Teel infoühiskonda - sedakorda Euroopa Liidu abiga / Katre Talviste, Anne Märdimäe

Index Scriptorium Estoniae

Talviste, Katre

1997-01-01

Euroopa Liidu infotehnika arendusprogrammid: ACTS - arenenud sidetehnika ja teenused, ESPRIT - infotehnika, TELEMATICS APPLICATIONS - telemaatikarakendused, FEMIRC Eesti (EL'i Innovatsiooniinfo keskus Eestis)

Looking back at the year 2003 / Herbert H. Payne

Index Scriptorium Estoniae

Payne, Herbert H.

2003-01-01

Eesti Raudtee juhatuse esimees ettevõttes erastamisel seatud eesmärkide - raudteetranspordi turvalisuse suurendamine, teenuse kvaliteedi parandamine ja efektiivsuse tõstmine - saavutamiseks tehtust

Promoting accessibility for disabled people using EU standardisation policy / David L. Hosking

Index Scriptorium Estoniae

Hosking, David L.

2017-01-01

Euroopa puuetega inimeste strateegiast juurdepääsetavusõiguste (tooted, teenused) aspektist ning ELi standardiseerimispoliitika osast selles ja ÜRO puuetega inimeste õiguste konventsiooni mõjust

Archaeological investigations on the site of the cistercian nunnery of st. Michael / Mauri Kiudsoo, Irita Kallis

Index Scriptorium Estoniae

Kiudsoo, Mauri

2005-01-01

2004. aasta suvel Tallinnas Suur-Kloostri 2 kinnistul toimunud kaevamistest. Leidis kinnitust hüpotees, mille kohaselt hävitati kloostri rajamisel mingi varasem asustusvorm. Arheoloogilise stratigraafia analüüsil ja fikseerimisel kasutati Edward C. Harrise koostatud stratigraafia teooria ja metoodika põhimõtteid ja nn. Harrise maatriksit

Arhitektuuriline vahendamine: kliima vs kultuur = Architectural mediations: climate vs culture / Franklin Lee, Anne Save de Beaurecueil

Index Scriptorium Estoniae

Lee, Franklin

2011-01-01

Tegelemisest Architectural Associationi 2. diplomistuudios ja büroos SUBdV keskkondlike ja kultuuriliste mõjurite duaalsusega arhitektuuris. Teemat on uuritud kolmes valdkonnas: sile vs artikuleeritud, keskkond vs ornament, kõrgtehnoloogia vs madaltehnoloogia. Architectural Association'i ja Hollandi Arhitektuuriinstituudi töötoast São Paulos 2010. a. suvel

Kvaliteedi uuringutest kvaliteediseireni / Elviine Uverskaja

Index Scriptorium Estoniae

Uverskaja, Elviine, 1948-

2009-01-01

Arvustus: Teenuse kvaliteet – raamatukogutöö tulemuslikkuse näitaja = Service quality – library perfomance indicator / Eesti Rahvusraamatukogu ; koostanud Anne Veinberg. (Eesti Rahvusraamatukogu toimetised ; 12). Tallinn, 2009.

Pilveteenuse osutamisel tekkiva õigussuhte kvalifitseerimine Eesti õiguses : [magistritöö] / Kristel Tuul ; Tartu Ülikool, õigusteaduskond ; juhendaja: Irene Kull

Index Scriptorium Estoniae

Tuul, Kristel, 1990-

2014-01-01

Pilveteenuse mõistest ja pilveteenuste liikidest, pilveteenuse osutamisel sõlmitava lepingu esemest, pilveteenuse lepingu subjektidest, pilveteenuse lepingu sisu kujunemisest, pilveteenuse lepingu sisu vastavusest litsentsi-, teenuse osutamise ja kasutuslepingu tunnustele

Business full of optimism

Index Scriptorium Estoniae

2004-01-01

Ülevaade reklaamindusest Baltimaades - ideede leidmine, töötajate professionaalsus, turu kujunemine, integreeritud turunduse teenus jm. Tabelid: Eesti ja Leedu agentuuride reiting ; Töötajate arv reklaamiagentuurides 2003

Success this year is due to past years' efforts / Layla Banks

Index Scriptorium Estoniae

Banks, Layla

2010-01-01

2009. aasta majanduskriisist. PR teenuse pakkuja A. W. Olsen & Partners, Baltic Beach Hotel Spa and Resorts ja ärikeskuste arendamisega tegeleva ettevõtte Linstow Center Management edust 2009. aastal

Serveri rentimine päästab suurest investeeringust / Enn Heinsoo

Index Scriptorium Estoniae

Heinsoo, Enn

2006-01-01

Ilmunud ka: Delovõje Vedomosti 2. aug. lk. 13. IT-outsourcing ehk IT-teenuse sisse ostmine annab ettevõttele võimaluse saada läbi oma serveriruumita ning IT-spetsialistideta, kasutades samas kõiki serveriga kaasnevaid mugavusi. Tabel: Serverit rentides võib hinnas võita kolmandiku. Vt. samas: Vladimiras Silkovas. Ühtne süsteem tagab töökindluse

[Lugejad küsivad - meie autorid vastavad] / Heino Siigur, Darja Roos, Jelizaveta Litau...[ jt.

Index Scriptorium Estoniae

2010-01-01

Ületunnitöö arvestusest, kapitali konventeerimisest ja ümberarvestamisest eurodeks, sotsiaalmaksu miinimumi maksmisest, elatise arvestamisest, teenuse osutamisest madala maksumääraga territooriumil, töötasu arvutamise viisidest

Unit Link insurance product catches on in Latvia, finally

Index Scriptorium Estoniae

2005-01-01

Lätis tuleb turule uus elukindlustuse teenus, mille kaudu on võimalik kindlustuslepinguid siduda investeerimisfondidega. Eesti, Läti ja Leedu kindlustusturust. Tabel: Eesti elukindlustus ettevõtted : Eesti mitteelukindlustus ettevõtted

Muutused lastekaitsetöös 2018. aastal / Kadi Lauri

Index Scriptorium Estoniae

Lauri, Kadi

2017-01-01

Sotsiaalhoolekande seaduse muudatustest, millega luuakse kinnise lasteasutuse teenus, ligipääs lepitusmenetlusele ning sisaldab ka muutusi süüteo toime pannud alaealiste kohtlemisel väär- ja kriminaalmenetluses

Notre Dame'i traagilised armastajad Pirita kloostri iidsete varemete vahel / Aigi Viira

Index Scriptorium Estoniae

Viira, Aigi

2003-01-01

Meelelahutustootja Comedy Productions eestvedamisel peaks etenduma 2004.a. suvel muusikal "Notre Dame de Paris" ("Jumalaema kirik Pariisis"). Lisaks sõnum "Muusikalivormi pakendatud kirjandusklassika"

Viru Vesi sai ISO sertifikaadid / Külli Kriis

Index Scriptorium Estoniae

Kriis, Külli, 1961-

2005-01-01

Ilmunud ka: Severnoje Poberezhje 23. märts lk. 4. AS Viru Vesi sai Eestis teise vee-ettevõttena veevarustuse, kanalisatsiooni ning reoveepuhastuse teenuse pakkumise alal keskkonna- ja kvaliteedijuhtimissüsteemi sertifikaadid

Mis saab Tallinna Polütehnikumist? / Sirje Tohver ; kommenteerib Mati Kask

Index Scriptorium Estoniae

Tohver, Sirje, 1948-

2000-01-01

Tallinna Polütehnikumi liitmisest Tallinna Kõrgema Tehnikakõrgkooliga. Arvamust avaldavad TPT õppealadirektor Jüri Mickfeldt ja AS Eesti Telefon IP Teenused turundusjuht Avo-Rein Tereping (TPT vilistlane, kooli nõukogu liige)

Loodushariduse mammutkongress Colombias / Aarne Tõldsepp

Index Scriptorium Estoniae

Tõldsepp, Aarne

2009-01-01

Sel suvel toimunud rahvusvahelisest matemaatika- ja loodushariduse kongressist Colombia ajaloolises sadamalinnas Cartagenas, mille peakorraldajaks oli 19 aastat tagasi Valgevenest Colombiasse emigreerunud professor Juri Orlik

Airlines itching to shuttle tourists to islands

Index Scriptorium Estoniae

2005-01-01

Soome ja Rootsi lennufirmad alustavad suvel lende Helsingist ja Stockholmist Kuressaarde. Saaremaa Laevakompanii Ventspilsi laevaliin hakkab plaanitud Mõntu sadama asemel väljuma Roomassaare sadamast

Suve kauge trummipõrin kutsub festivalidele / Mari Rebane

Index Scriptorium Estoniae

Rebane, Mari

2004-01-01

Euroopas suvel toimuvatest popmuusika festivalidest Provinssirock, Pori Jazz Festival, Midtfyns Rockfestival, Roskilde Festival, Glastonbury Festival, V Festivals, Rock Am Ring, Pepsi Sziget. Olulisematest festivalidest Eestis

Faktooring käibevahendite finantseerimise vahendina / Ivar Sikk, Kaido Kallas

Index Scriptorium Estoniae

Sikk, Ivar

2002-01-01

Faktooring on väga paindlik käibevahendite finantseerimise vahend, mis sobib kõikidele ettevõtetele, kes pakuvad või soovivad pakkuda oma kauba või teenuse ostjatele maksetähtaega. Tabelid. Joonised

Võlgade sissenõudmine rahvusvahelises äris / Jaan Õmblus

Index Scriptorium Estoniae

Õmblus, Jaan, 1971-

1996-01-01

Võlgade sissenõudmisel enamlevinud meetodid: ähvardused, vastavalt spetsialiseerunud firmade teenused, vara arestimine, võlanõuete turustamine, juriidilise kompetentsuse näitamine, vahendaja kasutamine, seaduslikud sunnimeetmed, võlgade ümbervormistamine ja juhtimisvõtete kasutamine

Wallenbergide Investor jätkab kasvustrateegiat / Olev Mait Makk

Index Scriptorium Estoniae

Makk, Olev Mait

2001-01-01

Wallenbergide kontrollitavast Rootsi investeerimisfirmast Investor, mille omanduses olevad firmad moodustavad kokku Euroopa suurima tööandja erasektoris. Investori gruppi kuuluvast ettevõttest SEB. Tabel: Investori portfellis olevad aktsiad; investori teenused tütarettevõtetele

Erakondade rahastamise õiguslik reguleering : [bakalaureusetöö] / Arne Koitmäe ; Tartu Ülikool, õigusteaduskond ; juhendaja: Kalle Merusk

Index Scriptorium Estoniae

Koitmäe, Arne, 1975-

1999-01-01

Erakonna mõiste ja funktsioonid, erakondade rahastamine: erainitsiatiiv (partei liikmemaks, liikmete lisamaksed, erakorralised maksed, annetused) ja riiklik toetus (maksusoodustused, riigi poolt osutatavad teenused, parteide riigipoolne rahastamine), erakondade tulude ja kulude kontroll ning avalikustamine, riigipoolne rahastamine

Eesti Post ei saanud laenajate tuvastamisest keelduda / Dannar Leitmaa

Index Scriptorium Estoniae

Leitmaa, Dannar, 1982-

2008-01-01

Eesti Post vastab kriitikale seoses kiirlaenuettevõtete klientide tuvastamisega, et isikutuvastamine on Eesti Posti hinnakirjaline teenus. Poliitikud nõuavad aru majandus- ja kommunikatsiooniministeeriumilt, mille haldusesse Eesti Post kuulub. Lisa: SMS Laen ärritas Eesti Posti

Välismaalasest majandusprofessori pilguheit Eestile / Douglas K. Peterson

Index Scriptorium Estoniae

Peterson, Douglas K.

2006-01-01

Eesti kiirelt arenevatest valdkondadest nagu turism, laevandus, IT- ja interneti-põhised teenused. Autor näeb ka ohte Eesti näiliselt silmipimestava majandusime jätkumisele: konkurents turismiturul, infrastruktuuride arengu aeglustumine, ühiskonna killustumine

Kliendid panid EMT alistuma / Sten-Aleks Pihlak

Index Scriptorium Estoniae

Pihlak, Sten-Aleks

2007-01-01

EMT loobus klientide reaktsiooni tõttu kavatsusest minna üle minutipõhisele kõneminutihinna kehtestamisele. Vt. samas: EMT üritas kliente veenda mitme argumendiga, kuid see ei õnnestunud; EMT teenus maksab juba praegu kõige rohkem

"Formula Student" / Malle Jürves

Index Scriptorium Estoniae

Jürves, Malle, 1950-

2008-01-01

Tehnikakõrgkooli ja tehnikaülikooli tudengite 17-liikmeline võiskond osales tänavu suvel Inglismaal Silverstone'i ringrajakompleksis peetaval tootearendusvõistlusel "Formula Student" omaehitatud vormelautoga

Meremuuseum võttis sihikule kuulsa miinilahingu kaardistamise / Marko Püüa

Index Scriptorium Estoniae

Püüa, Marko

2006-01-01

Meremuuseumi algatatud allveeuuringust, millega loodetakse päevavalgele tuua 1941. aasta suvel Soome lahes toimunud Juminda miinilahingu üksikasjad. Sisaldab skeemi : Mineeritud Soome lahe keskosa 1941. aastal

ISO sertifikaat aitab otsustada / Toomas Udu

Index Scriptorium Estoniae

Udu, Toomas

2005-01-01

Ilmunud ka: Delovõje Vedomosti : Transport i logistika 25. mai lk. 8. Teenuse kvaliteedi näitajad logistikafirmas ISO standardi alusel. Vt. samas: Eestis kasutatakse kolme kvaliteedistandardit; Kuidas mõjutada kvaliteeti läbi juhtimissüsteemi

Värske investeerija Eestis varakaim / Piret Reiljan

Index Scriptorium Estoniae

Reiljan, Piret, 1983-

2007-01-01

Vene kapitalil põhinev investeerimisühing KIT Finance Europe edestab varade mahult kõiki siinseid investeerimisühinguid ning keskendub suurklientidele. Vt. samas: KITi teenus kohalikele investeerijatele; Diagramm: Majandusnäitajad; Turuosad. Kommenteerib Rein Rätsep

Improvisatsioonil põhinev action-teater otsib Rakverest etenduseks talente / Eda Post

Index Scriptorium Estoniae

Post, Eda, 1983-

2005-01-01

A-teatri asutajad tegelevad noorteetenduse jaoks sobivate noorte näitlejate leidmisega, et suvel lavastada action-teatri vormis poolimprovisatsiooniline noortetükk. Teatritegijad Rakveres castingul "Action minu sees"

Pariisi kiri. Suvine raamatuhooaeg = A letter from Paris. Summer book season / Marek Tamm

Index Scriptorium Estoniae

Tamm, Marek, 1973-

2010-01-01

Prantsusmaal 1999. aasta suvel ilmunud raamatutest. Ka Ülemaailmsest Kultuuride Akadeemiast (Académie universelle des cultures) ja selle organisatsiooni korraldatud konverentsist "Mälu ja ajalugu" (Pariis, 1998)

Kohaliku omavalitsuse võimalused ettevõtluse arendamisel / Gert Schultz

Index Scriptorium Estoniae

Schultz, Gert

2003-01-01

Autor on seisukohal, et omavalitsus, kes on huvitatud elanikkonnale kvaliteetse teenuse pakkumisest ning laiemas mõttes elukeskkonna parandamisest, peab oma peamiseks prioriteediks pidama ettevõtlust ning eeskätt just väikeettevõtluse arendamist oma territooriumil. Tabel

Tarbijalepingute kohtualluvuse probleemid Brüsseli I määruses: milliste ohtudega peavad arvestama oma kaupu või teenuseid piiriüleselt pakkuvad ettevõtjad? / Karin Sein

Index Scriptorium Estoniae

Sein, Karin, 1974-

2014-01-01

Millal võib ühes liikmesriigis elav tarbija, kes on ostnud kauba või saanud teenuse teises liikmesriigis asuvalt ettevõtjalt, esitada ettevõtja vastu hagi oma elukohariigi kohtusse. Euroopa Kohtu lahenditest kohtuasjades Alpenhof, Mühlleitner ja Emrek

Segadus mõistetes seoses avaliku võimu ülesannetega / Nele Parrest

Index Scriptorium Estoniae

Parrest, Nele, 1978-

2014-01-01

Terminoloogilistest probleemidest avaliku võimu ülesannete määratlemisel ja võimalikest lahendustest neis süsteemi loomiseks. Mõistete kasutamisest ja korrastamise vajadusest kehtiva õiguse ja kohtupraktika põhjal. Mõisted "avalik ülesanne" ja "avalik teenus"

Kristian Taska tahab vändata lastefilmi / Neeme Korv

Index Scriptorium Estoniae

Korv, Neeme, 1974-

2003-01-01

European Film Promotion (EFP) valis K. Taska 20 lootustandva produtsendi hulka, keda Cannes'i festivalil tutvustatakse. Taska plaanib lastefilmi jõuluks ja suvel algavad thrilleri "Lilled Evale" võtted

Kroonika rokib Euroopas

Index Scriptorium Estoniae

2002-01-01

Kroonika ja Radio Sky Plus lähevad sel suvel suurele pop- ja rockifestivalituurile Euroopasse: Taani Roskilde festivalile, Belgiasse Douri festivalile, Paleo festivalile Šveitsi ja Ungarisse Pepsi Szigetile

5,5-Dimethyl-2-methylseleno-1,3,2-dioxaphosphorinan-2-one

Directory of Open Access Journals (Sweden)

Grzegorz Cholewinski

2010-04-01

Full Text Available The title compound, C6H13O3PSe, was obtained in the reaction of 5,5-dimethyl-2-oxo-2-seleno-1,3,2-dioxaphosphorinane potassium salt with methyl iodide. The selenomethyl group is in the axial position in relation to the six-membered dioxaphosphorinane ring.

Atonen ja Aaviksoo tegid eile esimese 3G kõne / Viktoria Korpan

Index Scriptorium Estoniae

Korpan, Viktoria, 1976-

2003-01-01

Majandusminister Meelis Atonen ja Eesti Mobiiltelefoni juht Peep Aaviksoo pidasid EMT tehnoloogiakeskuses esimese ametliku kõne 3G testvõrgus. Lisaks tavakõnele videokõnet ja kiiret andmesidet võimaldav teenus jõuab kommertskasutusse orienteeruvalt aastal 2005, lubas Aaviksoo

Internet nagu postiteenus / Anneli Ammas

Index Scriptorium Estoniae

Ammas, Anneli, 1962-

2004-01-01

Majandus- ja kommunikatsiooniminister Meelis Atoneni sõnul peaks Interneti-teenus muutuma sarnaseks postiteenusega, millel on ühtne hind üle Eesti. Bill Gates on huvitatud Eesti ettepanekust pakkuda Eesti kodutarbijale tarkvara tervikpaketist vaid seda osa, mida tarbija tegelikult kasutab

Urmas Ott tegutseb nüüd kirjastusrindel / Eve Heinla

Index Scriptorium Estoniae

Heinla, Eve, 1966-

2007-01-01

Mais ilmub Marie Underi luulekogu, koostajaks Urmas Ott ja suvel 2007 Neeme Järvi juubelikogumik "Viva la Musica", mille kokkupanekul on teleajakirjanik abiks. Kirjastuse SE&JS kaasomanik Sirje Endre tutvustab

Eesti keele ja kultuuri suvekursus : BALSSI 2006-BALSSI 2007 / Piibi-Kai Kivik

Index Scriptorium Estoniae

Kivik, Piibi-Kai

2007-01-01

eesti keele õpinguist Indiana Ülikoolis Bloomingtonis Balti keele ja kultuuri suvekoolis (BALSSI=Baltic Studies Summer Institute) 2006. a. suvel ja 2007. a. korraldatavast suvekoolist California Ülikoolis, Los Angeleses

Fischer matrices of Dempwolff group $2^{5}{^{cdot}}GL(5,2$

Directory of Open Access Journals (Sweden)

Ayoub Basheer Mohammed Basheer

2012-12-01

Full Text Available In cite{Demp2} Dempwolff proved the existence of a group of theform $2^{5}{^{cdot}}GL(5,2$ (a non split extension of theelementary abelian group $2^{5}$ by the general linear group$GL(5,2$. This group is the second largest maximal subgroup of thesporadic Thompson simple group $mathrm{Th}.$ In this paper wecalculate the Fischer matrices of Dempwolff group $overline{G} =2^{5}{^{cdot}}GL(5,2.$ The theory of projective characters isinvolved and we have computed the Schur multiplier together with aprojective character table of an inertia factor group. The fullcharacter table of $overline{G}$ is then can be calculated easily.

Piltsõnumid - uus massiteenus mobiilside turul? / Andrus Hiiepuu

Index Scriptorium Estoniae

Hiiepuu, Andrus, 1966-

2003-01-01

Autor analüüsib erinevaid teenuseid mobiilside turul ning tunnistab, et edu on neist saavutanud vaid kõne ja lühisõnumid. MMS teenuse levikut takistab vastava toetusega telefonide saadavus ja nende hind. Lisa: MMS (Multimedia Messaging Service)

EMT kiusab numbriga teise võrku lahkujaid / Toivo Tänavsuu

Index Scriptorium Estoniae

Tänavsuu, Toivo

2005-01-01

EMT võtab teise operaatori võrku kolida soovivatelt klientidelt võimaluse mobiiltelefoni teel kasutada nn m-parkimise teenust ja osta m-piletit, mis on EMT arendusjuhi Kuno Peegi sõnul kolmandate osapooltega seotud teenused. Lisa: Brezhnevi-kampaania oli PR-trikk?

IT-firmad pääsevad pooleks aastaks Silicon Valleysse / Holger Roonemaa

Index Scriptorium Estoniae

Roonemaa, Holger

2010-01-01

Tehnopol ja EAS toetavad nn. start-up-firmade saatmist pooleks aastaks USA-sse Silicon Valleysse kogemusi omandama, programm on mõeldud eelkõige neile ettevõtetele, kel on oma toode või teenus valmis ja kes soovivad sellega maailmaturule minna

Inessa Josing jälle fookuses

Index Scriptorium Estoniae

1999-01-01

Kunstiajakiri "Flash Art" illustreerib 1999. a. suvenumbris (nr. 207) uudist Euroopa noorte kunstnike biennaali Manifesta 3 toimumisest 2000. a. suvel Ljubljanas fotoga Inessa Josingu aknakujundusest (jõuluaken Tallinnas Viru t. teksasepoele)

Suvelõpu performance Karepal / Hannes Varblane

Index Scriptorium Estoniae

Varblane, Hannes, 1949-

2015-01-01

15. augustil 2009 Karepal Richard Sagritsa majamuuseumis toimunud performance'ist "Vana riist", milles osalesid Hannes Varblane, Jüri Ojaver, Alex Plutzer, Ilja Sundelevitš, Jaan Paavle, Üllar Saaremäe, Leonhard Lapin, väljapanekutega lisandusid Valeri Vinogradov ja Jaan Toomik. Projektijuht Teet Veispak

Suvelõpu performance Karepal / Hannes Varblane

Index Scriptorium Estoniae

Varblane, Hannes, 1949-

2009-01-01

15. augustil 2009 Karepal Richard Sagritsa majamuuseumis toimunud performance'ist "Vana riist", milles osalesid Hannes Varblane, Jüri Ojaver, Alex Plutzer, Ilja Sundelevitš, Jaan Paavle, Üllar Saaremäe, Leonhard Lapin, väljapanekutega lisandusid Valeri Vinogradov ja Jaan Toomik. Projektijuht Teet Veispak

Luzern saab uue kontserdimaja

Index Scriptorium Estoniae

1998-01-01

Mais algavad Luzerni uue kontserdisaali akustiliste jm. näitajate testkontserdid. Uuest kontserdisaalist saab ka Luzerni kuulsate rahvusvaheliste festivalide pealava nii suvel kui lihavõtte aegu. Arhitekt Jean Nouvel, akustik Russell Johnson.

Eesti tarbijate huvi 3G teenuste vastu on loid / Toivo Tänavsuu

Index Scriptorium Estoniae

Tänavsuu, Toivo

2005-01-01

Pärast EMT esimese 3G mobiilsidevõrgu avamist Tallinnas on selle teenuse kasutajate hulk kasvanud ligikaudu saja inimese võrra, 3G telefonide müük on hästi edenenud Lisa: EMT rajab 3G võrgu ka Tartusse

Staaride oma reality'd / Jaanus Noormets

Index Scriptorium Estoniae

Noormets, Jaanus

2005-01-01

Isiklikud tõsielusarjad televisioonis saavad sel suvel teiste seas endale ka poplaulja Britny Spears ("Britney and Kevin: Chaotic") ja rokkarid Bobby Brown ("Being Bobby Brown") ning Tommy Lee ("Tommy Lee Goes to Collage")

Tööpuudus hiilib kikivarvul Võrumaale / Arved Breidaks

Index Scriptorium Estoniae

Breidaks, Arved, 1975-

2008-01-01

Võrumaal on töötute arv eelmise aastaga võrreldes tõusma hakanud: mullu suvel maakonnas registreeritud 3,9%-line töötuse määr asendus tänavu juuli lõpus 5,4%-lise töötusega. Lisa: Töötus Võrumaal. Vt. samas: Kuidas iseloomustate olukorda Võrumaa tööjõuturul? Vastavad Martin Arula (AS Toftan), Kaido Mäesalu (AS Suwem), Meelis Munski (AS Semuehitus), Indrek Klampe (OÜ Selista Ehitus), Andres Visanpuu (Võru TÜ)

Loomaskulptuuride näitus Kadriorus / Aleksander Stern

Index Scriptorium Estoniae

Stern, Aleksander, 1948-

2009-01-01

2009. a suvel toimus Kadriorus Kastellaanimaja Galeriis Tallinna Loomaaia juubeliürituste raames näitus. Eksponeeriti Tallinna Loomaaias viiel korral aset leidnud Läänemeremaade animalistliku skulptuuri festivalide raames teostatud töid

Tony Blair - edukas ja ebasoosingus / Tõnis Arnover

Index Scriptorium Estoniae

Arnover, Tõnis, 1952-

2007-01-01

Tony Blairil saab suvel Suurbritannia peaministri kohal täis kümme aastat, kui ta erakonnakaaslaste korruptsiooniskandaali tõttu varem tagasi ei astu. Vt. samas: CV; Gordon Brown astub varjust välja

Kirjastamine 21. sajandil - trüki oma raamat ise / Rivo Sarapik, Andres Kütt, Stanislav Sinyagin

Index Scriptorium Estoniae

Sarapik, Rivo, 1981-

2008-01-01

Väikesetiraa̓iliste trükiste kirjastamise etappidest ja soovitusi trükifirmade valikul internetis ning erinevate inimeste kogemusi fotoraamatu või fotoajakirja trükkimisel, kasutades Blurb.com või Lulu.com teenust. Kuni väljatrükini on teenus valdavalt tasuta

Disain+juhtimine : disainjuhtimise peaauhind Eestisse / Triin Ojari

Index Scriptorium Estoniae

Ojari, Triin, 1974-

2012-01-01

Ühe 2012. a. Euroopa disainjuhtimise auhinna DME peaauhindadest sai Tallinna Transpordiameti uuendusprotsess kommunikatsiooni ja teenuse parandamiseks. Võidu taga on EKA tudengid Kristi Rummel, Brit Pavelson, Norman Orro ja Ronald Pihlapson, kes tegid seda alguses graafilise disaini osakonna 3. kursuse semestritööna

Steve Jürvetson: suureneb bioloogiateaduste tähtsus / Steve Jürvetson

Index Scriptorium Estoniae

Jürvetson, Steve, 1967-

2010-01-01

USA riskikapitalist panustaks kaugemas perspektiivis bioloogiateadustele, lähemas tulevikus on tema hinnangul perspektiivikad Internetiga seotud ärid, eelkõige tarbijaitele suunatud kaubad ja teenused. Finantskriis on ka muudatuste katalüsaator ning sektoreis, kus šokki polnud, pole eriti ka uut ettevõtlikkust

Ilmusid Rahvusraamatukogu uuenenud toimetised / Mihkel Volt

Index Scriptorium Estoniae

Volt, Mihkel

2009-01-01

Tutvustus: Ajalookirjutaja aeg = Aetas historicorum / Eesti Rahvusraamatukogu ; koostanud Piret Lotman. (Eesti Rahvusraamatukogu toimetised, nr. 11). Tallinn, 2008 ; Teenuse kvaliteet – raamatukogutöö tulemuslikkuse näitaja = Service quality – library perfomance indicator / Eesti Rahvusraamatukogu ; koostanud Anne Veinberg. (Eesti Rahvusraamatukogu toimetised ; 12). Tallinn, 2009.

