the chiral magnet Cu2OSeO3, specifically associated with the absence of inversion symmetry, the chiral crystallographic structure, and magnetic order. Through spectroscopic ellipsometry, we observe local crystal-field excitations below the charge-transfe

  15. Controlled assembly of single colloidal crystals using electro-osmotic micro-pumps

    OpenAIRE

    Niu, Ran; Oğuz, Erdal C.; Müller, Hannah; Reinmüller, Alexander; Botin, Denis; Löwen, Hartmut; Palberg, Thomas

    2016-01-01

    We assemble charged colloidal spheres at deliberately chosen locations on a charged unstructured glass substrate utilizing ion exchange based electro-osmotic micro-pumps. Using microscopy, a simple scaling theory and Brownian Dynamics simulations, we systematically explore the control parameters of crystal assembly and the mechanisms through which they depend on the experimental boundary conditions. We demonstrate that crystal quality depends crucially on the assembly distance of the colloids...

  16. Two Beam Energy Exchange in Hybrid Liquid Crystal Cells with Photorefractive Field Controlled Boundary Conditions (Postprint)

    Science.gov (United States)

    2016-09-12

    AFRL-RX-WP-JA-2017-0209 TWO BEAM ENERGY EXCHANGE IN HYBRID LIQUID CRYSTAL CELLS WITH PHOTOREFRACTIVE FIELD CONTROLLED BOUNDARY...DATES COVERED (From - To) 29 August 2016 Interim 26 October 2015 – 29 July 2016 4. TITLE AND SUBTITLE TWO BEAM ENERGY EXCHANGE IN HYBRID LIQUID... energy gain when two light beams intersect in a hybrid nematic liquid crystal (LC) cell with photorefractive crystalline substrates. A periodic space

  17. Spontaneous Resolution and Carbonation of Chiral Benzyllithium Complexes

    DEFF Research Database (Denmark)

    Lennartson, Anders; Sundberg, Jonas; Wiklund, Tove

    2010-01-01

    In search for new examples of absolute asymmetric synthesis (AAS), chiral α-substituted benzyllithium complexes have been prepared. While [Li(phet)(pmdta)] (1) (phet = 1-phenylethyl, pmdta = N,N,N′,N″,N″-pentamethyldiethylenetriamine) affords only racemic crystals, a promising candidate for AAS...... was indeed found: [Li(phet)(tmpda)], α-2, (tmpda = N,N,N′,N′-tetramethylpropylenediamine) crystallises as a conglomerate. Although concomitant polymorphism was not observed, a racemic phase (β-2) could also be isolated. Chiral crystals of α-2 gave 2-phenylpropionic acid in high yield on reaction with gaseous...

  18. Diffusion-controlled anisotropic growth of stable and metastable crystal polymorphs in the phase-field crystal model.

    Science.gov (United States)

    Tegze, G; Gránásy, L; Tóth, G I; Podmaniczky, F; Jaatinen, A; Ala-Nissila, T; Pusztai, T

    2009-07-17

    We use a simple density functional approach on a diffusional time scale, to address freezing to the body-centered cubic (bcc), hexagonal close-packed (hcp), and face-centered cubic (fcc) structures. We observe faceted equilibrium shapes and diffusion-controlled layerwise crystal growth consistent with two-dimensional nucleation. The predicted growth anisotropies are discussed in relation with results from experiment and atomistic simulations. We also demonstrate that varying the lattice constant of a simple cubic substrate, one can tune the epitaxially growing body-centered tetragonal structure between bcc and fcc, and observe a Mullins-Sekerka-Asaro-Tiller-Grinfeld-type instability.

  19. Controlling in situ crystallization of pharmaceutical particles within the spray dryer.

    Science.gov (United States)

    Woo, Meng Wai; Lee, May Ginn; Shakiba, Soroush; Mansouri, Shahnaz

    2016-12-20

    Simultaneous solidification and in situ crystallization (or partial crystallization) of droplets within the drying chamber are commonly encountered in the spray drying of pharmaceuticals. The crystallinity developed will determine the functionality of the powder and its stability during storage. This review discusses strategies that can be used to control the in situ crystallization process. Areas covered: The premise of the strategies discussed focuses on the manipulation of the droplet drying rate relative to the timescale of crystallization. This can be undertaken by the control of the spray drying operation, by the use of volatile materials and by the inclusion of additives. Several predictive approaches for in situ crystallization control and new spray dryer configuration strategies are further discussed. Expert opinion: Most reports, hitherto, have focused on the crystallinity of the spray dried material or the development of crystallinity during storage. More mechanistic understanding of the in situ crystallization process during spray drying is required to guide product formulation trials. The key challenge will be in adapting the mechanistic approach to the myriad possible formulations in the pharmaceutical industry.

  20. Controlled synthesis of bionic microstructure PbS crystals by mixed cationic/anionic surfactants

    Science.gov (United States)

    Li, Yanjie; Hu, Yongan; Zhang, Hui; Shen, Yuhua; Xie, Anjian

    2013-07-01

    Hexagonal starfish-like PbS crystals have been synthesized by the reaction of lead acetate and thioacetamide (TAA) controlled by mixture of cetyltrimethylammonium bromide/sodium dodecyl sulfate (STAB/SDS) at the molar ratio of 5: 1 through a hydrothermal process at 80°C. It has been found that the hexagonal starfish-like PbS single crystal is in cubic phase, and the six arms of the star extend along the six directions. By changing reaction conditions, such as the molar ratio of CTAB/SDS, temperature, and reaction time, the amounts of TAA and lead sources, the morphology and structure of the PbS crystals can be controlled. Furthermore, possible formation mechanism was preliminarily illustrated. The room-temperature photoluminescence spectra in solid state of the PbS single crystals obtained after different reaction times were investigated, which demonstrated that the PbS single crystals presented excellent optical properties. This work may open a novel route to the shaped-controllable synthesis of semiconductor crystals with various morphologies.

  1. Color chiral solitons

    CERN Document Server

    Novozhilov, V Yu; Novozhilov, Victor; Novozhilov, Yuri

    2002-01-01

    We discuss specific features of color chiral solitons (asymptotics, possibility of confainment, quantization) at example of isolated SU(2) color skyrmions, i.e. skyrmions in a background field which is the vacuum field forming the gluon condensate.

  2. Chiral brownian heat pump.

    Science.gov (United States)

    van den Broek, M; Van den Broeck, C

    2008-04-04

    We present the exact analysis of a chiral Brownian motor and heat pump. Optimization of the construction predicts, for a nanoscale device, frequencies of the order of kHz and cooling rates of the order of femtojoule per second.

  3. Chiral Brownian heat pump

    OpenAIRE

    Van Den Broek, Martijn; Van Den Broeck, Christian

    2007-01-01

    We present the exact analysis of a chiral Brownian motor and heat pump. Optimization of the construction predicts, for a nanoscale device, frequencies of the order of kHz and cooling rates of the order of femtojoule per second.

  4. Controlling flexural waves in semi-infinite platonic crystals

    CERN Document Server

    Haslinger, Stewart G; Movchan, Alexander B; Jones, Ian S; Craster, Richard V

    2016-01-01

    We address the problem of scattering and transmission of a plane flexural wave through a semi-infinite array of point scatterers/resonators, which take a variety of physically interesting forms. The mathematical model accounts for several classes of point defects, including mass-spring resonators attached to the top surface of the flexural plate and their limiting case of concentrated point masses. We also analyse the special case of resonators attached to opposite faces of the plate. The problem is reduced to a functional equation of the Wiener-Hopf type, whose kernel varies with the type of scatterer considered. A novel approach, which stems from the direct connection between the kernel function of the semi-infinite system and the quasi-periodic Green's functions for corresponding infinite systems, is used to identify special frequency regimes. We thereby demonstrate dynamically anisotropic wave effects in semi-infinite platonic crystals, with particular attention paid to designing systems to exhibit dynami...

  5. Incommensurate Chirality Density Wave Transition in a Hybrid Molecular Framework

    Science.gov (United States)

    Hill, Joshua A.; Christensen, Kirsten E.; Goodwin, Andrew L.

    2017-09-01

    Using single-crystal x-ray diffraction we characterize the 235 K incommensurate phase transition in the hybrid molecular framework tetraethylammonium silver(I) dicyanoargentate, [NEt4]Ag3(CN )4 . We demonstrate the transition to involve spontaneous resolution of chiral [NEt4]+ conformations, giving rise to a state in which molecular chirality is incommensurately modulated throughout the crystal lattice. We refer to this state as an incommensurate chirality density wave (XDW) phase, which represents a fundamentally new type of chiral symmetry breaking in the solid state. Drawing on parallels to the incommensurate ferroelectric transition of NaNO2 , we suggest the XDW state arises through coupling between acoustic (shear) and molecular rotoinversion modes. Such coupling is symmetry forbidden at the Brillouin zone center but symmetry allowed for small but finite modulation vectors q =[0 ,0 ,qz]* . The importance of long-wavelength chirality modulations in the physics of this hybrid framework may have implications for the generation of mesoscale chiral textures, as required for advanced photonic materials.

  6. Electrodynamics of chiral matter

    Science.gov (United States)

    Qiu, Zebin; Cao, Gaoqing; Huang, Xu-Guang

    2017-02-01

    Many-body systems with chiral fermions can exhibit novel transport phenomena that violate parity and time-reversal symmetries, such as the chiral magnetic effect, the anomalous Hall effect, and the anomalous generation of charge. Based on the Maxwell-Chern-Simons electrodynamics, we examine some electromagnetic and optical properties of such systems including the electrostatics, the magnetostatics, the propagation of electromagnetic waves, the novel optical effects, etc.

  7. Chiral Odd GPDs

    Directory of Open Access Journals (Sweden)

    Goldstein Gary R.

    2015-01-01

    Full Text Available Nucleon spin structure, transversity and the tensor charge are of central importance to understanding the role of QCD in hadronic physics. A new approach to measuring orbital angular momenta of quarks in the proton via twist 3 GPDs is shown. The “flexible parametrization” of chiral even GPDs is reviewed and its transformation into the chiral odd sector is discussed. The resulting parametrization is applied to recent data on π0 and η electroproduction.

  8. Resolution of the Chiral Drugs

    Institute of Scientific and Technical Information of China (English)

    DENG JinGen; ZHU Jin

    2001-01-01

    @@ Chiral drugs are generally not permitted to be used in racemic form so that unintended side effects and unnecessary environmental hazards are avoided. Moreover, homochiral molecules are required immediately to progress key toxicological and clinical studies in the drug discovery. One series of technologies which can rapidly supply homochiral compounds is the separation of racemates, and of those the technique of crystallization of diastereomers is extremely effective-principally because it is simple to operate and it affords both enantiomers. In classical resolution via diastereoisomeric salt formation, the resolved compounds are limited to a given racemic acid or base and the choice of a suitable resolving agent for a racemic target compound is achieved by time-consuming trial-and-error procedure.

  9. Resolution of the Chiral Drugs

    Institute of Scientific and Technical Information of China (English)

    DENG; JinGen

    2001-01-01

    Chiral drugs are generally not permitted to be used in racemic form so that unintended side effects and unnecessary environmental hazards are avoided. Moreover, homochiral molecules are required immediately to progress key toxicological and clinical studies in the drug discovery. One series of technologies which can rapidly supply homochiral compounds is the separation of racemates, and of those the technique of crystallization of diastereomers is extremely effective-principally because it is simple to operate and it affords both enantiomers. In classical resolution via diastereoisomeric salt formation, the resolved compounds are limited to a given racemic acid or base and the choice of a suitable resolving agent for a racemic target compound is achieved by time-consuming trial-and-error procedure.  ……

  10. Fano resonance control in a photonic crystal structure and its application to ultrafast switching

    DEFF Research Database (Denmark)

    Yu, Yi; Heuck, Mikkel; Hu, Hao;

    2014-01-01

    We experimentally demonstrate a photonic crystal structure that allows easy and robust control of the Fano spectrum. Its operation relies on controlling the amplitude of light propagating along one of the light paths in the structure from which the Fano resonance is obtained. Short-pulse dynamic...

  11. Symmetry Control of Polymer Colloidal Monolayers and Crystals by Electrophoretic Deposition on Patterned Surfaces

    NARCIS (Netherlands)

    Dziomkina, Nina V.; Hempenius, Mark A.; Vancso, G. Julius

    2005-01-01

    Colloidal crystals with body-centered cubic packing (see Figure) can be fabricated by electrophoretic deposition of charged latex particles onto patterned surfaces. Laser-interference lithography produces SiO2 layers patterned with controlled symmetry that can then be used to control the orientation

  12. Optimization of control parameters of CdZnTe ACRT-Bridgman single crystal growth

    Institute of Scientific and Technical Information of China (English)

    LIU Juncheng

    2004-01-01

    The CdZnTe vertical Bridgman single crystal process with accelerated crucible rotation technique (ACRT) has been simulated. Effects have been investigated of the ACRT wave parameters on the solid-liquid interface concavity and the solute segregation of the crystal. The results show that ACRT can result in the increase of both the solid-liquid interface concavity and the temperature gradient of the melt in the front of the solid-liquid interface, of which the magnitude varies from small to many times when the ACRT wave parameters change. Of the ACRT wave parameters, the increase of the crucible maximum rotation rate can hardly improve the radial solute segregation of the crystal, but the variation of the crucible acceleration time, the keep time at the maximum rotation rate, and the crucible deceleration time can affect the solute segregation of the single crystal extraordinarily. With suitable wave parameters, ACRT greatly decreases the radial solute segregation of the crystal, and even makes it disappear completely. However, it increases both the axial solute segregation and the radial one notably with bad wave parameters. An excellent single crystal could be gotten, of which a majority part is with no segregation, with ACRT-Bridgman method by adjusting both the ACRT wave parameters and the crystal growth control parameters, such as the initial temperature of the melt, the temperature gradient, and the crucible withdrawal rate, etc.

  13. Control of the wetting properties of ^{4}He crystals in superfluid.

    Science.gov (United States)

    Takahashi, T; Minezaki, H; Suzuki, A; Obara, K; Itaka, K; Nomura, R; Okuda, Y

    2016-05-01

    To investigate whether it is possible to control the wetting of ^{4}He crystals on a wall in superfluid, the contact angles of ^{4}He crystals were measured on rough and smooth walls at very low temperatures. A rough wall was prepared in a simple manner in which a commercially available coating agent for car mirrors, which makes the glass surface superhydrophobic, was used to coat a glass plate. The contact angles of ^{4}He crystals were increased by approximately 10^{∘} on the rough wall coated with the agent. Therefore, the increase in the repellency of ^{4}He crystals in superfluid was demonstrated to be possible on a very rough surface. The enhancement of the contact angles and a scanning electron microscopy image of the coated surface both suggest that a Cassie-Baxter state of ^{4}He crystals was realized on the surface; the crystals did not have full contact with the wall, but entrapped superfluid was present beneath the crystals in the hollow parts of the rough wall.

  14. Fabrication of size-controllable hexagonal non-close-packed colloidal crystals and binary colloidal crystals by pyrolysis combined with plasma-electron coirradiation of polystyrene colloidal monolayer.

    Science.gov (United States)

    Kim, Jae Joon; Li, Yue; Lee, Eun Je; Cho, Sung Oh

    2011-03-15

    We present an unprecedented and systematic route to controllably fabricate hexagonal non-close-packed (hncp) monolayer colloidal crystals and binary colloidal crystals (BCCs) based on plasma-electron coirradiation of polystyrene colloidal monolayers followed by thermal decomposition. Hncp colloidal crystals with tunable particle sizes and periods could be fabricated by changing the pristine colloidal particle size and the thermal decomposition time. In addition, BCCs and trimodal colloidal crystals that are composed of different-sized colloidal particles can also be fabricated by adding small particles on the prepared hncp colloidal crystals. Both the particle size ratio and the volume fraction of the BCCs can be widely tuned. These hncp colloidal crystals and BCCs have various potential applications as optical and photonic materials as well as in catalysis and sensors.

  15. Improvement of the chirality near avoided resonance crossing in optical microcavity

    Institute of Scientific and Technical Information of China (English)

    SONGQingHai[1,2; GUZhiYuan[1; ZHANGNan[1; WANGKaiYang[1; YINingBo[1; XIAOShuMin[1

    2015-01-01

    Chirality is one of the important phenomena at the vicinity of exceptional point (EP). The conventional understanding is that the chirality is determined by asymmetrical scattering efficiency (η), which reaches to zero only when the resonance ap- proaches EP. Here we study the possibility to enhance the chirality in open systems with a more robust mechanism. By com- bining chirality with avoided resonance crossing, we show that the chirality and 7 can be dramatically modified. Taking a spi- ral shaped annular cavity as an example, we show that the chirality of optical resonances can be significantly improved when two sets of chiral states approach each other, The imbalance between counterclockwise (CCW) components and clockwise (CW) components has been enhanced by more than an order of magnitude. Our research provides a new route to tailor and control the chirality in open systems.

