WorldWideScience

Sample records for arylsulfonates

  1. Photochemical surface modification of poly(arylsulfone) ultrafiltration membrane and covalent immobilization of enzyme

    Institute of Scientific and Technical Information of China (English)

    SONG Hua; WU Guang-xia; LIU Kai

    2004-01-01

    The sensitivity of poly(arylsulfone)(PSf) for UV irradiation in different solvents(water and ethanol) was investigated. It is confirmed that acrylic acid(AA) and acrylamide(AAm) are grafted only onto the surface of the membrane instead of the interior by FTIR and scanning electron microscope(SEM). The membrane performance(ΔJ/J0 and contact angleθ) after photografting was studied. In the range of conditions used, the grafting yield increases with irradiation time and monomer concentration growing. After photografting and N-3-dimethyl-aminopropyl-N' -ethycarbodiimide hydrochloride(EDC) activation, PSf membrane was immobilized with hydrogen peroxide oxidoreductase, and showed a higher activity than the control membrane.

  2. Double Heteroatom Functionalization of Arenes Using Benzyne Three‐Component Coupling†

    OpenAIRE

    García‐López, José‐Antonio; Çetin, Meliha; Greaney, Michael F.

    2015-01-01

    Abstract Arynes participate in three‐component coupling reactions with N, S, P, and Se functionalities to yield 1,2‐heteroatom‐difunctionalized arenes. Using 2‐iodophenyl arylsulfonates as benzyne precursors, we could effectively add magnesiated S‐, Se‐, and N‐nucleophilic components to the strained triple bond. In the same pot, addition of electrophilic N, S, or P reagents and a copper(I) catalyst trapped the intermediate aryl Grignard to produce a variety of 1,2‐difunctionalized arenes....

  3. Double Heteroatom Functionalization of Arenes Using Benzyne Three‐Component Coupling†

    Science.gov (United States)

    García‐López, José‐Antonio; Çetin, Meliha

    2015-01-01

    Abstract Arynes participate in three‐component coupling reactions with N, S, P, and Se functionalities to yield 1,2‐heteroatom‐difunctionalized arenes. Using 2‐iodophenyl arylsulfonates as benzyne precursors, we could effectively add magnesiated S‐, Se‐, and N‐nucleophilic components to the strained triple bond. In the same pot, addition of electrophilic N, S, or P reagents and a copper(I) catalyst trapped the intermediate aryl Grignard to produce a variety of 1,2‐difunctionalized arenes. PMID:25580700

  4. The ssu Locus Plays a Key Role in Organosulfur Metabolism in Pseudomonas putida S-313

    OpenAIRE

    Kahnert, Antje; Vermeij, Paul; Wietek, Claudia; James, Peter; Leisinger, Thomas; Kertesz, Michael A.

    2000-01-01

    Pseudomonas putida S-313 can utilize a broad range of aromatic sulfonates as sulfur sources for growth in sulfate-free minimal medium. The sulfonates are cleaved monooxygenolytically to yield the corresponding phenols. miniTn5 mutants of strain S-313 which were no longer able to desulfurize arylsulfonates were isolated and were found to carry transposon insertions in the ssuEADCBF operon, which contained genes for an ATP-binding cassette-type transporter (ssuABC), a two-component reduced flav...

  5. Thermochemical comparisons of homogeneous and heterogeneous acids and bases. 1. Sulfonic acid solutions and resins as prototype Broensted acids

    Energy Technology Data Exchange (ETDEWEB)

    Arnett, E.M.; Haaksma, R.A.; Chawla, B.; Healy, M.H.

    1986-08-06

    Heats of ionization by thermometric titration for a series of bases (or acids) can be used to compare solid acids (or bases) with liquid analogues bearing the same functionalities in homogeneous solutions. The method is demonstrated for Broensted acids by reacting a series of substituted nitrogen bases with solutions of p-toluenesulfonic acid (PTSA) in acetonitrile and with suspensions of the microporous polymeric arylsulfonic acid resin-Dowex 50W-X8 in the same solvent. Under well-controlled anhydrous conditions there is a good correlation (r = 0.992) between the heats of reaction of the bases with the homogeneous and heterogeneous acid systems, but the homogeneous system gives a more exothermic interaction by 3-4 kcal mol/sup -1/ for a series of 29 substituted pyrimidines, anilines, and some other amines. This difference may be attributed to homohydrogen bonding interactions between excess acid and sulfonate anion sites which are more restricted geometrically in the resin than in solution. Other factors which affect the enthalpy change for the acid-base interaction are the acid/base ratio, the water content of the sulfonic acid, the solvent, and the resin structure (e.g., microporous vs. macroporous). Steric hindrance in the base does not differentiate solid from homogeneous acid. In addition to the use of titration calorimetry, heats of immersion are reported for the Dowex-arylsulfonic acid resins and the Nafion-perfluorinated sulfonic acid resin in a series of basic liquids. The results are compared with each other and with those from a previous study of several varieties of coal.