Kuidas maitsevad võistlusroad? / Siiri Kirikal

Index Scriptorium Estoniae

Kirikal, Siiri, 1966-

2010-01-01

14. jaanuaril 2010 toimus KUMU kunstimuuseumi auditooriumis kokkade olümpiaks tituleeritud Bocuse d’Or 2010 Eesti kandidaadi väljaselgitamine. Suvel Genfis toimuval Bocuse d’Or Europe 2010 valikvõistlusel esindab Eestit Dmitri Rooz

Kunsti estica Rootsis ja Lätis

Index Scriptorium Estoniae

1999-01-01

Suvel hakkas Stockholmis ilmuma uus Põhjamaade kunstiajakiri "Nu", mis loodi Soome ajakirja "Siksi" ja Rootsi ajakirja "Index" ühendamisel. "NU" teises numbris "Nu" Eesti korrespondendi Harry Liivranna lühiartikkel Udo Siiast. Läti kunstiajakirjas Studija nr. 8 tutvustab Daiga Rudzate Veneetsia biennaaliga seoses Eesti ekspositsiooni, Irena Buzinska Tallinnas novembris avatavat inglise moefoto näitust. Läti kunstiajakirjas Acoustic.Space nr. 2 on Raivo Kelomehe informatsioon novembris Tallinnas toimuvast 2. meediakunsti festivalist ning Hanno Soansi videoprojekti tutvustus

3,4-Dibromo-2,2,5,5-tetraphenyl-2,5-dihydrofuran

Directory of Open Access Journals (Sweden)

Nadine Seidel

2018-04-01

Full Text Available The crystal structure of the title compound, C28H20Br2O, was solved in the orthorhombic space group P212121 with one molecule in the asymmetric unit. The phenyl rings are nearly planar and inclined at angles of 67.7 (1, 68.8 (1, 79.3 (1 and 62.3 (1° to the plane of the 2,5-dihydrofuran ring. The crystal structure features C—H...π and Br...Br interactions, which connect the molecules to a three-dimensional supramolecular network.

The 5s25p2 - (5s25p5d + 5s5p3 + 5s25p6s + 5s25p7s) transitions in Sb II and 5s25p - (5s5p2 + 5s2nl) transitions in Sb III

International Nuclear Information System (INIS)

Arcimowicz, B.; Joshi, Y.N.; Kaufman, V.

1989-01-01

The spectrum of antimony was photographed in the 575-2300 A region (1A 10 -10 m) using a hollow cathode and a triggered spark source. The analysis of the 5s 2 5p 2 - (5s 2 5p5d + 5s5p 3 + 5s 2 5p6s + 5s 2 5p7s) transitions in Sb II spectrum was revised and interpreted on the basis of multiconfiguration interaction calculations. Accurate wavelength measurements of Sb III lines lead to a revised ground-state 5s 2 5p 2 P interval value of 6574.5 cm -1 . (author). 15 refs., 9 tabs., 1 fig

Syntheses of [5-2H]-uracil, [5-2H]-cytosine, [6-2H]-uracil and [6-2H]-cytosine

International Nuclear Information System (INIS)

Kiritani, Reiko; Asano, Takeyoshi; Fujita, Shin-ichi; Dohmaru, Takaaki; Kawanishi, Tetsuro

1986-01-01

Syntheses of [5- 2 H]-, [6- 2 H]-uracil and [5- 2 H]-, [6- 2 H]-cytosine were investigated. The catalytic reaction of uracil or cytosine with 2 H 2 gas in alkaline media gave rise to [6- 2 H]-compounds almost exclusively. On the other hand, the reaction of 5-bromouracil or 5-bromocytosine with 2 H 2 gas gave rise to a mixture of [5- 2 H]-, [6- 2 H]- and [5- 2 H, 6- 2 H]-compounds depending on the experimental conditions. By controlling the temperature, the pressure of 2 H 2 gas and the amount of catalyst, [5- 2 H]-uracil and [5- 2 H]-cytosine were obtained. The isotopic distribution in each product was measured by 1 H NMR spectroscopy combined with an HPLC method. (author)

Activation of SO2 with [(η(5) -C5 Me5 )2 Ln(THF)2 ] (Ln=Eu, Yb) leading to dithionite and sulfinate complexes.

Science.gov (United States)

Klementyeva, Svetlana V; Gamer, Michael T; Schmidt, Anna-Corina; Meyer, Karsten; Konchenko, Sergey N; Roesky, Peter W

2014-10-13

The reaction of decamethylytterbocene [(η(5) -C5 Me5 )2 Yb(THF)2 ] with SO2 at low temperature gave two new compounds, namely, the Yb(III) dithionite/sulfinate complex [{(η(5) -C5 Me5 )2 Yb(μ3 ,1κ(2) O(1,3) ,2κ(3) O(2,2',4) -S2 O4 )}2 {(η(5) -C5 Me5 )Yb(μ,1κO,2κO'-C5 Me5 SO2 )}2 ] (1) and the Yb(III) dithionite complex [{(η(5) -C5 Me5 )2 Yb}2 (μ,1κ(2) O(1,3) ,2κ(2) O(2,4) -S2 O4 )] (2). After extraction of 1, the mixture was heated to give the dinuclear tetrasulfinate complex [{(η(5) -C5 Me5 )Yb}2 (μ,κO,κO'-C5 Me5 SO2 )4 ] (3 a). In contrast, from the reaction of [(η(5) -C5 Me5 )2 Eu(THF)2 ] with SO2 only the tetrasulfinate complex [{(η(5) -C5 Me5 )Eu}2 (μ,κO,κO'-C5 Me5 SO2 )4 ] (3 b) was isolated. Two major reaction pathways were observed: 1) reductive coupling of two SO2 molecules to form the dithionite anion S2 O4 (2-) ; and 2) nucleophilic attack of one metallocene C5 Me5 ligand on the sulfur atom of SO2 . The compounds presented are the first dithionite and sulfinate complexes of the f-elements. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

F.F.F.F. / Pille Väljataga

Index Scriptorium Estoniae

Väljataga, Pille

2001-01-01

Rühmituse F.F.F.F. (Berit Teeäär, Maria Valdma, Ketli Tiitsar, Kaire Rannik, Kristi Paap) esinemisest 2000. a. suvel Leedus Niida kunstnike majas. Ehteid eksponeeriti kõrvuti nende 20-kordse suurendusega fotodega.

Bernard Kangro preemia anti esimest korda näidendite eest / Liina Valper

Index Scriptorium Estoniae

Valper, Liina, 1941-

2006-01-01

3. oktoobril andis Võru maavanem Ülo Tuulik kirjanik Jan Rahmanile üle tänavuse Bernhard Kangro preemia. Esimest korda anti kirjandusauhind näidendite, sel suvel esietendunud võrukeelsete lavalugude "Painaja" ja "Sõit" eest

Bioloogiahuvi viis noored Bali saarele / Uku-Laur Tali

Index Scriptorium Estoniae

Tali, Uku-Laur, 1992-

2015-01-01

2014. aasta suvel Indoneesias rahvusvahelisel bioloogiaolümpiaadil esindas Eestit võistkond kosseisus Enna Elismäe ja Uku-Kaspar Uustalu (Tallinna Reaalkool), Siim Kurvits (Hugo Treffneri Gümnaasium) ning Riin Viigipuu (Kärdla Gümnaasium)

Nii ungarlane kui eestlane / Urmas Bereczki ; interv. Livia Viitol

Index Scriptorium Estoniae

Bereczki, Urmas, 1957-

2001-01-01

Intervjuu ajaloolase ja keraamiku, Ungari Instituudi direktori Urmas Bereczkiga, kes on sündinud Eestis ja kelle ema on eestlane. 2001. a. suvel Tallinna Kunstihoones Ungari Instituudi üritusena ungari kaasaegse kunsti ülevaatenäitus

10 CFR 960.5-2-5 - Environmental quality.

Science.gov (United States)

2010-01-01

... 10 Energy 4 2010-01-01 2010-01-01 false Environmental quality. 960.5-2-5 Section 960.5-2-5 Energy... REPOSITORY Preclosure Guidelines Environment, Socioeconomics, and Transportation § 960.5-2-5 Environmental... repository siting, construction, operation, closure, and decommissioning, and projected environmental impacts...

Nii võiks alata demokraatia lõpp / Tõnis Tõnisson

Index Scriptorium Estoniae

Tõnisson, Tõnis, 1945-

2005-01-01

Justiitsministeeriumis välja töötatud seaduseelnõust, mille eesmärgiks on piirata laimava või solvava sisuga internetikommentaare (elektroonilise side seaduse, infoühiskonna teenuse seaduse, jälitustegevuse seaduse, karistusseadustiku, kriminaalmenetluse seadustiku ja väärteomenetluse seadustiku muutmise seaduse eelnõu)

PÖFFi "Just Filmi" festival näitab suvekino

Index Scriptorium Estoniae

2002-01-01

Detsembris toimuvat Pimedate Ööde Filmifestivali laiendatakse ka suvele, et sobivates paikades näidata väärtfilme. Alates 6. juunist pakub PÖFFi laste- ja noortefilmide festival "Just Film" Nukuteatri suveõuel noortefilmide programmi

Lossi hoovis mälestati veretöö ohvreid / Veljo Kuivjõgi

Index Scriptorium Estoniae

Kuivjõgi, Veljo, 1951-

2006-01-01

Endel Püüa raamatu "Punane terror Saaremaal 1941. aastal" (Saaremaa : Saaremaa Muuseum, 2006) esitlusest ja mälestuspäevast, mis oli pühendatud kõigile ohvritele, kes hukati 1941. aasta suvel Kuressaare lossi hoovis

Rüütel tahab laulupidusid UNESCO maailmapärandisse

Index Scriptorium Estoniae

2003-01-01

Nimekiri 2003. aasta kevad-suvel toimunud laulupidusid, laulupäevi, laulupühasid jt. nimesid kandvatest muusikapäevadest. President Arnold Rüütel soovis kohtumisel UNESCO peadirektori Koichiro Matsuuraga, et laulupidude traditsioon kantaks UNESCO maailmapärandisse

Ehitusel käib pingeline töö tuisus ja tormis / Kristiina Viiron

Index Scriptorium Estoniae

Viiron, Kristiina, 1971-

2006-01-01

Ehitustööd pole enam seotud aastaajaga; nii Haapsalu Uksetehase AS, AS Lasita Aken kui ka AS Columbia Kivi valmistavad toodangut umbes samas koguses kui suvel. Ehitusmaterjalide tootmismahud on kasvanud umbes 20%. Lisa: Pausi nõuab tehnoloogia

Inglased küsisid FC Flora mängija ostmise eest Pohlakult altkäemaksu / Aivar Pohlak ; interv. Andrus Allika

Index Scriptorium Estoniae

Pohlak, Aivar, 1962-

2002-01-01

Londoni Everton pakkus läinud suvel Mart Poomi eest Derbyle viis miljonit Inglise naela. Intervjuu FC Flora presidendiga. Vt. samas ka art. "Derby peatreeneril lasub kahtlustus pistise võtmises. Lisa: Maailma kõige kallimad väravavahid

Kuulsused maitsevad Malaisias Robinsoni elu / Tarmo Michelson

Index Scriptorium Estoniae

Michelson, Tarmo, 1975-

2004-01-01

Telesaatetootja Ruut kavatseb suvel Malaisias vändata tõsielusarja, mille eeskujuks on Inglismaal ülimenukas "Olen kuulsus - laske mind siit välja". Eesti tuntud inimesed ütlevad välja oma arvamuse taolises projektis osalemise kohta

ETV katuse all keedeti salaseepi / Tiina Jõgeda

Index Scriptorium Estoniae

Jõgeda, Tiina, 1962-

2011-01-01

Rahvusringhäälingu (ERR) tootmisteenistuse juhataja Janno-Hans Arro, kes seoses pettustega vallandati augustis ERR-ist, valmistas mitu aastat ette suurejoonelist kodumaist teleseriaali. Seriaali filmiti sel suvel Madeiral. Põhjendustest, miks ETV seda ära osta ei taha

Homme algab Eesti festivalisuvi / Priit Pruul

Index Scriptorium Estoniae

Pruul, Priit

2006-01-01

Suvel Eestis toimuvatest muusikafestivalidest Rabarock 2006, Maailmaküla (muusikafestival), Hard Rock Laager 2006 (vabaõhufestival), Juu Jääb 2006 (retromuusikafestival), Sun Dance Music Festival, Plink Plonk (sõltumatu muusika festival), Viljandi pärimusmuusika festival 2006

Edukas outsourcing ehk iga keti tugevuse määrab tema nõrgim lüli / Riho Sarv

Index Scriptorium Estoniae

Sarv, Riho

2007-01-01

Tänapäeva ettevõtete edukuse aluseks on spetsialiseerumine ühele kindlale tegevusalale. Outsourcing ehk väljasttellimine on ettevõtte põhitegevust toetavate teenuste sisseostmine maksimaalse tulemuse saavutamiseks, konkreetne töölõik või projekt delegeeritakse teenuse pakkujale. Lisa: Olulisemad väljasttellimise kasutamise eelised

Lood erilistest inimestest / Erkki Luuk

Index Scriptorium Estoniae

Luuk, Erkki, 1971-

2002-01-01

Detsembris toimuvat Pimedate Ööde Filmifestivali on laiendatud ka suvele. Alates 6. juunist näidati Katariina kirikus kuuel õhtul Werner Herzogi (1942) filme. Režissöörist, tema lemmiknäitlejast Klaus Kinskist ja filmidest

Probleemtooted vajavad registreerimist / Peeter Eek

Index Scriptorium Estoniae

Eek, Peeter, 1963-

2006-01-01

2005. aasta suvel jäätmeseadusse tehti täiendus, millega nähti ette probleemtoodete registri loomine. Eelnõu kinnitati Vabariigi Valitsuse määrusena jaanuaris 2006. Tänased turuosalised on kohustatud ennast registreerima kas eraldi või kollektiivselt ehk nn. tootjavastutusorganisatsioonide (TVO) kaudu. Ilmunud ka Lääne Elu : Keskkonnaleht 18. märts 2006, lk. 3 ; Vooremaa 21. märts 2006, lk. 5 ; Koit : Keskkond 28. märts 2006, lk. 15 - 16 ; Järva Teataja : Järvamaa Keskkond 13. aprill 2006, lk. 3 ; Virumaa Teataja : Roheline Maakond 4. mai 2006, lk. 2 ; Võrumaa Teataja : Võrumaa Keskkonnaleht 25. mai 2006, lk. 3 ; Nädaline : Keskkonnaleht 23. sep. 2006, lk. 8 ; Hiiu Leht : Hiiumaa Looduse Leht 19. Dets. 2006, lk. 1

Värsked õpipoisid / Indrek Treufeldt

Index Scriptorium Estoniae

Treufeldt, Indrek, 1969-

2004-01-01

Euroopa Komisjoni kümme uut volinikku asuvad esialgu praeguste ametnike juures õppima protseduurireegleid ja vähem probleemide sisulist lahendamist. Kuna uus Euroopa Komisjon alustab sügisel, tuleb suvel selgeks vaielda, kes saab Romano Prodi järeltulijaks

Werner Herzogi üksiklased / Kristiina Davidjants

Index Scriptorium Estoniae

Davidjants, Kristiina, 1974-

2002-01-01

Detsembris toimuvat Pimedate Ööde Filmifestivali laiendatakse ka suvele, et sobivates paikades näidata väärtfilme. Alates 6. juunist näidatakse Katariina kirikus Werner Herzogi (1942) filme. Lähemalt režissöörist

Õhtumaa allakäik / Margit Tõnson

Index Scriptorium Estoniae

Tõnson, Margit, 1978-

2010-01-01

Eestlaste kaasosalusel vändatud režissöör Chris Krausi filmist "Polli päevikud" (Saksa-Austria-Eesti 2010). Suurem osa "Polli päevikutest" filmiti 2009. a. suvel Pärnumaal Varbla vallas. Muusika autor Annette Focks

Vene raha päästis Sedini kinnisvara / Anne Oja

Index Scriptorium Estoniae

Oja, Anne, 1970-

2008-01-01

Vene ärimehed ostsid Pjotr Sedinilt enamuse Lutheri kvartalit arendava firma aktsiapakis ning tasusid Swedbankile juba lootusetuks tembeldatud võla. Vt. samas: Grove Investi kinnistud müüdi maha suvel. Diagramm: Uute omanike käes pool Grove Investist

Hiinlased tahavad ehitada Ringtee silda

Index Scriptorium Estoniae

2007-01-01

2007. a. suvel kohtusid Tartu linnajuhtidega Shangai projekteerimisfirma Lin Tung-Yen & Li Guo-Hao Consultants Ltd ja Jiangsu provintsist pärit ehitusfirma Jiangyn Bridge Engineering Ltd esindajad, et esitada oma nägemus Tartusse planeeritavast Ringtee sillast. Anto Ili kommentaar

Uurimine paljastas Iisraeli suvesõja vead / Liisi Poll

Index Scriptorium Estoniae

Poll, Liisi, 1980-

2008-01-01

Iisraeli koostatud raporti järgi sai Iisraeli armee 2006. aasta suvel lüüa poolmilitaarse Liibanoni Hezbollahþ käest, uurimuses on viidatud vigadele ja väärtushinnangutele, mis sõjani viisid. Lisa: 2006. aasta suvesõda

Eesti meetod konkurentsivõime kaotamiseks / Kadri Kristjuhan

Index Scriptorium Estoniae

Kristjuhan, Kadri

2003-01-01

Deloitte & Touche poolt 2002. a. suvel läbi viidud tootmisuuringust, mis toob välja Eesti juhtide harjumatuse arvestada teiste töötajate ettepanekutega. Diagramm: 12% Eesti tööandjatest ei kuula oma töötajate ettepanekuid

Observation of the strongest 5s2 5p6 5d-(5s2 5p5 5d6s+5s25p6 7p) transitions in Au XI to Bi XV ions

International Nuclear Information System (INIS)

Churilov, S.S.; Joshi, Y.N.

2001-01-01

The spectra of gold till bismuth were studied in the 90-135 A region. Nine most intense lines belonging to the 5s 2 5p 6 5d-5s 2 5p 5 5d6s array were identified in Au XI to Bi XV ions. The 5s 2 5p 6 7p 2 P 3/2,1/2 levels in Au XI and the 5s 2 5p 6 7p 2 P 3/2 level in Hg XII were also identified. The observed wavelengths and intensities agree quite well with the Hartree-Fock calculations. (orig.)

Deliktiõiguslik vastutus teise isiku tekitatud kahju eest / Tambet Tampuu

Index Scriptorium Estoniae

Tampuu, Tambet, 1963-

2003-01-01

VÕS-s reguleeritud deliktiõiguslikust vastutusest: teenuse kasutaja vastutusest (ʹ 1054), alla 14-aastase isiku ja 14-18-aastase isiku vastutusest (ʹ 1053), eestkostja vastutusest vaimse puudega isiku eest (ʹ1053), kohustusliku vastutuskindlustuse andja vastutusest kindlustusvõtja tekitatud kahju eest ning juriidilise isiku vastutusest oma organi liikme tekitatud kahju eest

EMT kasvatab rate.ee-ga uusi kliente / Piret Reiljan

Index Scriptorium Estoniae

Reiljan, Piret, 1983-

2007-01-01

Suhtlusportaal rate.ee on olnud EMT jaoks edukas projekt ning ettevõtte juht Valdo Kalm peab tõstatatud eetikaküsimusi ebaõiglaselt esitatuks, sest rate.ee on tema sõnul teiste veebikanalitega võrreldes üks filtreeritumaid. Vt. samas: Mis on rate.ee; EMT loodud rate-mobiili teenused ja hinnakiri

Maydellide järeltulija teeb filmi oma juurtest / Maire Kõrver

Index Scriptorium Estoniae

Kõrver, Maire, 1961-

2009-01-01

Eestis, sh Raplamaal viibis Hollandis Haarlemi ülikoolis teletööd õppiv Maydellide järeltulija Sarah Albert, kes teeb koolitööna dokumentaalfilmi oma juurtest. Külaskäigust vanas mõisahoones asuvasse Maidla lastekodusse, Teenuse mõisa, Kullamaa kirikusse ja kalmistule ning Päri mõisa

Polarization dependence of double-resonance optical pumping and electromagnetically induced transparency in the 5S1/2-5P3/2-5D5/2 transition of 87Rb atoms

International Nuclear Information System (INIS)

Moon, Han Seb; Noh, Heung-Ryoul

2011-01-01

The polarization dependence of double-resonance optical pumping (DROP) in the ladder-type electromagnetically induced transparency (EIT) of the 5S 1/2 -5P 3/2 -5D 5/2 transition of 87 Rb atoms is studied. The transmittance spectra in the 5S 1/2 (F=2)-5P 3/2 (F'=3)-5D 5/2 (F''=2,3,4) transition were observed as caused by EIT, DROP, and saturation effects in the various polarization combinations between the probe and coupling lasers. The features of the double-structure transmittance spectra in the 5S 1/2 (F=2)-5P 3/2 (F'=3)-5D 5/2 (F''=4) cycling transition were attributed to the difference in saturation effect according to the transition routes between the Zeeman sublevels and the EIT according to the two-photon transition probability.

2′-deoxy-5,6-dihydro-5-azacytidine—a less toxic alternative of 2′-deoxy-5-azacytidine

Science.gov (United States)

Matoušová, Marika; Votruba, Ivan; Otmar, Miroslav; Tloušťová, Eva; Günterová, Jana

2011-01-01

Restoration of transcriptionally silenced genes by means of methyltransferases inhibitors plays a crucial role in the current therapy of myelodysplastic syndromes and certain types of leukemias. A comparative study of hypomethylating activities of a series of 5-azacytidine nucleosides: 5-azacytidine (AC), 2′-deoxy-5-azacytidine (DAC) and its α-anomer (α-DAC), 5,6-dihydro-5-azacytidine (DHAC), 2′-deoxy-5,6-dihydro-5-azacytidine (DHDAC, KP-1212) and its α-anomer (α-DHDAC), and of a 2-pyrimidone ribonucleoside (zebularine) was conducted. Methylation-specific PCR was employed to detect the efficiency of individual agents on cyclin-dependent kinase inhibitor 2B and thrombospondin-1 hypermethylated gene loci. Overall changes in DNA methylation level were quantified by direct estimation of 5-methyl-2′-deoxycytidine-5′-monophosphate by HPLC using digested genomic DNA. Flow cytometric analysis of cell cycle progression and apoptotic markers was used to determine cytotoxicity of the compounds. mRNA expression was measured using qRT-PCR. 2′-deoxy-5,6-dihydro-5-azacytidine was found to be less cytotoxic and more stable than 2′-deoxy-5-azacytidine at the doses that induce comparable DNA hypomethylation and gene reactivation. This makes it a valuable tool for epigenetic research and worth further investigations to elucidate its possible therapeutic potential. PMID:21566456

Seisukorrast Internatsionaalse Sõjakooli Eesti osakonnas / Aleksander Rupasov; vene keelest tõlkinud Tiit Noormets

Index Scriptorium Estoniae

Rupasov, Aleksander, 1960-

2015-01-01

Petrogradis töötanud Ühendatud Internatsionaalsest Sõjakoolist, kus kooli ülema ja komissari ametikohal töötas eestlane Aleksander Inno. Lisatud publitseeritud dokumendid Ajaloolis-poliitiliste Dokumentide Riiklikust Keskarhiivist Sankt-Peterburis valgustavad olukorda Ühendatud Internatsionaalses Sõjakoolis 1921. aasta suvel

Kirev suvelõpp Tallinna galeriides / Ants Juske

Index Scriptorium Estoniae

Juske, Ants, 1956-2016

2008-01-01

Lola Liivati näitus "Kogu" Tallinna Kunstihoone galeriis ja näitus "Kulg" Viinistu kunstikeskuses. Vano Allsalu "Öine Ikaros" Vaala galeriis. Soome kunstniku Ossi Pirkoneni näitus "In the Valley" Soome Instituudis

Rannus mängitakse suvel Barbara lugu

Index Scriptorium Estoniae

2007-01-01

Augustis on Rannus näitlejate ja näitejuhtide suvekool, mille tipphetk on ühine vabaõhuetendus "Barbara lugu", lavastajaks Jüri Lumiste. Artiklis ka lühidalt Barbara von Tiesenhuseni, kes oli Rannu lossi Tiesenhusenite 12 lapsest noorim, saatusest

Tuljakus on sarikapidu peetud, avamine juba suvel

Index Scriptorium Estoniae

2015-01-01

Ettevõte Baltek Arendus restaureerib lillepaviljoni kõrval asuva söögikoha, mis 1990. aastate alguses kandis nime Carina, võimalikult algupärasel kujul, nii nagu selle kohviku Tuljak nime all kavandas 1965. aastal tunnustatud arhitekt Valve Pormeister

Reaction of ether and thioether functionalised 1-alkenes with the cationic permethylzirconocene olefin polymerisation catalyst [(eta(5)-C5Me5)(2)ZrMe](+). Molecular structure of the insertion product [(eta(5)-C5Me5)(2)ZrCH2CH(Me)CH2OEt](+)

NARCIS (Netherlands)

Bijpost, Erik A; Zuideveld, Martin A.; Meetsma, Auke; Teuben, Jan H

1998-01-01

Reaction of [(η5-C5Me5)2ZrMe][MeB(C6F5)3] (1) with (thio)ether functionalised alkenes: 3-ethoxy-1-propene and 3-(methylthio)-1-propene gives stable insertion products [(η5-C5Me5)2ZrCH2CH(Me)CH2XR][MeB(C6F5)3] (2: X = O, R = Et; 3: X = S, R = Me) in which the (thio)ether function is intramolecularly

Energy, fine structure, and hyperfine structure of the core-excited states 1s2s2pnp 5P (n = 2-5) and 1s2p2mp 5S (m = 2-5) for Li- ion

International Nuclear Information System (INIS)

Wang, Z.B.; Gou, B.C.; Chen, F.

2006-01-01

The relativistic energies, the oscillator strength, and the lifetimes of high-lying core-excited states 1s2s2pnp 5 P (n=2-5) and 1s2p 2 mp 5 S 0 (m=2-5) of Li - ion are calculated with the saddle-point variational method and restricted variation method. The fine structure and the hyperfine structure of the core-excited states for this system are also explored. The results are compared with other theoretical and experimental data in the literature. The energy obtained in this work are much lower than the others previously published whereas the wavelengths and radiative life-times are in agreement

See keeruline Internet / Anu Uritam

Index Scriptorium Estoniae

Uritam, Anu, 1972-

2008-01-01

Võlaõigusseaduse sätete kohaldamisest ja infoühiskonna teenuse seadusest. Euroopa inimõiguste ja põhivabaduste konventsiooni ja Euroopa Nõukogu Ministrite Komitee seisukohtadest. Vastukaja artiklile: Liiv, Ele. Väljendusvabaduse ja üldiste isikuõiguste konflikt veebipäevikute ja -foorumite näitel // Juridica, 2008, nr. 7, lk. 473-481

Comparison of the one-electron oxidations of CO-bridged vs unbridged bimetallic complexes: Electron-transfer chemistry of Os2Cp2(CO)4 and Os2Cp∗2(μ-CO)2(CO)2 (Cp = η5-C5H5, Cp∗ = η5-C5Me5)

KAUST Repository

Laws, Derek R.

2014-09-22

The one-electron oxidations of two dimers of half-sandwich osmium carbonyl complexes have been examined by electrochemistry, spectro-electrochemistry, and computational methods. The all-terminal carbonyl complex Os2Cp2(CO)4 (1, Cp = η5-C5H5) undergoes a reversible one-electron anodic reaction at E1/2 = 0.41 V vs ferrocene in CH2Cl2/0.05 M [NBu4][B(C6F5)4], giving a rare example of a metal-metal bonded radical cation unsupported by bridging ligands. The IR spectrum of 1+ is consistent with an approximately 1:1 mixture of anti and gauche structures for the 33 e- radical cation in which it has retained all-terminal bonding of the CO ligands. Density functional theory (DFT) calculations, including orbital-occupancy-perturbed Mayer bond-order analyses, show that the highest-occupied molecular orbitals (HOMOs) of anti-1 and gauche-1 are metal-ligand delocalized. Removal of an electron from 1 has very little effect on the Os-Os bond order, accounting for the resistance of 1+ to heterolytic cleavage. The Os-Os bond distance is calculated to decrease by 0.10 å and 0.06 å as a consequence of one-electron oxidation of anti-1 and gauche-1, respectively. The CO-bridged complex Os2Cp∗2(μ-CO)2(CO)2 (Cp∗ = η5-C5Me5), trans-2, undergoes a more facile oxidation, E1/2 = -0.11 V, giving a persistent radical cation shown by solution IR analysis to preserve its bridged-carbonyl structure. However, ESR analysis of frozen solutions of 2+ is interpreted in terms of the presence of two isomers, most likely anti-2+ and trans-2+, at low temperature. Calculations show that the HOMO of trans-2 is highly delocalized over the metal-ligand framework, with the bridging carbonyls accounting for about half of the orbital makeup. The Os-Os bond order again changes very little with removal of an electron, and the Os-Os bond length actually undergoes minor shortening. Calculations suggest that the second isomer of 2+ has the anti all-terminal CO structure. (Figure Presented) © 2014 American

Bis(tetramethylcyclopentadienyl)titanium chemistry. Molecular structures of [(C(5)HMe(4))(mu-eta(1) : eta(5)-C(5)Me(4))Ti](2) and [(C(5)HMe(4))(2)Ti]N-2(2)

NARCIS (Netherlands)

deWolf, JM; Blaauw, R; Meetsma, A; Teuben, JH; Gyepes, R; Varga, [No Value; Mach, K; Veldman, N; Spek, AL

1996-01-01

Thermolysis of bis(tetramethylcyclopentadienyl)-stabilized titanium(III) compounds (C(5)HMe(4))(2)TiR (R = Me (2), Ph (3)) yields, in marked contrast with the bis(pentamethylcyclopentadienyl) analog, the dimeric product [(C(5)HMe(4))(mu-eta(1):eta(5)-C(5)Me(4))Ti](2) (4), With a bridging metalated

10 päeva Otepää väikejärvedel / Teet Krause

Index Scriptorium Estoniae

Krause, Teet, 1960-

2013-01-01

Eesti Maaülikooli kalastikuseirajad uurisid 2013. a suvel Otepää kandi 16 väikejärve kalavarusid. Huvipakkuvaks harrastuskalastajale tunnistati Mõrtsuka järv, Päidla Suurjärv, Pilkuse järv, Jaanuse järv, Restu paisjärv

"Polli päevikud" ei vaimusta kriitikuid / Kaarel Kressa

Index Scriptorium Estoniae

Kressa, Kaarel, 1983-

2010-01-01

Eestlaste kaasosalusel vändatud režissöör Chris Krausi filmi "Polli päevikud" vastuvõtust Toronto rahvusvahelisel filmifestivalil. Kriitik Dan Fainaru arvamusest. Suurem osa "Polli päevikutest" filmiti 2009. a. suvel Pärnumaal Varbla vallas. Meespeaosalist kehastab Tambet Tuisk

Mies kahes muuseumis korraga / Maria-Kristiina Soomre

Index Scriptorium Estoniae

Soomre, Maria-Kristiina, 1978-

2001-01-01

2001. a. suvel avab New Yorgi Museum of Modern Art arhitekt Ludwig Mies van der Rohe algusaastate tööle keskenduva näituse "Mies in Berlin" ja Whitney Museum of American Art arhitekti ameerika perioodi kajastava näituse "Mies in America".