  16. Controlling of magnetic vortex chirality and p olarity by spin-p olarized current%电流调控磁涡旋的极性和旋性∗

    Institute of Scientific and Technical Information of China (English)

    孙明娟; 刘要稳

    2015-01-01

    For a nanodisk, magnetic vortex characterized by a curling magnetization is an energetically stable state. The magnetization in the center of the magnetic vortex is directed upward or downward, namely, the vortex core polarity p=+1 or p=−1 refers to up or down, respectively. The curling direction of magnetization, namely, the vortex chirality, is either counter-clockwise or clockwise. Thus, different combinations of chirality and polarity in a vortex structure demonstrate four stable magnetic states, which can be used to design a multibit memory cell. Such a multibit memory application requires the independent controlling of both the vortex chirality and vortex polarity, which has received considerable attention recently. Switching the vortex polarity has been achieved by using either a magnetic field or a current. The vortex chirality can be controlled by introducing asymmetric geometry of nanodisks. In this article, by using micromagnetic simulations, we present an effective method to simultaneously control the vortex chirality and polarity in a spin valve structure, in which the fixed spin polarizer layer is magnetized in the film plane when the free layer has a magnetic vortex configuration. The free layer is designed into a ladder shape with the right part being thicker than the left part. Our simulations indicate that a combination of desirable vortex chirality and polarity can be easily controlled by a Gaussian current pulse with proper strength and pulse duration through the spin-transfer torque effect. The insight into physical mechanism of the controllable vortex is demonstrated by a series of snapshots. If the magnetic moment of the free layer is saturated in the direction of 0<θ<πduring the current pulse, whereθis the angle between the magnetization and +x axis, the vortex with the counter-clockwise chirality will be generated after the pulse. In contrast, if the free layer magnetization is saturated along the directionπ<θ<2π, after the pulse

  17. Chiral dynamics and peripheral transverse densities

    Energy Technology Data Exchange (ETDEWEB)

    Granados, Carlos G. [Uppsala University (Sweden); Weiss, Christian [JLAB, Newport News, VA (United States)

    2014-01-01

    In the partonic (or light-front) description of relativistic systems the electromagnetic form factors are expressed in terms of frame-independent charge and magnetization densities in transverse space. This formulation allows one to identify the chiral components of nucleon structure as the peripheral densities at transverse distances b = O(M{sub {pi}}{sup -1}) and compute them in a parametrically controlled manner. A dispersion relation connects the large-distance behavior of the transverse charge and magnetization densities to the spectral functions of the Dirac and Pauli form factors near the two--pion threshold at timelike t = 4 M{ sub {pi}}{sup 2}, which can be computed in relativistic chiral effective field theory. Using the leading-order approximation we (a) derive the asymptotic behavior (Yukawa tail) of the isovector transverse densities in the "chiral" region b = O(M{sub {pi}}{sup -1}) and the "molecular" region b = O(M{sub N}{sup 2}/M{sub {pi}}{sup 3}); (b) perform the heavy-baryon expansion of the transverse densities; (c) explain the relative magnitude of the peripheral charge and magnetization densities in a simple mechanical picture; (d) include Delta isobar intermediate states and study the peripheral transverse densities in the large-N{ sub c} limit of QCD; (e) quantify the region of transverse distances where the chiral components of the densities are numerically dominant; (f) calculate the chiral divergences of the b{sup 2}-weighted moments of the isovector transverse densities (charge and anomalous magnetic radii) in the limit M{sub {pi}} -> 0 and determine their spatial support. Our approach provides a concise formulation of the spatial structure of the nucleon's chiral component and offers new insights into basic properties of the chiral expansion. It relates the information extracted from low-t elastic form factors to the generalized parton distributions probed in peripheral high-energy scattering processes.

  18. Electromagnetic wave control of ceramic/resin photonic crystals with diamond structure

    Directory of Open Access Journals (Sweden)

    Soshu Kirihara, Mitsuo Takeda, Kazuaki Sakoda and Yoshinari Miyamoto

    2004-01-01

    Full Text Available Millimeter-order photonic crystals with the periodic arrangement of the dielectric constant were fabricated by infiltrating the mixed slurry of ceramics and polyester into the epoxy molds with an inverse form of a diamond structure. The epoxy molds are designed and processed by using a CAD/CAM process of stereolithography. The photonic crystals were prepared to have the diamond structure of the ceramic/polyester composite lattice, which is embedded in the epoxy matrix. The ceramic powders mixed with polyester are TiO2, SrTiO3, and BaTiO3 with high dielectric constant. It is possible to control more freely and widely the dielectric constant of the photonic crystals by this method. These ceramic/resin photonic crystals formed the complete photonic band gaps in the microwave band of 7–11 GHz, which can totally reflect the electromagnetic wave for all crystal directions. Attenuation profiles of the transmission amplitude in the band gaps were controlled with the dielectric constant of the composite lattice. The obtained results fairly agreed with the theoretical simulation of the electromagnetic wave propagation through photonic crystals.

  19. Controlling Interface States in 1D Photonic Crystals by tuning Bulk Geometric Phases

    CERN Document Server

    Gao, Wensheng; Chen, Baojie; Pun, Edwin Y B; Chan, C T; Tam, Wing Yim

    2016-01-01

    Interface states in photonic crystals usually require defects or surface/interface decorations. We show here that one can control interface states in 1D photonic crystals through the engineering of geometrical phase such that interface states can be guaranteed in even or odd, or in all photonic bandgaps. We verify experimentally the designed interface states in 1D multilayered photonic crystals fabricated by electron beam vapor deposition. We also obtain the geometrical phases by measuring the reflection phases at the bandgaps of the PCs and achieve good agreement with the theory. Our approach could provide a platform for the design of using interface states in photonic crystals for nonlinear optic, sensing, and lasing applications

  20. Chiral Random Matrix Theory and Chiral Perturbation Theory

    CERN Document Server

    Damgaard, P H

    2011-01-01

    Spontaneous breaking of chiral symmetry in QCD has traditionally been inferred indirectly through low-energy theorems and comparison with experiments. Thanks to the understanding of an unexpected connection between chiral Random Matrix Theory and chiral Perturbation Theory, the spontaneous breaking of chiral symmetry in QCD can now be shown unequivocally from first principles and lattice simulations. In these lectures I give an introduction to the subject, starting with an elementary discussion of spontaneous breaking of global symmetries.

  1. Chiral Random Matrix Theory and Chiral Perturbation Theory

    Energy Technology Data Exchange (ETDEWEB)

    Damgaard, Poul H, E-mail: phdamg@nbi.dk [Niels Bohr International Academy and Discovery Center, The Niels Bohr Institute, Blegdamsvej 17, DK-2100 Copenhagen (Denmark)

    2011-04-01

    Spontaneous breaking of chiral symmetry in QCD has traditionally been inferred indirectly through low-energy theorems and comparison with experiments. Thanks to the understanding of an unexpected connection between chiral Random Matrix Theory and chiral Perturbation Theory, the spontaneous breaking of chiral symmetry in QCD can now be shown unequivocally from first principles and lattice simulations. In these lectures I give an introduction to the subject, starting with an elementary discussion of spontaneous breaking of global symmetries.

  2. Chiral Graphene Quantum Dots.

    Science.gov (United States)

    Suzuki, Nozomu; Wang, Yichun; Elvati, Paolo; Qu, Zhi-Bei; Kim, Kyoungwon; Jiang, Shuang; Baumeister, Elizabeth; Lee, Jaewook; Yeom, Bongjun; Bahng, Joong Hwan; Lee, Jaebeom; Violi, Angela; Kotov, Nicholas A

    2016-02-23

    Chiral nanostructures from metals and semiconductors attract wide interest as components for polarization-enabled optoelectronic devices. Similarly to other fields of nanotechnology, graphene-based materials can greatly enrich physical and chemical phenomena associated with optical and electronic properties of chiral nanostructures and facilitate their applications in biology as well as other areas. Here, we report that covalent attachment of l/d-cysteine moieties to the edges of graphene quantum dots (GQDs) leads to their helical buckling due to chiral interactions at the "crowded" edges. Circular dichroism (CD) spectra of the GQDs revealed bands at ca. 210-220 and 250-265 nm that changed their signs for different chirality of the cysteine edge ligands. The high-energy chiroptical peaks at 210-220 nm correspond to the hybridized molecular orbitals involving the chiral center of amino acids and atoms of graphene edges. Diverse experimental and modeling data, including density functional theory calculations of CD spectra with probabilistic distribution of GQD isomers, indicate that the band at 250-265 nm originates from the three-dimensional twisting of the graphene sheet and can be attributed to the chiral excitonic transitions. The positive and negative low-energy CD bands correspond to the left and right helicity of GQDs, respectively. Exposure of liver HepG2 cells to L/D-GQDs reveals their general biocompatibility and a noticeable difference in the toxicity of the stereoisomers. Molecular dynamics simulations demonstrated that d-GQDs have a stronger tendency to accumulate within the cellular membrane than L-GQDs. Emergence of nanoscale chirality in GQDs decorated with biomolecules is expected to be a general stereochemical phenomenon for flexible sheets of nanomaterials.

  3. Chirality in distorted square planar Pd(O,N)2 compounds.

    Science.gov (United States)

    Brunner, Henri; Bodensteiner, Michael; Tsuno, Takashi

    2013-10-01

    Salicylidenimine palladium(II) complexes trans-Pd(O,N)2 adopt step and bowl arrangements. A stereochemical analysis subdivides 52 compounds into 41 step and 11 bowl types. Step complexes with chiral N-substituents and all the bowl complexes induce chiral distortions in the square planar system, resulting in Δ/Λ configuration of the Pd(O,N)2 unit. In complexes with enantiomerically pure N-substituents ligand chirality entails a specific square chirality and only one diastereomer assembles in the lattice. Dimeric Pd(O,N)2 complexes with bridging N-substituents in trans-arrangement are inherently chiral. For dimers different chirality patterns for the Pd(O,N)2 square are observed. The crystals contain racemates of enantiomers. In complex two independent molecules form a tight pair. The (RC) configuration of the ligand induces the same Δ chirality in the Pd(O,N)2 units of both molecules with varying square chirality due to the different crystallographic location of the independent molecules. In complexes and atrop isomerism induces specific configurations in the Pd(O,N)2 bowl systems. The square chirality is largest for complex [(Diop)Rh(PPh3 )Cl)], a catalyst for enantioselective hydrogenation. In the lattice of two diastereomers with the same (RC ,RC) configuration in the ligand Diop but opposite Δ and Λ square configurations co-crystallize, a rare phenomenon in stereochemistry.

  4. Conformational and Chiral Properties of Cyclic-tri(N-methyl-meta-benzamide) Bearing Amidino Groups.

    Science.gov (United States)

    Nishiyama, Shizuka; Urushibara, Ko; Masu, Hyuma; Azumaya, Isao; Kagechika, Hiroyuki; Tanatani, Aya

    2015-08-01

    Cyclic triamides bearing amidino groups at the meta position of the phenyl rings were synthesized, and their conformational properties in the crystal and in solution were examined. Compound exists as a capsule-type dimer of the enantiomers with a bowl-shaped syn conformation in the crystal state. Compound exists mainly in the syn form in solution, and chiral induction was observed upon addition of a chiral acid to a solution of.

  5. Molecular-level Design of Heterogeneous Chiral Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Gellman, Andrew John [Carnegie Mellon University; Sholl, David S. [Georgia Institute of Technology; Tysoe, Wilfred T. [University of Wisconsin - Milwaukee; Zaera, Francisco [University of California at Riverside

    2013-04-28

    Understanding and controlling selectivity is one of the key challenges in heterogeneous catalysis. Among problems in catalytic selectivity enantioselectivity is perhaps the most the most challenging. The primary goal of the project on “Molecular-level Design of Heterogeneous Chiral Catalysts” is to understand the origins of enantioselectivity on chiral heterogeneous surfaces and catalysts. The efforts of the project team include preparation of chiral surfaces, characterization of chiral surfaces, experimental detection of enantioselectivity on such surfaces and computational modeling of the interactions of chiral probe molecules with chiral surfaces. Over the course of the project period the team of PI’s has made some of the most detailed and insightful studies of enantioselective chemistry on chiral surfaces. This includes the measurement of fundamental interactions and reaction mechanisms of chiral molecules on chiral surfaces and leads all the way to rationale design and synthesis of chiral surfaces and materials for enantioselective surface chemistry. The PI’s have designed and prepared new materials for enantioselective adsorption and catalysis. Naturally Chiral Surfaces • Completion of a systematic study of the enantiospecific desorption kinetics of R-3-methylcyclohexanone (R-3-MCHO) on 9 achiral and 7 enantiomeric pairs of chiral Cu surfaces with orientations that span the stereographic triangle. • Discovery of super-enantioselective tartaric acid (TA) and aspartic acid (Asp) decomposition as a result of a surface explosion mechanism on Cu(643)R&S. Systematic study of super-enantiospecific TA and Asp decomposition on five enantiomeric pairs of chiral Cu surfaces. • Initial observation of the enantiospecific desorption of R- and S-propylene oxide (PO) from Cu(100) imprinted with {3,1,17} facets by L-lysine adsorption. Templated Chiral Surfaces • Initial observation of the enantiospecific desorption of R- and S-PO from Pt(111) and Pd(111

  6. Synthesis and Crystal Structure of a Novd Nickel (Ⅱ) Coordination Polymer with Chiral Schiff-base%新型手性希夫碱镍配位聚合物的合成及其晶体结构

    Institute of Scientific and Technical Information of China (English)

    班风俊; 盛恩宏; 龚腾飞; 叶诚诚

    2012-01-01

    A novel chiral nickel ( II ) coordination polymer with Schiff-base, Ni2(salen)2 { salen = (R,R)-( - )-N, N'-bis[3-tert-butyl-5-(4-ethynylpyridyl) salicyl-idene]-1,2-diaminocyclohexane} (1) , was synthesized. The structure was characterized by single-crystal X-ray crystallography and elemental analysis. The 1 belongs to monoclinic, space group C2 with a =25.060(5) A, b = 13.508 (3) A, c = ll.938(2) A, α=90(3)°, β = 104.82(3)°, γ =90(3)°, V = 3 906.7(14) A3, Z = 4, Mr = 828.24, Dc = 1.429 g · cm-3, F(000) = 1808, μ = 1. 027 mm-1, GOF = 1.068, R1=-0.051 0, wR2 =0.128 9. 1 is constructed by intermolecular π---Π interaction and assembled into a 2D structure via CH---Π interactions between the cyclohexanes and benzene rings.%以手性对称的Shiff碱为配体,合成了手性镍配合物[Ni2(salen)2(1)],其结构经X-单晶射线衍射和元素分析表征.1属单斜晶系,C2空间群,晶胞参数a =25.060(5)(A),b=13.508(3)(A),c= 11.938(2)(A),α=90(3)°,β=104.82(3)°,γ=90(3)°,V=3906.7(14)(A)3,Z=4,Mr=828.24,Dc=1.429 g·cm-3,F(000)=1808,μ=1.027mm-1,GOF=1.068,R1=0.051 0,wR2=0.1289.在1的分子结构中,环己胺和苯环之间通过分子间CH…π作用形成二维结构.

  7. Chiral anomalies and differential geometry

    Energy Technology Data Exchange (ETDEWEB)

    Zumino, B.

    1983-10-01

    Some properties of chiral anomalies are described from a geometric point of view. Topics include chiral anomalies and differential forms, transformation properties of the anomalies, identification and use of the anomalies, and normalization of the anomalies. 22 references. (WHK)

  8. Superconductivity in a chiral nanotube

    Science.gov (United States)

    Qin, F.; Shi, W.; Ideue, T.; Yoshida, M.; Zak, A.; Tenne, R.; Kikitsu, T.; Inoue, D.; Hashizume, D.; Iwasa, Y.

    2017-02-01

    Chirality of materials are known to affect optical, magnetic and electric properties, causing a variety of nontrivial phenomena such as circular dichiroism for chiral molecules, magnetic Skyrmions in chiral magnets and nonreciprocal carrier transport in chiral conductors. On the other hand, effect of chirality on superconducting transport has not been known. Here we report the nonreciprocity of superconductivity--unambiguous evidence of superconductivity reflecting chiral structure in which the forward and backward supercurrent flows are not equivalent because of inversion symmetry breaking. Such superconductivity is realized via ionic gating in individual chiral nanotubes of tungsten disulfide. The nonreciprocal signal is significantly enhanced in the superconducting state, being associated with unprecedented quantum Little-Parks oscillations originating from the interference of supercurrent along the circumference of the nanotube. The present results indicate that the nonreciprocity is a viable approach toward the superconductors with chiral or noncentrosymmetric structures.