Norma kasumlikkus kahanes / Annika Matson

Index Scriptorium Estoniae

Matson, Annika, 1976-

2005-01-01

Autodele turvavöösid tootva Norma ärikasum oli kolmandas kvartalis 23,7 miljonit krooni, mis on ligi viiendiku võrra vähem kui eelmisel aastal samal ajal. Diagramm. Vt. samas: Rootsi analüütik ennustas suvel Norma ülevõtmist

OXIDATIVE ALKYLATION OF (ETA-5-C5ME5)2TIR (R=CL, ME, ET, CH=CH2, PH, OME, N=C(H)TERT-BU) TO (ETA-5-C5ME5)2TI(ME)R BY GROUP-12 ORGANOMETALLIC COMPOUNDS MME2

NARCIS (Netherlands)

LUINSTRA, GA; TEUBEN, JH

1991-01-01

Oxidative alkylation of Cp*2TiX (Cp*: eta-5-C5Me5; X = OMe, Cl, N = C(H)tBu) and Cp*2TiMe by CdMe2 or ZnMe2 gives diamagnetic Cp*2Ti(Me)X and Cp*2TiMe2 respectively, and cadmium or zinc. The reactions of Cp*2TiR (R = Et, CH = CH2, Ph) with MMe2 (M = Cd, Zn) give statistical mixtures of Cp*2Ti(Me)R,

Tootedisaineri töö peenmehaanika ja olemise jaatus / Ene Läkk

Index Scriptorium Estoniae

Läkk, Ene, 1957-

2011-01-01

Tootjate ja riskikapitalistide huvist tootedisaineri teenuse vastu. Eesti disainibüroodest MaDis-Stuudio (Matti Õunapuu), Ten Twelve (asutaja: Jukka Halttunen), Keha3 (Margus Triibmann, Tarmo Luisk, Pavel Sidorenko, juht: Ville Jehe) ja Iseasi (Martin Pärn, Sven Sõrmus, Edina Dufala-Pärn, Pent Talvet, Kaspar Torn), pakutavatest teenustest ja töödest

Uusaastatervitus mitmelt monopolilt! / Peeter Tammistu

Index Scriptorium Estoniae

Tammistu, Peeter, 1953-

2011-01-01

AS Veolia on jätnud Tallinnas prügikonteinereid tühjendamata, põhjendades seda teede läbimatusega. Autor märgib, et kuna linn on andnud prügiveo ainuõiguse monopolile, pole tal ka võimalust teenusepakkujat vahetada, ning kui linnavõim ei tule toime monopoli ohjeldamisega, siis lasku teenus vabaks

Esma Auto ja Mazda on loodud kestma

Index Scriptorium Estoniae

2003-01-01

Ülevaade olulisematest sündmustest Esma Auto kümne tegevusaasta jooksul. Kommenteerivad Tarmo Järvoja, Mart Laar ja Enn Sau. Diagrammid ja skeemid: AS Esma Auto müügi statistika läbi aastate; AS Esma Auto kasum ja klientide arv aastate lõikes; Esma Auto esindused Eestis ja pakutavad teenused

Thermal and electrical properties of 60V2O5–5P2O5–(35− x) B2O3 ...

Indian Academy of Sciences (India)

The samples of composition 60V2O5–5P2O5–(35−)B2O3–CeO2, = 1, 2, 3, 4 and 5 mol% were prepared by the melt-quench method. The prepared samples were characterized by X-ray diffraction, thermogravimetric-differential thermal analysis and impedance spectroscopy. The activation energies were evaluated ...

(2,4-Dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylato-κ2O4,O5(4-oxido-2-oxo-1,2-dihydropyrimidine-5-carboxylato-κ2O4,O5bis(1,10-phenanthroline-κ2N,N′yttrium(III dihydrate

Directory of Open Access Journals (Sweden)

Zilu Chen

2008-09-01

Full Text Available In the title compound, [Y(C5H2N2O4(C5H3N2O4(C12H8N22]·2H2O, the YIII ion lies on a twofold rotation axis and exhibits a distorted square-antiprismatic coordination geometry. It is chelated by two 1,10-phenanthroline ligands, a 2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate monoanion and a 4-oxido-2-oxo-1,2-dihydropyrimidine-5-carboxylate dianion. The H atom involved in an N—H...N hydrogen bond between the 1,2-dihydropyrimidine units has half occupancy and is disordered around a twofold rotation axis.

THE DECEPTIVELY SIMPLE THERMOLYSIS OF TRIVALENT PERMETHYLTITANOCENE DERIVATIVES (ETA-5-C5ME5)2TIR - FORMATION OF A TETRAMETHYLFULVENE TITANIUM COMPOUND (ETA-6-C5ME4CH2)(ETA-5-C5ME5)TI AND RH, CATALYZED BY PERMETHYLTITANOCENE HYDRIDE, (ETA-5-C5ME5)2TIH

NARCIS (Netherlands)

LUINSTRA, GA; TEUBEN, JH

1992-01-01

The complexes Cp*2TiR (Cp* = eta-5-C5Me5; R = Me, Et, n-Pr, C2H3, CH2CMe3, Ph) undergo thermolysis to yield the fulvene complex Cp*FvTi (Fv = eta-6-C5Me4CH2) and RH. Kinetic measurements and deuterium labeling studies show that the decomposition is catalyzed by Cp*2TiH, which is formed either by

Synthesis and chemistry of the open-cage cobaltaheteroborane cluster [{(η(5)-C5Me5)Co}2B2H2Se2]: a combined experimental and theoretical study.

Science.gov (United States)

Barik, Subrat Kumar; Dorcet, Vincent; Roisnel, Thierry; Halet, Jean-François; Ghosh, Sundargopal

2015-08-28

Reaction of [(η(5)-C5Me5)CoCl]2 with a two-fold excess of [LiBH4·thf] followed by heating with an excess of Se powder produces the dicobaltaselenaborane species [{(η(5)-C5Me5)Co}2B2H2Se2], , in good yield. The geometry of resembles a nido pentagonal [Co2B2Se2] bipyramid with a missing equatorial vertex. It can alternatively be seen as an open cage triple-decker cluster. Isolation of permits its reaction with [Fe2(CO)9] to give heterometallic diselenametallaborane [{(η(5)-C5Me5)Co}Fe(CO)3B2H2Se2], . The geometry of is similar to that of with one of the [(η(5)-C5Me5)Co] groups replaced by the isolobal, two-electron fragment [Fe(CO)3]. Both new compounds have been characterized by mass spectrometry, and by (1)H, (11)B and (13)C NMR spectroscopy. The structural architectures have been unequivocally established by crystallographic analysis. In addition, density functional theory calculations were performed to investigate the bonding and electronic properties. The large HOMO-LUMO gaps computed for both clusters are consistent with their thermodynamic stability. Natural bond order calculations predict the absence of metal-metal bonding interaction.

2-Amino-5-bromopyridinium 2-hydroxybenzoate

Directory of Open Access Journals (Sweden)

Ching Kheng Quah

2010-08-01

Full Text Available In the title compound, C5H6BrN2+·C7H5O3−, the 2-amino-5-bromopyridinium cation and 2-hydroxybenzoate anion are essentially planar with maximum deviations of 0.020 (1 and 0.018 (2 Å, respectively. The anion is stabilized by an intramolecular O—H...O hydrogen bond, which generates an S(6 ring motif. In the crystal, the cations and anions are linked by N—H...O hydrogen bonds into chains propagating along [010]. The chains contain R22(8 ring motifs. The structure is further stabilized by π–π stacking interactions [centroid–centroid distances = 3.4908 (10 and 3.5927 (10 Å] and also features short Br...O contacts [2.9671 (13 Å].

Thermochemical study of 2,5-dimethyl-3-furancarboxylic acid, 4,5-dimethyl-2-furaldehyde, and 3-acetyl-2,5-dimethylfuran

International Nuclear Information System (INIS)

Ribeiro da Silva, Manuel A.V.; Amaral, Luisa M.P.F.

2011-01-01

The standard (p o = 0.1 MPa) molar enthalpies of formation, in the gaseous state, at T = 298.15 K, for 2,5-dimethyl-3-furancarboxylic acid, 3-acetyl-2,5-dimethylfuran, and 4,5-dimethyl-2-furaldehyde were derived from the values of the standard molar enthalpies of formation, in the condensed phase, and the standard molar enthalpies of phase transition from the condensed to the gaseous state. The values of the standard molar enthalpies of formation of the compounds in the condensed phases were calculated from the measurements of the standard massic energies of combustion obtained by static bomb combustion calorimetry. The enthalpies of vaporization/sublimation were measured by Calvet high temperature microcalorimetry. For 2,5-dimethyl-3-furancarboxylic acid the standard enthalpy of sublimation was also calculated, by the application of the Clausius-Clapeyron equation, to the temperature dependence of the vapor pressures measured by the Knudsen effusion technique. (table)

The 2s2p 4P0sub(5/2) - 2p24Psup(e)sub(5/2)-transition in O VI

International Nuclear Information System (INIS)

Sjoedin, R.; Pihl, J.; Hallin, R.; Lindskog, J.; Marelius, A.

1976-03-01

The Li-like doubly excited transitions 2s2p 4 P 0 sub(5/2) - 2p 2 4 Psup(e)sub(5/2) in O VI has been studied with the beam-foil technique. Oxygen ion beams with energies between 4.5 to 9 MeV were used. The wavelength of the transition was measured to 944.0+-0.5 A and the lifetime for the upper level 2p 2 4 Psup(e) was measured to be 0.51+-0.04 ns. (Auth.)

Interaction of covalent hydrides of transition metals with Lewis acids. Molecular and crystalline structures of (eta5-CΛ5HΛ5)Λ2Mo(μ-HΛ2)FeIΛ2xNCHΛ3C and (eta5-CΛ5HΛ5)Λ2Mo(μ-HΛ2)CoBrΛ2xNCHΛ3C

International Nuclear Information System (INIS)

Bel'skij, V.K.; Bulychev, B.M.; Aripovskij, A.V.

1985-01-01

Using the methods of X-ray structural and IR spectroscopy analyses the structure of the complexes of molybdenocene dihydride with halides of iron triad has been investigated. (eta 5 -C 5 H 5 ) 2 Mo(μ-H 2 )CoBr 2 xNCH 3 C is crystallized in monoclinic cell with the parameters: a=7.821(1), b=12488(2), c=16.275(3)A, γ=105.74(1), sp. gr. P2 1 /n, Z=4. (eta 5 -C 5 H 5 ) 2 xMo(μ-H 2 )FeI 2 xNCH 3 C is crystallized in triclinic cell with the parameters: a=8.572(2), b=8.067(2), c=12496(3)A, α=87.72(2). β=90.82(2), γ=71.22(2), sp.gr. P anti 1, Z=2. The conclusion is made, that the structural type of bimetallic complexes of a sipilar type is determined by the ratio of iron triad halide acidity, halogen atom nucleophility and solvent basicity

Synthesis of (R)-5-(Di[2,3-3H2]propylamino)-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one-([3H]U-86170) and (R)-5-([2,3-3H2]propylamino)-5,6-dihydro-4H-imidazo(4,5,1-ij) quinolin-2(1H)-one ([3H]U-91356)

International Nuclear Information System (INIS)

Moon, M.W.; Hsi, R.S.P.

1992-01-01

(R)-5-(diallylamino)-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (12b) was prepared in 9% overall yield from 3-aminoquinoline. Reaction of 12b in ethyl acetate with tritium gas in presence of a 5% platinum on carbon catalyst afforded a mixture of (R)-5-(di[2,3- 3 H 2 ]propylamino)-5,6-dihydro-4H-imidazo[4,5,1-ij]-quinolin-2(1H)-one ([ 3 H]U-86170, 69 Ci/mmol) and (R)-5-([2,3- 3 H 2 ]-propylamino)5,6-dihydro-4H-imidazo-[4,5,1-ij]quinolin-2(1H)-one ( [ 3 H]U-91356, 34 Ci/mmol) which was separated by preparative reverse-phase chromatography. U-86170 and U-91356 are potent dopamine D2 agonists. The labelled compounds are useful for drug disposition studies. [ 3 H]U-86170 is also useful as a dopamine D2 agonist radioligand for receptor binding studies. (author)

Suveetendus eksootilises paigas / Heli Salong

Index Scriptorium Estoniae

Salong, Heli, 1958-

2004-01-01

Eeloleval suvel on teatrihuvilistel võimalik näha vabaõhuetendust väga erilises kohas - Pöide vallas asuval Udriku laiul, kus etendatakse P. Vallaku "Relvad vastamisi", lavastaja E. Klemets. Korraldajateks on MTÜ Lihtsad Lahendused koostöös AS Fix Ideed Estonia ja Ugala teatriga

PR aitab tulemusi saavutada piirangute kiuste / Jekaterina Eilart

Index Scriptorium Estoniae

Eilart, Jekaterina

2014-01-01

Olympic Entertainment Group laiendas 2013. aasta suvel oma online-äri ning sisenes "OlyBet" kaubamärgi all spordiennustuse turule. Suhtekorralduse Auhind 2013 erasektori kategooria võitnud projektist "PR-toetus OlyBeti kaubamärgi lansseerimisele" - kaubamärgi tutvustamiseks korraldatud kommunikatsioonist ja meediasuhete loomise projektist

Eesti ja Läti rahvusväeosade loomine Esimeses maailmasõjas 1914-1918. Sarnasused ja erinevused / Hanno Ojalo

Index Scriptorium Estoniae

Ojalo, Hanno, 1961-

2013-01-01

Rahvusväeosadest Esimeses maailmasõjas. Läti kütipataljonide loomisest. Eesti rahvusväeosade loomisest Vene sõjaväes.Läti küttide viimaseks suureks lahinguks oli Riia kaitsmine 1917. aasta suvel. Läti küttide saatusest pärast Riia langemist

Kasahstani nafta : närvide mäng / Steve LeVine

Index Scriptorium Estoniae

LeVine, Steve

2008-01-01

Nafta ja gaasi väljaveost Kasahstanist ja Kesk-Aasiast. USA naftakompanii Chevroni naftaekspordile on tõkkeid seadnud Venemaa pidevad jõudemonstratsioonid ning kohalike riikide soov Venemaale mitte vastu astuda, samuti 2008. aasta suvel toimunud Vene-Gruusia sõda, mis raskendas nafta jõudmist Euroopasse. Kaart

Prantslanna tallinlaste kodus

Index Scriptorium Estoniae

2002-01-01

Tallinna Kunstihoone galeriis Eléonore de Montesquiou (s. 1970) näitus "Minu maja on minu maa (home my sweet home)". Tervikprojekt koosneb videost, fotodest, häältest ja installatsioonist. Kunstiprojekt on filmitud suvel 2001 Eestis. Kuraatorid Aurélie Wacquant, Léa Gauthier

Jean Nouveli supermodernism Barcelonas / Raili Seppänen

Index Scriptorium Estoniae

Seppänen, Raili

2005-01-01

2005. a. suvel valmivast prantsuse arhitekti Jean Nouveli (sünd. 1945) projekteeritud tornmajast Torre Agbar Barcelonas Avinguda Diagonal 209-211. Abiks hispaania arhitekt Fermin Vazquez arhitektibüroost b720 Arquitectura S.L. Jean Nouveli tuntud projekte. Ill.: J. Nouveli portreefoto, tornmaja välisvaade

Direct preparation of 14C-labelled 5-allyl- and 5-propyl-2'-deoxyuridine from [2-14C]2'-deoxyuridine

International Nuclear Information System (INIS)

Ruth, J.L.; White, S.K.; Bergstrom, D.E.

1982-01-01

[2- 14 C]5-Allyl-2'-deoxyuridine was synthesized directly from [2- 14 C]2'-deoxyuridine using mercury, palladium, and 3-chloropropene. [2- 14 C]5-Propyl-2'-deoxyuridine was obtained by hydrogenation of the [ 14 C]5-allyl-2'-deoxyuridine. Advantages of the synthetic method and its application to the preparation of other radiolabeled 5-alkyl/alkenyl-2'-deoxyuridines are discussed. (author)

Energetics of the interaction of the antitumour agent titanocene dichloride with glycine: enthalpy of formation of [Ti(η5-C5H5)2(OOCCH2NH3)2]Cl2

International Nuclear Information System (INIS)

Nunes, Paulo M.; Minas da Piedade, Manuel E.

2004-01-01

The standard molar enthalpy of formation of [Ti(η 5 -C 5 H 5 ) 2 (OOCCH 2 NH 3 ) 2 ]Cl 2 in the crystalline state, at T=298.15 K, was determined as Δ f H m 0 {[Ti(η 5 -C 5 H 5 ) 2 (OOCCH 2 NH 3 ) 2 ]Cl 2 , cr}=-(1447.6 ± 8.1) kJ · mol -1 , by reaction-solution calorimetry. A discussion of the energetics of the direct interaction of the antitumour agent Ti(η 5 -C 5 H 5 ) 2 Cl 2 with glycine is also presented

Outsourcing is the Solution / Janis Berzins

Index Scriptorium Estoniae

Berzins, Janis

2011-01-01

Autor leiab, et Läti poliitikute arusaam neoliberalismist on vale ja et Läti on nõrk riik, kuna ei suuda enam ise majandust ja julgeolekut kontrollida. Autor toob näiteid ja märgib, et riik võiks ka haldusjuhtimise ja juriidilise poolega seotud teenused Rootsi, Saksamaa või EL-i käest sisse osta

Teenusestandardid kasvatavad kliendi usaldust / Kate-Riin Kont

Index Scriptorium Estoniae

Kont, Kate-Riin, 1971-

2007-01-01

16.-18. oktoobril 2007 toimus Tallinnas CHESS Initiativeþi world café seminar. Euroopa Standardikomitee teenuste horisontaalse standardimise strateegia ehk CHESS Initiative on loodud selleks, et anda hinnang teenuste standardimise teostatavusele. Euroopa Standardikomitee teenuste horisontaalse standardimise programmist (CHESS Initiative) ja selle raames korraldatavatest world café seminaridest, teenusestandardite vajalikkusest, teenuse osutamise ohuriskidest, kaebuste käsitlemisest

Google annab kõigi pihta turmtuld / Erik Aru

Index Scriptorium Estoniae

Aru, Erik

2010-01-01

Google'ile kuuluva operatsioonisüsteemiga Android varustatud telefonide müük edestas II kvartalis Microsofti Windows Mobile'i rakendavate müüki üle kolme korra, II kvartalis jõudis Android müüginäitajate poolest ette ka Apple'ist. Google kavatseb käivitada YouTube'i baasil tasuliste videote teenuse

The Deceptively Simple Thermolysis of Trivalent Permethyltitanocene Derivatives (η5-C5Me5)2TiR. Formation of a Tetramethylfulvene Titanium Compound (η6-C5Me4CH2)(η5-C5Me5)Ti and RH, Catalyzed by Permethyltitanocene Hydride, (η5-C5Me5)2TiH

NARCIS (Netherlands)

Luinstra, Gerrit A.; Teuben, Jan H.

1992-01-01

The complexes Cp*2TiR (Cp* = η5-C5Me5; R = Me, Et, n-Pr, C2H3, CH2CMe3, Ph) undergo thermolysis to yield the fulvene complex Cp*FvTi (Fv = η6-C5Me4CH2) and RH. Kinetic measurements and deuterium labeling studies show that the decomposition is catalyzed by Cp*2TiH, which is formed either by

Synthesis and optical properties of new 5'-aryl-substituted 2,5-bis(3-decyl-2,2'-bithiophen-5-yl-1,3,4-oxadiazoles

Directory of Open Access Journals (Sweden)

Anastasia S. Kostyuchenko

2017-02-01

Full Text Available New photoluminescent donor–acceptor–donor (DAD molecules, namely 5'-aryl-substituted 2,5-bis(3-decyl-2,2'-bithiophen-5-yl-1,3,4-oxadiazoles were prepared by palladium-catalyzed coupling from readily available compounds such as ethyl 3-decyl-2,2'-bithiophene-5-carboxylate and aryl halides. The obtained compounds feature increasing bathochromic shifts in their emission spectra with increasing aryl-substituent size yielding blue to bluish-green emissions. At the same time, their absorption spectra are almost independent from the identity of the terminal substituent with λmax values ranging from 395 to 405 nm. The observed trends are perfectly predicted by quantum chemical DFT/TDDFT calculations carried out for these new molecules.

Photoassociation spectroscopy of 87Rb2 (5s1/2+5p1/2)0u+ long-range molecular states: Coupling with the (5s1/2+5p3/2)0u+ series analyzed using the Lu-Fano approach

International Nuclear Information System (INIS)

Jelassi, H.; Viaris de Lesegno, B.; Pruvost, L.

2006-01-01

We report on photoassociation of cold 87 Rb atoms providing the spectroscopy of (5s 1/2 +5p 1/2 )0 u + long-range molecular states, in the energy range of [-12.5, -0.7 cm -1 ] below the dissociation limit. A Lu-Fano approach coupled to the LeRoy-Bernstein formula is used to analyze the data. The Lu-Fano graph exhibits the coupling of the molecular series with the (5s 1/2 +5p 3/2 )0 u + one, which is due to spin effects in the molecule. A two-channel model involving an improved LeRoy-Bernstein formula allows us to characterize the molecular series, to localize (5s 1/2 +5p 3/2 )0 u + levels, to evaluate the coupling, and to predict the energy and width of the first predissociated level of (5s 1/2 +5p 3/2 )0 u + series. An experimental spectrum confirms the prediction

Sõnal on suurem jõud kui relval / Marianne Mikko

Index Scriptorium Estoniae

Mikko, Marianne, 1961-

2008-01-01

Terroristliku rühmituse FARC käes pantvangis olnud Colombia naispoliitik, endine presidendikandidaat Ingrid Betancourt, pääses sel suvel prantslaste erioperatsiooniga vabadusse. Oktoobris esines Ingrid Betancourt Euroopa Parlamendis. Ilmunud ka Pärnu Postimees 18. okt. lk. 19; Hiiu Leht : Nädalalõpp 24. okt. lk. 6

Suvekino näitab Herzogi filme / Andres Laasik

Index Scriptorium Estoniae

Laasik, Andres, 1960-2016

2002-01-01

Detsembris toimuvat Pimedate Ööde Filmifestivali laiendatakse ka suvele, et sobivates paikades näidata väärtfilme. Alates 6. juunist näidatakse Katariina kirikus kuuel õhtul algusega kell 22 Werner Herzogi (1942) filme. Režissöörist ja näidatavatest filmidest

Werner Herzog Tallinnas / Aare Ermel

Index Scriptorium Estoniae

Ermel, Aare, 1957-2013

2002-01-01

Detsembris toimuvat Pimedate Ööde Filmifestivali laiendatakse ka suvele, et sobivates paikades näidata väärtfilme. Alates 6. juunist näidatakse Katariina kirikus kuuel õhtul algusega kell 22 Werner Herzogi (1942) filme. Režissöörist ja näidatavatest filmidest

A scalable synthesis of 5,5'-dibromo-2,2'-bipyridine and its stepwise functionalization via Stille couplings.

Science.gov (United States)

D'Souza, Daniel M; Leigh, David A; Papmeyer, Marcus; Woltering, Steffen L

2012-11-01

The synthesis of 5,5'-dibromo-2,2'-bipyridine and 5-bromo-2,2'-bipyridine, useful intermediates for elaboration into more complex ligands through metal-catalyzed coupling reactions, can be efficiently conducted on a multigram scale from inexpensive starting materials. The described procedure is reliably scalable and suitable for the synthesis of tens of grams of 5,5'-dibromo-2,2'-bipyridine. 5-Bromo-2,2'-bipyridine is produced as a minor product. The 5,5'-disubstituted-2,2'-bipyridine motif has excellent coordination properties and is a versatile building block for the synthesis of functional materials (including biodiagnostics, photovoltaics and organic light-emitting diodes) and complex molecular topologies (including catenanes and trefoil and pentafoil knots). The selective stepwise functionalization of 5,5'-dibromo-2,2'-bipyridine by consecutive Stille couplings is therefore illustrated and documented in detail. The synthesis of 5,5'-dibromo-2,2'-bipyridine takes 4-5 d: 1 d to prepare the key intermediate 2,2'-bipyridine dihydrobromide, 3 d for its reaction with bromine in a steel bomb reaction vessel and 8 h to isolate and purify the final product.

Adducts of UF5 with SbF5 and structure of UF5 . 2SbF5

International Nuclear Information System (INIS)

Sawodny, W.; Rediess, K.

1980-01-01

Both α-UF 5 and β-UF 5 form only a 1:2 compound UF 5 . 2SbF 5 reacting directly with SbF 5 , from which UF 5 . SbF 5 can be obtained by thermal decomposition. UF 5 . 2SbF 5 crystallizes in the monoclinic space group P2 1 /c with the following lattice constants a = 8.110(4), b = 14.129(6), c = 10.032(6) A and β = 96.97(5) 0 ; Z = 4. An X-ray study shows centrosymmetric four-membered rings of alternating UF 8 and SbF 6 polyhedra connected by other SbF 6 entities. This structure is similar to that of UOF 5 . 2SbF 5 , but the distorted pentagonal-bipyramidal coordination of the U atom found there is increased to a dodecahedral coordination by an additional U-F-Sb bridge, though with a somewaht larger UF distance. (author)

44 CFR 5.2 - Application.

Science.gov (United States)

2010-10-01

... 44 Emergency Management and Assistance 1 2010-10-01 2010-10-01 false Application. 5.2 Section 5.2 Emergency Management and Assistance FEDERAL EMERGENCY MANAGEMENT AGENCY, DEPARTMENT OF HOMELAND SECURITY GENERAL PRODUCTION OR DISCLOSURE OF INFORMATION General Provisions § 5.2 Application. This part applies to...

Optical properties of nanocrystalline potassium lithium niobate in the glass system (100-x) TeO2-x(1.5K2O-Li2O-2.5Nb2O5).

Science.gov (United States)

Ahamad, M Niyaz; Varma, K B R

2009-08-01

Optically clear glasses of various compositions in the system (100-x) TeO2-x(1.5K2O-Li2O-2.5Nb2O5) (2 glasses comprising potassium lithium niobate (K3Li2Nb5O15) microcrystallites on the surface and nanocrystallites within the glass were obtained by controlled heat-treatment of the as-quenched glasses just above the glass transition temperature (T(g)). The optical transmission spectra of these glasses and glass-crystal composites of various compositions were recorded in the 200-2500 nm wavelength range. Various optical parameters such as optical band gap, Urbach energy, refractive index were determined. Second order optical non-linearity was established in the heat-treated samples by employing the Maker-Fringe method.

4-[125I]iodo-(2,5-dimethoxy)phenylisopropylamine and [3H]ketanserin labeling of 5-hydroxytryptamine2 (5HT2) receptors in mammalian cells transfected with a rat 5HT2 cDNA: Evidence for multiple states and not multiple 5HT2 receptor subtypes

International Nuclear Information System (INIS)

Teitler, M.; Leonhardt, S.; Weisberg, E.L.; Hoffman, B.J.

1990-01-01

Evidence has accumulated indicating that the radioactive hallucinogens 4-bromo-[3H](2,5-dimethoxy)phenylisopropylamine ([3H]DOB) and 4-[125I]iodo-(2,5-dimethoxy)phenylisopropylamine ([125I]DOI) label an agonist high affinity state of the 5-hydroxytryptamine2 (5HT2) receptor and [3H]ketanserin labels both agonist high and low affinity states. Recently, an alternative hypothesis has been put forward proposing that the radioactive hallucinogens are labeling a 5HT2 receptor subtype distinct from the receptor labeled by [3H]ketanserin. In order to provide definitive evidence as to which of these hypotheses is correct, the rat 5HT2 receptor gene was transfected into NIH-3T3 cells and COS cells. Neither nontransfected cell type expresses 5HT2 receptors; the transfected cells expressed high affinity binding sites for both [125I] DOI (KD = 0.8 nM and Bmax = 363 fmol/mg in NIH-3T3 cells; KD = 0.2 nM and Bmax = 26 fmol/mg in COS cells) and [3H]ketanserin (KD = 0.4 nM and Bmax = 5034 fmol/mg in NIH-3T3 cells; KD = 1.0 nM and Bmax = 432 fmol/mg in COS cells). The affinities of agonists and antagonists for the [125I]DOI-labeled receptor were significantly higher than for the [3H]ketanserin-labeled receptor. The affinities of agonists and antagonists for these binding sites were essentially identical to their affinities for the sites radiolabeled by these radioligands in mammalian brain homogenates. The [125I]DOI binding was guanyl nucleotide sensitive, indicating a coupling to a GTP-binding protein. These data indicate that the 5HT2 receptor gene product contains both the guanyl nucleotide-sensitive [125I]DOI binding site and the [3H]ketanserin binding site. Therefore, these data indicate that the 5HT2 receptor gene product can produce a high affinity binding site for the phenylisopropylamine hallucinogen agonists as well as for the 5HT2 receptor antagonists

Voore Farm Teenused : nagu Agritechnica näitus

Index Scriptorium Estoniae

2016-01-01

Voore Farm Teenuste tehnikapargis on kokku üle 80 erineva masina. Efektiivne tehnikapark võimaldab pakkuda mõistliku hinna eest teenust ka teistele põllumajandusettevõtetele. Vestlusest ettevõtte juhatuse liikme Henrik Klammeriga

Siim Nestor soovitab : Teenage Kicks. Bängin / Siim Nestor

Index Scriptorium Estoniae

Nestor, Siim, 1974-

2002-01-01

12. aprillil alustatakse Pif-Pafi klubis live-muusikale orienteeritud muusikaõhtute sarjaga Teenage Kicks. Esinevad ansamblid BAP ja Id Rev ( andis 2001. aasta suvel välja albumi "Sina Ei"). Bängin on väike technopidu 13. apr. Wimbledonis, kus valivad technot Erkki Tero, Orav, Ilmar Kerm ja Raul Saaremets

Mobiilne töötaja võib tööd teha isegi pargipingil / Alar Pardla

Index Scriptorium Estoniae

Pardla, Alar, 1970-

2004-01-01

Ilmunud ka: Delovõje Vedomosti 8. sept. lk. 21. GPRS-i ja WiFi kasutajaid puudutavatest turvalisuse ja maksumuse küsimustest. Tabel: GPRS-andmeside hind erineb kuni 20 korda; WiFi-teenuse hindu on raske võrrelda. Vt. samas: Ka Motorola hakkab WiFi-mobiiltelefone tootma. Lisa: Nipid, kuidas mobiilne e-posti kasutaja saab kulusid kokku hoida; Neli kulutust kontori mobiilsemaks muutmisel

Rong viib autod ohutult rööbastel Euroopasse / Mirko Ojakivi

Index Scriptorium Estoniae

Ojakivi, Mirko

2007-01-01

Helsingi-Rovaniemi reisirongi külge on haagitud autotreiler reisijate autodega. Edelaraudtee juhi Kalvi Pukka väitel on selline idee liikvel olnud ka Edelaraudtees, kuid niisugune teenus õigustab end, kui linnadevaheline kaugus on umbes 600 km. Rail Baltica valmimisel on mõeldav, et rongiga Lätti või Leetu sõites saab kaasa võtta ka auto. Lisa: Rongi autotreilerid

Ettevõtjaks juba koolis / Kersti Loor

Index Scriptorium Estoniae

Loor, Kersti

2009-01-01

Õpilasfirma on JAA (Junior Achievmenti Arengufond) ettevõtlusõppe programm, mille käigus keskkooliõpilased moodustavad oma firma, mõtlevad välja toote või teenuse, turustavad ja arendavad seda. Tänavuse Eesti võistluse võitja oli Tallinna 21. Kooli õpilasfirma Roheline Jälg, teiseks tuli Toila Gümnaasiumi firma Aktsioon ja kolmandaks Kohila Gümnaasiumi õpilasfirma Stuupak

39 CFR 2.5 - Authority.

Science.gov (United States)

2010-07-01

... 39 Postal Service 1 2010-07-01 2010-07-01 false Authority. 2.5 Section 2.5 Postal Service UNITED STATES POSTAL SERVICE THE BOARD OF GOVERNORS OF THE U.S. POSTAL SERVICE GENERAL AND TECHNICAL PROVISIONS (ARTICLE II) § 2.5 Authority. These bylaws are adopted by the Board under the authority conferred upon the...

Pressure broadening and frequency shift of the 5S1/2 → 5D5/2 and 5S1/2 → 7S1/2 two photon transitions in 85Rb by the noble gases and N2

International Nuclear Information System (INIS)

Zameroski, Nathan D; Hager, Gordon D; Erickson, Christopher J; Burke, John H

2014-01-01

Doppler free two photon absorption spectroscopy was employed to measure the pressure broadening and frequency shift rates of the 5S 1/2 (F = 3) → 5D 5/2 (F = 5, 4, 3, 2, 1) (778.105 nm) and the 5S 1/2 (F = 2) → 7S 1/2 (F = 2) (760.126 nm) two photon transitions in 85 Rb by the noble gases and N 2 . To our knowledge, these rates are reported on for the first time. The self-broadening and shift rate of the 5S 1/2 (F = 3) → 5D 5/2 (F = 5, 4, 3, 2, 1) transition and self -broadening rate of the 5S 1/2 (F = 2) → 7S 1/2 (F = 2) transition were also measured. The temperature dependence of the self-frequency shift (Rb-Rb collisions) of these transitions is presented. Helium diffusion rates through Quartz and Pyrex cells are also calculated and the implication of helium diffusion through glass vapor cells is discussed in regards to atomic frequency standards based on these transitions. Experimental pressure broadening and shift rates are compared to theoretically calculated rates assuming a 6, 8 or 6, 8, 10 difference potential and pseudo potential model. Reasonable agreement is achieved between experimental and theoretical values. (paper)

SYNTHESIS AND CHARACTERIZATION OF (MU-5-C5ME5)2TI(R)CL (R = ME, ET, NORMAL-PR, CH=CH2, PH, O-NORMAL-PR) AND THEIR SALT METATHESIS REACTIONS - THERMAL-DECOMPOSITION PATHWAYS OF (MU-5-C5ME5)2TI(ME)R' (R' = ET, CH=CH2, PH, CH2PH)

NARCIS (Netherlands)

LUINSTRA, GA; TEUBEN, JH

Complexes Cp*2Ti(R)Cl (Cp* = eta-5-C5Me5; R = Me (1), Et (2), n-Pr (3), CH=CH2 (4), Ph (5), O-n-Pr (6)) have been prepared by oxidation Of CP*2TiR with lead dichloride. Not every compound Cp*2Ti(R)Cl was accessible and for R = CH2CMe3 and CH2Ph reduction to Cp*2TiCl and R. was observed. Homolysis of

Synthesis and Characterization of (η5-C5Me5)2Ti(R)Cl (R = Me, Et, n-Pr, CH=CH2, Ph, O-n-Pr) and Their Salt Metathesis Reactions. Thermal Decomposition Pathways of (η5-C5Me5)2Ti(Me)R' (R' = Et, CH=CH2, Ph, CH2Ph)

NARCIS (Netherlands)

Luinstra, Gerrit A.; Teuben, Jan H.

1992-01-01

Complexes Cp*2Ti(R)Cl (Cp* = η5-C5Me5; R = Me (1), Et (2), n-Pr (3), CH=CH2 (41, Ph (5), O-n-Pr (6)) have been prepared by oxidation of Cp*2TiR with lead dichloride. Not every compound Cp*2Ti(R)Cl was accessible and for R = CH2CMe3 and CH2Ph reduction to Cp*2TiCl and R· was observed. Homolysis of

Crystallographic characterization of divalent organosamarium compound (C5H5)2Sm(THF)2

International Nuclear Information System (INIS)

Jagannatha Swamy, S.

2002-01-01

The single pot reaction between SmX 2 (X = Cl - , I - ) and BuLi in THF at -40 degC, followed by the addition of C 5 H 5 - Na + results in a dark red solution. Leaving the concentrated reaction mixture at -25 degC for two days in a deep freezer results in the formation of the crystals of the compound, (C 5 H 5 ) 2 ; Sm(THF) 2 . The compound is insoluble in any solvent and it has been characterized by conventional methods. The crystals are monoclinic with space group C2/c, and a = 13.416(1), b = 9.644(1), c = 14.129(2) pm, β109.873(9) 0 and z = 4 for ρcalcd = 1.64 g cm -3 . Least squares refinement on the basis of 1804 observed reflections has led to a final R value of 0.037 and R w = 0.054. (author)

Vene keele 1. suvekool / Dimitri Mironov

Index Scriptorium Estoniae

Mironov, Dimitri

2001-01-01

2001.a. suvel korraldas TPÜ slaavi filoloogia osakond koostöös välissuhete osakonnaga vene keele suvekooli, mis oli mõeldud välisüliõpilastele. Kaks ja pool nädalat kestnud kursuste jooksul õppisid tudengid Soomest, Inglismaalt ja Hispaaniast intensiivselt vene keelt ning osalesid vene kultuuri tutvustavas programmis

Kunstiteaduslikke Uurimusi tõusis teadusajakirjade nomenklatuuris / Virve Sarapik

Index Scriptorium Estoniae

Sarapik, Virve, 1961-

2011-01-01

Thomson Reutersi Web of Science koostab ka humanitaarajakirjade andmebaase Arts & Humanities Citation Index ja Current Contents. Web of Science indeksitesse jõudnud Eestis väljaantavaid humanitaariaväljaandeid, millede hulka 2011. a. suvel lisandus Eesti Kunstiteadlaste Ühingu poolt väljaantav Kunstiteaduslikke Uurimusi. Suhteliselt algstaadiumis olevast Euroopa-kesksest humanitaarajakirjade andmebaasist ERIH

Ründo Mülts: "Vanemad on suunanud mind rahvuskultuuri austamise vaimus" / Raivo Raigna ; kommenteerinud Hanno Tamm, Priit Adler

Index Scriptorium Estoniae

Raigna, Raivo

2011-01-01

Päinurme koduloomuuseumist, mille rajaja ja omanik on Ründo Mülts. Sel suvel valminud Ründo Mültsi filmist "Võhmuta mõis ja asundus aegade tuules". Tallinna Ülikooli ajalootudengina asus ta uurimisöö raames uurima antud piirkonna minevikku ning otsustas jäädvustada nähtu-kuuldu ka filmilindile

Õigus tõhusale menetlusele enda kaitseks. Euroopa Inimõiguste Kohtu käsitluse ja Eesti õigusruumi näitel / Mart Susi

Index Scriptorium Estoniae

Susi, Mart, 1965-

2009-01-01

Autori ülevaade 2008. aasta suvel Tartu Ülikooli õigusteaduskonnas kaitstud doktoridissertatsioonist "Õigus tõhusale menetlusele enda kaitseks - Euroopa inimõiguste ja põhivabaduste kaitse konventsiooni artikkel 13 Euroopa Inimõiguste Kohtu dünaamilises käsitluses". Euroopa Inimõiguste Kohtu lahendites kasutatavate õigusmõistete ja õigusinstrumentide puutepunktidest Eesti õigusruumiga

(E-2-((4R,5R-5-((Benzyloxymethyl-2,2-dimethyl-1,3-dioxolan-4-ylbut-2-ene-1,4-diol

Directory of Open Access Journals (Sweden)

Carlos R. Carreras

2010-04-01

Full Text Available The synthesis of (E-2-((4R,5R-5-((benzyloxymethyl-2,2-dimethyl-1,3-dioxolan-4-ylbut-2-ene-1,4-diol by a one-step reduction of the appropriate 2-substituted butenolide is reported. Product characterization was carried out by IR, 1H NMR, 13C NMR, MS, elemental analysis and optical rotation.

Estonia hukk jõuab suvel kinodesse / Tarmo Michelson

Index Scriptorium Estoniae

Michelson, Tarmo, 1975-

2002-01-01

Nädal tagasi alustati Berliinis poliitilise põnevusfilmi "Baltic Storm" võtetega, mis kujutab parvlaev "Estonia" hukku venelaste vandenõu tulemusena. Produtsendid on Jutta Rabe ja Kaj Holmberg, režissöör Reuben Leder, peaosades Greta Scacchi ja Jürgen Prochnow

Ajaloolasena Tallinna linnaarhiivis 1960. aasta suvel / Jorma Ahvenainen

Index Scriptorium Estoniae

Ahvenainen, Jorma

2008-01-01

Arvi Korhoneni õpilase Jorma Ahvenaineni muljeid tööst Tallinna linnaarhiivis. Autor külastas Eestit 1960. aastal, et koguda materjale väitekirja "Der Getreidehandel Livlands im Mittelalter" jaoks

4-[4-(4-Fluorophenyl-2-methyl-5-oxo-2,5-dihydroisoxazol-3-yl]-1-methylpyridinium iodide–4-[3-(4-fluorophenyl-2-methyl-5-oxo-2,5-dihydroisoxazol-4-yl]-1-methylpyridinium iodide (0.6/0.4

Directory of Open Access Journals (Sweden)

Simona Margutti

2008-01-01

Full Text Available The crystal structure of the title compound, C16H16FN2O2+·I−, was determined as part of a study of the biological activity of isoxazolone derivatives as p38 mitogen-activated protein kinase (MAPK inhibitors. The X-ray crystal structure of 4-[4-(4-fluorophenyl-2-methyl-5-oxo-2,5-dihydroisoxazol-3-yl]-1-methylpyridinium iodide showed the presence of the regioisomer 4-[3-(4-fluorophenyl-2-methyl-5-oxo-2,5-dihydroisoxazol-4-yl]-1-methylpyridinium iodide. The synthesis of the former compound was achieved by reacting 4-(4-fluorophenyl-3-(4-pyridylisoxazol-5(2H-one after treatment with Et3N in dimethylformamide, with iodomethane. The unexpected formation of the regioisomer could be explained by a rearrangement occurring via aziridine of the isoxazolone compound. The regioisomers have site occupancies of 0.632 (4/0.368 (4. The two six members rings make a dihedral angle of 66.8 (2°.

A 2.5-kW industrial CO2 laser

Science.gov (United States)

Golov, V. K.; Ivanchenko, A. I.; Krasheninnikov, V. V.; Ponomarenko, A. G.; Shepelenko, A. A.

1986-06-01

A fast-flow laser is reported in which the active medium is excited by a self-sustained dc discharge produced by an electric-discharge device with nonsectioned electrodes. In the laser, two discharge gaps are formed by a flat anode and two cathodes, one on each side of the anode. A gas mixture is driven through the gasdynamic channel by a centrifugal fan rotating at 6000 rpm/min. With a mixture of CO2:N2:He = 2.5:7.5:5 mm Hg, the rated power is 2.5 kW; the maximum power is 4 kW with the mixture 2.5:7.5:10 mm Hg. The general design of the laser is described, and its principal performance characteristics are given.

Miniaturized printed K shaped monopole antenna with truncated ground plane for 2.4/5.2/5.5/5.8 wireless lan applications

Science.gov (United States)

Chandan, Bharti, Gagandeep; Srivastava, Toolika; Rai, B. S.

2018-04-01

A novel truncated ground plane monopole antenna is proposed for wide band wireless local area network (WLAN) applications. The antenna contains a rectangular patch with a rectangular ring, a circular slot and a truncated ground plane printed on opposite sides of a low cost substrate FR4. The operating frequency bands for the antenna are band1 (2.4-2.88 GHz) and band 2 (4.8-6.3 GHz) with ≤ - 10 dB return loss which covers 2.4/5.2/5.5/5.8 GHz WLAN bands. The antenna is compact with overall dimension 26×40×0.8 mmł and with the dimension of patch 16×16×0.8 mm3. The two bands of antenna is obtained by cutting a rectangular ring and a circular slot in the patch and return loss is improved by cutting two rectangular slot in the ground plane. Performance measures of the antenna are shown in terms of return loss, current distribution, radiation pattern and gain. To verify the simulated results, the antenna is also fabricated and tested. The simulated and fabricated results have been found in good agreement.

Properties and Crystallization Phenomena in Li2Si2O5–Ca5(PO4)3F and Li2Si2O5–Sr5(PO4)3F Glass–Ceramics Via Twofold Internal Crystallization

Science.gov (United States)

Rampf, Markus; Dittmer, Marc; Ritzberger, Christian; Schweiger, Marcel; Höland, Wolfram

2015-01-01

The combination of specific mechanical, esthetic, and chemical properties is decisive for the application of materials in prosthodontics. Controlled twofold crystallization provides a powerful tool to produce special property combinations for glass–ceramic materials. The present study outlines the potential of precipitating Ca5(PO4)3F as well as Sr5(PO4)3F as minor crystal phases in Li2Si2O5 glass–ceramics. Base glasses with different contents of CaO/SrO, P2O5, and F− were prepared within the glasses of the SiO2–Li2O–K2O–CaO/SrO–Al2O3–P2O5–F system. Preliminary studies of nucleation by means of XRD and scanning electron microscopy (SEM) of the nucleated base glasses revealed X-ray amorphous phase separation phenomena. Qualitative and quantitative crystal phase analyses after crystallization were conducted using XRD in combination with Rietveld refinement. As a main result, a direct proportional relationship between the content of apatite-forming components in the base glasses and the content of apatite in the glass–ceramics was established. The microstructures of the glass–ceramics were investigated using SEM. Microstructural and mechanical properties were found to be dominated by Li2Si2O5 crystals and quite independent of the content of the apatite present in the glass–ceramics. Biaxial strengths of up to 540 MPa were detected. Ca5(PO4)3F and Sr5(PO4)3F influence the translucency of the glass–ceramics and, hence, help to precisely tailor the properties of Li2Si2O5 glass–ceramics. The authors conclude that the twofold crystallization of Li2Si2O5–Ca5(PO4)3F or Li2Si2O5–Sr5(PO4)3F glass–ceramics involves independent solid-state reactions, which can be controlled via the chemical composition of the base glasses. The influence of the minor apatite phase on the optical properties helps to achieve new combinations of features of the glass–ceramics and, hence, displays new potential for dental applications. PMID:26389112

2-Amino-5-chloropyridinium nitrate

Directory of Open Access Journals (Sweden)

Donia Zaouali Zgolli

2009-11-01

Full Text Available The title structure, C5H6ClN2+·NO3−, is held together by extensive hydrogen bonding between the NO3− ions and 2-amino-5-chloropyridinium H atoms. The cation–anion N—H...O hydrogen bonds link the ions into a zigzag- chain which develops parallel to the b axis. The structure may be compared with that of the related 2-amino-5-cyanopyridinium nitrate.

GLOBE-koolide õpilased assisteerivad NASA teadlasi / Imbi Henno

Index Scriptorium Estoniae

Henno, Imbi

2004-01-01

GLOBE (Global Learning and Observations to Benefit Environment) on õpilastele suunatud uurimuslikku ja praktilist tegevust pakkuv haridus- ja teadusprogramm. Õpilased teevad keskkonnavaatlusi ja mõõtmisi, saadavad oma tulemused interneti kaudu GLOBE'i andmebaasi ja kasutavad andmebaase koolitöös. Suvel toimus USA-s Boulderis GLOBE'i 10. tegevusaastale pühendatud konverents

The Iron Age and 13th-18th century Cemetery and Chapel Site of Niklusmägi : Grave Looting and Archaeology / Heiki Valk, Pikne Kama, Riina Rammo ... [jt.

Index Scriptorium Estoniae

2013-01-01

2011. aastal anti arheoloogilidele vihje Niklusmäe kalme lõhkumisest. 2012. aasta suvel leidsid projekti "Arheoloogia, võim ja ühiskond" raames aset arheoloogilised päästeuuringud. Ilmnes, et kalmet oli rüüstatud 4-5 aasta jooksul. Leitud luustikest, hauapanustest. Niklusmäest Läti Henriku kroonika andmetel. Tänini räägib pärimus Lätist tulnud, Niklusmäe metsa läbivast ja Sangaste poole suunduvast sõjateest. Leiud on tõstatanud küsimusi Eesti lõunaserva matmiskommete ja etnokultuuriliste olude kohta. Kuna kalmesüdamik on rüüstatud, jäävad küsimused vastuseta

2-(6-Bromobenzo[d]thiazol-2-yl-5,5-dimethylthiazol-4(5H-one

Directory of Open Access Journals (Sweden)

Rainer Beckert

2013-12-01

Full Text Available The title compound, C12H9BrN2OS2, was obtained by reacting 6-bromobenzo[d]thiazole-2-carbonitrile in iso-propanol with ethyl 2-mercapto-2-methylpropanoate at reflux temperature for several hours. The resulting dimethyloxyluciferin derivative shows partial double-bond character of the carbon–carbon bond between the two heterocyclic moieties [C—C = 1.461 (3 Å]. This double bond restricts rotation around this C—C axis, therefore leading to an almost planar molecular structure [N—C—C—S torsion angle = 9.7 (3°]. The five-membered thiazoline ring is not completely planar as a result of the bulky S atom [C—S—C—C torsion angle = 5.17 (12°].

Operation JANGLE. Particle Studies. Projects 2.5a-1, 2.5a-2, 2.5a-3, 2. 8,

Science.gov (United States)

1979-10-01

air with time. 26.1 Brookhaven Air Monitor A filter paper feed system traveling at 4 inches per hour combined with a vacuum pump (3.5 ou ft/min) was...Monitor This Instrument also employs an air pumping system (2.6 cu.ft/min) with filter paper 6 Inohes wide traveling at 7 inches per hour or multiples...JANGLE of the Portable Air Sampler (PAS) used previously by Test Division, CRL and Dug.way Proving Ground, Utah. Its purpose was to pro- vde an

5-Methyl-3,8-di-(2-amino-4-bromophenyl-4,9-dioxa-1,2,6,7-tetraaza-5λ5-phosphaspiro[4.4]nona-2,7-diene

Directory of Open Access Journals (Sweden)

Sławomir Kasperowicz

2018-01-01

Full Text Available 5-Methyl-3,8-di-(2-amino-4-bromophenyl-4,9-dioxa-1,2,6,7-tetraaza-5λ5-phosphaspiro[4.4]nona-2,7-diene was obtained by condensation of 2-amino-5-bromobenzohydrazide and methylphosphonyl dichloride in the presence of triethylamine. An initial biological screening was performed for the resulting product. The synthesized compound showed relatively strong cytotoxic activity, which was, however, similar for cancer and non-cancer cell lines.

Multiferroic properties of Pb2Fe2O5 ceramics

International Nuclear Information System (INIS)

Wang, Min; Tan, Guolong

2011-01-01

Research highlights: → Simultaneous occurrence of ferromagnetism and ferroelectricity in Pb 2 Fe 2 O 5 ceramics. → The off-centers of shifted Pb 2+ ions as well as the FeO 6 octahedra in the 'Pb 2 Fe 2 O 5 ' lead to a ferroelectric polarization. → Pb 2 Fe 2 O 5 ceramic demonstrates ferromagnetic order state due to the spin arrangement in the double chains of FeO 5 tetrahedral pyramids. -- Abstract: Pb 2 Fe 2 O 5 (PFO) powders in monoclinic structure have been synthesized using lead acetate in glycerin and ferric acetylacetonate as the precursor. The powders were pressed into pellets, which were sintered into ceramics at 800 o C for 1 h. The morphology and structure have been determined by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). Polarization was observed in Pb 2 Fe 2 O 5 ceramics at room temperature, exhibiting a clear ferroelectric hysteresis loop. The remanent polarization of Pb 2 Fe 2 O 5 ceramic is estimated to be Pr ∼ 0.22 μC/cm 2 . The origin of the polarization may be attributed to the off-centers of shifted Pb 2+ ions as well as the FeO 6 octahedra in the perovskite-based structure of Pb 2 Fe 2 O 5 . Magnetic hysteresis loop was also observed at room temperature. The Pb 2 Fe 2 O 5 ceramic shows coexistence of ferroelectricity and ferromagnetism. It provides a new field of research for complex oxides with multiferroic properties.

La5Zn2Sn

Directory of Open Access Journals (Sweden)

Igor Oshchapovsky

2011-11-01

Full Text Available A single crystal of pentalanthanum dizinc stannide, La5Zn2Sn, was obtained from the elements in a resistance furnace. It belongs to the Mo5SiB2 structure type, which is a ternary ordered variant of the Cr5B3 structure type. The space is filled by bicapped tetragonal antiprisms from lanthanum atoms around tin atoms sharing their vertices. Zinc atoms fill voids between these bicapped tetragonal antiprisms. All four atoms in the asymmetric unit reside on special positions with the following site symmetries: La1 (..m; La2 (4/m..; Zn (m.2m; Sn (422.

Kino kolib suveks õue / Janno Zõbin

Index Scriptorium Estoniae

Zõbin, Janno

2002-01-01

Detsembris toimuvat Pimedate Ööde Filmifestivali laiendatakse ka suvele, et sobivates paikades näidata väärtfilme. Tallinnas Katariina kirikus ja Theatrumis juba näidati K. Kieslowski filmide retrospektiivi. Juunis näidatakse Werner Herzogi filme ning Tallinna Linnaarhiivi siseõues hakkab tegutsema juba traditsiooniks saanud vabaõhukino. Noortefilme näidatakse Nukuteatri hoovis

Eesti tüübid : meie siin maal / Maris Rosenthal

Index Scriptorium Estoniae

Rosenthal, Maris

2009-01-01

Eesti Rahva Muuseumi ja fotograaf Alar Madissoni projekti "Eesti tüübid" raames valminud fotonäitus "Meie siin maal" Tartus Raadi mõisapargis. Kaasaega dokumenteeriva projekti eesmärgiks oli jäädvustada kõigis Eesti maakondades elavaid eri generatsioonide ja sotsiaalsete rühmade esindajaid ERMi fotokogu täiendamiseks. Meenutusi pildistamistelt 2008. aasta suvel

Muusika / Priit Kuusk

Index Scriptorium Estoniae

Kuusk, Priit, 1938-

2004-01-01

EMA muusikateaduste osakonna uurimisprojektist "Muusikaelu Eestis XX sajandi algupoolel". Algab sari "Noored pianistid I - VII". Kristjan Järvi suvelõpp ja sügis. Rahvusooper Estonia otsib peaosatäitjat ooperisse "Väike Napoleon". Andres Mustonen toob 24. IX Eestisse V. Silvestrovi "Reekviemi" ja V. Martõnovi "Klaverikontserdi" teise maailmaettekande. Modern Fox '38 esitles oma uut plaati "Oober"

Cobalt(II), nickel(II), copper(II), and zinc(II) complexes with [3(5)]adamanzane, 1,5,9,13-tetraazabicyclo[7.7.3]nonadecane and [(2.3)(2).2(1)]adamanzane, 1,5,9,12-tetraazabicyclo[7.5.2]hexadecane

DEFF Research Database (Denmark)

Broge, Louise; Pretzmann, Ulla; Jensen, Nicolai

2001-01-01

) and of three cobalt(II), four nickel(II), one copper(II), and two zinc(II) complexes with [3(5)]adamanzane. For nine of these compounds (2-8, 10b, and 12) the single-crystal X-ray structures were determined. The coordination geometry around the metal ion is square pyramidal in [Cu([(2.3)(2).2(1)]adz)Br]ClO4 (2......) and trigonal bipyramidal in the isostructural structures [Cu([3(5)]adz)Br]Br (3), [Ni-([3(5)]adz)Cl]Cl (5), [Ni([3(5)]adz)Br]Br (6), and [Co([3(5)]adz)Cl]Cl (8). In [Ni([3(5)]adz)(NO3)]NO3 (4) and [Ni([3(5)]-adz)(ClO4)]ClO4 (7) the coordination geometry around nickel(II) is a distorted octahedron...... with the inorganic ligands at cis positions. The coordination polyhedron around the metal ion in [Co([3(5)]adz)][ZnCl4] (10b) and [Zn([3(5)]adz)][ZnCl4] (12) is a slightly distorted tetrahedron. Anation equilibrium constants were determined spectrophotometrically for complexes 2-6 at 25 and 40 degreesC and fall...

Structural aspects of B2O3-substituted (PbO)0.5(SiO2)0.5 glasses

International Nuclear Information System (INIS)

Sudarsan, V.; Kulshreshtha, S.K.; Shrikhande, V.K.; Kothiyal, G.P.

2002-01-01

Lead borosilicate glasses having general formulae (PbO) 0.5-x (SiO 2 ) 0.5 (B 2 O 3 ) x with 0.0≤x≤0.4 and (PbO) 0.5 (SiO 2 ) 0.5-y (B 2 O 3 ) y with 0.0≤y≤0.5 have been prepared by a conventional melt-quench method and characterized by 29 Si, 11 B magic angle spinning (MAS) NMR techniques and infrared spectroscopy, as regards their structural features. From 29 Si NMR results, it has been inferred that with increasing concentration of boron oxide, (PbO) 0.5-x (SiO 2 ) 0.5 (B 2 O 3 )x glasses exhibit a systematic increase in the number of Q 4 structural units of Si at the expense of Q 2 structural units, along with the formation of Si-O-B linkages. On the other hand, for (PbO) 0.5 (SiO 2 ) 0.5-y (B 2 O 3 ) y glasses, there is no direct interaction between SiO 2 and B 2 O 3 in the glass network, as revealed by the 29 Si MAS NMR studies. Boron exists in both trigonal and tetrahedral configurations for these two series of glasses and for the (PbO) 0.5 (SiO 2 ) 0.5-y (B 2 O 3 ) y series of glasses; the relative concentration of these two structural units remains almost constant with increasing B 2 O 3 concentration. In contrast, for (PbO) 0.5-x (SiO 2 ) 0.5 (B 2 O 3 ) x glasses, there is a slight increase in the number of BO 3 structural units above x = 0.2, as there is a competition between SiO 2 and B 2 O 3 for interaction with Pb 2+ , thereby leading to the formation of BO 3 structural units. For both series of glasses, the thermal expansion coefficient is found to decrease with increasing B 2 O 3 concentration, the effect being more pronounced for the (PbO) 0.5-x (SiO 2 ) 0.5 (B 2 O 3 ) x series of glasses due to the increased concentration of Q 4 structural units of silicon and better cross-linking as a result of the formation of Si-O-B-type linkages. (author)

Metabolism of 1,2,3,4-, 1,2,3,5-, and 1,2,4,5-tetrachlorobenzene in the squirrel monkey

International Nuclear Information System (INIS)

Schwartz, H.; Chu, I.; Villeneuve, D.C.; Benoit, F.M.