  9. A Helical Polymer with a Cooperative Response to Chiral Information

    Science.gov (United States)

    Green, Mark M.; Peterson, Norman C.; Sato, Takahiro; Teramoto, Akio; Cook, Robert; Lifson, Shneior

    1995-06-01

    Polyisocyanates, long studied as theoretical models for wormlike chains in dilute solution and liquid crystals, differ from their biological helical analogs in the absence of a predetermined helical sense. These polymers have an unusual sensitivity to chiral effects that arises from a structure in which alternating right- and left-handed long helical blocks are separated by infrequent and mobile helical reversals. Statistical thermodynamic methods yield an exact description of the polymer and the cooperative nature of its chiral properties. Minute energies that favor one of the helical senses drive easily measurable conformational changes, even though such energies may be extremely difficult to calculate from structural theory. In addition, the chiral nature of the polymer can be used to test theoretical ideas concerned with cholesteric liquid crystals, one of which solves the problem of assigning the helical sense.

  10. Spontaneous Generation of Chirality in Simple Diaryl Ethers.

    Science.gov (United States)

    Lennartson, Anders; Hedström, Anna; Håkansson, Mikael

    2015-07-01

    We studied the spontaneous formation of chiral crystals of four diaryl ethers, 3-phenoxybenzaldehyde, 1; 1,3-dimethyl-2-phenoxybenzene, 2; di(4-aminophenyl) ether, 3; and di(p-tolyl) ether, 4. Compounds 1, 3, and 4 form conformationally chiral molecules in the solid state, while the chirality of 2 arises from the formation of supramolecular helices. Compound 1 is a liquid at ambient temperature, but 2-4 are crystalline, and solid-state CD-spectroscopy showed that they could be obtained as optically active bulk samples. It should be noted that the optical activity arise upon crystallization, and no optically active precursors were used. Indeed, even commercial samples of 3 and 4 were found to be optically active, giving evidence for the ease at which total spontaneous resolution may occur in certain systems.

  11. Nucleation Controlled Growth of Cadmium Oxalate Crystals in Agar Gel and Their Characterization

    Directory of Open Access Journals (Sweden)

    P. V. Dalal

    2013-01-01

    Full Text Available Perfect single crystals of cadmium oxalate have been grown using the slow and controlled reaction between cadmium acetate and oxalic acid in agar gel media at ambient temperature, resulting in the formation of insoluble product Cd(COO2. Different methods for growing crystals were adopted. The optimum conditions were employed in each method by varying the concentration of gel and reactants, gel setting time, and so forth. Prismatic, transparent single crystal about 20 times larger than the crystals obtained in various other methods at the interstitial by adding impurities in the gel was obtained. The grown crystals was characterized with the help of FT-IR studies and triclinic system of crystals were supported with lattice parameters a = 8.803 A0, b = 22.352 A0, c = 5.706 A0, α = 95.74 A0, β = 90.92 A0, γ = 117.01 A0, and V = 994.69 A03, calculated from X-ray diffractogram.

  12. Influence of controlling vibrations on heat transfer in floating zone crystal growth*

    Science.gov (United States)

    Fedyushkin, A. I.

    The crystal growth processes of monocrystals are strongly vibrational sensitive systems and in particular it concerns to a floating zone method as presence of a free surface and two fronts of crystallization and melting that aggravate it The given work is devoted to numerical investigations of the influence of controlling vibrations on heat transfer during crystal growth by floating zone technique Normal and weightless environment conditions are considered Mathematical simulation is performed on the numerical solutions of basis unsteady Navier-Stokes equations for incompressible fluid flows and energy equation 2D axisymmetric geometry was used in model Marangoni convection and radiation condition on the curvature free surface were taken in account The calculations of the shape of a free surface of a liquid zone and influences on it of a corner of wetting force of weight and size of factor of a superficial tension are carried out The simulations of convective heat transfer for real curvature free surface of a liquid zone with and without the taking into account of the following factors parameters of radiation rotations natural and Marangoni convection and vibrations are carried out The given calculations are carried out for semiconductors melts with Prandtl number Pr 1 and for oxides Pr 1 The influence of vibrations of a crystal on melt flow and on the wide of dynamic and thermal boundary layers at melt-crystal interface is studied The action of vibrations on an enhancement of heat fluxes at the melt crystal interface is shown

  13. Control of nucleation and growth in protein crystal growth

    Science.gov (United States)

    Rosenberger, Franz; Meehan, Edward J.

    1988-01-01

    The potential advantages of nucleation and growth control through temperature, rather than the addition of precipitants or removal of solvent, are discussed. A simple light scattering arrangement for the characterization of nucleation and growth conditions in solutions is described. The temperature dependence of the solubility of low ionic strength lysozyme solutions is applied in preliminary nucleation and growth experiments.

  14. Dynamic self-assembly and control of microfluidic particle crystals

    Science.gov (United States)

    Lee, Wonhee; Amini, Hamed; Stone, Howard A.; Di Carlo, Dino

    2010-01-01

    Engineered two-phase microfluidic systems have recently shown promise for computation, encryption, and biological processing. For many of these systems, complex control of dispersed-phase frequency and switching is enabled by nonlinearities associated with interfacial stresses. Introducing nonlinearity associated with fluid inertia has recently been identified as an easy to implement strategy to control two-phase (solid-liquid) microscale flows. By taking advantage of inertial effects we demonstrate controllable self-assembling particle systems, uncover dynamics suggesting a unique mechanism of dynamic self-assembly, and establish a framework for engineering microfluidic structures with the possibility of spatial frequency filtering. Focusing on the dynamics of the particle–particle interactions reveals a mechanism for the dynamic self-assembly process; inertial lift forces and a parabolic flow field act together to stabilize interparticle spacings that otherwise would diverge to infinity due to viscous disturbance flows. The interplay of the repulsive viscous interaction and inertial lift also allow us to design and implement microfluidic structures that irreversibly change interparticle spacing, similar to a low-pass filter. Although often not considered at the microscale, nonlinearity due to inertia can provide a platform for high-throughput passive control of particle positions in all directions, which will be useful for applications in flow cytometry, tissue engineering, and metamaterial synthesis. PMID:21149674

  15. Quarkyonic Chiral Spirals

    CERN Document Server

    Kojo, Toru; McLerran, Larry; Pisarski, Robert D

    2009-01-01

    We consider the formation of chiral density waves in Quarkyonic matter, which is a phase where cold, dense quarks experience confining forces. We model confinement following Gribov and Zwanziger, taking the gluon propagator, in Coulomb gauge and momentum space, as 1/(p^2)^2. We assume that the number of colors, N, is large, and that the quark chemical potential, mu, is much larger than renormalization mass scale, Lambda_QCD. To leading order in 1/N and Lambda_QCD, a gauge theory with Nf flavors of massless quarks in 3+1 dimensions naturally reduces to a gauge theory in 1+1 dimensions, with an enlarged flavor symmetry of SU(2Nf). Through an anomalous chiral rotation, in two dimensions a Fermi sea of massless quarks maps directly onto the corresponding theory in vacuum. A chiral condensate forms locally, and varies with the spatial position, z, as . Following Schon and Thies, we term this two dimensional pion condensate a (Quarkyonic) chiral spiral. Massive quarks also exhibit chiral spirals, with the magnitude...

  16. Conformational Chirality of the Biphenyl Groups Induced by the Aggregation of Poly{bis[4-(4'-(S)-2-methylbutoxy)- Biphenoxy] Phosphazene}

    Institute of Scientific and Technical Information of China (English)

    TANG Xianhui; LI Baozong; LI Yi; YANG Yonggang

    2016-01-01

    Poly{bis[4-(4'-(S)-2-methylbutoxy)biphenyloxy]phosphazene}(PP-C) was designed and successfully synthesized, and then characterized by means of FT-IR spectroscopy,1H- and31P-NMR, GPC spectroscopy, wide angle X-ray diffraction and differential scanning calorimetry. The results indicated that for PP-C, theMw is 2.18×105 and the PDI is 1.96. PP-C was a kind of crystallized polymer with a crystallizing point of -2.0℃ and a melting point of 28℃. The conformational chirality of the PP-C molecules was studied using circular dichroism spectrum. It was found that in dilute THF solution, the biphenyl groups in the PP-C molecules twisted randomly. However, when the PP-C formed aggregates, the biphenyl groups tended to twist single-handedly, which was controlled by the adjacent chiral alkoxy groups.

  17. Chiral patterning in Paenibacillus colonies under stress

    Science.gov (United States)

    Levine, Herbert

    2012-02-01

    One of the most striking examples of bacterial colony patterning occurs in the C-morphotype of Paenibacillus strains. Here, macroscopic chirality results from the interaction of local liquid-crystal ordering of the long bacterial cells with the self-propelled motility driven by the non-reflection-symmetric flagella. This talk will review some of the original experimental data from the Ben-Jacob lab as well as recent insight obtained via genomics. I will then discuss attempts to model and simulate the chiral patterns via solving reaction-diffusion equations on random lattices. At the end, I will introduce the challenges still to be faced in understanding transitions between these patterns and more common branching structures

  18. Chiral Synthons in Pesticide Syntheses

    NARCIS (Netherlands)

    Feringa, Bernard

    1988-01-01

    The use of chiral synthons in the preparation of enantiomerically pure pesticides is described in this chapter. Several routes to chiral synthons based on asymmetric synthesis or on natural products are illustrated. Important sources of chiral building blocks are reviewed. Furthermore the implicatio

  19. Chiral fermions on the lattice

    CERN Document Server

    Jahn, O; Jahn, Oliver; Pawlowski, Jan M.

    2002-01-01

    We discuss topological obstructions to putting chiral fermions on an even dimensional lattice. The setting includes Ginsparg-Wilson fermions, but is more general. We prove a theorem which relates the total chirality to the difference of generalised winding numbers of chiral projection operators. For an odd number of Weyl fermions this implies that particles and anti-particles live in topologically different spaces.

  20. Control of heat transfer in continuous-feeding Czochralski-silicon crystal growth with a water-cooled jacket

    Science.gov (United States)

    Zhao, Wenhan; Liu, Lijun

    2017-01-01

    The continuous-feeding Czochralski method is an effective method to reduce the cost of single crystal silicon. By promoting the crystal growth rate, the cost can be reduced further. However, more latent heat will be released at the melt-crystal interface under a high crystal growth rate. In this study, a water-cooled jacket was applied to enhance the heat transfer at the melt-crystal interface. Quasi-steady-state numerical calculation was employed to investigate the impact of the water-cooled jacket on the heat transfer at the melt-crystal interface. Latent heat released during the crystal growth process at the melt-crystal interface and absorbed during feedstock melting at the feeding zone was modeled in the simulations. The results show that, by using the water-cooled jacket, heat transfer in the growing crystal is enhanced significantly. Melt-crystal interface deflection and thermal stress increase simultaneously due to the increase of radial temperature at the melt-crystal interface. With a modified heat shield design, heat transfer at the melt-crystal interface is well controlled. The crystal growth rate can be increased by 20%.

  1. Implications of Chirality of Drugs and Excipients in Physical Pharmacy.

    Science.gov (United States)

    Duddu, Sarma P.

    1993-01-01

    The interactions of enantiomers of a chiral drug with other chemical entities, which may lead to changes and stereoselective differences in the physicochemical properties of the drug, were investigated. The various interactions described below employed ephedrine, pseudoephedrine and some of their salts, and to a minor extent, propranolol hydrochloride. The interaction of ephedrinium or pseudoephedrinium with the achiral anion, salicylate, yielded crystalline salts with the notable exception of homochiral ephedrine. Racemic ephedrinium salicylate exists as a centrosymmetric crystal (P2_1/n) whereas racemic pseudoephedrinium salicylate is a mixture of homochiral crystals (P2 _1). The inability of ephedrinium to exist as a homochiral salicylate salt is attributed to a high energy conformation of the ephedrinium cation, following conformational analysis. Arising from conformationally favorable interactions, the crystallization of racemic ephedrinium salicylate from aqueous solutions was utilized to improve the enantiomeric purity of a partially resolved mixture of ephedrine from 60% to 82% in one crystallization step. Interaction of the opposite enantiomers of ephedrine and pseudoephedrine in the solid, liquid, solution and vapor state produced the respective racemic compounds. The formation of racemic ephedrine in the solid state as predominantly second order (k = 392 mol^{-1} hr^{-1}), probably mediated by the vapor phase. The formation of racemic pseudoephedrine was predominantly diffusion-controlled in the solid state via an intermediate non-crystalline phase. The interaction with traces of the opposite enantiomer during crystallization of (RS)-(-)-ephedrinium 2-naphthalenesulfonate and (SS)-(+)-pseudoephedrinium salicylate changed pharmaceutically important solid state properties, including dissolution rate. Uptake of the enantiomeric impurity was measured by a new, sensitive HPLC method. The enantiomeric impurity, at mole fractions drug with other chemical

  2. Doped Chiral Polymer Metamaterials

    Science.gov (United States)

    Park, Cheol (Inventor); Kang, Jin Ho (Inventor); Gordon, Keith L. (Inventor); Sauti, Godfrey (Inventor); Lowther, Sharon E. (Inventor); Bryant, Robert G. (Inventor)

    2017-01-01

    Some implementations provide a composite material that includes a first material and a second material. In some implementations, the composite material is a metamaterial. The first material includes a chiral polymer (e.g., crystalline chiral helical polymer, poly-.gamma.-benzyl-L-glutamate (PBLG), poly-L-lactic acid (PLA), polypeptide, and/or polyacetylene). The second material is within the chiral polymer. The first material and the second material are configured to provide an effective index of refraction value for the composite material of 1 or less. In some implementations, the effective index of refraction value for the composite material is negative. In some implementations, the effective index of refraction value for the composite material of 1 or less is at least in a wavelength of one of at least a visible spectrum, an infrared spectrum, a microwave spectrum, and/or an ultraviolet spectrum.

  3. [Chirality and drugs].

    Science.gov (United States)

    Testa, B; Reist, M; Carrupt, P A

    2000-07-01

    The two enantiomers of a chiral drug may have vastly different pharmacodynamic and pharmacokinetic properties. As a result, the research and development of chiral drugs raises specific problems some of which are discussed here. Thus, various pharmacokinetic interactions may involve two enantiomers, as seen for example when one enantiomer inhibits the metabolism of the other and modifies its effects. A different situation occurs when a third compound stereoselectively inhibits the metabolism of one of the two enantiomers. Another problem examined here results from the lack of configurational stability of some chiral drugs, a little known phenomenon whose consequences can be of pharmacological or pharmaceutical significance depending on the rate of the reaction of racemization or epimerisation. In-depth investigations are needed before choosing between a eutomer or a racemate.

  4. Temperature influence on electrically controlled liquid crystal filled photonic bandgap fiber devices

    DEFF Research Database (Denmark)

    Wei, Lei; Alkeskjold, Thomas Tanggaard; Bjarklev, Anders Overgaard

    2009-01-01

    We experimentally investigate the temperature influence on electrically controlled liquid crystal filled photonic bandgap fiber device. The phase shift in the wavelength range 1520nm-1600nm for realizing quarter and half wave plates at different temperatures by applying a certain voltage...

  5. Nonlinear Control of Absorption in Graphene-based 1D Photonic Crystal

    CERN Document Server

    Vincenti, M A; Grande, M; D'Orazio, A; Scalora, M

    2013-01-01

    Perfect, narrow-band absorption is achieved in an asymmetric 1D photonic crystal with a monolayer graphene defect. Thanks to the large third order nonlinearity of graphene and field localization in the defect layer we demonstrate the possibility to achieve controllable, saturable absorption for the pump frequency.

  6. A cell for the controllable thermal treatment and electrochemical characterisation of single crystal alloy electrodes

    DEFF Research Database (Denmark)

    Bondarenko, Alexander S.; Stephens, Ifan E.L.; Chorkendorff, Ib

    2012-01-01

    A new electrochemical cell is described which provides the opportunity to perform electrochemical experiments and apply a controllable thermal treatment without exposing the sample to the laboratory atmosphere. We report typical model experiments with Pt(111) single crystal electrodes which can...

  7. Control of optically induced currents in semiconductor crystals

    Energy Technology Data Exchange (ETDEWEB)

    Kohli, Kapil Kumar

    2010-06-01

    The generation and control of optically induced currents has the potential to become an important building block for optical computers. Here, shift and rectification currents are investigated that emerge from a divergence of the optical susceptibility. It is known that these currents react to the shape of the impinging laser pulse, and especially to the shape of the pulse envelope. The main goal is the systematic manipulation of the pulse envelope with an optical pulse shaper that is integrated into a standard THz emission setup. The initial approach, the chirping of the laser pulse only has a weak influence on the envelope and the currents. Instead, a second approach is suggested that uses the combined envelope of a phase-stable pulse-pair as a parameter. In a laser pulse, the position of the maxima of the electrical field and the pulse envelope are shifted relative to each other. This shift is known as the Carrier-Envelope Phase (CEP). It is a new degree of freedom that is usually only accessible in specially stabilized systems. It is shown, that in a phase-stable pulse-pair, at least the relative CEP is usable as a new degree of freedom. It has a great influence on the shape of the pulse envelope and thus on the current density. It is shown that this approach enables the coherent control of the current density. The experiments are corroborated by a theoretical model of the system. The potential of this approach is demonstrated in an application. A framework is presented that uses an iterative genetic algorithm to create arbitrarily shaped THz traces. The algorithm controls the optical pulse shaper, and varies the phase of the impinging laser pulses until the desired target trace is found. (orig.)

  8. Syntheses and molecular self-assembly of chiral phosphorami dates

    Institute of Scientific and Technical Information of China (English)

    DU, Da-Ming; HUA, Wen-Ting; WANG, Jian-Wu

    2000-01-01

    Two chiral phosphoramidates, ( R )-( - )-1, 1′-binaphthyl-2, 2′-dihydroxy-N-[ α-( S)-methylbenzyl] phosphoramidate and (-)-l,1′-biphenyl-2,2′-dihydroxy-N-[ α-( S)-methylbenzyl]- phosphoramidate were synthesized. Their crystal structures were determined by X-ray single crystal diffraction analysis. The phoshorramidate molecules are self-associated by inter molecular N-H…… O = P hydrogen bonds and aromatic edge to face interactions.

  9. Chiral quark model

    Indian Academy of Sciences (India)

    H Weigel

    2003-11-01

    In this talk I review studies of hadron properties in bosonized chiral quark models for the quark flavor dynamics. Mesons are constructed from Bethe–Salpeter equations and baryons emerge as chiral solitons. Such models require regularization and I show that the two-fold Pauli–Villars regularization scheme not only fully regularizes the effective action but also leads the scaling laws for structure functions. For the nucleon structure functions the present approach serves to determine the regularization prescription for structure functions whose leading moments are not given by matrix elements of local operators. Some numerical results are presented for the spin structure functions.

  10. Preparation of Ultrafine TATB and the Technology for Crystal Morphology Control%Preparation of Ultrafine TATB and the Technology for Crystal Morphology Control

    Institute of Scientific and Technical Information of China (English)

    Yang, Li; Ren, Xiaoting; Li, Tiecheng; Wang, Shiwei; Zhang, Tonglai

    2012-01-01

    The ultrafine 1,3,5-triamino-2,4,6-trinitrobenzene (TATB) has been prepared by using solvent and non-solvent method, and the influencing factors in close relationship with the grain size and crystal morphology control such as categories and dosage of surfactants, volume ratio of solvent to non-solvent have also been considered in this paper. It showed that these factors had remarkable effect on the crystal morphology, particle size and agglomeration during the crystallization process. By using 0.095% (mass percentage) ionic surfactant (S) as the additive and using spray-drops feeding device as the dropping equipment, 1.06 g TATB raw materials have been refined into free-running ellipsoid and spherical TATB grains with the grain size from 30 to 50 nm. By using 0.014% (mass percentage) non-ionic surfactant (P) as the additive, spherical TATB grains with the particle diameter of 50 nm and with narrow particle-size distribution have also been obtained. It was shown by the characterizations that the ultrafine particle of TATB had better heat resisting evenness and its 5 seconds ignition point is advanced by 7.5 K.

  11. Novel Design Integrating a Microwave Applicator into a Crystallizer for Rapid Temperature Cycling. A Direct Nucleation Control Study

    Science.gov (United States)

    2017-01-01

    The control of nucleation in crystallization processes is a challenging task due to the often lacking knowledge on the process kinetics. Inflexible (predetermined) control strategies fail to grow the nucleated crystals to the desired quality because of the variability in the process conditions, disturbances, and the stochastic nature of crystal nucleation. Previously, the concept of microwave assisted direct nucleation control (DNC) was demonstrated in a laboratory setup to control the crystal size distribution in a batch crystallization process by manipulating the number of particles in the system. Rapid temperature cycling was used to manipulate the super(under)saturation and hence the number of crystals. The rapid heating response achieved with the microwave heating improved the DNC control efficiency, resulting in halving of the batch time. As an extension, this work presents a novel design in which the microwave applicator is integrated in the crystallizer, hence avoiding the external loop though the microwaves oven. DNC implemented in the 4 L unseeded crystallizer, at various count set points, resulted in strong efficiency enhancement of DNC, when compared to the performance with a slow responding system. The demonstrated crystallizer design is a basis for extending the enhanced process control opportunity to other applications. PMID:28729813

  12. Density of states controls Anderson localization in disordered photonic crystal waveguides

    DEFF Research Database (Denmark)

    Garcia-Fernández, David; Smolka, Stephan; Stobbe, Søren

    2010-01-01

    -of-plane losses are non-negligible, ℓe can be approximated to be the localization length ξ. The extinction mean-free path shows a fivefold variation between the low- and the high-DOS regime, and it becomes shorter than the sample length thus giving rise to strongly confined modes. The dispersive behavior of ℓe......We prove Anderson localization in a disordered photonic crystal waveguide by measuring the ensemble-averaged extinction mean-free path, ℓe, which is controlled by the dispersion in the photon density of states (DOS) of the photonic crystal waveguide. Except for the very low DOS case, where out...

  13. Controlling factors for the brittle-to-ductile transition in tungsten single crystals

    Science.gov (United States)

    Gumbsch; Riedle; Hartmaier; Fischmeister

    1998-11-13

    Materials performance in structural applications is often restricted by a transition from ductile response to brittle fracture with decreasing temperature. This transition is currently viewed as being controlled either by dislocation mobility or by the nucleation of dislocations. Fracture experiments on tungsten single crystals reported here provide evidence for the importance of dislocation nucleation for the fracture toughness in the semibrittle regime. However, it is shown that the transition itself, in general, is controlled by dislocation mobility rather than by nucleation.

  14. Electromagnetic induction heating for single crystal graphene growth: morphology control by rapid heating and quenching.

    Science.gov (United States)

    Wu, Chaoxing; Li, Fushan; Chen, Wei; Veeramalai, Chandrasekar Perumal; Ooi, Poh Choon; Guo, Tailiang

    2015-03-12

    The direct observation of single crystal graphene growth and its shape evolution is of fundamental importance to the understanding of graphene growth physicochemical mechanisms and the achievement of wafer-scale single crystalline graphene. Here we demonstrate the controlled formation of single crystal graphene with varying shapes, and directly observe the shape evolution of single crystal graphene by developing a localized-heating and rapid-quenching chemical vapor deposition (CVD) system based on electromagnetic induction heating. Importantly, rational control of circular, hexagonal, and dendritic single crystalline graphene domains can be readily obtained for the first time by changing the growth condition. Systematic studies suggest that the graphene nucleation only occurs during the initial stage, while the domain density is independent of the growth temperatures due to the surface-limiting effect. In addition, the direct observation of graphene domain shape evolution is employed for the identification of competing growth mechanisms including diffusion-limited, attachment-limited, and detachment-limited processes. Our study not only provides a novel method for morphology-controlled graphene synthesis, but also offers fundamental insights into the kinetics of single crystal graphene growth.

  15. A numerical model including PID control of a multizone crystal growth furnace

    Science.gov (United States)

    Panzarella, Charles H.; Kassemi, Mohammad

    This paper presents a 2D axisymmetric combined conduction and radiation model of a multizone crystal growth furnace. The model is based on a programmable multizone furnace (PMZF) designed and built at NASA Lewis Research Center for growing high quality semiconductor crystals. A novel feature of this model is a control algorithm which automatically adjusts the power in any number of independently controlled heaters to establish the desired crystal temperatures in the furnace model. The control algorithm eliminates the need for numerous trial and error runs previously required to obtain the same results. The finite element code, FIDAP, used to develop the furnace model, was modified to directly incorporate the control algorithm. This algorithm, which presently uses PID control, and the associated heat transfer model are briefly discussed. Together, they have been used to predict the heater power distributions for a variety of furnace configurations and desired temperature profiles. Examples are included to demonstrate the effectiveness of the PID controlled model in establishing isothermal, Bridgman, and other complicated temperature profies in the sample. Finally, an example is given to show how the algorithm can be used to change the desired profile with time according to a prescribed temperature-time evolution.

  16. Nucleation of protein crystals: critical nuclei, phase behavior, and control pathways

    Science.gov (United States)

    Galkin, Oleg; Vekilov, Peter G.

    2001-11-01

    We have studied the nucleation of crystals of the model protein lysozyme using a novel technique that allows direct determinations of homogeneous nucleation rates. At constant temperature of 12.6°C we varied the thermodynamic supersaturation by changing the concentrations of protein and precipitant. We found a broken dependence of the homogeneous nucleation rate on supersaturation that is beyond the predictions of the classical nucleation theory. The nucleation theorem allows us to relate this to discrete changes of the size of the crystal nuclei with increasing supersaturation as (10 or 11)→(4 or 5)→(1 or 2). Furthermore, we observe that the existence of a second liquid phase at high protein concentrations strongly affects crystal nucleation kinetics. We show that the rate of homogeneous nucleation of lysozyme crystals passes through a maximum in the vicinity of the liquid-liquid phase boundary hidden below the liquidus (solubility) line in the phase diagram of the protein solution. We found that glycerol and polyethylene glycol (PEG), which do not specifically bind to proteins, shift this phase boundary and significantly suppress or enhance the crystal nucleation rates, although no simple correlation exists between the action of PEG on the phase diagram and the nucleation kinetics. This provides for a control mechanism which does not require changes in the protein concentration, or the acidity and ionicity of the solution. The effects of the two additives on the phase diagram strongly depend on their concentration and this provides opportunities for further tuning of nucleation rates.

  17. Development of simultaneous control of polymorphism and morphology in indomethacin crystallization

    Science.gov (United States)

    Wada, Shuichi; Kudo, Shoji; Takiyama, Hiroshi

    2016-02-01

    In order to improve the bioavailability, it is desired to obtain the polymorph which has the higher solubility of indomethacin (IMC α-form). However, when α-form crystals were obtained by conventional anti-solvent crystallization, the stirring operation could not be continued because cotton agglomerates were formed in the solution. In order to simultaneously satisfy the bioavailability of IMC and the operability of IMC production, the modification of the morphology (external shape) of α-form agglomerates is important. So, the purpose of this present study is the development of the crystallization method. In order to modify the cotton agglomerates, the anti-solvent crystallization was carried out by using electrolyte aqueous solution (NaCl aq. solution) as the anti-solvent. By using the electrolyte aqueous solution, the liquid-liquid phase separation (LLPS) was observed depending on the solution composition. From the experimental results, under the condition both of high electrolyte concentration and of high stirring speed, dispersion of droplets was obtained, and spherical agglomerates of α-form were formed in the slurry. The stirring operation could be continued in the slurry because the modification of α-form cotton agglomerates was achieved. So, the simultaneous control method of the polymorphism and the morphology in IMC crystallization was realized.

  18. Study of Fluid Flow Control in Protein Crystallization using Strong Magnetic Fields

    Science.gov (United States)

    Ramachandran, Narayanan; Leslie, Fred; Ciszak, Ewa

    2002-11-01

    An important component in biotechnology, particularly in the area of protein engineering and rational drug design is the knowledge of the precise three-dimensional molecular structure of proteins. The quality of structural information obtained from X-ray diffraction methods is directly dependent on the degree of perfection of the protein crystals. As a consequence, the growth of high quality macromolecular crystals for diffraction analyses has been the central focus for biochemists, biologists, and bioengineers. Macromolecular crystals are obtained from solutions that contain the crystallizing species in equilibrium with higher aggregates, ions, precipitants, other possible phases of the protein, foreign particles, the walls of the container, and a likely host of other impurities. By changing transport modes in general, i.e., reduction of convection and sedimentation, as is achieved in "microgravity", researchers have been able to dramatically affect the movement and distribution of macromolecules in the fluid, and thus their transport, formation of crystal nuclei, and adsorption to the crystal surface. While a limited number of high quality crystals from space flights have been obtained, as the recent National Research Council (NRC) review of the NASA microgravity crystallization program pointed out, the scientific approach and research in crystallization of proteins has been mainly empirical yielding inconclusive results. We postulate that we can reduce convection in ground-based experiments and we can understand the different aspects of convection control through the use of strong magnetic fields and field gradients. Whether this limited convection in a magnetic field will provide the environment for the growth of high quality crystals is still a matter of conjecture that our research will address. The approach exploits the variation of fluid magnetic susceptibility with concentration for this purpose and the convective damping is realized by appropriately

  19. A novel laser-based method for controlled crystallization in dental prosthesis materials

    Science.gov (United States)

    Cam, Peter; Neuenschwander, Beat; Schwaller, Patrick; Köhli, Benjamin; Lüscher, Beat; Senn, Florian; Kounga, Alain; Appert, Christoph

    2015-02-01

    Glass-ceramic materials are increasingly becoming the material of choice in the field of dental prosthetics, as they can feature both high strength and very good aesthetics. It is believed that their color, microstructure and mechanical properties can be tuned such as to achieve an optimal lifelike performance. In order to reach that ultimate perfection a controlled arrangement of amorphous and crystalline phases in the material is required. A phase transformation from amorphous to crystalline is achieved by a heat treatment at defined temperature levels. The traditional approach is to perform the heat treatment in a furnace. This, however, only allows a homogeneous degree of crystallization over the whole volume of the parent glass material. Here a novel approach using a local heat treatment by laser irradiation is presented. To investigate the potential of this approach the crystallization process of SiO2-Li2O-Al2O3-based glass has been studied with laser systems (pulsed and continuous wave) operating at different wavelengths. Our results show the feasibility of gradual and partial crystallization of the base material using continuous laser irradiation. A dental prosthesis machined from an amorphous glassy state can be effectively treated with laser irradiation and crystallized within a confined region of a few millimeters starting from the body surface. Very good aesthetics have been achieved. Preliminary investigation with pulsed nanosecond lasers of a few hundreds nanoseconds pulse width has enabled more refinement of crystallization and possibility to place start of phase change within the material bulk.

  20. The development of chiral nematic mesoporous materials.

    Science.gov (United States)

    Kelly, Joel A; Giese, Michael; Shopsowitz, Kevin E; Hamad, Wadood Y; MacLachlan, Mark J

    2014-04-15

    Cellulose nanocrystals (CNCs) are obtained from the sulfuric acid-catalyzed hydrolysis of bulk cellulose. The nanocrystals have diameters of ~5-15 nm and lengths of ~100-300 nm (depending on the cellulose source and hydrolysis conditions). This lightweight material has mostly been investigated to reinforce composites and polymers because it has remarkable strength that rivals carbon nanotubes. But CNCs have an additional, less explored property: they organize into a chiral nematic (historically referred to as cholesteric) liquid crystal in water. When dried into a thin solid film, the CNCs retain the helicoidal chiral nematic order and assemble into a layered structure where the CNCs have aligned orientation within each layer, and their orientation rotates through the stack with a characteristic pitch (repeating distance). The cholesteric ordering can act as a 1-D photonic structure, selectively reflecting circularly polarized light that has a wavelength nearly matching the pitch. During CNC self-assembly, it is possible to add sol-gel precursors, such as Si(OMe)4, that undergo hydrolysis and condensation as the solvent evaporates, leading to a chiral nematic silica/CNC composite material. Calcination of the material in air destroys the cellulose template, leaving a high surface area mesoporous silica film that has pore diameters of ~3-10 nm. Importantly, the silica is brilliantly iridescent because the pores in its interior replicate the chiral nematic structure. These films may be useful as optical filters, reflectors, and membranes. In this Account, we describe our recent research into mesoporous films with chiral nematic order. Taking advantage of the chiral nematic order and nanoscale of the CNC templates, new functional materials can be prepared. For example, heating the silica/CNC composites under an inert atmosphere followed by removal of the silica leaves highly ordered, mesoporous carbon films that can be used as supercapacitor electrodes. The composition

  1. Chirality Relay in 2,2'-Substituted 1,1'-Binaphthyl: Access to Propeller Chirality of the Tricoordinate Boron Center.

    Science.gov (United States)

    Wang, Chen; Sun, Zuo-Bang; Xu, Qing-Wen; Zhao, Cui-Hua

    2016-11-14

    It is a challenging issue to achieve propeller chirality for triarylboranes owing to the low transition barrier between the P and M forms of the boron center. Herein, we report a new strategy to achieve propeller chirality of triarylboranes. It was found that the chirality relay from axially chiral 1,1'-binaphthyl to propeller chirality of the trivalent boron center can be realized when a Me2 N and a Mes2 B group (Mes=mesityl) are introduced at the 2,2'-positions of the 1,1'-binaphthyl skeleton (BN-BNaph) owing to the strong π-π interaction between the Me2 N-bonded naphthyl ring and the phenyl ring of one adjacent Mes group, which not only exerts great steric hindrance on the rotation of the two Mes groups but also gives unequal stability to the two configurations of the boron center for a given configuration of the binaphthyl moiety. The stereostructures of the boron center were fully characterized through (1) H NMR spectroscopy, X-ray crystal analyses, and theoretical calculations. Detailed comparisons with the analog BN-Ph-BNaph, in which the Mes2 B group is separated from 1,1'-binaphthyl by a para-phenylene spacer, confirmed the essential role of π-π interaction for the successful chirality relay in BN-BNaph.