1987-01-01

The metabolism of three tetrachlorobenzene isomers (TeCB) was investigated in the squirrel monkey. The animals were administered orally 6 single doses of 14 C-labeled 1,2,3,4-, 1,2,4,5-, or 1,2,3,5-tetrachlorobenzene over a 3-wk period at levels ranging from 50 to 100 mg/kg body weight (b.w) and kept in individual metabolism cages to collect urine and feces for radioassay. Approximately 38% (1,2,3,4-TeCB), 36% (1,2,3,5-TeCB), and 18% (1,2,4,5-TeCB) of the doses were excreted respectively in the feces 48 h post administration. In monkeys dosed with 1,2,3,4-TeCB, unchanged compound accounted for 50% of the fecal radioactivity. Unchanged compound accounted for more than 50% of the fecal radioactivity found in the monkeys dosed with 1,2,3,5-TeCB. The fecal metabolites were identified in both groups. No metabolites were detected in the feces of monkeys dosed with 1,2,4,5-TeCB. While the fecal route represented the major route of excretion for 1,2,3,4-TeCB, the other two isomers were eliminated exclusively in the feces. The above data in the squirrel monkey are different from those obtained with the rat and the rabbit, and demonstrate the different metabolic pathways for the isomers

Oxidation of 5-Chloromethylfurfural (CMF to 2,5-Diformylfuran (DFF

Directory of Open Access Journals (Sweden)

Ana I. Vicente

2017-02-01

Full Text Available 2,5-Diformylfuran (DFF is an important biorenewable building block, namely for the manufacture of new polymers that may replace existing materials derived from limited fossil fuel resources. The current reported methods for the preparation of DFF are mainly derived from the oxidation of 5-hydroxymethylfurfural (HMF and, to a lesser extent, directly from fructose. 5-Chloromethylfurfural (CMF has been considered an alternative to HMF as an intermediate building block due to its advantages regarding stability, polarity, and availability from glucose and cellulose. The only reported method for the transformation of CMF to DFF is restricted to the use of DMSO as the solvent and oxidant. We envisioned that the transformation could be performed using more attractive conditions. To that end, we explored the oxidation of CMF to DFF by screening several oxidants such as H2O2, oxone, and pyridine N-oxide (PNO; different heating methods, namely thermal and microwave irradiation (MWI; and also flow conditions. The combination of PNO (4 equiv. and Cu(OTf2 (0.5 equiv. in acetonitrile was identified as the best system, which lead to the formation of DFF in 54% yield under MWI for 5 min at 160 °C. Consequently, a range of different heterogeneous copper catalysts were tested, which allowed for catalyst reuse. Similar results were also observed under flow conditions using copper immobilized on silica under thermal heating at 160 °C for a residence time of 2.7 min. Finally, HMF and 5,5′-oxybis(5-methylene-2-furaldehyde (OBMF were the only byproducts identified under the reaction conditions studied.

Weekly cycle of magnetic characteristics of PM2.5 and PM2.5-10 in Beijing, China

Science.gov (United States)

SHI, M.; Wu, H.; Zhang, S.; Li, H.; Yang, T.

2013-12-01

In urban areas,fine particle matter with aerodynamic diameter between 2.5 um and 10 um (PM2.5-10), and 2.5 um (PM2.5), as an important source of urban particulate matter (PM) pollutants, have significant negative effects on health, atmospheric visibility and climate. PM has increasingly become a significant index of indicating the atmospheric pollution of city. In recent years, Beijing, China has been listed as one of the most serious air pollution city in the world. In order to investigate the sources of air pollutants, a total of 283 pairs of PM2.5 and PM2.5-10 samples were collected daily from July, 2010 to June, 2011 in Beijing. Mineral magnetic properties and Scanning electron microscope (SEM) observations and energy dispersive X-ray spectroscopy (EDS) analyses of PM2.5 and PM2.5-10 were measured to verify the magnetic materials. Magnetic measures for PM indicated that the major magnetic phase was coarse-grained magnetite-like material. The χlf, χarm, SIRM and χarm/SIRM series of the PM2.5 and PM2.5-10 show seasonal dependences: high values in winter and low values in summer. In additional the parameters analyzed by Time-series methods show a strong cycle about 7 days above 95% confidence level. Weekly cycle of magnetic characteristics of PM2.5 and PM2.5-10 show different pattern: the concentration of magnetic particles in PM2.5-10 show high values in mid-week, and particle sizes is steady, while the concentration of magnetic particles in PM2.5 show reverse a weekly cycle pattern, and particle sizes is smaller in the mid-week.Microscopy analyses reveal basically three morphologies of magnetic grains: aggregate, spherules and angular particles. The ultrafine carbonaceous particles which tend to form complex clusters and chain-like structures, most likely come from coal burning and motor vehicle exhaust. Spherical particles in PM2.5 are dominantly composed of Fe, O and C, grain-diameters of particles range from 0.3 to 2 um. Angular particles of Fe

The synthesis of 7-chloro-5-pentadeuteriophenyl-1-methyl-1H-1, 5-benzodiazepine-2,4(3H, 5H)dione ([2H5]clobazam)

International Nuclear Information System (INIS)

Borel, A.G.; Abbott, F.S.

1990-01-01

Pentadeuteriophenyl clobazam was synthesized in essentially quantitative isotopic purity, and characterized by 1 H-NMR and mass spectroscopy. The title compound was found to be >98% pure by HPLC, and its retention time (t R 6.17 min) was less than that of an authentic clobazam standard (t R 6.32 min). Of the five steps in the synthesis of clobazam, the most susceptible to deuterium exchange was the nucleophilic substitution of 2,4-dichloronitrobenzene by aniline-d 7 to form N-(5-chloro-2-nitrophenyl)penta-deuteriophenylamine. In this step, the isotopic impurity aniline-2,3,4,5-d 5 introduced protons from nitrogen into the ortho and para positions of the deuteriophenyl ring of N-(5-chloro-2-nitrophenyl)pentadeuteriophenylamine. (author)

BLOCKAGE 2.5 user's manual

International Nuclear Information System (INIS)

Rao, D.V.; Brideau, J.; Shaffer, C.; Souto, F.; Bernahl, W.

1996-12-01

The BLOCKAGE 2.5 code described in this User's Manual was developed by the US Nuclear Regulatory Commission (NRC) as a tool to evaluate licensee compliance with NRC Bulletin 96-03, ''Potential Plugging of Emergency Core Cooling Suction Strainers by Debris in Boiling Water Reactors.'' As such, BLOCKAGE 2.5 provides a generalized framework into which a user can input plant-specific and insulation-specific data for performing analyses in accordance with Regulatory Guide 1.82, Rev. 2. This user's manual describes the capabilities of BLOCKAGE 2.5 along with a description of the graphics user's interface provided for data entry. Each input/output dialog is described in detail along with special considerations related to developing and executing BLOCKAGE. Also, several sample problems are provided such that user can easily modify them to suit a particular plant of interest. The models used in BLOCKAGE 2.5 and their validation are presented in the accompanying NUREG/CR-6371. The BLOCKAGE models were designed to be parametric in nature, allowing the user flexibility to examine the impact of several modeling assumptions and to conduct sensitivity analyses. As a result, BLOCKAGE 2.5 results are known to be very sensitive to the user provided input. It is therefore strongly recommended that users become thoroughly familiar with BLOCKAGE models and their limitations as described in NUREG/CR-6224

Regioselective intramolecular ring closure of 2-amino-6-bromo-2,6-dideoxyhexono-1,4-lactones to 5- or 6-membered iminuronic acid analogues:synthesis of 1-deoxymannojirimycin and 2,5-dideoxy-2,5-imino-D-glucitol

DEFF Research Database (Denmark)

Malle, Birgitte Mølholm; Lundt, Inge; Wrodnigg, Tanja M.

2008-01-01

closure took place by 5-exo attack on the 5,6-epoxide leading to 2,5-dideoxy-2,5-imino-L-gulonic acid (9b), which was reduced to 2,5-dideoxy-2,5-imino-D-glucitol (9c). The method was further applied to 2-amino-6-bromo-2,6-dideoxy-D-galacto- as well as D-talo-1,4-lactones (14 and 15). However, only......-galacto- as well as L-talo-2-amino-6-bromo-2,6-dideoxy-1,4-lactones ent-14 and ent-15, reacted accordingly to give the D-galacto- and L-altro-1,5-iminuronic acid mimetics, (2S,3S,4R,5S)-3,4,5-trihydroxypipecolic acid (2,6-dideoxy-2,6-imino-L-galactonic acid, ent-16) and (2R,3S,4R,5S)-3,4,5-trihydroxypipecolic...

Roles of Human CYP2A6 and Monkey CYP2A24 and 2A26 Cytochrome P450 Enzymes in the Oxidation of 2,5,2',5'-Tetrachlorobiphenyl.

Science.gov (United States)

Shimada, Tsutomu; Kakimoto, Kensaku; Takenaka, Shigeo; Koga, Nobuyuki; Uehara, Shotaro; Murayama, Norie; Yamazaki, Hiroshi; Kim, Donghak; Guengerich, F Peter; Komori, Masayuki

2016-12-01

2,5,2',5'-Tetrachlorobiphenyl (TCB) induced type I binding spectra with cytochrome P450 (P450) 2A6 and 2A13, with K s values of 9.4 and 0.51 µM, respectively. However, CYP2A6 oxidized 2,5,2',5'-TCB to form 4-hydroxylated products at a much higher rate (∼1.0 minute -1 ) than CYP2A13 (∼0.02 minute -1 ) based on analysis by liquid chromatography-tandem mass spectrometry. Formation of 4-hydroxy-2,5,2',5'-TCB by CYP2A6 was greater than that of 3-hydroxy-2,5,2',5'-TCB and three other hydroxylated products. Several human P450 enzymes, including CYP1A1, 1A2, 1B1, 2B6, 2D6, 2E1, 2C9, and 3A4, did not show any detectable activities in oxidizing 2,5,2',5'-TCB. Cynomolgus monkey CYP2A24, which shows 95% amino acid identity to human CYP2A6, catalyzed 4-hydroxylation of 2,5,2',5'-TCB at a higher rate (∼0.3 minute -1 ) than CYP2A26 (93% identity to CYP2A6, ∼0.13 minute -1 ) and CYP2A23 (94% identity to CYP2A13, ∼0.008 minute -1 ). None of these human and monkey CYP2A enzymes were catalytically active in oxidizing other TCB congeners, such as 2,4,3',4'-, 3,4,3',4'-, and 3,5,3',5'-TCB. Molecular docking analysis suggested that there are different orientations of interaction of 2,5,2',5'-TCB with the active sites (over the heme) of human and monkey CYP2A enzymes, and that ligand interaction energies (U values) of bound protein-ligand complexes show structural relationships of interaction of TCBs and other ligands with active sites of CYP2A enzymes. Catalytic differences in human and monkey CYP2A enzymes in the oxidation of 2,5,2',5'-TCB are suggested to be due to amino acid changes at substrate recognition sites, i.e., V110L, I209S, I300F, V365M, S369G, and R372H, based on the comparison of primary sequences. Copyright © 2016 by The American Society for Pharmacology and Experimental Therapeutics.

Three-component synthesis of C2F5-substituted pyrazoles from C2F5CH2NH2·HCl, NaNO2 and electron-deficient alkynes

Directory of Open Access Journals (Sweden)

Pavel K. Mykhailiuk

2015-01-01

Full Text Available A one-pot reaction between C2F5CH2NH2·HCl, NaNO2 and electron-deficient alkynes gives C2F5-substituted pyrazoles in excellent yields. The transformation smoothly proceeds in dichloromethane/water, tolerates the presence of air, and requires no purification of products by column chromatography. Mechanistically, C2F5CH2NH2·HCl and NaNO2 react first in water to generate C2F5CHN2, that participates in a [3 + 2] cycloaddition with electron-deficient alkynes in dichloromethane.

27 CFR 5.2 - Related regulations.

Science.gov (United States)

2010-04-01

... 27 Alcohol, Tobacco Products and Firearms 1 2010-04-01 2010-04-01 false Related regulations. 5.2 Section 5.2 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT OF THE TREASURY LIQUORS LABELING AND ADVERTISING OF DISTILLED SPIRITS Scope § 5.2 Related regulations...

Synthesis and Antibacterial Activities of Novel 2,5-Diphenylindolo[2,3-e] Pyrazolo[1',5':3",4"]pyrimido[2",1"-c] [1,2,4]triazines

Directory of Open Access Journals (Sweden)

Mohamed G. Marei

2011-12-01

Full Text Available The formation of (E-3-{2-(2,5-diphenylpyrazolo[1,5-c]pyrimidin-7-ylhydrazono}indolin-2-ones 3 has been achieved by condensation of equimolar amounts of 7-hydrazino-2,5-diphenylpyrazolo[1,5-c]pyrimidine (1 and isatin (or isatin derivatives 2 at room temperature. The (E-products could be isomerized into corresponding the (Z-3 isomers. Reactions of the latter fused heterocyclic hydrazones towards different electro-philic reagents yielded the corresponding 3-substituted derivatives 4–7. Dehydrative cyclisation of the hydrazones 3 using phosphorus oxychloride afforded the 2,5-diphenyl- indolo[2,3-e]pyrazolo[1',5':3",4"]pyrimido[2",1"-c][1,2,4] triazines 13. The polyfused heterocyclic ring system 13 underwent electrophilic substitution reactions at position 4 rather than at position 3. The 3-bromo isomer of 17 was prepared by a sequence of reactions starting from 2,5-diphenylpyrazolo[1,5-c]pyrimidine-7(6H-thione (11. The orientation of the electrophilic attack was supported by spectroscopic and chemical evidence. Some of the synthesized compounds were found to possess slight to moderate activity against the microorganisms Bacillus subtilis, Micrococcus luteus, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa.

trans-(Cl)-[Ru(5,5'-diamide-2,2'-bipyridine)(CO)2 Cl2 ]: Synthesis, Structure, and Photocatalytic CO2 Reduction Activity.

Science.gov (United States)

Kuramochi, Yusuke; Fukaya, Kyohei; Yoshida, Makoto; Ishida, Hitoshi

2015-07-06

A series of trans-(Cl)-[Ru(L)(CO)2 Cl2 ]-type complexes, in which the ligands L are 2,2'-bipyridyl derivatives with amide groups at the 5,5'-positions, are synthesized. The C-connected amide group bound to the bipyridyl ligand through the carbonyl carbon atom is twisted with respect to the bipyridyl plane, whereas the N-connected amide group is in the plane. DFT calculations reveal that the twisted structure of the C-connected amide group raises the level of the LUMO, which results in a negative shift of the first reduction potential (Ep ) of the ruthenium complex. The catalytic abilities for CO2 reduction are evaluated in photoreactions (λ>400 nm) with the ruthenium complexes (the catalyst), [Ru(bpy)3 ](2+) (bpy=2,2'-bipyridine; the photosensitizer), and 1-benzyl-1,4-dihydronicotinamide (the electron donor) in CO2 -saturated N,N-dimethylacetamide/water. The logarithm of the turnover frequency increases by shifting Ep a negative value until it reaches the reduction potential of the photosensitizer. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Kuidas möödus majandusaasta 2006 / Lembo Tanning, Toivo Tanning

Index Scriptorium Estoniae

Tanning, Lembo

2007-01-01

Ilmunud ka: Buhgalterskije Novosti, nr. 4, 2007, lk. 36-40. Ülevaade viimase kümne aasta maailmamajanduse arengutest sisemajanduse kogutoodangu ja väliskaubanduse põhjal. Tabelid: G-7 SKP 2000. aasta hindades ja rahavahetuskursiga, mld USD; USA väliskaubandus ja -teenused, mld USD-d, 2004-2006. Graafik: Hiina RV SKP, triljon jüaani, 1990-2006. Diagramm: Maailma suurimad eksportöörid, mld USD, 2004-2006

39 CFR 5.2 - Committee procedure.

Science.gov (United States)

2010-07-01

... 39 Postal Service 1 2010-07-01 2010-07-01 false Committee procedure. 5.2 Section 5.2 Postal Service UNITED STATES POSTAL SERVICE THE BOARD OF GOVERNORS OF THE U.S. POSTAL SERVICE COMMITTEES (ARTICLE V) § 5.2 Committee procedure. Each committee establishes its own rules of procedure, consistent with...

Dual band monopole antenna for WLAN 2.4/5.2/5.8 with truncated ground

Science.gov (United States)

Chandan, Bharti, Gagandeep; Srivastava, Toolika; Rai, B. S.

2018-04-01

A dual-band mono-pole antenna is proposed for Wireless LAN applications. The WLAN band is obtained by cutting a rectangular ring and a circular slot in the radiating patch. The overall dimension of antenna is 17×16.5×0.8 mmł. The frequency bands obtained are 2.38-2.9 GHz and 4.7-6.1 GHz with ≤ - 10 dB return loss which covers WLAN 2.4/5.2/5.8 GHz bands. The behavior of the antenna is analyzed in terms of radiation pattern, peak realized gain, radiation efficiency and surface current density. It has dipole like radiation pattern with gain of 2.33 - 4.31 dBi for lower frequency band and 4.29 - 5.16 dBi for upper frequency band with radiation efficiency of 95-98% and 93-96% respectively. The parametric analysis is carried out to understand the consequence of the various shape parameters and to get an optimum design. The simulation and measurement gave the results having close agreement.

Ca2Cr0.5Ga1.5O5—An extremely redox-stable brownmillerite phase

International Nuclear Information System (INIS)

Luo, Kun; Amano Patino, Midori; Hayward, Michael A.

2015-01-01

Investigation of the Ca 2 Cr x Ga 2−x O 5 compositional series reveals a maximum chromium solubility of 25%. The most chromium rich composition, Ca 2 Cr 0.5 Ga 1.5 O 5 , adopts a brownmillerite-type anion deficient perovskite structure described in space group Pnma (a=5.368 Å, b=14.547 Å, c=5.593 Å). Neutron powder diffraction data reveals rigorous B-site cation order, with all of the tetrahedral coordination sites occupied exclusively by gallium and the octahedral coordination sites occupied by gallium or chromium. Annealing studies reveals Ca 2 Cr 0.5 Ga 1.5 O 5 is stable in both oxidizing (100% O 2 ) and reducing (5% H 2 in N 2 ) conditions up to 800 °C, suggesting it could find application as a stable host lattice for fuel cell electrodes or electrolytes with suitable doping to enhance catalytic behaviour and/or anionic conductivity. - Graphical abstract: Ca 2 Cr 0.5 Ga 1.5 O 5 , adopts a brownmillerite-type anion deficient perovskite structure yet it is stable in both oxidizing (100% O 2 ) and reducing (5% H 2 in N 2 ) conditions up to 800 °C. - Highlights: • Anion deficient oxide stable to both oxidation and reduction up to 800 °C. • Cation-ordered brownmillerite structure determined by powder neutron diffraction. • Low solubility of Cr 3+ in framework due to spherical d 3 electron configuration

2´-deoxy-5,6-dihydro-5-azacytidine - a less toxic alternative of 2´-deoxy-5-azacytidine: a comparative study of hypomethylating potential.

Science.gov (United States)

Matoušová, Marika; Votruba, Ivan; Otmar, Miroslav; Tloušťová, Eva; Günterová, Jana; Mertlíková-Kaiserová, Helena

2011-06-01

Restoration of transcriptionally silenced genes by means of methyltransferases inhibitors plays a crucial role in the current therapy of myelodysplastic syndromes and certain types of leukemias. A comparative study of hypomethylating activities of a series of 5-azacytidine nucleosides: 5-azacytidine (AC), 2'-deoxy-5-azacytidine (DAC) and its α-anomer (α-DAC), 5,6-dihydro-5-azacytidine (DHAC), 2'-deoxy-5,6-dihydro-5-azacytidine (DHDAC, KP-1212) and its α-anomer (α-DHDAC), and of a 2-pyrimidone ribonucleoside (zebularine) was conducted. Methylation-specific PCR was employed to detect the efficiency of individual agents on cyclin-dependent kinase inhibitor 2B and thrombospondin-1 hypermethylated gene loci. Overall changes in DNA methylation level were quantified by direct estimation of 5-methyl-2'-deoxycytidine-5'-monophosphate by HPLC using digested genomic DNA. Flow cytometric analysis of cell cycle progression and apoptotic markers was used to determine cytotoxicity of the compounds. mRNA expression was measured using qRT-PCR. 2'-deoxy-5,6-dihydro-5-azacytidine was found to be less cytotoxic and more stable than 2'-deoxy-5-azacytidine at the doses that induce comparable DNA hypomethylation and gene reactivation. This makes it a valuable tool for epigenetic research and worth further investigations to elucidate its possible therapeutic potential.

Magnetic properties of two new compounds: Pr2Ni3Si5 and Ho2Ni3Si5

International Nuclear Information System (INIS)

Mazumdar, C.; Padalia, B.D.; Godart, C.

1994-01-01

Formation of two more new materials, Pr 2 Ni 3 Si 5 and Ho 2 Ni 3 Si 5 , of the series, R 2 Ni 3 Si 5 (R = rare earth and Y) and their magnetic properties are reported here. These materials crystallize in the orthorhombic U 2 Co 3 Si 5 -type structure (space group Ibam). Magnetic susceptibility measurement in the temperature range 5 K--300 K show that the compound Pr 2 Ni 3 Si 5 order antiferromagnetically at T N ∼ 8.5 K and Ho 2 Ni 3 Si 5 at ∼ 6 K. Considering T N (Gd 2 Ni 3 Si 5 ) ∼ 15 K, T N (Pr 2 Ni 3 Si 5 ) ∼ 8.5 K is rather high. The magnetic susceptibility of both of the materials, in the paramagnetic state, follows a Curie-Weiss law with effective moment close to that of the corresponding free trivalent rare earth ion

Sc2[Se2O5]3: The First Rare-Earth Metal Oxoselenate(IV with Exclusively [Se2O5]2− Anions

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Stefan Greiner

2018-04-01

Full Text Available The scandium oxodiselenate(IV Sc2[Se2O5]3 was synthesized via solid-state reactions between scandium sesquioxide (Sc2O3 and selenium dioxide (SeO2 with thallium(I chloride (TlCl as fluxing agent in molar ratios of 1:4:2. Evacuated fused silica ampoules were used as reactions vessels for annealing the mixtures for five days at 800 °C. The new scandium compound crystallizes in the triclinic space group P 1 ¯ with the lattice parameters a = 663.71(5 pm, b = 1024.32(7 pm, c = 1057.49(8 pm, α = 81.034(2°, β = 87.468(2°, γ = 89.237(2° and Z = 2. There are two distinct Sc3+ positions, which show six-fold coordination by oxygen atoms as [ScO6]9− octahedra (d(Sc–O = 205–212 pm. Three different [Se2O5]2− anions provide these oxygen atoms with their terminal ligands (Ot. Each of the six selenium(IV central atoms exhibit a stereochemically active lone pair of electrons, so that all [Se2O5]2− anions consist of two ψ1-tetrahedral [SeO3]2− subunits (d(Se–Ot = 164–167 pm, d(Se–Ob = 176–185 pm, ∢(O–Se–O = 93–104° sharing one bridging oxygen atom (Ob with ∢(Se–Ob–Se = 121–128°. The vibrational modes of the complex anionic [Se2O5]2− entities were characterized via single-crystal Raman spectroscopy.

Molecular dynamics simulation based on the multi-component molecular orbital method: Application to H5O2+,D5O2+,andT5O2+

International Nuclear Information System (INIS)

Ishimoto, Takayoshi; Koyama, Michihisa

2012-01-01

Graphical abstract: Molecular dynamics method based on multi-component molecular orbital method was applied to basic hydrogen bonding systems, H 5 O 2 + , and its isotopomers (D 5 O 2 + andT 5 O 2 + ). Highlights: ► Molecular dynamics method with nuclear quantum effect was developed. ► Multi-component molecular orbital method was used as ab initio MO calculation. ► Developed method applied to basic hydrogen bonding system, H 5 O 2 + , and isotopomers. ► O ⋯ O vibrational stretching reflected to the distribution of protonic wavefunctions. ► H/D/T isotope effect was also analyzed. - Abstract: We propose a molecular dynamics (MD) method based on the multi-component molecular orbital (MC M O) method, which takes into account the quantum effect of proton directly, for the detailed analyses of proton transfer in hydrogen bonding system. The MC M O based MD (MC M O-MD) method is applied to the basic structures, H 5 O 2 + (called “Zundel ion”), and its isotopomers (D 5 O 2 + andT 5 O 2 + ). We clearly demonstrate the geometrical difference of hydrogen bonded O ⋯ O distance induced by H/D/T isotope effect because the O ⋯ O in H-compound was longer than that in D- or T-compound. We also find the strong relation between stretching vibration of O ⋯ O and the distribution of hydrogen bonded protonic wavefunction because the protonic wavefunction tends to delocalize when the O ⋯ O distance becomes short during the dynamics. Our proposed MC M O-MD simulation is expected as a powerful tool to analyze the proton dynamics in hydrogen bonding systems.

N-[(2S-4-Chloro-2-(l-menthyloxy-5-oxo-2,5-dihydro-3-furyl]-l-alanine

Directory of Open Access Journals (Sweden)

Kai Yang

2009-05-01

Full Text Available The title compound, C17H26ClNO5, was prepared via a tandem asymmetric Michael addition–elimination reaction of (5S-3,4-dichloro-5-(l-menthyloxyfuran-2(5H-one and l-alanine in the presence of potassium hydroxide. The five-membered furanone ring is approximately planar while the six-membered menthyloxy ring adopts a chair conformation. The crystal packing is stabilized by intermolecular O—H...O and N—H...O hydrogen bonds.

5-[3-(2,5-Dimethoxyphenylprop-2-enylidene]-1,3-diethyl-2-thioxohexahydropyrimidine-4,6-dione

Directory of Open Access Journals (Sweden)

Abdullah Mohamed Asiri

2009-08-01

Full Text Available 1,3-Diethyl-2-thiobarbituric acid reacts with 2,5-dimethoxybenzaldehyde to form the title Knoevenagel product, C19H22N2O4S. In the compound, the two six-membered rings at either end of the three-membered –CHCHCH– chain are nearly coplanar with this fragment (r.m.s. deviation of the two six-membered rings and the three chain atoms = 0.08 Å.

(5/2-→5/2+) 803 keV beta transition in 147Nd

International Nuclear Information System (INIS)

Lakshminarayana, S.; Srinivasa Rao, M.; Seshagiri Rao, V.; Sastry, D.L.

1978-01-01

The existing experimental results on the 5/2 - →5/2 + 803 keV beta transition in 147 Nd are mutually contradictory to classify it under xi-approximation. To resolve this contradiction, the β-γ directional correlations are performed carefully as a function of energy using a conventional fast-slow coincidence scintillation system. The attenuation factor G 2 in this case turns out to be 0.64 +- 0.05. The results on the longitudinal electron polarization and the shape measurements are combined with the present results and an attempt is made to extract the nuclear matrix elements governing this first forbidden non-unique beta transition following Simm's formalism. Results are discussed based on the final sets of matrix elements. (auth.)

Phase Content and Equilibrium Relationships in Ternary Systems MOx/VO2,5/PO2,5 (M = TiIV, ZrIV, NbV; x = 2 or 2,5) with Additions for Four-Component System Ti/Cr/P/O

International Nuclear Information System (INIS)

Titlbach, Sven

2014-01-01

In the systems TiO 2 / V 2 O 5 / P 2 O 5 , ZrO 2 / V 2 O 5 / P 2 O 5 and Nb 2 O 5 / V 2 O 5 / P 2 O 5 studies on phase composition and the equilibrium relations were performed in the context of the heterogeneously catalyzed gas-phase oxidation of n-butane to maleic anhydride. Here is a selection of the research findings: in the system TiO 2 / V 2 O 5 / P 2 O 5 the hitherto unknown orthophosphate (VO)Ti 6 (PO 4 ) 9 and the mixed crystal series Ti(P 1-x V x ) 2 O 7 (0 ≤ x ≤ 0,24; 0,30 ≤ x ≤ 0,43) with miscibility gap was detected. In the quasi-ternary system ZrO 2 / V 2 O 5 / P 2 O 5 the literature well described gapless solid solution Zr(P 1-x V x ) 2 O 7 was confirmed and investigated radiographically and by NMR spectroscopy. In the system Nb 2 O 5 / V 2 O 5 / P 2 O 5 the mixed crystal series Nb 1-x V x O(PO 4 ) (0 ≤ x ≤ 0,36), P 1-x V x Nb 9 O 25 (0 ≤ x ≤ 1) and NbOP 1-x V x O 4 (0 ≤ x ≤ 0,20) were found.