  2. Interweaving Chiral Spirals

    CERN Document Server

    Kojo, Toru; Fukushima, Kenji; McLerran, Larry; Pisarski, Robert D

    2011-01-01

    We elaborate how to construct the interweaving chiral spirals in (2+1) dimensions, that is defined as a superposition of differently oriented chiral spirals. We divide the two-dimensional Fermi sea into distinct wedges characterized by the opening angle 2 Theta and the depth Q \\simeq pF, where pF is the Fermi momentum. Each wedge earns an energy gain by forming a single chiral spiral. The optimal values for Theta and Q are chosen by the balance between this energy gain and the energy costs from the deformed Fermi surface (dominant at large Theta) and patch-patch interactions (dominant at small Theta). We estimate these energy gains and costs by means of the expansions in terms of 1/Nc, Lambda_QCD/Q, and Theta using a non-local four-Fermi interaction model: At small 1/Nc the mass gap (chiral condensate) is large enough and the interaction among quarks and the condensate is local in momentum space thanks to the form factor in our non-local model. The fact that patch-patch interactions lie only near the patch bo...

  3. Simplicial chiral models

    CERN Document Server

    Rossi, P; Rossi, Paolo; Tan, Chung I

    1995-01-01

    Principal chiral models on a d-1 dimensional simplex are introduced and studied analytically in the large N limit. The d = 0 , 2, 4 and \\infty models are explicitly solved. Relationship with standard lattice models and with few-matrix systems in the double scaling limit are discussed.

  4. Controlling the morphology of TiO{sub 2} nano crystals with different capping agents

    Energy Technology Data Exchange (ETDEWEB)

    Calatayud, D. G.; Rodriguez, M.; Jardiel, T.

    2015-10-01

    This paper provides direct evidence to support the role of capping agents in controlling the evolution of TiO{sub 2} seeds into nano crystals with a specific shape. Starting with Ti(OBut){sub 4} and using oleid acid, oleylamine, dioleamide, 11-aminoundecanoic acid, arginine, trifluroacetic acid or HF as capping agents, mainly TiO{sub 2} truncated octahedrons enclosed by {1 0 1} and {0 0 1} facets were obtained. We could also selectively obtain square, rods and rounded rhombic-shaped nanoparticles by growing of {0 1 0} facets by adding oleic acid and oleylamine in ratio 6:4, respectively, while all other parameters were kept the same. This research not only offers new insights into the role played by a capping agent in shape-controlled synthesis but also provides, a versatile approach to controlling the shape of metal oxide nano crystals. (Author)

  5. Chiral magnetic effect without chirality source in asymmetric Weyl semimetals

    CERN Document Server

    Kharzeev, Dmitri; Meyer, Rene

    2016-01-01

    We describe a new type of the Chiral Magnetic Effect (CME) that should occur in Weyl semimetals with an asymmetry in the dispersion relations of the left- and right-handed chiral Weyl fermions. In such materials, time-dependent pumping of electrons from a non-chiral external source generates a non-vanishing chiral chemical potential. This is due to the different capacities of the left- and right-handed (LH and RH) chiral Weyl cones arising from the difference in the density of states in the LH and RH cones. The chiral chemical potential then generates, via the chiral anomaly, a current along the direction of an applied magnetic field even in the absence of an external electric field. The source of chirality imbalance in this new setup is thus due to the band structure of the system and the presence of (non-chiral) electron source, and not due to the parallel electric and magnetic fields. We illustrate the effect by an argument based on the effective field theory, and by the chiral kinetic theory calculation f...

  6. Shape-Evolution Control of hybrid perovskite CH3NH3PbI3 crystals via solvothermal synthesis

    Science.gov (United States)

    Zhang, Baohua; Guo, Fuqiang; Yang, Lianhong; Jia, Xiuling; Liu, Bin; Xie, Zili; Chen, Dunjun; Lu, Hai; Zhang, Rong; Zheng, Youdou

    2017-02-01

    We systematically synthesized CH3NH3PbI3 crystals using solvothermal process, and the reaction conditions such as concentration of the precursor, temperature, time, and lead source have been comprehensively investigated to obtain shape-controlled CH3NH3PbI3 crystals. The results showed that the CH3NH3PbI3 crystals exhibit tetragonal phase and the crystals change from nanoparticles to hopper-faced cuboids. Photoluminescence spectra of the crystals obtained with different lead sources show a blue shift due to the presence of defects in the crystals, and the peak intensity is very sensitive to the lead sources. Moreover, impurities (undesirable byproducts and excess components like HI or CH3NH2) presented during crystal growth can result in hopper growth.

  7. Structure and Magnetic Property Control of Copper Hydroxide Acetate by Non-Classical Crystallization.

    Science.gov (United States)

    Song, RuiQi; Krasia-Christoforou, Theodora; Debus, Christian; Cölfen, Helmut

    2017-03-01

    Copper hydroxide acetate (CHA), one layered hydroxide compound with tunable magnetism, attracts great interest because of its potential applications in memory devices. However, ferromagnetism for CHA is only demonstrated by means of GPa pressure. Herein, a new method is reported, involving the combination of different crystallization pathways to control crystallization of amorphous CHA toward the formation of CHA/polymer composites with tunable magnetic properties and even a tunability that can be tested at room temperature. By using poly[(ethylene glycol)6 methyl ether methacrylate]-block-poly[2-(acetoacetoxy) ethyl methacrylate] (PEGMA-b-PAEMA) diblock copolymers as additives in combination with a post-treatment process by ultracentrifugation, it is demonstrated that CHA and PEGMA-b-PAEMA form composites exhibiting different magnetic properties, depending on CHA in-plane nanostructures. Analytical characterization reveals that crystallization of CHA is induced by ultracentrifugation, during which CHA nanostructures can be well controlled by changing the degrees of polymerization of the PEGMA and PAEMA blocks and their block length ratios. These findings not only present the first example of using crystallization from polymer stabilized amorphous precursors toward the generation of magnetic nanomaterials with tunable magnetism but also pave the way for the future design of functional composite materials.

  8. Novel approach to protein crystallizations: Control of the phase behavior of aqueous solutions using microfluidics

    Science.gov (United States)

    Shim, Jung Uk

    A microfluidic device denoted the Phase Chip has been developed to exploit the permeation of water through poly(dimethylsiloxane) (PDMS) in order to vary the concentration of aqueous nanoliter volume microdrops stored in wells. The permeation of water in the Phase Chip is modeled using the diffusion equation and good agreement between experiment and theory is obtained. The phase diagram of a polymer/salt mixture is measured employing the Phase Chip and agrees well with the phase diagram obtained off-chip. The Phase Chip first creates drops of the polymer/salt mixture whose composition varies sequentially. Subsequently the drops are docked in storage wells and the concentration of each stored drop is controlled by varying the water activity of a reservoir that is separated from the drops by a thin layer of PDMS through which water, but not the solutes, permeates. The Phase Chip, incorporating a dialysis membrane on-chip, presents several advantages for protein crystallizations. First, protein crystallization is a non-equilibrium process so it makes sense to have dynamic control over the key thermodynamic variable; concentration. The Phase Chip, with its ability to reversibly control protein and precipitant concentrations, renders varying concentration as convenient as varying temperature. Second, by varying the water content of each drop we can explore many different crystallization conditions in the same drop. Finally, we have demonstrated that we can first formulate stable protein solutions, next induce nucleation and then grow large protein crystals. For these reasons, the Phase Chip promises to be a faster, better, and cheaper method for protein crystallization.

  9. A Simple and Novel Route for The Preparation of Chiral Sodium Zincophosphate

    Institute of Scientific and Technical Information of China (English)

    LIAO Sen; WU Wen-Wei; SUN Ya-Bo; SONG Bao-Ling

    2008-01-01

    A simple and novel route for the preparation of chiral sodium zincophosphate (NaZnPO4·H2O) (CZP) was studied, and the target product was obtained with Na3PO4·12H2O and ZnSO4·7H2O as raw materials and polyethylene glycol-400 (PEG-400) as a surfactant via one step low heat solid state reaction.The product was characterized with TG/DTG, XRD, TEM and SEM.The experimental results showed that the NaZnPO4·H2O, which was all obtained from different P/Zn atomic ratios (0.9-1.15) of Na3PO4·12H2O to ZnSO4·7H2O and different ageing time (2.0-8.0 h) at 60 ℃, had the same chiral crystal structures except slight difference in their crystallinity.The comparison experimental results suggest that the ageing temperature and anion control the enantiomorphism of NaZnPO4·H2O,that is, if ZnSO4·7H2O or Zn(NO3)2·6H2O were used as Zn source, the first chiral structure of space group P6122 was formed when the reaction mixture was aged at 60℃,and the second chiral structure of space group P6522 was got when the reaction mixture was aged at room temperature.

  10. Detecting the chirality for coupled quantum dots

    Energy Technology Data Exchange (ETDEWEB)

    Cao Huijuan [Institute for Condensed Matter Physics, School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510631 (China); Hu Lian [Institute for Condensed Matter Physics, School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510631 (China)], E-mail: huliancaohj@yahoo.com

    2008-04-21

    We propose a scheme to detect the chirality for a system consisting of three coupled quantum dots. The chirality is found to be determined by the frequency of the transition between chiral states under the chiral symmetry broken perturbation. The results are important to construct quantum gates and to demonstrate chiral entangle states in the triangle spin dots.

  11. Chlorophylls, Symmetry, Chirality, and Photosynthesis

    Directory of Open Access Journals (Sweden)

    Mathias O. Senge

    2014-09-01

    Full Text Available Chlorophylls are a fundamental class of tetrapyrroles and function as the central reaction center, accessory and photoprotective pigments in photosynthesis. Their unique individual photochemical properties are a consequence of the tetrapyrrole macrocycle, the structural chemistry and coordination behavior of the phytochlorin system, and specific substituent pattern. They achieve their full potential in solar energy conversion by working in concert in highly complex, supramolecular structures such as the reaction centers and light-harvesting complexes of photobiology. The biochemical function of these structures depends on the controlled interplay of structural and functional principles of the apoprotein and pigment cofactors. Chlorophylls and bacteriochlorophylls are optically active molecules with several chiral centers, which are necessary for their natural biological function and the assembly of their supramolecular complexes. However, in many cases the exact role of chromophore stereochemistry in the biological context is unknown. This review gives an overview of chlorophyll research in terms of basic function, biosynthesis and their functional and structural role in photosynthesis. It highlights aspects of chirality and symmetry of chlorophylls to elicit further interest in their role in nature.

  12. Asymmetric aza-[2,3]-Wittig sigmatropic rearrangements: chiral auxiliary control and formal asymmetric synthesis of (2S, 3R, 4R)-4-hydroxy-3-methylproline and (-)-kainic acid.

    Science.gov (United States)

    Anderson, James C; O'Loughlin, Julian M A; Tornos, James A

    2005-08-07

    A survey of 16 different chiral auxiliaries and a variety of strategies found that an (-)-8-phenylmenthol ester of a glycine derived migrating group can control the absolute stereochemistry of aza-[2,3]-Wittig sigmatropic rearrangements with diastereoselectivities of ca. 3 : 1 with respect to the auxiliary. In two specific examples, ca. 50% yields of enantiomerically pure products were obtained after chromatographic purification. These were synthetically manipulated with no erosion of stereochemistry into intermediates that completed formal asymmetric syntheses of (+)-HyMePro and (-)-kainic acid.

  13. Chiral habit selection on nanostructured epitaxial quartz films.

    Science.gov (United States)

    Carretero-Genevrier, Adrián; Gich, Martí; Picas, Laura; Sanchez, Clément; Rodriguez-Carvajal, Juan

    2015-01-01

    Understanding the crystallization of enantiomorphically pure systems can be relevant to diverse fields such as the study of the origins of life or the purification of racemates. Here we report on polycrystalline epitaxial thin films of quartz on Si substrates displaying two distinct types of chiral habits that never coexist in the same film. We combine Atomic Force Microscopy (AFM) analysis and computer-assisted crystallographic calculations to make a detailed study of these habits of quartz. By estimating the surface energies of the observed crystallites we argue that the films are enantiomorphically pure and we briefly outline a possible mechanism to explain the habit and chiral selection in this system.

  14. Characterization of a chiral nematic mesoporous organosilica using NMR

    Science.gov (United States)

    Manning, Alan; Shopsowitz, Kevin; Giese, Michael; MacLachlan, Mark; Dong, Ronald; Michal, Carl

    2012-10-01

    Using templation with nanocrystalline cellulose, a mesoporous organosilica film with a chiral nematic pore structure has recently been developed. [1] We have used a variety of Nuclear Magnetic Resonance (NMR) techniques to characterize the pore structure. The pore size distribution has been found by analyzing the freezing point depression of absorbed water via NMR cryoporometry. The effective longitudinal and transverse pore diameters for diffusing water were investigated with Pulsed-Field Gradient (PFG) NMR and compared to a 1-D connected-pore model. Preliminary data on testing imposed chiral ordering in absorbed liquid crystals is also presented. [4pt] [1] K.E. Shopsowitz et al. JACS 134(2), 867 (2012)

  15. Explanation for the Emergence of a Single Chiral Solid State during Attrition-Enhanced Ostwald Ripening : Survival of the Fittest

    NARCIS (Netherlands)

    Noorduin, Wim L.; Meekes, Hugo; Bode, Arno A.C.; Enckevort, Willem J.P. van; Kaptein, Bernard; Kellogg, Richard M.; Vlieg, Elias

    2008-01-01

    The overabundant occurrence of single-handed chiral molecules in living systems has inspired scientists for well more than a century. A route to the evolution of a single chiral solid phase, using abrasive grinding of the crystals in contact with a saturated solution, has been demonstrated for the a

  16. Controlling light with high-Q silicon photonic crystal nanocavities: Photon confinement, nonlinearity and coherence

    Science.gov (United States)

    Yang, Xiaodong

    The strong light localization and long photon lifetimes in two-dimensional silicon photonic crystal nanocavities with high quality factor (Q ) and subwavelength modal volume (V) significantly enhance the light-matter interactions, presenting many opportunities to explore new functionalities in silicon nanophotonic integrated circuits for on-chip all-optical information processing, optical computation and optical communications. This thesis will focus on the design, nanofabrication, and experimental characterization of both passive and active silicon nanophotonic devices based on two-dimensional high-Q silicon photonic crystal nanocavities. Three topics of controlling light with these high-Q nanocavities will be presented, including (1) photon confinement mechanism and cavity resonance tuning, (2) enhancement of optical nonlinearities, and (3) all-optical analogue to coherent interferences. The first topic is photon confinement in two-dimensional high- Q silicon photonic crystal nanocavities. In Chapter 2, the role of Q/V as the figure of merit for the enhanced light-matter interaction in optical microcavities and nanocavities is explained and different types of high-Q optical microcavities and nanocavities are reviewed with an emphasis on two-dimensional photonic crystal nanocavities. Then the nanofabrication process and the Q characterization are illustrated for the two-dimensional silicon photonic crystal nanocavities. In Chapter 3, the post-fabrication digital resonance tuning of high-Q silicon photonic crystal nanocavities using atomic layer deposition is proposed and demonstrated, with wide tuning range and precise control of cavity resonances while preserving high quality factors. The second topic is the enhancement of optical nonlinearities in two-dimensional high-Q silicon photonic crystal nanocavities, including stimulated Raman scattering and thermo-optical nonlinearities. In Chapter 4, the enhanced stimulated Raman scattering for low threshold Raman

  17. Modal liquid crystal lens driven by low voltage produced from a wireless controlling and driving system

    Science.gov (United States)

    Zhang, Xinyu; Loktev, Mikhail; Vdovin, Gleb

    2005-04-01

    A wireless driving and controlling setup constructed by a coil system and a simple power metal-oxide-semiconductor field effect transistor switch circuit for modal liquid crystal lens has been designed, fabricated and characterized. Electrical and structural modeling and analysis have been applied to the design of the wireless power transforming and controlling system. Some key electrical characteristics of coils with different diameter and winding, such as resistance, impedance, capacitance, inductance, and Q factor, which determine the driving and controlling behaviors of the coil system constructed, are given. The liquid crystal lens can be operated under relatively low driving voltage ranging from about 1.5to12Vrms. Under dynamic operation, the prototype system has shown a stable driving and controlling performance to liquid crystal lens under the condition of switching mode of a few KHz. The possibility of integrating very small coils connected in series onto a small-size silicon chip as an integrated receiver in biomedicine application has been shown experimentally.

  18. Controllable synthesis of rice-shape Alq3 nanoparticles with single crystal structure

    Science.gov (United States)

    Xie, Wanfeng; Fan, Jihui; Song, Hui; Jiang, Feng; Yuan, Huimin; Wei, Zhixian; Ji, Ziwu; Pang, Zhiyong; Han, Shenghao

    2016-10-01

    We report the controllable growth of rice-shape nanoparticles of Alq3 by an extremely facile self-assembly approach. Possible mechanisms have been proposed to interpret the formation and controlled process of the single crystal nanoparticles. The field-emission performances (turn-on field 7 V μm-1, maximum current density 2.9 mA cm-2) indicate the potential application on miniaturized nano-optoelectronics devices of Alq3-based. This facile method can potentially be used for the controlled synthesis of other functional complexes and organic nanostructures.

  19. Crystal structures of {[Cu(Lpn2][Fe(CN5(NO]·H2O}n and {[Cu(Lpn2]3[Cr(CN6]2·5H2O}n [where Lpn = (R-propane-1,2-diamine]: two heterometallic chiral cyanide-bridged coordination polymers

    Directory of Open Access Journals (Sweden)

    Olha Sereda

    2015-04-01

    Full Text Available The title compounds, catena-poly[[[bis[(R-propane-1,2-diamine-κ2N,N′]copper(II]-μ-cyanido-κ2N:C-[tris(cyanido-κC(nitroso-κNiron(III]-μ-cyanido-κ2C:N] monohydrate], {[Cu(Lpn2][Fe(CN5(NO]·H2O}n, (I, and poly[[hexa-μ-cyanido-κ12C:N-hexacyanido-κ6C-hexakis[(R-propane-1,2-diamine-κ2N,N′]dichromium(IIItricopper(II] pentahydrate], {[Cu(Lpn2]3[Cr(CN6]2·5H2O}n, (II [where Lpn = (R-propane-1,2-diamine, C3H10N2], are new chiral cyanide-bridged bimetallic coordination polymers. The asymmetric unit of compound (I is composed of two independent cation–anion units of {[Cu(Lpn2][Fe(CN5(NO]} and two water molecules. The FeIII atoms have distorted octahedral geometries, while the CuII atoms can be considered to be pentacoordinate. In the crystal, however, the units align to form zigzag cyanide-bridged chains propagating along [101]. Hence, the CuII atoms have distorted octahedral coordination spheres with extremely long semicoordination Cu—N(cyanido bridging bonds. The chains are linked by O—H...N and N—H...N hydrogen bonds, forming two-dimensional networks parallel to (010, and the networks are linked via N—H...O and N—H...N hydrogen bonds, forming a three-dimensional framework. Compound (II is a two-dimensional cyanide-bridged coordination polymer. The asymmetric unit is composed of two chiral {[Cu(Lpn2][Cr(CN6]}− anions bridged by a chiral [Cu(Lpn2]2+ cation and five water molecules of crystallization. Both the CrIII atoms and the central CuII atom have distorted octahedral geometries. The coordination spheres of the outer CuII atoms of the asymmetric unit can be considered to be pentacoordinate. In the crystal, these units are bridged by long semicoordination Cu—N(cyanide bridging bonds forming a two-dimensional network, hence these CuII atoms now have distorted octahedral geometries. The networks, which lie parallel to (10-1, are linked via O—H...O, O—H...N, N—H...O and N—H...N hydrogen bonds involving all five non

  20. Self-assembly mechanism of 1,3:2,4-di(3,4-dichlorobenzylidene)-D-sorbitol and control of the supramolecular chirality.

    Science.gov (United States)

    Li, Jingjing; Fan, Kaiqi; Guan, Xidong; Yu, Yingzhe; Song, Jian

    2014-11-11

    effective means of realizing in situ tuning of nanostructures and control of the expression of chirality at supramolecular levels.

  1. Control of parabolic PDEs with time-varying spatial domain: Czochralski crystal growth process

    Science.gov (United States)

    Ng, James; Aksikas, Ilyasse; Dubljevic, Stevan

    2013-09-01

    This paper considers the optimal control problem for a class of convection-diffusion-reaction systems modelled by partial differential equations (PDEs) defined on time-varying spatial domains. The class of PDEs is characterised by the presence of a time-dependent convective-transport term which is associated with the time evolution of the spatial domain boundary. The functional analytic description of the PDE yields the representation of the initial and boundary value problem as a nonautonomous parabolic evolution equation on an appropriately defined infinite-dimensional function space. The properties of the time-varying evolution operator to guarantee existence and well posedness of the initial and boundary value problem are demonstrated which serves as the basis for the optimal control problem synthesis. An industrial application of the crystal temperature regulation problem for the Czochralski crystal growth process is considered and numerical simulation results are provided.

  2. Band gap control in a line-defect magnonic crystal waveguide

    Energy Technology Data Exchange (ETDEWEB)

    Morozova, M. A., E-mail: mamorozovama@yandex.ru; Grishin, S. V.; Sadovnikov, A. V.; Romanenko, D. V.; Sharaevskii, Yu. P.; Nikitov, S. A. [Laboratory ' Metamaterials,' Saratov State University, Astrakhanskaya 83, Saratov 410012 (Russian Federation)

    2015-12-14

    We report on the experimental observation of the spin wave spectrum control in a line-defect magnonic crystal (MC) waveguide. We demonstrate the possibility to control the forbidden frequency band (band gap) for spin waves tuning the line-defect width. In particular, this frequency may be greater or lower than the one of 1D MC waveguide without line-defect. By means of space-resolved Brillouin light scattering technique, we study the localization of magnetization amplitude in the line-defect area. We show that the length of this localization region depends on the line-defect width. These results agree well with theoretical calculations of spin wave spectrum using the proposed model of two coupled magnonic crystal waveguides. The proposed simple geometry of MC with line-defect can be used as a logic and multiplexing block for application in the novel field of magnonic devices.

  3. Cell chirality: emergence of asymmetry from cell culture.

    Science.gov (United States)

    Wan, Leo Q; Chin, Amanda S; Worley, Kathryn E; Ray, Poulomi

    2016-12-19

    Increasing evidence suggests that intrinsic cell chirality significantly contributes to the left-right (LR) asymmetry in embryonic development, which is a well-conserved characteristic of living organisms. With animal embryos, several theories have been established, but there are still controversies regarding mechanisms associated with embryonic LR symmetry breaking and the formation of asymmetric internal organs. Recently, in vitro systems have been developed to determine cell chirality and to recapitulate multicellular chiral morphogenesis on a chip. These studies demonstrate that chirality is indeed a universal property of the cell that can be observed with well-controlled experiments such as micropatterning. In this paper, we discuss the possible benefits of these in vitro systems to research in LR asymmetry, categorize available platforms for single-cell chirality and multicellular chiral morphogenesis, and review mathematical models used for in vitro cell chirality and its applications in in vivo embryonic development. These recent developments enable the interrogation of the intracellular machinery in LR axis establishment and accelerate research in birth defects in laterality.This article is part of the themed issue 'Provocative questions in left-right asymmetry'.

  4. Control of calcium carbonate crystallization by using anionic polymethylsiloxanes as templates

    Energy Technology Data Exchange (ETDEWEB)

    Neira-Carrillo, Andronico, E-mail: aneira@uchile.cl [Faculty of Veterinary and Animal Sciences, University of Chile, Santa Rosa 11735, PO Box 2-15, Santiago (Chile); Vasquez-Quitral, Patricio; Paz Diaz, Maria; Soledad Fernandez, Maria; Luis Arias, Jose [Faculty of Veterinary and Animal Sciences, University of Chile, Santa Rosa 11735, PO Box 2-15, Santiago (Chile); Yazdani-Pedram, Mehrdad [Faculty of Chemical and Pharmaceutical Science, University of Chile, S. Livingstone 1007, PO Box 233, Santiago (Chile)

    2012-10-15

    Sulfonated (SO{sub 3}H-PMS) and carboxylated (CO{sub 2}H-PMS) polymethylsiloxanes were synthesized and their effects as anionic template modifier on the CaCO{sub 3} crystal morphologies were evaluated. In vitro crystallization assays of CaCO{sub 3} were performed at room temperature by using gas diffusion method at different concentration, pH and time. SEM images of CaCO{sub 3} showed well-defined short calcite piles (ca. 5 {mu}m) and elongated calcite (ca. 20 {mu}m) when SO{sub 3}H-PMS was used. When CO{sub 2}H-PMS was used, the morphology of CaCO{sub 3} crystals was single-truncated at pH 7-9 and aggregated-modified calcite at pH 10-11. However, at pH 12 the least stable donut-shaped vaterite crystals were formed. EDS and XRD confirmed the presence of Si from anionic PMS templates on the CaCO{sub 3} surfaces and its polymorphism, respectively. Results showed that the selective morphologies of CaCO{sub 3} reflect the electrostatic interaction of anionic groups of functionalized PMS with Ca{sup 2+} adsorbed on CaCO{sub 3} crystals. Rounded and truncated-modified fluorescent CaCO{sub 3} was also produced by the inclusion of functionalized PMS into the lattice of CaCO{sub 3} matrix. We demonstrated that the anionic PMS offer a good modifier for polymer-controlled crystallization and a convenient approach for understanding the biomineralization field. - Graphical abstract: Optical photographs of rounded and truncated-modified fluorescent CaCO{sub 3} produced by the inclusion of sulfonated (SO{sub 3}H-PMS) polymethylsiloxanes into the lattice of CaCO{sub 3} matrix. Insert represents the simulation of modified and fluorescent CaCO{sub 3} crystals using Software JCrystal, (2008). Highlights: Black-Right-Pointing-Pointer We prepared two anionic polymethylsiloxanes (PMS) as templates. Black-Right-Pointing-Pointer Their modifier capacity on the CaCO{sub 3} crystal morphologies was demonstrated. Black-Right-Pointing-Pointer At pH 12, the least stable donut-shaped vaterite

  5. Dynamic increase and decrease of photonic crystal nanocavity Q factors for optical pulse control.

    Science.gov (United States)

    Upham, Jeremy; Tanaka, Yoshinori; Asano, Takashi; Noda, Susumu

    2008-12-22

    We introduce recent advances in dynamic control over the Q factor of a photonic crystal nanocavity system. By carefully timing a rapid increase of the Q factor from 3800 to 22,000, we succeed in capturing a 4ps signal pulse within the nanocavity with a photon lifetime of 18ps. By performing an additional transition of the Q factor within the photon lifetime, the held light is once again ejected from of the system on demand.

  6. Controlling the focusing properties of a triangular-lattice metallic photonic-crystal slab

    Institute of Scientific and Technical Information of China (English)

    Feng Shuai; Wang Yi-Quan; Li Zhi-Yuan; Cheng Bing-Ying; Zhang Dao-Zhong

    2007-01-01

    This paper studies the focusing properties of a two-dimensional photonic crystal (PC) slab consisting of a triangular lattice of metallic cylinders immersed in a dielectric background. Through the analysis of the equifrequency-surface contours and the field patterns of a point source placed in the vicinity of the PC slab, it finds that both the image distance and image quality can be controlled by simply adjusting the refractive index of the background material.

  7. Sensing and tuning microfiber chirality with nematic chirogyral effect

    Science.gov (United States)

    Čopar, Simon; Seč, David; Aguirre, Luis E.; Almeida, Pedro L.; Dazza, Mallory; Ravnik, Miha; Godinho, Maria H.; Pieranski, Pawel; Žumer, Slobodan

    2016-03-01

    Microfibers with their elongated shape and translation symmetry can act as important components in various soft materials, notably for their mechanics on the microscopic level. Here we demonstrate the mechanical response of a micro-object to imposed chirality, in this case, the tilt of disclination rings in an achiral nematic medium caused by the chiral surface anchoring on an immersed microfiber. This coupling between chirality and mechanical response, used to demonstrate sensing of chirality of electrospun cellulose microfibers, is revealed in the optical micrographs due to anisotropy in the elastic response of the host medium. We provide an analytical explanation of the chirogyral effect supported with numerical simulations and perform an experiment to test the effect of the cell confinement and fiber size. We controllably twist the microfibers and demonstrate the response of the nematic medium. More generally the demonstrated study provides means for experimental discrimination of surface properties and allows mechanical control over the shape of disclination rings.

  8. Research of polishing process to control the iron contamination on the magnetorheological finished KDP crystal surface.

    Science.gov (United States)

    Chen, Shaoshan; Li, Shengyi; Peng, Xiaoqiang; Hu, Hao; Tie, Guipeng

    2015-02-20

    A new nonaqueous and abrasive-free magnetorheological finishing (MRF) method is adopted for processing a KDP crystal. MRF polishing is easy to result in the embedding of carbonyl iron (CI) powders; meanwhile, Fe contamination on the KDP crystal surface will affect the laser induced damage threshold seriously. This paper puts forward an appropriate MRF polishing process to avoid the embedding. Polishing results show that the embedding of CI powders can be avoided by controlling the polishing parameters. Furthermore, on the KDP crystal surface, magnetorheological fluids residua inevitably exist after polishing and in which the Fe contamination cannot be removed completely by initial ultrasonic cleaning. To solve this problem, a kind of ion beam figuring (IBF) polishing is introduced to remove the impurity layer. Then the content of Fe element contamination and the depth of impurity elements are measured by time of flight secondary ion mass spectrometry. The measurement results show that there are no CI powders embedding in the MRF polished surface and no Fe contamination after the IBF polishing process, respectively. That verifies the feasibility of MRF polishing-IBF polishing (cleaning) for processing a KDP crystal.

  9. Polymorphism control of p-aminobenzoic acid by isothermal anti-solvent crystallization

    Science.gov (United States)

    Garg, Rakesh Kumar; Sarkar, Debasis

    2016-11-01

    We report, for the first time, the control of polymorphism of p-aminobenzoic acid by isothermal anti-solvent crystallization using ethanol as solvent and water as anti-solvent. p-aminobenzoic (p-ABA) acid crystallizes in two distinct polymorphic forms: the α-polymorph, which is commercially available form and appears as long fibrous needles; and the β-polymorph, which appears in the form of prisms. The solubility of p-ABA was determined gravimetrically for various water/ethanol mixtures at 15 °C and isothermal anti-solvent crystallization experiments were conducted at 15 °C over a range of supersaturation ratio from 1.01 to 1.30 and at different anti-solvent addition rates of 4, 6, 8, and10 ml/h. The needle-type α-polymorph was always obtained at higher supersaturation ratio and higher flow-rates of anti-solvent addition. The prismatic β-polymorph was obtained at lower supersaturation range of 1.01-1.06 when anti-solvent was added at 4 and 6 ml/h. The obtained polymorphs were characterized using scanning electron microscopy, powder x-ray diffraction, and differential scanning calorimetry. The region of occurrence of each polymorph with respect to supersaturation ratio and anti-solvent wt% is presented for these addition rates. The careful selection of supersaturation ratio and anti-solvent addition rate can produce desired polymorph of p-ABA by anti-solvent crystallization.

  10. Soldering Chiralities; 2, Non-Abelian Case

    CERN Document Server

    Wotzasek, C

    1996-01-01

    We study the non-abelian extension of the soldering process of two chiral WZW models of opposite chiralities, resulting in a (non-chiral) WZW model living in a 2D space-time with non trivial Riemanian curvature.