2′-deoxy-5,6-dihydro-5-azacytidine—a less toxic alternative of 2′-deoxy-5-azacytidine: A comparative study of hypomethylating potential

OpenAIRE

Matoušová, Marika; Votruba, Ivan; Otmar, Miroslav; Tloušťová, Eva; Günterová, Jana; Mertlíková-Kaiserová, Helena

2011-01-01

Restoration of transcriptionally silenced genes by means of methyltransferases inhibitors plays a crucial role in the current therapy of myelodysplastic syndromes and certain types of leukemias. A comparative study of hypomethylating activities of a series of 5-azacytidine nucleosides: 5-azacytidine (AC), 2′-deoxy-5-azacytidine (DAC) and its α-anomer (α-DAC), 5,6-dihydro-5-azacytidine (DHAC), 2′-deoxy-5,6-dihydro-5-azacytidine (DHDAC, KP-1212) and its α-anomer (α-DHDAC), and of a 2-pyrimidone...

On the anisotropy energies for YCo5, RCo5, Y2Co17, and R2Co17

International Nuclear Information System (INIS)

Takahashi, H.; Hikosaka, K.; Ohtsuka, S.; Seo, A.; Ukai, T.; Mori, N.

1988-01-01

The approximate d bands for YCo 5 , RCo 5 , Y 2 Co 17 , and R 2 Co 17 (Th 2 Zn 17 and Th 2 Ni 17 type) are formulated by Deegan's prescription and the formulas of Slater and Koster. The experimental results of YCo 5 and Y 2 Co 17 are discussed by using these approximate d bands. For RCo 5 and R 2 Co 17 the discussions are made by adopting the localized model and the band model for 4f electrons

SO2 and NO removal from flue gas over V2O5/AC at lower temperatures - role of V2O5 on SO2 removal

International Nuclear Information System (INIS)

Ma, Jianrong; Liu, Zhenyu; Liu, Qingya; Guo, Shijie; Huang, Zhanggen; Xiao, Yong

2008-01-01

Supporting V 2 O 5 onto an activated coke (AC) has been reported to significantly increase the AC's activity in simultaneous SO 2 and NO removal from flue gas. To understand the role of V 2 O 5 on SO 2 removal, V 2 O 5 /AC is studied through SO 2 removal reaction, surface analysis, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) techniques. It is found that the main role of V 2 O 5 in SO 2 removal over V 2 O 5 /AC is to catalyze SO 2 oxidation through a VOSO 4 -like intermediate species, which reacts with O 2 to form SO 3 and V 2 O 5 . The SO 3 formed transfers from the V sites to AC sites and then reacts with H 2 O to form H 2 SO 4 . At low V 2 O 5 loadings, a V atom is able to catalyze as many as 8 SO 2 molecules to SO 3 . At high V 2 O 5 loadings, however, the number of SO 2 molecules catalyzed by a V atom is much less, due possibly to excessive amounts of V 2 O 5 sites in comparison to the pores available for SO 3 and H 2 SO 4 storage. (author)

RELAP5/MOD2 code assessment

International Nuclear Information System (INIS)

Nithianandan, C.K.; Shah, N.H.; Schomaker, R.J.; Miller, F.R.

1985-01-01

Babcock and Wilcox (B and W) has been working with the code developers at EG and G and the US Nuclear Regulatory Commission in assessing the RELAP5/MOD2 computer code for the past year by simulating selected separate-effects tests. The purpose of this assessment has been to evaluate the code for use in MIST (Ref. 2) and OTIS integral system tests simulations and in the prediction of pressurized water reactor transients. B and W evaluated various versions of the code and made recommendations to improve code performance. As a result, the currently released version (cycle 36.1) has been improved considerably over earlier versions. However, further refinements to some of the constitutive models may still be needed to further improve the predictive capability of RELAP5/MOD2. The following versions of the code were evaluated. (1) RELAP/MOD2/Cycle 22 - first released version; (2) YELAP5/Cycle 32 - EG and G test version of RELAP5/MOD2/Cycle 32; (3) RELAP5/MOD2/Cycle 36 - frozen cycle for international code assessment; (4) updates to cycle 36 based on recommendations developed by B and W during the simulation of a Massachusetts Institute of Technology (MIT) pressurizer test; and (5) cycle 36.1 updates received from EG and G

RELAP5/MOD2 code assessment

Energy Technology Data Exchange (ETDEWEB)

Nithianandan, C.K.; Shah, N.H.; Schomaker, R.J.; Miller, F.R.

1985-11-01

Babcock and Wilcox (B and W) has been working with the code developers at EG and G and the US Nuclear Regulatory Commission in assessing the RELAP5/MOD2 computer code for the past year by simulating selected separate-effects tests. The purpose of this assessment has been to evaluate the code for use in MIST (Ref. 2) and OTIS integral system tests simulations and in the prediction of pressurized water reactor transients. B and W evaluated various versions of the code and made recommendations to improve code performance. As a result, the currently released version (cycle 36.1) has been improved considerably over earlier versions. However, further refinements to some of the constitutive models may still be needed to further improve the predictive capability of RELAP5/MOD2. The following versions of the code were evaluated. (1) RELAP/MOD2/Cycle 22 - first released version; (2) YELAP5/Cycle 32 - EG and G test version of RELAP5/MOD2/Cycle 32; (3) RELAP5/MOD2/Cycle 36 - frozen cycle for international code assessment; (4) updates to cycle 36 based on recommendations developed by B and W during the simulation of a Massachusetts Institute of Technology (MIT) pressurizer test; and (5) cycle 36.1 updates received from EG and G.

Formation pathways in the synthesis and properties of (Tl0.5Pb0.5)(Sr0.9Ba0.1)2Ca2Cu3Oz and (Tl0.5Pb0.5)(Sr0.8Ba0.2)2Ca2Cu3Oz-1223 superconductors

International Nuclear Information System (INIS)

Auinger, M; Gritzner, G; Bertrand, Ch; Galez, Ph; Soubeyroux, J-L

2007-01-01

The formation pathway of (Tl 0.5 Pb 0.5 )(Sr 0.9 Ba 0.1 ) 2 Ca 2 Cu 3 O z and (Tl 0.5 Pb 0.5 )(Sr 0.8 Ba 0.2 ) 2 Ca 2 Cu 3 O z was studied by neutron and x-ray diffraction. The following reaction pathway was proposed: thallium oxide and lead oxide react with Sr-rich (Sr 1-x Ca x )CuO 2 and Ca-rich (Ca x Sr 1-x )O to form Sr 4 Tl 2 O 7 and (Ca x Sr 1-x )PbO 3 , respectively. The thallate and the plumbate compounds then form the (Tl 0.5 Pb 0.5 )-1212 phase starting at a temperature of 600 deg. C. Finally, between 850 and 900 deg. C, the 1223 phase is formed from (Tl 0.5 Pb 0.5 )-1212 (Ca x Sr 1-x ) 2 CuO 3 and CuO. Parallel experiments to fabricate the (Tl, Pb)-1223 superconductor resulted in specimens with critical temperatures of 117.5 K and 116 K, respectively, and transition widths of 2 K. Differences between the pathways for the formation of Pb-doped, Sr-rich and Pb-free, Ba-rich Tl-1223 superconductors are discussed

Taimne linn - fantaasia saab tegelikkuseks / Kadri Kalle

Index Scriptorium Estoniae

Kalle, Kadri, 1984-

2009-01-01

Belgia arhitektist Luc Schuitenist ja tema töödest Brüsselis 2009. a. suvel eksponeeritud näitusel "Vegetal City". Arhitekt pakub loovaid lähenemisi sellele, kuidas linnad võiksid rohkem sarnaneda looduslike elupaikadega. Juba 1970. aastatel ehitas ta maja, mis kasutab päikese- ja tuuleenergiat, tema ideekavandite hulka kuuluvad ka üllatava disainiga keskkonnasõbralikud sõidukid

Kuidas valiti president 1996. aastal? / Rein Toomla

Index Scriptorium Estoniae

Toomla, Rein, 1951-

2002-01-01

Autor leiab 1996. aasta presidendivalimisi analüüsides, et oluliseks tuleb pidada seda, et valimised suudeti põhiseaduses ettenähtud korras läbi viia ning ei pidanud käivituma erakorraliste valimiste mehhanism. Tabelid: 1995. a. Riigikogu valimised; Riigikogu fraktsioonid 1996. a. suvel; Toetus presidendikandidaatidele; Presidendivalimised Riigikogus; Arvatavasti Lennart Meri poolt; Arvatavasti Arnold Rüütli poolt; Presidendivalimised Valimiskogus

Eesti Filharmoonia Kammerkoor esineb kanalis Mezzo

Index Scriptorium Estoniae

2004-01-01

Üleeuroopalise klassikalise muusika telekanali Mezzo ja ETV koostöös valiti välja kolm telesaadet telekanalis Mezzo tutvustamaks Euroopale Eesti süvakultuuri: 2002 suvel Tallinna Rootsi Mihkli kirikus Tallinna Kammerorkestri ja Kammerkoori kontsert kavaga "Baltic Voices" on eetris 14-16. apr.õhtul, teistel õhtutel ka Erkki-Sve Tüüri teos "Ardor" ning Vanemuise teatri balletitrupi tantsuetendus "Fluxus"

Pyridinium 5-[(1,3-diethyl-6-hydroxy-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidin-5-yl(2-methoxyphenylmethyl]-1,3-diethyl-4,6-dioxo-2-thioxopyrimidin-5-ide

Directory of Open Access Journals (Sweden)

Abdullah Mohamed Asiri

2009-08-01

Full Text Available 1,3-Diethyl-2-thiobarbituric acid reacts with 2-anisaldehyde to form the Michael addition product 2-anisylbis(1,3-diethyl-2-thiobarbitur-5-ylmethanate, which crystallizes as the title pyridinium salt, C5H6N+·C24H29N4O5S2−, when it reacts with the pyridine used to catalyse the reaction. There are two independent ion pairs in the crystal structure. The anion features a methine C atom connected to three six-membered rings; one of the rings carries a hydroxy group, which engages in hydrogen bonding with the carbonyl group belonging to another ring. The monoclinic unit cell emulates an orthorhombic unit cell, and is a twin with a minor twin component of 35%.

Abacavir methanol 2.5-solvate

Directory of Open Access Journals (Sweden)

Phuong-Truc T. Pham

2009-08-01

Full Text Available The structure of abacavir (systematic name: {(1S,4R-4-[2-amino-6-(cyclopropylamino-9H-purin-9-yl]cyclopent-2-en-1-yl}methanol, C14H18N6O·2.5CH3OH, consists of hydrogen-bonded ribbons which are further held together by additional hydrogen bonds involving the hydroxyl group and two N atoms on an adjacent purine. The asymmetric unit also contains 2.5 molecules of methanol solvate which were grossly disordered and were excluded using SQUEEZE subroutine in PLATON [Spek, (2009. Acta Cryst. D65, 148–155].

2-Amino-5-chloropyridinium trifluoroacetate

Directory of Open Access Journals (Sweden)

Madhukar Hemamalini

2010-04-01

Full Text Available The asymmetric unit of the title salt, C5H6ClN2+·C2F3O2−, contains two independent 2-amino-5-chloropyridinium cations and two independent trifluoroacetate anions. The F atoms of both anions are disordered over two sets of positions, with occupancy ratios of 0.672 (12:0.328 (12 and 0.587 (15:0.413 (15. In the crystal, the cations and anions are linked via N—H...O and C—H...O hydrogen bonds, forming a two-dimensional network parallel to (001.

Rietveld refinement of the orthorhombic Pbca structures of Rb2CdSi5O12, Cs2MnSiO5O12, Cs2CoSi5O12 and Cs2NiSi5O12 leucites by synchrotron X-ray powder diffraction

International Nuclear Information System (INIS)

Bell, A.M.T.; Henderson, C.M.B.

1996-01-01

Analysis of high-resolution synchrotron X-ray powder diffraction patterns for hydrothermally synthesized Rb 2 CdSi 5 O 12 and Cs 2 MnSi 5 O 12 leucite analogues, and dry-synthesized Cs 2 CoSi 5 O 12 and Cs 2 NiSi 5 O 12 leucite analogues showed that they have an orthorhombic Pbca structure. The structures have been refined by the Rietveld method, showing that the tetrahedrally coordinated atoms (Si, Cd, Mn, Co and Ni) are ordered on separate sites. The Cs 2 MnSi 5 O 12 , Cs 2 CoSi 5 O 12 and Cs 2 NiSi 5 O 12 leucite samples are unusual in containing SiO 4 tetrahedra which are more distorted, on average, than the larger MnO 4 , CoO 4 and NiO 4 tetrahedra. The JCPDS file numbers for Rb 2 CdSi 5 O 12 , Cs 2 MnSi 5 O 12 and Cs 2 CoSi 5 O 12 are 46-1491, 46-1492 and 46-1493, respectively. (orig.)

(Carbonato-κ(2)O,O')bis-(5,5'-dimethyl-2,2'-bipyridyl-κ(2)N,N')cobalt(III) bromide trihydrate.

Science.gov (United States)

Arun Kumar, Kannan; Meera, Parthsarathi; Amutha Selvi, Madhavan; Dayalan, Arunachalam

2012-04-01

In the title complex, [Co(CO(3))(C(12)H(12)N(2))(2)]Br·3H(2)O, the Co(III) cation has a distorted octa-hedral coordination environment. It is chelated by four N atoms of two different 5,5'-dimethyl-2,2'-bipyridyl (dmbpy) ligands in axial and equatorial positions, and by two O atoms of a carbonate anion completing the equatorial positions. Although the water mol-ecules are disordered and their H atoms were not located, there are typical O⋯O distances between 2.8 and 3.0 Å, indicating O-H⋯O hydrogen bonding. The crystal packing is consolidated by C-H⋯O and C-H⋯Br hydrogen bonds, as well as π-π stacking inter-actions between adjacent pyridine rings of the dmbpy ligands, with centroid-centroid distances of 3.694 (3) and 3.7053 (3) Å.

Diaquabis[5-(2-pyridyltetrazolato-κ2N1,N5]iron(II

Directory of Open Access Journals (Sweden)

Min Hu

2009-04-01

Full Text Available The title complex, [Fe(C6H4N52(H2O2], was synthesized by the reaction of ferrous sulfate with 5-(2-pyridyl-2H-tetrazole (HL. The FeII atom, located on a crystallographic center of inversion, is coordinated by four N-atom donors from two planar trans-related deprotonated L ligands and two O atoms from two axial water molecules in a distorted octahedral geometry. The FeII mononuclear units are further connected by intermolecular O—H...N and C—H...O hydrogen-bonding interactions, forming a three-dimensional framework.

2'-deoxy-5,6-dihydro-5-azacytidine-a less toxic alternative of 2'-deoxy-5-azacytidine. A comparative study of hypomethylating potential

Czech Academy of Sciences Publication Activity Database

Matoušová, Marika; Votruba, Ivan; Otmar, Miroslav; Tloušťová, Eva; Günterová, Jana; Mertlíková-Kaiserová, Helena

2011-01-01

Roč. 6, č. 6 (2011), s. 769-776 ISSN 1559-2294 R&D Projects: GA MŠk 1M0508 Institutional research plan: CEZ:AV0Z40550506 Keywords : epigenetic therapy * nucleoside analogs * DNA methylation * 2'-deoxy-5-azacytidine * 2'-deoxy-5,6-dihydro-5-azacytidine Subject RIV: CE - Biochemistry Impact factor: 4.318, year: 2011

One-pot oxidation and bromination of 3,4-diaryl-2,5-dihydrothiophenes using Br2: synthesis and application of 3,4-diaryl-2,5-dibromothiophenes.

Science.gov (United States)

Dang, Yizhe; Chen, Yi

2007-08-31

A class of 3,4-diaryl-2,5-dibromothiophenes (1b-5b) was synthesized by a one-pot reaction of 3,4-diaryl-2,5-dihydrothiophenes with Br2 reagent in excellent yield (83-92%). It was found that Br2 performed a double function (oxidation and bromination) during the conversion of 3,4-diaryl-2,5-dihydrothiophenes to 3,4-diaryl-2,5-dibromothiophenes. The application of 3,4-diaryl-2,5-dibromothiophenes used as building blocks was also investigated. Employing 3,4-diphenyl-2,5-dibromothiophene (1b) as a template, a class of 2,3,4,5-tetraarylthiophenes was prepared by the Suzuki coupling reaction. This provided a new and simple approach to the preparation of 2,3,4,5-tetraarylthiophenes.

Hallucinogenic 5-HT2AR agonists LSD and DOI enhance dopamine D2R protomer recognition and signaling of D2-5-HT2A heteroreceptor complexes.

Science.gov (United States)

Borroto-Escuela, Dasiel O; Romero-Fernandez, Wilber; Narvaez, Manuel; Oflijan, Julia; Agnati, Luigi F; Fuxe, Kjell

2014-01-03

Dopamine D2LR-serotonin 5-HT2AR heteromers were demonstrated in HEK293 cells after cotransfection of the two receptors and shown to have bidirectional receptor-receptor interactions. In the current study the existence of D2L-5-HT2A heteroreceptor complexes was demonstrated also in discrete regions of the ventral and dorsal striatum with in situ proximity ligation assays (PLA). The hallucinogenic 5-HT2AR agonists LSD and DOI but not the standard 5-HT2AR agonist TCB2 and 5-HT significantly increased the density of D2like antagonist (3)H-raclopride binding sites and significantly reduced the pKiH values of the high affinity D2R agonist binding sites in (3)H-raclopride/DA competition experiments. Similar results were obtained in HEK293 cells and in ventral striatum. The effects of the hallucinogenic 5-HT2AR agonists on D2R density and affinity were blocked by the 5-HT2A antagonist ketanserin. In a forskolin-induced CRE-luciferase reporter gene assay using cotransfected but not D2R singly transfected HEK293 cells DOI and LSD but not TCB2 significantly enhanced the D2LR agonist quinpirole induced inhibition of CRE-luciferase activity. Haloperidol blocked the effects of both quinpirole alone and the enhancing actions of DOI and LSD while ketanserin only blocked the enhancing actions of DOI and LSD. The mechanism for the allosteric enhancement of the D2R protomer recognition and signalling observed is likely mediated by a biased agonist action of the hallucinogenic 5-HT2AR agonists at the orthosteric site of the 5-HT2AR protomer. This mechanism may contribute to the psychotic actions of LSD and DOI and the D2-5-HT2A heteroreceptor complex may thus be a target for the psychotic actions of hallunicogenic 5-HT2A agonists. Copyright © 2013 Elsevier Inc. All rights reserved.

Photocatalytic activity of TiO2/Nb2O5/PANI and TiO2/Nb2O5/RGO as new nanocomposites for degradation of organic pollutants.

Science.gov (United States)

Zarrin, Saviz; Heshmatpour, Felora

2018-06-05

In this study, highly active titanium dioxide modified by niobium oxide (Nb 2 O 5 ), polymer (PANI) and reduced graphene oxide (RGO) were successfully prepared. The morphology, structure, surface area and light absorption properties of the present nanocomposites for removal of methylene blue (MB) and methyl orange (MO) were investigated and compared with those of TiO 2 /Nb 2 O 5 and TiO 2 nanoparticles. The characterization techniques such as XRD, FT-IR, UV-vis, SEM, EDX, BET and TEM were employed in order to identify the nanocomposites. Also, photocatalytic properties of TiO 2 /Nb 2 O 5 /PANI and TiO 2 /Nb 2 O 5 /RGO nanocomposites under visible light irradiation were studied. In this way, the obtained results were compared to each other and also compared to TiO 2 /Nb 2 O 5 and TiO 2 nanoparticles. In this context, the chemical oxygen demand (COD) removal follows the photodegradation in observed performance. The results indicate that reduced TiO 2 /Nb 2 O 5 nanocomposite is effectively modified by graphene oxide to give TiO 2 /Nb 2 O 5 /RGO composite. The TiO 2 /Nb 2 O 5 /RGO exhibits significantly higher photocatalytic activity in degradation of organic dyes under visible light rather than that of TiO 2 /Nb 2 O 5 /PANI, TiO 2 /Nb 2 O 5 and pure TiO 2 . Copyright © 2018 Elsevier B.V. All rights reserved.

7-{[2-(4-Hydroxyphenylmethylidene]amino}-1,3-thiazol-4-yl-2-(methoxyiminoacetyl]amino}-3-{[(2-methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-ylsulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid

Directory of Open Access Journals (Sweden)

Ghulam Fareed

2012-05-01

Full Text Available Novel 7-{[2-(4-hydroxyphenylmethylidene]amino}-1,3-thiazol-4-yl-2-(methoxyiminoacetyl]amino}-3-{[(2-methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-ylsulfanyl]methyl}-8-oxo-5-thia-1azabicyclo [4.2.0]oct-2-ene-2-carboxylic acid was prepared by condensation of ceftriaxone disodium (1 with 4-hydroxybenzaldehyde (2 in ethanol under reflux conditions for 3–4 h. The structure of synthesized compound was elucidated using LCMS, ¹H-NMR, and CHN techniques.

Atmospheric chemistry of C2F5CHO: mechanism of the C2F5C(O)O-2+HO2 reaction

DEFF Research Database (Denmark)

Andersen, Mads Peter Sulbæk; Hurley, MD; Wallington, TJ

2003-01-01

in a yield of 76 +/- 4 The gas phase reaction of CnF2n+1C(O)O-2 with HO2 radicals offers a potential explanation for at least part of the observed environmental burden of fluorinated carboxylic acids, CnF2n+1C(O)OH. As part of this work an upper limit for the rate constant of reaction of Cl atorns with C2F5C......(O)OH at 296 K was determined; k(Cl + C2F5C(O)OH) 1 x 10(-11) cm(3) molecule(-1) s(-1). (C) 2003 Published by Elsevier B.V....

Two polymeric nickel(II) complexes with aromatic benzene-1,2,4,5-tetracarboxylate and pyridine-2,5-dicarboxylate linkers.

Science.gov (United States)

Atria, Ana María; Corsini, Gino; González, Lissette; Garland, Maria Teresa; Baggio, Ricardo

2009-07-01

(Mu-benzene-1,2,4,5-tetracarboxylato-kappa(2)O(1):O(4))bis[aquabis(2,2-methylpropane-1,3-diamine-kappa(2)N,N')nickel(II)] methanol disolvate tetrahydrate, [Ni(2)(C(10)H(2)O(8))(C(5)H(14)N(2))(4)(H(2)O)(2)].2CH(4)O.4H(2)O, (I), is dinuclear, with elemental units built up around an inversion centre halving the benzene-1,2,4,5-tetracarboxylate (btc) anion, which bridges two symmetry-related Ni(II) cations. The octahedral Ni polyhedron is completed by two chelating 2,2-methylpropane-1,3-diamine (dmpda) groups and a terminal aqua ligand. Two methanol and four water solvent molecules are involved in a number of N-H...O and O-H...O hydrogen bonds which define a strongly bound two-dimensional supramolecular structure. The structure of catena-poly[[[bis(2,2-methylpropane-1,3-diamine-kappa(2)N,N')nickel(II)]-mu-pyridine-2,5-dicarboxylato-kappa(3)O(5):N,O(2)-[(2,2-methylpropane-1,3-diamine-kappa(2)N,N')nickel(II)]-mu-pyridine-2,5-dicarboxylato-kappa(3)N,O(2):O(5)] octahydrate], {[Ni(2)(C(7)H(3)NO(4))(2)(C(5)H(14)N(2))(3)].8H(2)O}(n), (II), is polymeric, forming twisted chains around three independent Ni centres, two of which lie on inversion centres and the third in a general position. There are three chelating dmpda ligands (one disordered over two equally populated positions), which are each attached to a different cation, and two pyridine-2,5-dicarboxylate (pdc) anions, both chelating the Ni centre in general positions through an -O-C-C-N- loop, while acting as bridges to the remaining two centrosymmetric Ni atoms. There are, in addition, eight noncoordinated water molecules in the structure, some of which are disordered.

Synthesis and characterization of lanthanum complex (5-choloro-8-hydroxy quinoline) bis (2-2'bipyridine) lanthanum La(Bpy)2(5-Clq)

Science.gov (United States)

Kumar, Rahul; Soam, Ankur; Bhargava, Parag

2017-05-01

Lanthanum complex, (5-choloro 8-hydroxy quinoline) bis (2-2'bipyridine) has been synthesized and characterized by different techniques. Lanthanum complex, La(Bpy)2(5-Clq) was characterized for structural, thermal and photoluminescence analysis. Structural analysis of this material was done by Fourier transformed infrared spectroscopy (FTIR) and mass spectroscopy. Thermal analysis of this material was done by thermal gravimetric analysis (TGA) and material shows the thermal stability up to 400°C. Absorption and emission spectra of the material was measured by UV-visible spectroscopy and photoluminescence spectroscopy. Solution of this material La(Bpy)2(5-Clq) in ethanol showed absorption peak at 332 nm, which may be attributed due to (π - π*) transitions. The photoluminescence spectra of La(Bpy)2(5-Clq) in ethanol solution showed intense peak at 505 nm.

Abnormal reaction of 2,5-Dimethylfuran

International Nuclear Information System (INIS)

Pevzner, L.M.; Ignat'ev, V.M.

1987-01-01

The authors have shown that the expected hydroxymethylation at position 3 of the furan ring does not occur in the reaction of 2,5-dimethylfuran with paraform in acetic acid at 70-80 0 C with the dimethylfuran and paraform in molar ratios of 2:1-1:2, but the products from substitution in the side chain are formed. By vacuum distillation of the reaction mass the authors isolated 2-(5-methyl-2-furyl)- ethanol and a hygroscopic viscous product melting at 136 0 C (5 mm Hg). The yield of the reaction products depends on the molar ratio of the dimethylfuran and paraform. The PMR spectrum of the product contains signals for the β-protons of the furan ring with chemical shifts of 5.81 and 5.90 ppm, a signal for the methyl group in the furan ring at 2.22 ppm, a doublet at 3.72 ppm with spin-spin coupling constant of 6 Hz, a weak quintet at 3.20 ppm with the same constant, and a broadened signal in the region of 4.66 ppm for the proton of the hydroxyl group

Crystal and molecular structure of the coordination compounds of Er3+ with 1-(methoxydiphenylphosphoryl)-2-diphenylphosphorylbenzene [ErL21(NO3)2]2[Er(NO3)2(H2O)5]0.333(NO3)2.333 · 2.833H2O and its ethyl substituted derivative [ErL22(NO3)2][Er(NO3)5]0.5 · 0.5H2O

International Nuclear Information System (INIS)

Polyakova, I. N.; Baulin, V. E.; Ivanova, I. S.; Pyatova, E. N.; Sergienko, V. S.; Tsivadze, A. Yu.

2015-01-01

The coordination compounds of Er 3+ with 1-(methoxydiphenylphosphoryl)-2-diphenylphosphorylbenzene [ErL 2 1 (NO 3 ) 2 ] 2 [Er(NO 3 ) 2 (H 2 O) 5 ] 0.333 (NO 3 ) 2.333 · 2.833H 2 O (I) and its ethyl substituted derivative [ErL 2 2 (NO 3 ) 2 ][Er(NO 3 ) 5 ] 0.5 · 0.5H 2 O (II) are synthesized and their crystal structures are studied. I and II contain [ErL 2 (NO 3 ) 2 ] + complex cations of identical composition and close structure. The eight-vertex polyhedron of the Er atom in the shape of a distorted octahedron with two split trans vertices is formed by the O atoms of the phosphoryl groups of L ligands and nitrate anions. L ligands close nine-membered metallocycles. The structures contain spacious channels which are populated differently, namely, by disordered [Er(NO 3 ) 2 (H 2 O) 5 ] + complex cations, NO 3 − anions, and crystallization water molecules in I and disordered [Er(NO 3 ) 5 ] 2− complex anions and crystallization water molecules in II. The IR spectra of I and II are studied

Liquid crystal europium(III) β-diketonato complex with 5,5'-di(heptadecyl)-2,2'-bipyridine

International Nuclear Information System (INIS)

Knyazev, A.A.; Lobkov, V.S.; Galyametdinov, Yu.G.