  11. Imaging photonic crystals using Fourier plane imaging and Fourier ptychographic microscopy techniques implemented with a computer controlled hemispherical digital condenser

    Science.gov (United States)

    Sen, Sanchari; Desai, Darshan B.; Alsubaie, Meznh H.; Zhelyeznyakov, Maksym V.; Molina, L.; Sarraf, Hamed Sari; Bernussi, Ayrton A.; Peralta, Luis Grave de

    2017-01-01

    Fourier plane imaging (FPIM) and Fourier ptychographic (FPM) microscopy techniques were used to image photonic crystals. A computer-controlled hemispherical digital condenser provided required sample illumination with variable inclination. Notable improvement in image resolution was obtained with both methods. However, it was determined that the FPM technique cannot surpass the Rayleigh resolution limit when imaging photonic crystals.

  12. Beta tricalcium phosphate ceramics with controlled crystal orientation fabricated by application of external magnetic field during the slip casting process.

    Science.gov (United States)

    Hagio, Takeshi; Yamauchi, Kazushige; Kohama, Takenori; Matsuzaki, Toshiya; Iwai, Kazuhiko

    2013-07-01

    Beta tricalcium phosphate (β-TCP) is a resorbable bioceramic that has hitherto been utilized in the medical field. Since it crystallizes in the anisotropic hexagonal system, properties such as chemical and physical ones are expected to depend on its crystal axis direction and/or on its crystal plane (anisotropy). Control of crystal orientation is thus important when used in polycrystalline form. Meanwhile, application of a strong magnetic field has been found to be a promising technique to control crystal orientation of anisotropic shape or structured crystals. In this work, we attempted to fabricate β-TCP ceramics with controlled crystal orientation by applying an external magnetic field during the slip casting process and subsequently sintering them at 1050°C, below the β-α transition temperature. Application of a vertical magnetic field increased intensities of planes perpendicular to c-plane on the top surface, while a horizontal one with simultaneous mechanical mold rotation decreased it. These results indicated that crystal orientation of β-TCP ceramics were successfully controlled by the external magnetic field and together that the magnetic susceptibility of β-TCP is χ(c[perpendicular])>χ(c//).

  13. Circular dichroism induced by Fano resonances in planar chiral oligomers

    CERN Document Server

    Hopkins, Ben; Miroshnichenko, Andrey E; Kivshar, Yuri S

    2016-01-01

    We present a general theory of circular dichroism induced in planar chiral nanostructures with rotational symmetry. It is demonstrated, analytically, that the handedness of the incident field's polarization can control whether a nanostructure induces either absorption or scattering losses, even when the total loss (extinction) is polarization-independent. We then show that this effect is a consequence of modal interference so that strong circular dichroism in absorption and scattering can be engineered by combining Fano resonances with chiral nanoparticle clusters.

  14. Spiral Galaxies as Chiral Objects?

    CERN Document Server

    Capozziello, S; Capozziello, Salvatore; Lattanzi, Alessandra

    2005-01-01

    Spiral galaxies show axial symmetry and an intrinsic 2D-chirality. Environmental effects can influence the chirality of originally isolated stellar systems and a progressive loss of chirality can be recognised in the Hubble sequence. We point out a preferential modality for genetic galaxies as in microscopic systems like aminoacids, sugars or neutrinos. This feature could be the remnant of a primordial symmetry breaking characterizing systems at all scales.

  15. Chiral Dynamics 2006

    Science.gov (United States)

    Ahmed, Mohammad W.; Gao, Haiyan; Weller, Henry R.; Holstein, Barry

    2007-10-01

    pt. A. Plenary session. Opening remarks: experimental tests of chiral symmetry breaking / A. M. Bernstein. [Double pie symbols] scattering / H. Leutwyler. Chiral effective field theory in a [Triangle]-resonance region / V. Pascalutsa. Some recent developments in chiral perturbation theory / Ulf-G. Mei ner. Chiral extrapolation and nucleon structure from the lattice / R.D. Young. Recent results from HAPPEX / R. Michaels. Chiral symmetries and low energy searches for new physics / M.J. Ramsey-Musolf. Kaon physics: recent experimental progress / M. Moulson. Status of the Cabibbo angle / V. Cirigliano. Lattice QCD and nucleon spin structure / J.W. Negele. Spin sum rules and polarizabilities: results from Jefferson lab / J-P Chen. Compton scattering and nucleon polarisabilities / Judith A. McGovern. Virtual compton scattering at MIT-bates / R. Miskimen. Physics results from the BLAST detector at the BATES accelerator / R.P. Redwine. The [Pie sympbol]NN system, recent progress / C. Hanhart. Application of chiral nuclear forces to light nuclei / A. Nogga. New results on few-body experiments at low energy / Y. Nagai. Few-body lattice calculations / M.J. Savage. Research opportunities at the upgraded HI?S facility / H.R. Weller -- pt. B. Goldstone boson dynamics. Working group summary: Goldstone Boson dynamics / G. Colangelo and S. Giovannella. Recent results on radiative Kaon decays from NA48 and NA48/2 / S.G. López. Cusps in K-->3 [Pie symbol] decays / B. Kubis. Recent KTeV results on radiative Kaon decays / M.C. Ronquest. The [Double pie symbols] scattering amplitude / J.R. Peláez. Determination of the Regge parameters in the [Double pie symbols] scattering amplitude / I. Caprini. e+e- Hadronic cross section measurement at DA[symbol]NE with the KLOE detector / P. Beltrame. Measurement of the form factors of e+e- -->2([Pie symbol]+[Pie symbol]-), pp and the resonant parameters of the heavy charmonia at BES / H. Hu. Measurement of e+e- multihadronic cross section below 4

  16. Optical chiral metamaterial based on the resonant behaviour of nanodiscs

    Science.gov (United States)

    Kordi, Mahdi; Mojtaba Mirsalehi, Mir

    2016-08-01

    Circular dichorism and optical activity have been achieved by chiral metamaterials in the optical spectrum, but for the case of negative index of refraction, remarkable achievements have not been obtained in this region so far. We employ nanoparticles to shift the resonant frequency of a chiral metamaterial based on twisted cross wires to optical domain. Our proposed structure provides giant optical activity, strong circular dichorism and also negative refractive index in the optical wavelengths. Optical activity in our structure has a rotary power similar to a gyrotropic crystal of quartz, but in a thickness which is four orders of magnitude smaller. The foundation of our method for realizing such an optical chiral metamaterial is based on creating a different coupling between longitudinal modes of localized surface plasmons for right and left circularly polarized incident waves.

  17. Chirality-dependent vapor-phase epitaxial growth and termination of single-wall carbon nanotubes.

    Science.gov (United States)

    Liu, Bilu; Liu, Jia; Tu, Xiaomin; Zhang, Jialu; Zheng, Ming; Zhou, Chongwu

    2013-09-11

    Structurally uniform and chirality-pure single-wall carbon nanotubes are highly desired for both fundamental study and many of their technological applications, such as electronics, optoelectronics, and biomedical imaging. Considerable efforts have been invested in the synthesis of nanotubes with defined chiralities by tuning the growth recipes but the approach has only limited success. Recently, we have shown that chirality-pure short nanotubes can be used as seeds for vapor-phase epitaxial cloning growth, opening up a new route toward chirality-controlled carbon nanotube synthesis. Nevertheless, the yield of vapor-phase epitaxial growth is rather limited at the present stage, due in large part to the lack of mechanistic understanding of the process. Here we report chirality-dependent growth kinetics and termination mechanism for the vapor-phase epitaxial growth of seven single-chirality nanotubes of (9, 1), (6, 5), (8, 3), (7, 6), (10, 2), (6, 6), and (7, 7), covering near zigzag, medium chiral angle, and near armchair semiconductors, as well as armchair metallic nanotubes. Our results reveal that the growth rates of nanotubes increase with their chiral angles while the active lifetimes of the growth hold opposite trend. Consequently, the chirality distribution of a nanotube ensemble is jointly determined by both growth rates and lifetimes. These results correlate nanotube structures and properties with their growth behaviors and deepen our understanding of chirality-controlled growth of nanotubes.

  18. Recrystallization and shape control of crystals of the organic dye acid green 27 in a mixed solvent.

    Science.gov (United States)

    Cong, Huai-Ping; Yu, Shu-Hong

    2007-01-01

    Recrystallization of the unstructured dye acid green 27 (AG27) in a mixed solvent of alcohol (ethanol or methanol) and water was systematically studied. The results demonstrated that AG27 crystals with uniform sizes and controllable shapes can be produced by simply changing the volume ratio of ethanol (or methanol) and deionized water (DIW). Rodlike and shuttlelike AG27 crystals can be selectively synthesized. The XRD analyses revealed the periodic structures of the organic crystals. Furthermore, crystallization in another mixed solvent of N,N-dimethylformamide (DMF) and DIW results in the formation of longer fibers with high aspect ratio, which further validates the remarkable effects of mixed solvent on the shape of the AG27 crystals. This method of recrystallization in a mixed solvent is expected to facilitate the synthesis of other functional organic crystals with unusual shapes.

  19. Generalized simplicial chiral models

    CERN Document Server

    Alimohammadi, M

    2000-01-01

    Using the auxiliary field representation of the simplicial chiral models on a (d-1)-dimensional simplex, we generalize the simplicial chiral models by replacing the term Tr$(AA^{\\d})$ in the Lagrangian of these models, by an arbitrary class function of $AA^{\\d}; V(AA^{\\d})$. This is the same method that has been used in defining the generalized two-dimensional Yang-Mills theories (gYM_2) from ordinary YM_2. We call these models, the " generalized simplicial chiral models ". With the help of the results of one-link integral over a U(N) matrix, we compute the large-N saddle-point equations for eigenvalue density function $\\ro (z)$ in the weak ($\\b >\\b_c$) and strong ($\\b <\\b_c$) regions. In d=2, where the model somehow relates to gYM_2 theory, we solve the saddle-point equations and find $\\ro (z)$ in two region, and calculate the explicit value of critical point $\\b_c$ for $V(B)=TrB^n (B=AA^{\\d})$. For $V(B)=Tr B^2,Tr B^3$ and Tr$B^4$, we study the critical behaviour of the model at d=2, and by calculating t...

  20. Chiral nuclear thermodynamics

    CERN Document Server

    Fiorilla, Salvatore; Weise, Wolfram

    2011-01-01

    We calculate the equation of state of nuclear matter for arbitrary isospin-asymmetry up to three loop order in the free energy density in the framework of in-medium chiral perturbation theory. In our approach 1\\pi- and 2\\pi-exchange dynamics with the inclusion of the \\Delta-isobar excitation as an explicit degree of freedom, corresponding to the long- and intermediate-range correlations, are treated explicitly. Few contact terms fixed to reproduce selected known properties of nuclear matter encode the short-distance physics. Two-body as well as three-body forces are systematically included. We find a critical temperature of about 15 MeV for symmetric nuclear matter. We investigate the dependence of the liquid-gas first-order phase transition on isospin-asymmetry. In the same chiral framework we calculate the chiral condensate of isospin-symmetric nuclear matter at finite temperatures. The contribution of the \\Delta-isobar excitation is essential for stabilizing the condensate. As a result, we find no indicati...

  1. Free-standing chiral plasmonics

    Science.gov (United States)

    Leong, Eunice Sok Ping; Deng, Jie; Wu, Siji; Khoo, Eng Huat; Liu, Yan Jun

    2014-11-01

    Chiral plasmonic nanostructures offer the ability to achieve strong optical circular dichroism (CD) activity over a broad spectral range, which has been challenging for chiral molecules. Chiral plasmonic nanostructures have been extensively studied based on top-down and bottom-up fabrication techniques. Particularly, in the top-down electron-beam lithography, 3D plasmonic nanostructure fabrication involves layer-by-layer patterning and complex alignment, which is time-consuming and causes many defects in the structures. Here, we present a free-standing 3D chiral plamonic nanostructures using the electron-beam lithography technique with much simplified fabrication processes. The 3D chiral plasmonic nanostructures consist of a free-standing ultrathin silicon nitride membrane with well-aligned L-shape metal nanostructures on one side and disk-shape ones on the other side. The free-standing membrane provides an ultra-smooth metal/dielectric interface and uniformly defines the gap between the upper and lower layers in an array of chiral nanostructures. Such free-standing chiral plasmonic nanostructures exhibit strong CD at optical frequencies, which can be engineered by simply changing the disk size on one side of the membrane. Experimental results are in good agreement with the finite-difference time-domain simulations. Such free-standing chiral plasmonics holds great potential for chirality analysis of biomolecules, drugs, and chemicals.

  2. Crystal front shape control by use of an additional heater in a Czochralski sapphire single crystal growth system

    Science.gov (United States)

    Hur, Min-Jae; Han, Xue-Feng; Choi, Ho-Gil; Yi, Kyung-Woo

    2017-09-01

    The quality of sapphire single crystals used as substrates for LED production is largely influenced by two defects: dislocation density and bubbles trapped in the crystal. In particular, the dislocation density has a higher value in sapphire grown by the Czochralski (CZ) method than by other methods. In the present study, we predict a decreased value for the convexity and thermal gradient at the crystal front (CF) through the use of an additional heater in an induction-heated CZ system. In addition, we develop a solute concentration model by which the location of bubble formation in CZ growth is calculated, and the results are compared with experimental results. We further calculate the location of bubble entrapment corresponding with the use of an additional heater. We find that sapphire crystal growth with an additional heater yields a decreased thermal gradient at the CF, together with decreased CF convexity, improved energy efficiency, and improvements in terms of bubble formation location.

  3. Spontaneous emission control of single quantum dots by electromechanical tuning of a photonic crystal cavity

    CERN Document Server

    Midolo, L; Hoang, T B; Xia, T; van Otten, F W M; Li, L H; Linfield, E; Lermer, M; Höfling, S; Fiore, A

    2012-01-01

    We demonstrate the control of the spontaneous emission rate of single InAs quantum dots embedded in a double-membrane photonic crystal cavity by the electromechanical tuning of the cavity resonance. Controlling the separation between the two membranes with an electrostatic field we obtain the real-time spectral alignment of the cavity mode to the excitonic line and we observe an enhancement of the spontaneous emission rate at resonance. The cavity has been tuned over 13 nm without shifting the exciton energies. A spontaneous emission enhancement of 4.5 has been achieved with a coupling efficiency of the dot to the mode 92%.

  4. Growth of optical-quality anthracene crystals doped with dibenzoterrylene for controlled single photon production

    Energy Technology Data Exchange (ETDEWEB)

    Major, Kyle D., E-mail: kyle.major11@imperial.ac.uk; Lien, Yu-Hung; Polisseni, Claudio; Grandi, Samuele; Kho, Kiang Wei; Clark, Alex S.; Hwang, J.; Hinds, E. A., E-mail: ed.hinds@imperial.ac.uk [Centre for Cold Matter, Department of Physics, Blackett Laboratory, Imperial College London, Prince Consort Road, London SW7 2AZ (United Kingdom)

    2015-08-15

    Dibenzoterrylene (DBT) molecules within a crystalline anthracene matrix show promise as quantum emitters for controlled, single photon production. We present the design and construction of a chamber in which we reproducibly grow doped anthracene crystals of optical quality that are several mm across and a few μm thick. We demonstrate control of the DBT concentration over the range 6–300 parts per trillion and show that these DBT molecules are stable single-photon emitters. We interpret our data with a simple model that provides some information on the vapour pressure of DBT.

  5. Low-molecular-weight poly-carboxylate as crystal growth modifier in biomineralization

    Indian Academy of Sciences (India)

    Ballav Moni Borah; Bhaskar Jyoti Bhuyan; Gopal Das

    2006-11-01

    Construction of modified inorganic mineral with controlled mineralization analogues of those produced by nature is now of current interest for understanding the mechanism of the in vivo biomineralization processes, as well as looking for fresh industrial and technological applications. Lowmolecular-weight chiral poly-carboxylate ligands derived from naturally occurring L--amino acids have been used as model systems to study the effect of molecular properties on crystal growth modification.

  6. Structure and Growth Control of Organic–Inorganic Halide Perovskites for Optoelectronics: From Polycrystalline Films to Single Crystals

    Science.gov (United States)

    Chen, Yani; He, Minhong; Peng, Jiajun; Sun, Yong

    2016-01-01

    Recently, organic–inorganic halide perovskites have sparked tremendous research interest because of their ground‐breaking photovoltaic performance. The crystallization process and crystal shape of perovskites have striking impacts on their optoelectronic properties. Polycrystalline films and single crystals are two main forms of perovskites. Currently, perovskite thin films have been under intensive investigation while studies of perovskite single crystals are just in their infancy. This review article is concentrated upon the control of perovskite structures and growth, which are intimately correlated for improvements of not only solar cells but also light‐emitting diodes, lasers, and photodetectors. We begin with the survey of the film formation process of perovskites including deposition methods and morphological optimization avenues. Strategies such as the use of additives, thermal annealing, solvent annealing, atmospheric control, and solvent engineering have been successfully employed to yield high‐quality perovskite films. Next, we turn to summarize the shape evolution of perovskites single crystals from three‐dimensional large sized single crystals, two‐dimensional nanoplates, one‐dimensional nanowires, to zero‐dimensional quantum dots. Siginificant functions of perovskites single crystals are highlighted, which benefit fundamental studies of intrinsic photophysics. Then, the growth mechanisms of the previously mentioned perovskite crystals are unveiled. Lastly, perspectives for structure and growth control of perovskites are outlined towards high‐performance (opto)electronic devices.