2004-01-01

Liquid crystal europium(III) complex containing β-diketone and 5,5-di(heptadecyl)-2,2'-bipyridine as ligands was prepared in ethanol solution and was isolated as a yellow precipitate with 62% yield. The product was characterized by data of elementary analysis, thermography, IR spectroscopy and luminescence spectra. Temperatures of crystal-mesophase and mesophase-isotropic liquid phase transitions amount to 95 and 130 Deg C respectively [ru

Structure and magnetism of the Sm{sub 7.5}Y{sub 2.5}Fe{sub 90−x}Si{sub x} (x=0.0, 2.5, 5.0, 7.5 and 10) alloys

Energy Technology Data Exchange (ETDEWEB)

Yang, W.Y.; Zhao, H.; Lai, Y.F.; Du, H.L.; Liu, S.Q.; Wang, C.S.; Han, J.Z.; Yang, Y.C. [State Key Laboratory for Mesoscopic Physics, School of Physics, Peking University, Beijing 100871 (China); Yu, X.; Qi, Z.Q. [GanZhou Fortune Electronic Co. Ltd., Jiangxi (China); Yang, J.B. [State Key Laboratory for Mesoscopic Physics, School of Physics, Peking University, Beijing 100871 (China); Collaborative Innovation Center of Quantum Matter, Beijing (China)

2017-03-15

Sm{sub 7.5}Y{sub 2.5}Fe{sub 90−x}Si{sub x} (x=0.0, 2.5, 5.0, 7.5 and 10) alloys have been prepared by arc melting method and equilibrium disordered Th{sub 2}Zn{sub 17}-type phases, (Sm,Y){sub 2−y}(Fe,Si){sub 17+2y}, with relative lower rare-earth content than the ordered Th{sub 2}Zn{sub 17}-type phase, have been obtained. Compared to the ordered Th{sub 2}Zn{sub 17}-type structure, the X-ray diffraction (XRD) intensity of the superstructure lines of the (Sm,Y){sub 2−y}(Fe,Si){sub 17+2y} decreases with the increase of the Si content and becomes zero for x=10. According to the refinement with the disordered Th{sub 2}Zn{sub 17}-type structure, the occupation rates of the R atoms at (3a) and (6c) sites tend to reach the same value with the increase of the Si content, and the lattice parameter a decreases while the lattice parameter c increases, leading to an increase of c/a. It was found that the atomic ratio of Fe(Si)/Sm(Y) in the disordered Th{sub 2}Zn{sub 17}-type structure increases with the increase of Si content and reaches a maximum value of 9.07 with x=10. The XRD diagrams of the magnetic aligned samples indicate that the easy magnetization direction (EMD) of the (Sm,Y){sub 2−y}(Fe,Si){sub 17+2y} is in the a-b plane, and the change of the EMD in a-b plane has also been observed due to the Si preferred site occupation. The remanence ratios along the easy direction are higher than that along hard direction; however, all the remanence ratios are less than 0.5. The magnetocrystalline anisotropy constant K increases first and then decreases with increasing the Si content. The Curie temperature of Sm{sub 7.5}Y{sub 2.5}Fe{sub 90−x}Si{sub x} alloys increases by about 65 K per Si. The saturation magnetization increases first and then decreases with a maximum of 135.5 emu/g observed for x=2.5 at room temperature. - Highlights: • Equilibrium disordered Th{sub 2}Zn{sub 17}-type phases (Sm,Y){sub 2-y}(Fe,Si){sub 17+2y} have been obtained. • The atomic ratio of

Genotype-Dependent Difference in 5-HT2C Receptor-Induced Hypolocomotion: Comparison with 5-HT2A Receptor Functional Activity

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Darya V. Bazovkina

2015-01-01

Full Text Available In the present study behavioral effects of the 5-HT2C serotonin receptor were investigated in different mouse strains. The 5-HT2C receptor agonist MK-212 applied intraperitoneally induced significant dose-dependent reduction of distance traveled in the open field test in CBA/Lac mice. This effect was receptor-specific because it was inhibited by the 5-HT2C receptor antagonist RS102221. To study the role of genotype in 5-HT2C receptor-induced hypolocomotion, locomotor activity of seven inbred mouse strains was measured after MK-212 acute treatment. We found that the 5-HT2C receptor stimulation by MK-212 decreased distance traveled in the open field test in CBA/Lac, C57Bl/6, C3H/He, and ICR mice, whereas it failed to affect locomotor activity in DBA/2J, Asn, and Balb/c mice. We also compared the interstrain differences in functional response to 5-HT2C and 5-HT2A receptors activation measured by the quantification of receptor-mediated head-twitches. These experiments revealed significant positive correlation between 5-HT2C and 5-HT2A receptors functional responses for all investigated mouse strains. Moreover, we found that 5-HT2A receptor activation with DOI did not change locomotor activity in CBA/Lac mice. Taken together, our data indicate the implication of 5-HT2C receptors in regulation of locomotor activity and suggest the shared mechanism for functional responses mediated by 5-HT2C and 5-HT2A receptors.

1,4-Disilacyclohexa-2,5-diene

DEFF Research Database (Denmark)

Tibbelin, Julius; Wallner, Andreas; Emanuelsson, Rikard

2014-01-01

2,3,5,6-Tetraethyl-1,4-disilacyclohexa-2,5-dienes with either four chloro (1a), methyl (1b), or trimethylsilyl (TMS) (1c) substituents at the two silicon atoms were examined in an effort to design rigid compounds with strong neutral cross-hyperconjugation between π- and σ-bonded molecular segments......). Furthermore, 1,4-disilacyclohexadiene 1c absorbs strongly at 273 nm (4.55 eV), whereas 1a and 1b have no symmetry allowed excitations above 215 nm (below 5.77 eV). Thus, suitably substituted 1,4-disilacyclohexa-2,5-dienes could represent novel building blocks for the design of larger cross...

The synthesis of 7-chloro-5-pentadeuteriophenyl-1-methyl-1H-1, 5-benzodiazepine-2,4(3H, 5H)dione (( sup 2 H sub 5 )clobazam)

Energy Technology Data Exchange (ETDEWEB)

Borel, A.G.; Abbott, F.S. (British Columbia Univ., Vancouver, BC (Canada). Dept. of Pharmaceutical Sciences)

1990-07-01

Pentadeuteriophenyl clobazam was synthesized in essentially quantitative isotopic purity, and characterized by {sup 1}H-NMR and mass spectroscopy. The title compound was found to be >98% pure by HPLC, and its retention time (t{sub R} 6.17 min) was less than that of an authentic clobazam standard (t{sub R} 6.32 min). Of the five steps in the synthesis of clobazam, the most susceptible to deuterium exchange was the nucleophilic substitution of 2,4-dichloronitrobenzene by aniline-d{sub 7} to form N-(5-chloro-2-nitrophenyl)penta-deuteriophenylamine. In this step, the isotopic impurity aniline-2,3,4,5-d{sub 5} introduced protons from nitrogen into the ortho and para positions of the deuteriophenyl ring of N-(5-chloro-2-nitrophenyl)pentadeuteriophenylamine. (author).

New perovskite-based manganite Pb2Mn2O5

International Nuclear Information System (INIS)

Hadermann, Joke; Abakumov, Artem M.; Perkisas, Tyche; D'Hondt, Hans; Tan Haiyan; Verbeeck, Johan; Filonenko, Vladimir P.; Antipov, Evgeny V.; Van Tendeloo, Gustaaf

2010-01-01

A new perovskite based compound Pb 2 Mn 2 O 5 has been synthesized using a high pressure high temperature technique. The structure model of Pb 2 Mn 2 O 5 is proposed based on electron diffraction, high angle annular dark field scanning transmission electron microscopy and high resolution transmission electron microscopy. The compound crystallizes in an orthorhombic unit cell with parameters a=5.736(1) A∼√2a p , b=3.800(1) A∼a p , c=21.562(6) A∼4√2a p (a p -the parameter of the perovskite subcell) and space group Pnma. The Pb 2 Mn 2 O 5 structure consists of quasi two-dimensional perovskite blocks separated by 1/2[110] p (101) p crystallographic shear planes. The blocks are connected to each other by chains of edge-sharing MnO 5 distorted tetragonal pyramids. The chains of MnO 5 pyramids and the MnO 6 octahedra of the perovskite blocks delimit six-sided tunnels accommodating double chains of Pb atoms. The tunnels and pyramidal chains adopt two mirror-related configurations ('left' L and 'right' R) and layers consisting of chains and tunnels of the same configuration alternate in the structure according to an -L-R-L-R-sequence. The sequence is sometimes locally violated by the appearance of -L-L- or -R-R-fragments. A scheme is proposed with a Jahn-Teller distortion of the MnO 6 octahedra with two long and two short bonds lying in the a-c plane, along two perpendicular orientations within this plane, forming a d-type pattern. - Graphical abstract: Order of the Jahn-Teller distorted MnO 6 octahedra in Pb 2 Mn 2 O 5 . Two long and two short bonds lie in the a-c plane, along two perpendicular orientations within this plane, forming a d-type pattern.

Indoor PM1, PM2.5, PM10 and outdoor PM2.5 concentrations in primary schools in Sari, Iran.

Science.gov (United States)

Mohammadyan, Mahmoud; Shabankhani, Bijan

2013-09-01

This study was carried out to determine the distribution of particles in classrooms in primary schools located in the centre of the city of Sari, Iran and identify the relationship between indoor classroom particle levels and outdoor PM2.5 concentrations. Outdoor PM2.5 and indoor PM1, PM2.5, and PM10 were monitored using a real-time Micro Dust Pro monitor and a GRIMM monitor, respectively. Both monitors were calibrated by gravimetric method using filters. The Kolmogorov-Smirnov test showed that all indoor and outdoor data fitted normal distribution. Mean indoor PM1, PM2.5, PM10 and outdoor PM2.5 concentrations for all of the classrooms were 17.6 μg m(-3), 46.6 μg m(-3), 400.9 μg m(-3), and 36.9 μg m(-3), respectively. The highest levels of indoor and outdoor PM2.5 concentrations were measured at the Shahed Boys School (69.1 μg m(-3) and 115.8 μg m(-3), respectively). The Kazemi school had the lowest levels of indoor and outdoor PM2.5 (29.1 μg m(-3) and 15.5 μg m(-3), respectively). In schools located near both main and small roads, the association between indoor fine particle (PM2.5 and PM1) and outdoor PM2.5 levels was stronger than that between indoor PM10 and outdoor PM2.5 levels. Mean indoor PM2.5 and PM10 and outdoor PM2.5 were higher than the standards for PM2.5 and PM10, and there was a good correlation between indoor and outdoor fine particle concentrations.

Photogeneration of metastable side-on N2 linkage isomers in [Ru(NH3)5N2]Cl2, [Ru(NH3)5N2]Br2 and [Os(NH3)5N2]Cl2.

Science.gov (United States)

Schaniel, Dominik; Woike, Theo; Delley, Bernard; Boskovic, Colette; Güdel, Hans-Ueli

2008-09-28

Photogeneration of side-on N2 linkage isomers in [Ru(NH3)5N2]2+ and [Os(NH3)5N2]2+ is achieved by irradiation with lambda = 325 nm of powder samples at T = 80 K and detected by the downshift of the nu(N-N) vibration and by the heat release at elevated temperature due to the back switching of the side-on configuration to the ground state. The concentration of the transferred molecules is evaluated by the decrease of the area of the nu(N-N) or 2nu(N-N) vibrational bands. All characteristic changes between the linear Ru-N-N and side-on configuration are predicted by DFT calculations: the structure of the anion, shifts of the vibrations, electronic excitation energy, energetic position and sequence of the electronic orbitals, the potentials of the ground and relaxed metastable state with the activation energy, saddle points and energetic position of the minimum.

Phase transition in the (Li 0.5-( x/2) K 0.5-( x/2) Cs x) 2SO 4 system

Science.gov (United States)

Hamed, A. E.; El-Aziz, Y. M. Abd.; Madi, N. K.; Kassem, M. E.

1995-12-01

Phase transition in the (Li 0.5-( x/2) K 0.5-( x/2) Cs x) 2SO 4 system was studied by measuring the specific heat at constant pressure, C p, as a function of temperature in the temperature range 300-800 K. For non-zero values of X ( X = 0.2%, 0.5%, 1% and 2%) the critical behaviour of the phase transition was found to change considerably compared with that of X = 0 or pure LiKSO 4. The observed change in the phase transition with increase of Cs 2SO 4 content ( X) was accompanied by a decrease in the thermodynamic parameters: the value of the specific heat at the transition point (Δ C P) max, the transition temperature, T1, and the value of the energy of ordering. The results were interpreted within the Landau thermodynamic theory of the phase transition.

Analysis of effects of 2,2',5,5'-tetracholorobiphenyl on the flux control in oxidative phosphorylation system in rat liver mitochondria.

NARCIS (Netherlands)

Mildaziene, V.; Nauciene, Z.; Baniene, R.; Demin, O.V.; Krab, K.

2002-01-01

Modular kinetic analysis reveals that the environmental pollutant 2,2′,5,5′tetrachlorobiphenyl (2,2′,5,5′-TCB) affects a large number of steps in oxidative phosphorylation in rat liver mitochondria. 2,2′,5,5′-TCB increases membrane permeability to ions, and inhibits NADH dehydrogenase, cytochrome

Magnesium and nickel(II) furan-2,5-dicarboxylate

DEFF Research Database (Denmark)

Schau-Magnussen, Magnus; Gorbanev, Yury; Kegnæs, Søren

2011-01-01

The salts hexaaquamagnesium furan-2,5-dicarboxylate, [Mg(H2O)(6)](C6H2O5), (I), and hexaaquanickel furan-2,5-dicarboxylate, [Ni(H2O)(6)](C6H2O5), (II), provide the first crystallographic characterization of the furan-2,5-dicarboxylate dianion. Both structures exhibit extensive three-dimensional h...

Effective role of CaO/P2O5 ratio on SiO2-CaO-P2O5 glass system

Directory of Open Access Journals (Sweden)

P. Kiran

2017-05-01

Full Text Available In the present work, the effect of the CaO/P2O5 ratio on the composition of sol-gel synthesized 58SiO2-(19 − xP2O5–(23 + xCaO (x = 0, 5, 10 and 15 mol% glass samples was studied. Further, the effect of NBO/BO ratio on hydroxy carbonated apatite layer (HCA forming ability based on dissolution behavior in simulated body fluid (SBF solution was also investigated. CaO/P2O5 ratios of synthesized glass samples were 1.2, 2, 3.6, and 9.5, respectively. NBO/BO ratios were obtained using Raman spectroscopic analysis as 0.58, 1.20, 1.46, and 1.78, respectively. All samples were soaked in the SBF solution for 7 days. The calculated weight losses of these samples were 58%, 64%, 83%, and 89% for corresponding NBO/BO ratios. The increase in CaO/P2O5 ratio increases the NBO/BO ratios. However, the increase in NBO/BO ratio increases HCA forming ability of SBF treated samples. The HCA crystalline layer formation was confirmed through X-ray Diffraction (XRD, Transmission Electron Microscopy (TEM, Scanning Electron Microscopy (SEM, Raman and Infrared spectroscopic analysis. Higher CaO/P2O5 ratio favors the increase in HCA formation for SBF treated calcium phospho silicate glasses.

Synthesis of carbon-14 labelled (5Z)-4-bromo-5-(bromomethylene)-2(5H)-furanone:

DEFF Research Database (Denmark)

Persson, T.; Johansen, S.K.; Martiny, L.

2004-01-01

The potent quorum sensing inhibitor (5Z)-4-bromo-5-(bromomethylene)-2(5H)-[2-C-14]furanone has been prepared in five steps in 7.7% overall yield starting from bromo[1-C-14]acetic acid. Condensation of ethyl bromo[1-C-14]acetate with ethyl acetoacetate followed by decarboxylation was accelerated...... by microwave heating to afford [1-C-14]levulinic acid. Subsequently, bromination and oxidation gave the targeted furan-2-one with a radiochemical purity of > 97% and a specific activity of 57 mCi/mmol....

(2E-3-(3,5-Dimethyl-1-phenyl-1H-pyrazol-4-yl-1-(2,5-dimethyl-3-thienylprop-2-en-1-one

Directory of Open Access Journals (Sweden)

Salman A. Khan

2010-04-01

Full Text Available The title compound, (2E-3-(3,5-dimethyl-1-phenyl-1H-pyrazol-4-yl-1-(2,5-dimethyl-3-thienylprop-2-en-1-one (3 was synthesized in high yield by aldol condensation of 3-acetyl-2,5-dimethylthiophene and 3,5-dimethyl-1-phenylpyrazole-4-carboxaldehyde in ethanolic NaOH at room temperature. Its structure was fully characterized by elemental analysis, IR, 1H NMR, 13C NMR and EI-MS spectral analysis.

"7 vaprat" ei lõpeta ka suvel / H. S.

Index Scriptorium Estoniae

H. S.

2002-01-01

Populaarne muusikaedetabelisaade "7 vaprat" läheb juunis ansamblitega Terminaator, Tuberkuloited, No Big Silence, Blacky, Speed Free ja Hell Can Wait suvetuurile. 11. juunil antakse kontsert Tartus, 12. juunil Rakveres, 13. juunil Pärnus ja 15. juunil Tallinnas. Kontsertidest valmivad ka telesaated, saatejuht Villu Tamme

The cation-deficient Ruddlesden-Popper oxysulfide Y2Ti2O5S2 as a layered sulfide: topotactic potassium intercalation to form KY2Ti2O5S2.

Science.gov (United States)

Rutt, Oliver J; Hill, Timothy L; Gál, Zoltán A; Hayward, Michael A; Clarke, Simon J

2003-12-01

Potassium intercalation into the cation-deficient n = 2 Ruddlesden-Popper oxysulfide Y(2)Ti(2)O(5)S(2) to form KY(2)Ti(2)O(5)S(2) has been carried out by reaction of the oxysulfide with potassium vapor in sealed metal tubes at 400 degrees C, potassium naphthalide in THF at 50 degrees C, or potassium in liquid ammonia at temperatures as low as -78 degrees C. Insertion of potassium is topotactic, and although a site 12-coordinate by oxide ions is vacant in the perovskite-type oxide slabs of the structure, potassium is too large to enter this site via the 4-coordinate window, and instead enters the rock-salt-type sulfide layers of the structure which necessitates a 30% increase in the lattice parameter c normal to the layers. In contrast with one of the sodium intercalates of Y(2)Ti(2)O(5)S(2) (beta-NaY(2)Ti(2)O(5)S(2)) in which sodium occupies a tetrahedral site in the sulfide layers, potassium favors an 8-coordinate site which necessitates a relative translation of adjacent oxide slabs. KY(2)Ti(2)O(5)S(2) is tetragonal: P4/mmm, a = 3.71563(4) A, c = 14.8682(2) A (at 298 K), Z = 1. Although the resistivity (3.4(1) x 10(3) Omega cm) is larger than would be expected for a metal, temperature independent paramagnetism dominates the magnetic susceptibility, and the material is electronically very similar to the analogous sodium intercalate beta-NaY(2)Ti(2)O(5)S(2) which features reduced-titanium-containing oxide layers of very similar geometry and electron count.

C. R. Jakobsoni kaks senitundmatut käsikirja / Vello Paatsi

Index Scriptorium Estoniae

Paatsi, Vello, 1948-2015

2006-01-01

Läti Riiklikust Ajalooarhiivist 2005. aasta suvel leitud kahest, usureformaatoritelele Brescia Arnoldile ja John Wycliffe'le pühendatud C. R. Jakobsoni käsikirjast (Valguse riigi vägevad võitlejad. Kirja pannud C. R. Jakobson. I Breshja Arnold ;Valguse riigi vägevad võitlejad. Kirja pannud C. R. Jakobson. II Juhan Wikliffe). Ka C. R. Jakobsoni seisukohtadest kiriku ja usu küsimustes

Projektimeeskonnad vahefinišis / Katre Ratassepp

Index Scriptorium Estoniae

Ratassepp, Katre

2015-01-01

Projektimeeskondadele pandi alus mullu suvel, kui esimest korda kogunes laiendatud RMK juhtgrupp, et arutada RMK arengukava aastateks 2015-2020. Struktuuriüksuste juhtidest ja tegevusvaldkondade peaspetsialistidest moodustati mõttekoda, kes aasta jooksul koos käis. 25 käima lükatud arendusprojektist 17 on tänaseks staadiumis "tehtud", 4 peaks kohe-kohe tulemini jõudma ning 4 projekti vajavad jätkutegevusi

Poly[dimethanolbis[μ-5-(3-pyridyltetrazolato-κ2N2:N5]copper(II

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Xiao-Hong Wei

2010-05-01

Full Text Available In the crystal structure of the title complex, [Cu(C6H4N52(CH3OH2]n, the CuII cation lies on an inversion center and is coordinated by four 5-(3-pyridyltetrazolate anions and two methanol molecules in an elongated distorted CuN4O2 octahedral geometry. Each 5-(3-pyridyltetrazolate anion bridges two CuII cations, forming a two-dimensional polymeric complex with (4,4 network topology. In the crystal structure, the two-dimensional layers are connected by intermolecular O—H...N hydrogen bonding, forming a three-dimensional supramolecular architecture.

2,2,3,3,5,5,6,6-Octa-p-tolyl-1,4-dioxa-2,3,5,6-tetragermacyclohexane dichloromethane disolvate

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Monika L. Amadoruge

2009-09-01

Full Text Available The title compound, C56H56Ge4O2·2CH2Cl2 or Tol8Ge4O2·2CH2Cl2 (Tol = p-CH3C6H4, was obtained serendipitously during the attempted synthesis of a branched oligogermane from Tol3GeNMe2 and PhGeH3. The molecule contains an inversion center in the middle of the Ge4O2 ring which is in a chair conformation. The Ge—Ge bond distance is 2.4418 (5 Å and the Ge—O bond distances are 1.790 (2 and 1.785 (2 Å. The torsion angles within the Ge4O2 ring are −56.7 (1 and 56.1 (1° for the Ge—Ge—O—Ge angles and −43.9 (1° for the O—Ge—Ge—O angle.

5-HT2A and 5-HT2C receptors as hypothalamic targets of developmental programming in male rats

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Malgorzata S. Martin-Gronert

2016-04-01

Full Text Available Although obesity is a global epidemic, the physiological mechanisms involved are not well understood. Recent advances reveal that susceptibility to obesity can be programmed by maternal and neonatal nutrition. Specifically, a maternal low-protein diet during pregnancy causes decreased intrauterine growth, rapid postnatal catch-up growth and an increased risk for diet-induced obesity. Given that the synthesis of the neurotransmitter 5-hydroxytryptamine (5-HT is nutritionally regulated and 5-HT is a trophic factor, we hypothesised that maternal diet influences fetal 5-HT exposure, which then influences development of the central appetite network and the subsequent efficacy of 5-HT to control energy balance in later life. Consistent with our hypothesis, pregnant rats fed a low-protein diet exhibited elevated serum levels of 5-HT, which was also evident in the placenta and fetal brains at embryonic day 16.5. This increase was associated with reduced levels of 5-HT2CR, the primary 5-HT receptor influencing appetite, in the fetal, neonatal and adult hypothalamus. As expected, a reduction of 5-HT2CR was associated with impaired sensitivity to 5-HT-mediated appetite suppression in adulthood. 5-HT primarily achieves effects on appetite by 5-HT2CR stimulation of pro-opiomelanocortin (POMC peptides within the arcuate nucleus of the hypothalamus (ARC. We show that 5-HT2ARs are also anatomically positioned to influence the activity of ARC POMC neurons and that mRNA encoding 5-HT2AR is increased in the hypothalamus of in utero growth-restricted offspring that underwent rapid postnatal catch-up growth. Furthermore, these animals at 3 months of age are more sensitive to appetite suppression induced by 5-HT2AR agonists. These findings not only reveal a 5-HT-mediated mechanism underlying the programming of susceptibility to obesity, but also provide a promising means to correct it, by treatment with a 5-HT2AR agonist.

5-HT2A and 5-HT2C receptors as hypothalamic targets of developmental programming in male rats.

Science.gov (United States)

Martin-Gronert, Malgorzata S; Stocker, Claire J; Wargent, Edward T; Cripps, Roselle L; Garfield, Alastair S; Jovanovic, Zorica; D'Agostino, Giuseppe; Yeo, Giles S H; Cawthorne, Michael A; Arch, Jonathan R S; Heisler, Lora K; Ozanne, Susan E

2016-04-01

Although obesity is a global epidemic, the physiological mechanisms involved are not well understood. Recent advances reveal that susceptibility to obesity can be programmed by maternal and neonatal nutrition. Specifically, a maternal low-protein diet during pregnancy causes decreased intrauterine growth, rapid postnatal catch-up growth and an increased risk for diet-induced obesity. Given that the synthesis of the neurotransmitter 5-hydroxytryptamine (5-HT) is nutritionally regulated and 5-HT is a trophic factor, we hypothesised that maternal diet influences fetal 5-HT exposure, which then influences development of the central appetite network and the subsequent efficacy of 5-HT to control energy balance in later life. Consistent with our hypothesis, pregnant rats fed a low-protein diet exhibited elevated serum levels of 5-HT, which was also evident in the placenta and fetal brains at embryonic day 16.5. This increase was associated with reduced levels of 5-HT2CR, the primary 5-HT receptor influencing appetite, in the fetal, neonatal and adult hypothalamus. As expected, a reduction of 5-HT2CR was associated with impaired sensitivity to 5-HT-mediated appetite suppression in adulthood. 5-HT primarily achieves effects on appetite by 5-HT2CR stimulation of pro-opiomelanocortin (POMC) peptides within the arcuate nucleus of the hypothalamus (ARC). We show that 5-HT2ARs are also anatomically positioned to influence the activity of ARC POMC neurons and that mRNA encoding 5-HT2AR is increased in the hypothalamus ofin uterogrowth-restricted offspring that underwent rapid postnatal catch-up growth. Furthermore, these animals at 3 months of age are more sensitive to appetite suppression induced by 5-HT2AR agonists. These findings not only reveal a 5-HT-mediated mechanism underlying the programming of susceptibility to obesity, but also provide a promising means to correct it, by treatment with a 5-HT2AR agonist. © 2016. Published by The Company of Biologists Ltd.

Synthesis and crystal structures of 2-methyl-4-aryl-5-oxo-5H-indeno [1,2-b] pyridine carboxylate derivatives

DEFF Research Database (Denmark)

Pandian, Ramesh; Naushad, Edayadulla; Vijayakumar, Vinodhkumar

2014-01-01

pyridine derivatives through oxidation. Consequently, the interest in this aromatization reaction, investigation of a wide range of 1, 4-DHPs continues to attract the attention of researchers. Herein, we report the preparation of pyridine derivatives and the crystal structures determined by X......-ray crystallographic methods.Results: The crystal structures and conformational studies of two organic compounds, namely ethyl 2-methyl-4-phenyl-5-oxo-5H-indeno [1,2-b] pyridine-3-carboxylate (I) and ethyl 2-methyl-4-(4 chlorophenyl)-5-oxo-5H-indeno [1,2-b] pyridine-3-carboxylate (II) are reported. The terminal ethyl......) dimer running along 011 direction.Conclusion: The crystal structures ethyl 2-methyl-4-phenyl-5-oxo-5H-indeno [1,2-b] pyridine-3-carboxylate and ethyl 2-methyl-4-(4 chlorophenyl)-5-oxo-5H-indeno [1,2-b] pyridine-3-carboxylate have been investigated in detail. The terminal ethyl group of compound I...

1,4-Di(2-butoxycarbonyl-trans-vinyl-2,5-dimethoxybenzene

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William A. Molano

2015-11-01

Full Text Available The title compound 1,4-di(2-butoxycarbonyl-trans-vinyl-2,5-dimethoxybenzene was synthesized in 94% yield through the Heck reaction between 2,5-diiodo-1,4-dimethoxybenzene and n-butyl acrylate, using bis(dibenzylideneacetone palladium(0 as homogeneous catalyst.

10 CFR 960.5-2-7 - Transportation.

Science.gov (United States)

2010-01-01

... 10 Energy 4 2010-01-01 2010-01-01 false Transportation. 960.5-2-7 Section 960.5-2-7 Energy... REPOSITORY Preclosure Guidelines Environment, Socioeconomics, and Transportation § 960.5-2-7 Transportation... using reasonably available technology; (iii) will not require transportation system components to meet...

trans-Diaquabis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato-κ2O,O′cobalt(II dihydrate

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Takumi Tominaga

2017-01-01

Full Text Available The CoII atom in the mononuclear title compound, [Co(C5HF6O22(H2O2]·2H2O, is situated on an inversion centre and exhibits a slightly distorted octahedral coordination sphere. In the crystal, molecules are arranged in layers parallel to (100, held together by O—H...O and O—H...F hydrogen bonds.

Comparison of in vivo immunomodulatory effects of 5-hydroxymethylfurfural and 5, 5'-oxydimethylenebis (2-furfural).

Science.gov (United States)

Lin, Ni; Liu, Tiantian; Lin, Lin; Lin, Sheng; Zang, Qingce; He, Jiuming; Abliz, Zeper; Li, Chao; Wang, Aiping; Jin, Hongtao

2016-11-01

The standard of 5-Hydroxymethylfurfural (5-HMF) existed in dextrose injection as an inevitable by-product during high-temperature setrilization has been included in pharmacopoeias considering its hazardous effects on human health. We found that the concentrations of 5-HMF in some traditional Chinese medicine injections (TCMIs) far exceeded its limit in dextrose injection. Besides, we detected 5, 5'-Oxydimethylenebis (2-furfural) (OMBF) in those TCMIs containing high concentrations of 5-HMF. We investigated the in vivo immunomodulatory effects of 5-HMF and OMBF at three dose levels using the reporter antigen popliteal lymph node assay (RA-PLNA), which allows the straightforward examination and mechanistic study of immunotoxicity of low molecular weight compounds. We found that 5-HMF increased the production of IgG 2a and IFN-γ when co-injected with TNP-OVA, indicating its capability of providing a co-stimulatory signal to evoke a typical type-1 immune response. Compared with the 5-HMF, OMBF elevated the production of IgG 1 , IgG 2 , IL-4 and IFN-γ in response to both reporter antigens, suggesting that OMBF can act as a neo-antigen or neo-epitope to elicit a mixed type-1 and type-2 immune response. It indicates that both 5-HMF and OMBF have immunosensitizing potential with different mechanisms, and exposure to 5-HMF and OMBF may represent a safety concern for humans. Copyright © 2016 Elsevier Inc. All rights reserved.