  7. Structure and Growth Control of Organic-Inorganic Halide Perovskites for Optoelectronics: From Polycrystalline Films to Single Crystals.

    Science.gov (United States)

    Chen, Yani; He, Minhong; Peng, Jiajun; Sun, Yong; Liang, Ziqi

    2016-04-01

    Recently, organic-inorganic halide perovskites have sparked tremendous research interest because of their ground-breaking photovoltaic performance. The crystallization process and crystal shape of perovskites have striking impacts on their optoelectronic properties. Polycrystalline films and single crystals are two main forms of perovskites. Currently, perovskite thin films have been under intensive investigation while studies of perovskite single crystals are just in their infancy. This review article is concentrated upon the control of perovskite structures and growth, which are intimately correlated for improvements of not only solar cells but also light-emitting diodes, lasers, and photodetectors. We begin with the survey of the film formation process of perovskites including deposition methods and morphological optimization avenues. Strategies such as the use of additives, thermal annealing, solvent annealing, atmospheric control, and solvent engineering have been successfully employed to yield high-quality perovskite films. Next, we turn to summarize the shape evolution of perovskites single crystals from three-dimensional large sized single crystals, two-dimensional nanoplates, one-dimensional nanowires, to zero-dimensional quantum dots. Siginificant functions of perovskites single crystals are highlighted, which benefit fundamental studies of intrinsic photophysics. Then, the growth mechanisms of the previously mentioned perovskite crystals are unveiled. Lastly, perspectives for structure and growth control of perovskites are outlined towards high-performance (opto)electronic devices.

  8. Controlled vapor phase growth of single crystalline, two-dimensional GaSe crystals with high photoresponse.

    Science.gov (United States)

    Li, Xufan; Lin, Ming-Wei; Puretzky, Alexander A; Idrobo, Juan C; Ma, Cheng; Chi, Miaofang; Yoon, Mina; Rouleau, Christopher M; Kravchenko, Ivan I; Geohegan, David B; Xiao, Kai

    2014-06-30

    Compared with their bulk counterparts, atomically thin two-dimensional (2D) crystals exhibit new physical properties, and have the potential to enable next-generation electronic and optoelectronic devices. However, controlled synthesis of large uniform monolayer and multi-layer 2D crystals is still challenging. Here, we report the controlled synthesis of 2D GaSe crystals on SiO2/Si substrates using a vapor phase deposition method. For the first time, uniform, large (up to ~60 μm in lateral size), single-crystalline, triangular monolayer GaSe crystals were obtained and their structure and orientation were characterized from atomic scale to micrometer scale. The size, density, shape, thickness, and uniformity of the 2D GaSe crystals were shown to be controllable by growth duration, growth region, growth temperature, and argon carrier gas flow rate. The theoretical modeling of the electronic structure and Raman spectroscopy demonstrate a direct-to-indirect bandgap transition and progressive confinement-induced bandgap shifts for 2D GaSe crystals. The 2D GaSe crystals show p-type semiconductor characteristics and high photoresponsivity (~1.7 A/W under white light illumination) comparable to exfoliated GaSe nanosheets. These 2D GaSe crystals are potentially useful for next-generation electronic and optoelectronic devices such as photodetectors and field-effect transistors.

  9. Towards true 3-dimensional BCC colloidal crystals with controlled lattice orientation

    NARCIS (Netherlands)

    Dziomkina, N.; Hempenius, Mark A.; Vancso, Gyula J.

    2009-01-01

    A fabrication method of colloidal crystals possessing the BCC crystal structure is described. BCC colloidal crystals with a thickness of up to seven colloidal layers were grown in the direction of the (100) crystal plane. Defect free colloidal crystals with a homogeneous surface coverage were

  10. Anchoring energy enhancement and pretilt angle control of liquid crystal alignment on polymerized surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Weng, Libo; Chien, Liang-Chy [Liquid Crystal Institute, Kent State University, Kent, Ohio 44242 (United States); Liao, Pei-Chun [Liquid Crystal Institute, Kent State University, Kent, Ohio 44242 (United States); AU Optronics Corporation, Hsinchu, 300, Taiwan (China); Lin, Chen-Chun; Ting, Tien-Lun; Hsu, Wen-Hao; Su, Jenn-Jia [AU Optronics Corporation, Hsinchu, 300, Taiwan (China)

    2015-09-15

    We demonstrate enhanced surface anchoring energy and control of pretilt angle in a nematic liquid crystal cell with vertical alignment and polymerized surfaces (PS-VA). The polymerized surfaces are formed by ultraviolet (UV) irradiation-induced phase separation of a minute amount of a reactive monomer in the vertical-aligned nematic liquid crystal. By introducing a bias voltage during UV curing, surface-localized polymer protrusions with a dimension of 100nm and a field-induced pretilt angle are observed. Experimental evidences and theoretical analyses validate that PS-VA has increased surface anchoring strength by two folds and pretilt angle has been changed from 89° to 86° compared to those of a VA cell. The enabling PS-VA cell technique with excel electro-optical properties such as very good dark state, high optical contrast, and fast rise and decay times may lead to development of a wide range of applications.

  11. Phononic Crystal Plate with Hollow Pillars Actively Controlled by Fluid Filling

    Directory of Open Access Journals (Sweden)

    Yabin Jin

    2016-05-01

    Full Text Available We investigate theoretically the properties of phononic crystal plates with hollow pillars. Such crystals can exhibit confined whispering gallery modes around the hollow parts of the pillars whose localization can be increased by separating the pillar from the plate by a full cylinder. We discuss the behaviors of these modes and their potential applications in guiding and filtering. Filling the hollow parts with a fluid gives rise to new localized modes, which depend on the physical properties and height of the fluid. Thus, these modes can be actively controlled for the purpose of multichannel multiplexing. In particular, one can obtain localized modes associated with the compressional vibrations of the fluid along its height. They can be used for the purpose of sensing the acoustic properties of the fluid or their variations with temperature.

  12. Controlled chemical modification of the internal surface of photonic crystal fibers for application as biosensitive elements

    Science.gov (United States)

    Pidenko, Sergey A.; Burmistrova, Natalia A.; Pidenko, Pavel S.; Shuvalov, Andrey A.; Chibrova, Anastasiya A.; Skibina, Yulia S.; Goryacheva, Irina Y.

    2016-10-01

    Photonic crystal fibers (PCF) are one of the most promising materials for creation of constructive elements for bio-, drug and contaminant sensing based on unique optical properties of the PCF as effective nanosized optical signal collectors. In order to provide efficient and controllable binding of biomolecules, the internal surface of glass hollow core photonic crystal fibers (HC-PCF) has been chemically modified with silanol groups and functionalized with (3-aminopropyl) triethoxysilane (APTES). The shift of local maxima in the HC-PCF transmission spectrum has been selected as a signal for estimating the amount of silanol groups on the HC-PCF inner surface. The relationship between amount of silanol groups on the HC-PCF inner surface and efficiency of following APTES functionalization has been evaluated. Covalent binding of horseradish peroxidase (chosen as a model protein) on functionalized PCF inner surface has been performed successively, thus verifying the possibility of creating a biosensitive element.

  13. Controlling and measuring quantum transport of heat in trapped-ion crystals.

    Science.gov (United States)

    Bermudez, A; Bruderer, M; Plenio, M B

    2013-07-26

    Measuring heat flow through nanoscale devices poses formidable practical difficulties as there is no "ampere meter" for heat. We propose to overcome this problem in a chain of trapped ions, where laser cooling the chain edges to different temperatures induces a heat current of local vibrations (vibrons). We show how to efficiently control and measure this current, including fluctuations, by coupling vibrons to internal ion states. This demonstrates that ion crystals provide an ideal platform for studying quantum transport, e.g., through thermal analogues of quantum wires and quantum dots. Notably, ion crystals may give access to measurements of the elusive bosonic fluctuations in heat currents and the onset of Fourier's law. Our results are strongly supported by numerical simulations for a realistic implementation with specific ions and system parameters.

  14. Anchoring energy enhancement and pretilt angle control of liquid crystal alignment on polymerized surfaces

    Directory of Open Access Journals (Sweden)

    Libo Weng

    2015-09-01

    Full Text Available We demonstrate enhanced surface anchoring energy and control of pretilt angle in a nematic liquid crystal cell with vertical alignment and polymerized surfaces (PS-VA. The polymerized surfaces are formed by ultraviolet (UV irradiation-induced phase separation of a minute amount of a reactive monomer in the vertical-aligned nematic liquid crystal. By introducing a bias voltage during UV curing, surface-localized polymer protrusions with a dimension of 100nm and a field-induced pretilt angle are observed. Experimental evidences and theoretical analyses validate that PS-VA has increased surface anchoring strength by two folds and pretilt angle has been changed from 89° to 86° compared to those of a VA cell. The enabling PS-VA cell technique with excel electro-optical properties such as very good dark state, high optical contrast, and fast rise and decay times may lead to development of a wide range of applications.

  15. Crowded Star Mesogens: Guest-Controlled Stability of Mesophases from Unconventional Liquid-Crystal Molecules.

    Science.gov (United States)

    Lehmann, Matthias; Maier, Philipp; Grüne, Matthias; Hügel, Markus

    2017-01-23

    The molecular design of crowded hexasubstituted star mesogens based on a benzene core and alternating substitution with oligo(phenylenevinylene) arms and aryl units generates free space between the conjugated arm scaffolds. Various arylcarboxy building blocks, decorated with alkoxy chains, have been incorporated in the void by mixing, hydrogen bonding or covalent bonds to the aryl groups. The mesogens assemble in columnar stacks ranging from soft crystals to rectangular and hexagonal columnar liquid crystals, revealed by polarized optical microscopy, differential scanning calorimetry, X-ray scattering and modelling. The stability of the mesophases is crucially influenced by the binding mode of the arylcarboxy guest building blocks. The origin of the variation in clearing temperature is unravelled by modelling, cohesive energy density considerations and solid-state NMR spectroscopy. The control over the transition temperature is important for the formation of aligned thin films and thus for potential applications.

  16. Preparation of drug nanocrystals by controlled crystallization : Application of a 3-way nozzle to prevent premature crystallization for large scale production

    NARCIS (Netherlands)

    de Waard, Hans; Grasmeijer, Niels; Hinrichs, Wouter L.J.; Eissens, Anko C.; Pfaffenbach, Peter P.F.; Frijlink, Henderik W.

    2009-01-01

    In a previous study we have developed a novel process to produce drug nanocrystals. This process, "controlled crystallization during freeze-drying" has shown to be a successful method to increase the dissolution rate of poorly water-soluble drugs [de Waard, H., Hinrichs, W.L.J., Frijlink, H.W., 2008

  17. Control of Process Operations and Monitoring of Product Qualities through Generic Model-based Framework in Crystallization Processes

    DEFF Research Database (Denmark)

    Abdul Samad, Noor Asma Fazli Bin

    A generic and systematic model-based framework for the design of a process monitoring and control system to achieve the desired crystal size distribution (CSD) and crystal shape for a wide range of crystallization processes has been developed. This framework combines a generic multi......-dimensional to a twodimensional description; b) the systematic framework is used in a case study to design a monitoring and control (PAT) system for a potassium dichromate and KDP crystallization processes to achieve the desired target CSD respectively; and c) Based on the PAT system design in b), the application of uncertainty......-dimensional modelling framework, tools for design of set point profiles, for design of PAT (Process Analytical Technology) systems as well as option to perform the uncertainty and sensitivity analysis of the PAT system design. Through this framework, it is possible for a wide range of crystallization processes...

  18. Inhomogeneous chiral symmetry breaking in dense neutron-star matter

    Energy Technology Data Exchange (ETDEWEB)

    Buballa, Michael; Carignano, Stefano [Technische Universitaet Darmstadt, Theoriezentrum, Institut fuer Kernphysik, Darmstadt (Germany)

    2016-03-15

    An increasing number of model results suggests that chiral symmetry is broken inhomogeneously in a certain window at intermediate densities in the QCD phase diagram. This could have significant effects on the properties of compact stars, possibly leading to new astrophysical signatures. In this contribution we discuss this idea by reviewing recent results on inhomogeneous chiral symmetry breaking under an astrophysics-oriented perspective. After introducing two commonly studied spatial modulations of the chiral condensate, the chiral density wave and the real kink crystal, we focus on their properties and their effect on the equation of state of quark matter. We also describe how these crystalline phases are affected by different elements which are required for a realistic description of a compact star, such as charge neutrality, the presence of magnetic fields, vector interactions and the interplay with color superconductivity. Finally, we discuss possible signatures of inhomogeneous chiral symmetry breaking in the core of compact stars, considering the cases of mass-radius relations and neutrino emissivity explicitly. (orig.)

  19. Control of fluid flow during Bridgman crystal growth using low-frequency vibrational stirring

    Science.gov (United States)

    Zawilski, Kevin Thomas

    The goal of this research program was to develop an in depth understanding of a promising new method for stirring crystal growth melts called coupled vibrational stirring (CVS). CVS is a mixing technique that can be used in sealed systems and produces rapid mixing through vortex flows. Under normal operating conditions, CVS uses low-frequency vibrations to move the growth crucible along a circular path, producing a surface wave and convection in the melt. This research focused on the application of CVS to the vertical Bridgman technique. CVS generated flows were directly studied using a physical modeling system containing water/glycerin solutions. Sodium nitrate was chosen as a model growth system because the growth process could be directly observed using a transparent furnace. Lead magnesium niobate-lead titanate (PMNT) was chosen as the third system because of its potential application for high performance solid state transducers and actuators. In this study, the critical parameters for controlling CVS flows in cylindrical Bridgman systems were established. One of the most important results obtained was the dependence of an axial velocity gradient on the vibrational frequency. By changing the frequency, the intensity of fluid flow at a given depth can be easily manipulated. The intensity of CVS flows near the crystal-melt interface was found to be important. When flow intensity near the interface increased during growth, large growth rate fluctuations and significant changes in interface shape were observed. To eliminate such fluctuations, a constant flow rate near the crystal-melt interface was maintained by decreasing the vibrational frequency. A continuous frequency ramp was found to be essential to grow crystals of good quality under strong CVS flows. CVS generated flows were also useful in controlling the shape of the growth interface. In the sodium nitrate system without stirring, high growth rates produced a very concave interface. By adjusting the flow

  20. Crystal Orientation Controlled Photovoltaic Properties of Multilayer GaAs Nanowire Arrays.

    Science.gov (United States)

    Han, Ning; Yang, Zai-Xing; Wang, Fengyun; Yip, SenPo; Li, Dapan; Hung, Tak Fu; Chen, Yunfa; Ho, Johnny C

    2016-06-28

    In recent years, despite significant progress in the synthesis, characterization, and integration of various nanowire (NW) material systems, crystal orientation controlled NW growth as well as real-time assessment of their growth-structure-property relationships still presents one of the major challenges in deploying NWs for practical large-scale applications. In this study, we propose, design, and develop a multilayer NW printing scheme for the determination of crystal orientation controlled photovoltaic properties of parallel GaAs NW arrays. By tuning the catalyst thickness and nucleation and growth temperatures in the two-step chemical vapor deposition, crystalline GaAs NWs with uniform, pure ⟨110⟩ and ⟨111⟩ orientations and other mixture ratios can be successfully prepared. Employing lift-off resists, three-layer NW parallel arrays can be easily attained for X-ray diffraction in order to evaluate their growth orientation along with the fabrication of NW parallel array based Schottky photovoltaic devices for the subsequent performance assessment. Notably, the open-circuit voltage of purely ⟨111⟩-oriented NW arrayed cells is far higher than that of ⟨110⟩-oriented NW arrayed counterparts, which can be interpreted by the different surface Fermi level pinning that exists on various NW crystal surface planes due to the different As dangling bond densities. All this indicates the profound effect of NW crystal orientation on physical and chemical properties of GaAs NWs, suggesting the careful NW design considerations for achieving optimal photovoltaic performances. The approach presented here could also serve as a versatile and powerful platform for in situ characterization of other NW materials.