2-Methylsulfanyl-5,6-dihydro-2H-1,3-dithiolo[4,5-b][1,4]dioxin-2-ium tetrafluoroborate

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Guoquan Zhou

2012-04-01

Full Text Available The title compound, C6H7O2S3+·BF4−, consists of a planar 2-thioxo-1,3-dithiol-4,5-yl unit [maximum deviation from the ring plane = 0.020 (3 Å], with an ethylenedioxy group fused at the 4,5-positions; the ethylenedioxy C atoms are disordered over two positions with site-occupancy factors of 0.5. The 1,4-dioxine ring has a twist-chair conformation. Weak cation–anion S...F interactions [3.022 (4–3.095 (4 Å] and an S...O [3.247 (4 Å] interaction are present.

Laser-probing measurements and calculations of lifetimes of the 5d 2D3 at ∼sol∼ at 2 and 5d 2D5 at ∼sol∼ at 2 metastable levels in Ba II

International Nuclear Information System (INIS)

Gurell, J.; Lundin, P.; Mannervik, S.; Royen, P.; Schef, P.; Biemont, E.; Quinet, P.; Blagoev, K.; Fivet, V.; Norlin, L.-O.; Rostohar, D.

2007-01-01

The two metastable levels 5d 2 D 3 at ∼sol∼ at 2 and 5d 2 D 5 at ∼sol∼ at 2 in Ba II both show extremely long lifetimes of the order of several tens of seconds each. This has been found both by experiments and by theoretical predictions. The small transition probabilities associated with these two levels make them interesting and challenging for theoreticians as well as for experimentalists. Several calculations and measurements of these two lifetimes have been made previously but discrepancies between the results are present. This article presents values of τ=89.4±15.6 s for the 2 D 3 at ∼sol∼ at 2 level and τ=32.0±4.6 s for the 2 D 5 at ∼sol∼ at 2 level measured in a beam-laser experiment performed at the ion storage ring CRYRING. These values are supported by our new calculations resulting in τ=82.0 s for the 2 D 3 at ∼sol∼ at 2 level and τ=31.6 s for the 2 D 5 at ∼sol∼ at 2 level

10 CFR 960.5-2-3 - Meteorology.

Science.gov (United States)

2010-01-01

... 10 Energy 4 2010-01-01 2010-01-01 false Meteorology. 960.5-2-3 Section 960.5-2-3 Energy DEPARTMENT OF ENERGY GENERAL GUIDELINES FOR THE PRELIMINARY SCREENING OF POTENTIAL SITES FOR A NUCLEAR WASTE REPOSITORY Preclosure Guidelines Preclosure Radiological Safety § 960.5-2-3 Meteorology. (a) Qualifying...

Ce2Co3Ge5: a new U2Co3Si5 - type valance fluctuating compound

International Nuclear Information System (INIS)

Layek, Samar; Hossain, Zakir

2010-01-01

Poly crystalline sample of Ce 2 Co 3 Ge 5 have been prepared by arc melting and consequently annealing at 1100 deg C. Rietveld refinement of XRD shows that it crystallize in the orthorhombic U 2 Co 3 Si 5 structure (space group Ibam) with crystal parameters a= 9.802A, b= 11.777A and c= 5.941A and unit cell volume V= 684.8 A 3 The unit cell volume of Ce 2 Co 3 Ge 5 is seen clearly to deviate from that expected on the basis of lanthanide contraction. From susceptibility measurement, effective magnetic moment of this compound μ eff = 0.95 μ B which is lower than magnetic moment free for Ce 3+ ions (2.54 μB) but higher than that of non-magnetic Ce 4+ state (0 μ B ). All these results clearly indicated Ce 2 Co 3 Ge 5 to be a mixed valance compound. (author)

10 CFR 960.5-2 - Technical guidelines.

Science.gov (United States)

2010-01-01

... 10 Energy 4 2010-01-01 2010-01-01 false Technical guidelines. 960.5-2 Section 960.5-2 Energy DEPARTMENT OF ENERGY GENERAL GUIDELINES FOR THE PRELIMINARY SCREENING OF POTENTIAL SITES FOR A NUCLEAR WASTE REPOSITORY Preclosure Guidelines § 960.5-2 Technical guidelines. The technical guidelines in this subpart set...

Synthesis, Properties and Stereochemistry of 2-Halo-1,2λ5-oxaphosphetanes

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Anastasy O. Kolodiazhna

2016-10-01

Full Text Available Results of research into four-membered 2-halo-1,2λ5-oxaphosphetane phosphorus(V-heterocycles are presented. The preparation of 2-halo-1,2λ5-oxaphosphetanes by reaction of P-haloylides with carbonyl compounds is described. The mechanism of asynchronous [2+2]-сycloaddition of ylides to aldehydes was proposed on the base of low-temperature NMR investigations. 2-Halo-1,2λ5-oxaphosphetanes were isolated as individual compounds and their structures were confirmed by 1Н-, 13C-, 19F- and 31Р-NMR spectra. These compounds are convenient reagents for preparing of various organic and organophosphorus compounds hardly available by other methods. Chemical and physical properties of the 2-halo-1,2λ5-oxaphosphetanes are reviewed. The 2-chloro-1,2λ5-oxaphosphetanes, rearrange with formation of 2-chloroalkyl-phosphonates or convert into trans-phosphorylated alkenes depending on the substituents at the α-carbon atom. Prospective synthetic applications of 2-halo-1,2λ5-oxaphosphetanes are analyzed. The 2-halo-1,2λ5-oxaphosphetanes may be easily converted to various alkenylphosphonates: allyl- or vinylphosphonates, phosphorus ketenes, thioketenes, ketenimines.

SYNTHESIS, SPECTRAL AND THEORETICAL CHARACTERIZATION OF 5,6-DICHLORO/DIMETHYL-2-(2´,3´/2´,4´/2´,5´/3´,4´/3´,5´-DIMETHOXYPHENYL-1H-BENZIMIDAZOLES

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Demet Gürbüz

2016-12-01

Full Text Available 5,6-Dichloro/dimethyl-2-(2´,3´/2´,4´/2´,5´/3´,4´/3´,5´-dimethoxyphenyl-1H-benzimidazoles were synthesized and characterized by using analytical data, FT-IR, FT-Raman, NMR, ESI-MS and fl uorescence spectroscopy. The optimized molecular geometry, zero point energy, dipole moment, ESE, band gap and charge distributions were calculated by Gaussian 09 using Density Functional Theory (DFT, RB3LYP with 6-31++G(d,p basis set. According to the calculations, the molecules have structures with various torsion angles between the benzimidazole and benzene rings from 9.7º to 47.8º. The calculated energy values with ZPE correction and DFT show that the methyl derivatives are more stable than the chloro forms. 3´,4´-Dimethoxy derivatives have higher decomposition points in comparison with the other compounds in series. The chlorine atoms of 5,6-dichloro-2- (2´,3´/2´,4´/2´,5´/3´,4´/3´,5´-dimethoxyphenyl-1H-benzimidazoles are positively charged whereas the C5 and C6 carbon atoms are negatively charged due to the attached chlorine atoms, in virtue of the electron withdrawing characteristic of the imidazole part of the benzimidazole ring. Also, some calculated prominent bond lengths and bond angles were discussed.

Octabutylbis(μ2-2-chloro-5-nitrobenzoatobis(2-chloro-5-nitrobenzoatodi-μ3-oxido-tetratin(IV

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Hoong-Kun Fun

2010-12-01

Full Text Available The title complex, [Sn4(C4H98(C7H3ClNO44O2], is a cluster formed by a crystallographic inversion center around the central Sn2O2 ring. Both of the two independent Sn atoms are five-coordinated, with distorted trigonal–bipyramidal SnC2O3 geometries. One Sn atom is coordinated by two butyl groups, one O atom of the benzoate anion and two bridging O atoms, whereas the other Sn atom is coordinated by two butyl groups, two O atoms of the benzoate anions and a bridging O atom. The O atoms of the bridging benzoate anion are disordered over two sites with an occupancy ratio of 0.862 (12:0.138 (12. One of the butyl groups coordinated to the Sn2O2 ring is disordered over two sites with an occupancy ratio of 0.780 (8:0.220 (8, whereas both of the two butyl groups coordinated to the other Sn atom are disordered over two sites with occupancy ratios of 0.788 (5:0.212 (5 and 0.827 (10:0.173 (10. All the butyl groups are equatorial with respect to the SnO3 trigonal plane. In the crystal, complex molecules are stacked down [010] with weak intermolecular C—H...π interactions stabilizing the crystal structure.

Microstructural morphologies of slag based glass-ceramics nucleated with 5 wt% Cr{sub 2}O{sub 3} and 5 wt% Cr{sub 2}O{sub 3} + 5 wt% TiO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Oevecoglu, M.L.; Oezkal, B. [Istanbul Technical Univ. (Turkey). Dept. of Metallurgical and Materials Enginering; Catakli, E. [Mimar Sinan Univ., Istanbul (Turkey). Faculty of Science and Literature; Erkmen, Z.E. [Istnabul Univ. (Turkey). Dept. of Metallurgical Engineering

2002-07-01

Glass-ceramic materials were developed from the blast-furnace slags by mixing 5 wt% Cr{sub 2}O{sub 3} and 5 wt% Cr{sub 2}O{sub 3} + 5 wt% TiO{sub 2}. The samples were nucleated for 18 h at 780 C and crystallized for 20 min. at 905 C, respectively. SEM and SEM/EDS investigations revealed the presence of clover-shaped TiO{sub 2} particles in the glassy matrix of the sample nucleated with 5 wt% Cr{sub 2}O{sub 3} + 5 wt% TiO{sub 2} and polygonal-shaped Cr{sub 2}O{sub 3} platelets for both samples. XRD scans revealed the presence of akermanite (2CaO.MgO.2SiO{sub 2}) and gehlenite (2CaO.Al{sub 2}O{sub 3}.SiO{sub 2}) peaks indicating the existence of the mellilite solid solution for the crystallized glass-ceramic samples. (orig.)

One-pot synthesis of 4,8-dibromobenzo[1,2-c;4,5-c']bis[1,2,5]thiadiazole.

Science.gov (United States)

Tam, Teck Lip; Li, Hairong; Wei, Fengxia; Tan, Ke Jie; Kloc, Christian; Lam, Yeng Ming; Mhaisalkar, Subodh G; Grimsdale, Andrew C

2010-08-06

A one-step synthesis of 4,8-dibromobenzo[1,2-c;4,5-c']bis[1,2,5]thiadiazole with use of 1,2,4,5-tetraaminobenzene tetrahydrobromide and thionyl bromide in good yield is reported. This unit can then be used in the synthesis of low bandgap materials via palladium-catalyzed coupling reactions. The approach offers a quick and easy way to prepare low bandgap materials as compared to the current literature methods.

THESEUS Deliverable ID2.5

DEFF Research Database (Denmark)

Nørgaard, Jørgen Harck; Andersen, Thomas Lykke; Burcharth, Hans F.

2012-01-01

As a consequence of climate changes, coastal defenses are worldwide at higher risk of failure. Climate changes can lead to problems in terms of function, stability, and safety of goods and persons. To overcome the problems, different scenarios can be adopted, such as; 1) no upgrade actions...... and repairing the damages 2) upgrade of existing defences by e.g. changing the structure dimensions 3) perform strategic retreat and decommissioning. Within the THESEUS project, the present work task, WT 2.5, focus on upgrading existing rubble mound breakwater defences. Solutions for upgrading parts of rubble...... mound structures are investigated by means of modifying the structure profile and/or adding structure elements. Results from this study will be incorporated in the THESEUS decision tool (DSS-tool) and in the guidelines in work package 5 (WP.5)....

Ferrielectricity in DyMn2O5: A golden touchstone for multiferroicity of RMn2O5 family

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J.-M. Liu

2015-06-01

Full Text Available The RMn2O5 manganite compounds represent one class of multiferroic family with magnetic origins, which has been receiving continuous attention in the past decade. So far, our understanding of the magnetic origins for ferroelectricity in RMn2O5 is associated with the nearly collinear antiferromagnetic structure of Mn ions, while the exchange striction induced ionic displacements are the consequence of the spin frustration competitions. While this scenario may be applied to almost all RMn2O5 members, its limitation is either clear: the temperature-dependent behaviors of electric polarization and its responses to external stimuli are seriously materials dependent. These inconsistences raise substantial concern with the state-of-the-art physics of ferroelectricity in RMn2O5. In this mini-review, we present our recent experimental results on the roles of the 4f moments from R ions which are intimately coupled with the 3d moments from Mn ions. DyMn2O5 is a golden figure for illustrating these roles. It is demonstrated that the spin structure accommodates two nearly collinear sublattices which generate respectively two ferroelectric (FE sublattices, enabling DyMn2O5 an emergent ferrielectric (FIE system rarely identified in magnetically induced FEs. The evidence is presented from several aspects, including FIE-like phenomena and magnetoelectric responses, proposed structural model, and experimental check by nonmagnetic substitutions of the 3d and 4f moments. Additional perspectives regarding possible challenges in understanding the multiferroicity of RMn2O5 as a generalized scenario are discussed.

Intrinsic radioactivity of KSr2I5:Eu2+

International Nuclear Information System (INIS)

Rust, M.; Melcher, C.; Lukosi, E.

2016-01-01

A current need in nuclear security is an economical, yet high energy resolution (near 2%), scintillation detector suitable for gamma-ray spectroscopy. For current scintillators on the market, there is an inverse relationship between scintillator energy resolution and cost of production. A new promising scintillator, KSr 2 I 5 :Eu 2+ , under development at the University of Tennessee, has achieved an energy resolution of 2.4% at 662 keV at room temperature, with potential growth rates exceeding several millimeters per hour. However, the internal background due to the 40 K content could present a hurdle for effective source detection/identification in nuclear security applications. As a first step in addressing this question, this paper reports on a computational investigation of the intrinsic differential pulse height spectrum (DPHS) generated by 40 K within the KSr 2 I 5 :Eu 2+ scintillator as a function of crystal geometry. It was found that the DPHS remains relatively equal to a constant multiplicative factor of the negatron emission spectrum with a direct increase of the 1.46 MeV photopeak relative height to the negatron spectrum with volume. Further, peak pileup does not readily manifest itself for practical KSr 2 I 5 :Eu 2+ volumes.

Magnetic ordering in the monoclinic structure of Nd5Si1.45Ge2.55 and Pr5Si1.5Ge2.5 studied by means of neutron powder diffraction

International Nuclear Information System (INIS)

Magen, C; Ritter, C; Morellon, L; Algarabel, P A; Ibarra, M R

2004-01-01

The compounds Nd 5 Si 1.45 Ge 2.55 and Pr 5 Si 1.5 Ge 2.5 have been investigated by means of magnetization measurements and neutron powder diffraction techniques. These alloys present a room-temperature monoclinic Gd 5 Si 2 Ge 2 -type crystallographic structure and, on cooling, both systems order ferromagnetically, at T C = 56 and 32 K, respectively, from a high-temperature paramagnetic to a low-temperature complex canted ferromagnetic state. The monoclinic crystallographic structure remains unchanged upon cooling down to 4 K, demonstrating the existence of a monoclinic ferromagnetic phase, and the possibility of a full decoupling of magnetic and crystallographic degrees of freedom in the 5:4 lanthanide intermetallic compounds

Synthesis of 14C-labelled polychlorobiphenyls derived from the labelled 4-chloro-, 2,5-dichloro-, 3,4-dichloro-, 2,3-dichloro-2,4,5-trichloro- and 2,3,6-trichloroanilines

International Nuclear Information System (INIS)

Bergman, A.; Bamford, I.; Wachtmeister, C.A.

1981-01-01

[ 14 C]Aniline hydrogen sulphate was acetylated, and the acetanilide obtained was chlorinated with N-chlorosuccinimide to 2-chloro, 4-chloro- and 2,4-dichloroacet[ 14 C]anilide. The labelled 2- and 4-chloroacet[ 14 C]anilides were hydrolyzed and treated with aluminium chloride, hydrogen chloride and chlorine in dry dichloromethane to give the major products 2,5-dichloro-and 3,4-dichloro[ 14 C]aniline. The labelled 2,3-dichloro- and 2,3,6-trichloroanilines were obtained as minor products from the chlorination of 2-chloro[ 14 C]aniline, likewise 2,4,5-trichloroaniline was obtained from 4-chloro[ 14 C]aniline. The [ 14 C]anilines prepared were coupled with benzene, 1,4-dichloro-, 1,2-dichloro- or 1,3-dichlorobenzene to give 4-chloro-, 2,3',4',5-tetrachloro-, 2,3,3',4'-tetrachloro-, 3,3',4,4'-tetrachloro-, 2,2',5,5'-tetrachloro-, 2,2',3,3'-tetrachloro-, 2,2',3,5',6-pentachloro-, 2,2',4,4',5-pentachloro- and 2,3',4,5,5'-pentachloro[ 14 C]biphenyl. 3,4-Dichloro[ 14 C]aniline and biphenyls prepared from this aniline were found to be contaminated by bromoanalogues. The origin of these have been studied. (author)

Phase formation of V2O5.xNb2O5 compounds via gels and freeze-dried precursors

International Nuclear Information System (INIS)

Langbein, Hubert; Mayer-Uhma, Tobias

2009-01-01

An X-ray powder diffraction study of the phase formation in the system V 2 O 5 /Nb 2 O 5 is performed. Freeze-dried ammonium vanadate and ammonium oxalato niobate, alkoxide-derived xerogels and a mixture of active oxides are used as precursors to compare the resulting phase composition. Thermal decomposition of the freeze-dried precursor is monitored with DTA/TG and mass spectrometry. In the quasi-binary system V 2 O 5 -Nb 2 O 5 metastable VNbO 5 , V 4 Nb 18 O 55 , VNb 9 O 25 and solid solutions of V 2 O 5 in TT-Nb 2 O 5 as also thermodynamically stable VNb 9 O 25 exist. The thermal decomposition of freeze-dried vanadate-oxalatoniobate solution allows the synthesis of all these phases in a relative simple manner. Structural relationships between an intermediate phase and the product, or, in the case of solid-state reactions, between one of the starting oxide and the product, favour the desired reaction. Therefore, the structure of a former phase influences or directs the structure of the product similar to a topotactic reaction

Fragrance material review on 1-[5(or 6)-methyl-7(or 8)-1-(methylethyl)bicyclo[2.2.2]oct-5-en-2-yl]ethan-1-one.

Science.gov (United States)

Scognamiglio, J; Letizia, C S; Api, A M

2013-12-01

A toxicologic and dermatologic review of 1-[5(Or 6)-Methyl-7(or 8)-1-(methylethyl)bicyclo[2.2.2]oct-5-en-2-yl]ethan-1-one when used as a fragrance ingredient is presented. 1-[5(Or 6)-Methyl-7(or 8)-1-(methylethyl)bicyclo[2.2.2]oct-5-en-2-yl]ethan-1-one is a member of the fragrance structural group Alkyl Cyclic Ketones. These fragrances can be described as being composed of an alkyl, R1, and various substituted and bicyclic saturated or unsaturated cyclic hydrocarbons, R2, in which one of the rings may include up to 12 carbons. Alternatively, R2 may be a carbon bridge of C2-C4 carbon chain length between the ketone and cyclic hydrocarbon. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for 1-[5(Or 6)-Methyl-7(or 8)-1-(methylethyl)bicyclo[2.2.2]oct-5-en-2-yl]ethan-1-one were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, phototoxicity, photoallergy, and genotoxicity, data. A safety assessment of the entire Alkyl Cyclic Ketones will be published simultaneously with this document; please refer to Belsito et al., Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M., Fryer, A.D., Greim, H., Miyachi, Y., Saurat, J.H., Sipes, I.G., 2013. A Toxicologic and Dermatologic Assessment of Alkyl Cyclic Ketones When Used as Fragrance Ingredients. (submitted for publication)). for an overall assessment of the safe use of this material and all Alkyl Cyclic Ketones in fragrances. Copyright © 2013 Elsevier Ltd. All rights reserved.

5 CFR 1315.2 - Definitions.

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2010-01-01

.... Determination of such dates is discussed in § 1315.4(g). (q) Electronic commerce means the end to end electronic... 5 Administrative Personnel 3 2010-01-01 2010-01-01 false Definitions. 1315.2 Section 1315.2 Administrative Personnel OFFICE OF MANAGEMENT AND BUDGET OMB DIRECTIVES PROMPT PAYMENT § 1315.2 Definitions. (a...

Synthesis and Biological Activity of 2,5-Bisubstituted Derivatives of 1,3,4-Thiadiazol-2,5-dithiol

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T. S. Zhivotova

2013-01-01

Full Text Available By reaction of 1,3,4-thiadiazol-2,5-dithiol with different organohalogens, chlorides of carboxylic acids, acrylic acid derivatives, alkaloids, and secondary amines, various derivatives of 2,5-bi-substituted 1,3,4-thiadiazole were synthesized, and biological properties of some of them were studied.

CATALYTIC KINETIC RESOLUTION OF 5-ALKOXY-2(5H)-FURANONES

NARCIS (Netherlands)

FABER, WS; Kok, Johan C; DELANGE, B; FERINGA, BL; Faber, Wijnand S.; Lange, Ben de; Feringa, Bernard

1994-01-01

The kinetic resolution of racemic 5-alkoxy-2(5H)-furanones, using a chiral aminoalcohol catalyzed 1-4-addition of arylthiols, was examined. Using various butenolides it was shown that a gamma-alkoxy substituent appears to be essential to reach high enantioselectivities whereas electron-donating

Comparative Investigation of 0.5Li2MnO3·0.5LiNi0.5Co0.2Mn0.3O2 Cathode Materials Synthesized by Using Different Lithium Sources

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Peng-Bo Wang

2018-05-01

Full Text Available Lithium-rich manganese-based cathode materials has been attracted enormous interests as one of the most promising candidates of cathode materials for next-generation lithium ion batteries because of its high theoretic capacity and low cost. In this study, 0.5Li2MnO3·0.5LiNi0.5Co0.2Mn0.3O2 materials are synthesized through a solid-state reaction by using different lithium sources, and the synthesis process and the reaction mechanism are investigated in detail. The morphology, structure, and electrochemical performances of the material synthesized by using LiOH·H2O, Li2CO3, and CH3COOLi·2H2O have been analyzed by using Thermo gravimetric analysis (TGA, X-ray diffraction (XRD, Scanning electron microscope (SEM, Transmission electron microscope (TEM, X-ray photoelectron spectroscopy (XPS, and electrochemical measurements. The 0.5Li2MnO3·0.5LiNi0.5Co0.2Mn0.3O2 material prepared by using LiOH·H2O displays uniform morphology with nano particle and stable layer structure so that it suppresses the first cycle irreversible reaction and structure transfer, and it delivers the best electrochemical performance. The results indicate that LiOH·H2O is the best choice for the synthesis of the 0.5Li2MnO3·0.5LiNi0.5Co0.2Mn0.3O2 material.

Improvement of thermoelectric properties induced by uniquely ordered lattice field in Bi2Se0.5Te2.5 pillar array

International Nuclear Information System (INIS)

Tan, Ming; Hao, Yanming; Wang, Gangzhi

2014-01-01

In this study, it was found that uniquely ordered lattice field favors transport of carriers but hinder that of phonons. The n-Bi 2 Se 0.5 Te 2.5 pillar array film was successfully achieved by a simple ion beam assisted deposition technique. This oriented pillar array structure is clear with pillar diameter of about 30 nm, exhibiting a uniquely ordered lattice field. The properties of the ordered Bi 2 Se 0.5 Te 2.5 pillar array were greatly enhanced in comparison with those of the ordinary film. The Bi 2 Se 0.5 Te 2.5 pillar array with a thermoelectric dimensionless figure-of-merit ZT=1.28 was obtained at room temperature. The in-plane transport mechanisms of the ordered pillar array and the ordinary structures, lattice field model, are proposed and investigated. The specially ordered lattice field is the main reason for the properties enhancement observed in the Bi 2 Se 0.5 Te 2.5 film. Introduction of such ordered lattice field into TE films is therefore a very promising approach. - Graphical abstract: In this study, it was found that uniquely ordered lattice field favors transport of carriers but hinder that of phonons. The Bi 2 Se 0.5 Te 2.5 pillar array film with a thermoelectric dimensionless figure-of-merit ZT=1.28 was obtained at room temperature. The in-plane transport mechanisms of the ordered pillar array and the ordinary structures, the lattice field model, are proposed and investigated. The specially ordered lattice field is the main reason for the properties enhancement observed in the Bi 2 Se 0.5 Te 2.5 pillar array. Introduction of such uniquely ordered lattice field into TE films is therefore a very promising approach. In (a) TEM and (b) HRTEM images of the ordered Bi 2 Se 0.5 Te 2.5 column array. - Highlights: • Uniquely ordered Bi 2 Se 0.5 Te 2.5 pillar array was achieved by an IBAD method. • The pillar array with an ordered lattice field exhibits attractive TE property. • The transport mechanism of such ordered pillar array is proposed and

Regulation of steroid 5-{alpha} reductase type 2 (Srd5a2) by sterol regulatory element binding proteins and statin

Energy Technology Data Exchange (ETDEWEB)

Seo, Young-Kyo [Department of Molecular Biology and Biochemistry, 3244 McGaugh Hall, University of California, UC Irvine, Irvine, CA 92697-3900 (United States); Zhu, Bing [Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555-0144 (United States); Jeon, Tae-Il [Department of Molecular Biology and Biochemistry, 3244 McGaugh Hall, University of California, UC Irvine, Irvine, CA 92697-3900 (United States); Osborne, Timothy F., E-mail: tfosborn@uci.edu [Department of Molecular Biology and Biochemistry, 3244 McGaugh Hall, University of California, UC Irvine, Irvine, CA 92697-3900 (United States)

2009-11-01

In this study, we show that sterol regulatory element binding proteins (SREBPs) regulate expression of Srd5a2, an enzyme that catalyzes the irreversible conversion of testosterone to dihydroxytestosterone in the male reproductive tract and is highly expressed in androgen-sensitive tissues such as the prostate and skin. We show that Srd5a2 is induced in livers and prostate from mice fed a chow diet supplemented with lovastatin plus ezitimibe (L/E), which increases the activity of nuclear SREBP-2. The three fold increase in Srd5a2 mRNA mediated by L/E treatment was accompanied by the induction of SREBP-2 binding to the Srd5a2 promoter detected by a ChIP-chip assay in liver. We identified a SREBP-2 responsive region within the first 300 upstream bases of the mouse Srd5a2 promoter by co-transfection assays which contain a site that bound SREBP-2 in vitro by an EMSA. Srd5a2 protein was also induced in cells over-expressing SREBP-2 in culture. The induction of Srd5a2 through SREBP-2 provides a mechanistic explanation for why even though statin therapy is effective in reducing cholesterol levels in treating hypercholesterolemia it does not compromise androgen production in clinical studies.

Regulation of steroid 5-α reductase type 2 (Srd5a2) by sterol regulatory element binding proteins and statin

International Nuclear Information System (INIS)

Seo, Young-Kyo; Zhu, Bing; Jeon, Tae-Il; Osborne, Timothy F.

2009-01-01

In this study, we show that sterol regulatory element binding proteins (SREBPs) regulate expression of Srd5a2, an enzyme that catalyzes the irreversible conversion of testosterone to dihydroxytestosterone in the male reproductive tract and is highly expressed in androgen-sensitive tissues such as the prostate and skin. We show that Srd5a2 is induced in livers and prostate from mice fed a chow diet supplemented with lovastatin plus ezitimibe (L/E), which increases the activity of nuclear SREBP-2. The three fold increase in Srd5a2 mRNA mediated by L/E treatment was accompanied by the induction of SREBP-2 binding to the Srd5a2 promoter detected by a ChIP-chip assay in liver. We identified a SREBP-2 responsive region within the first 300 upstream bases of the mouse Srd5a2 promoter by co-transfection assays which contain a site that bound SREBP-2 in vitro by an EMSA. Srd5a2 protein was also induced in cells over-expressing SREBP-2 in culture. The induction of Srd5a2 through SREBP-2 provides a mechanistic explanation for why even though statin therapy is effective in reducing cholesterol levels in treating hypercholesterolemia it does not compromise androgen production in clinical studies.

Assembly of bicyclic or monocyclic clusters from [(η5-C5Me5)2Mo2(μ3-S)4(CuMeCN)2]2+ with tetraphosphine or N,P mixed ligands: syntheses, structures and enhanced third-order NLO performances.

Science.gov (United States)

Ren, Zhi-Gang; Sun, Sha; Dai, Min; Wang, Hui-Fang; Lü, Chun-Ning; Lang, Jian-Ping; Sun, Zhen-Rong

2011-09-07

Reactions of the preformed cluster [(η(5)-C(5)Me(5))(2)Mo(2)(μ(3)-S)(4)Cu(2)(MeCN)(2)](ClO(4))(2) (1) with two tetraphosphine ligands, 1,4-N,N,N',N'-tetra(diphenylphosphanylmethyl)benzene diamine (dpppda) and N,N,N',N'-tetra(diphenylphosphanylmethyl)ethylene diamine (dppeda), produced two bicyclic clusters {[(η(5)-C(5)Me(5))(2)Mo(2)(μ(3)-S)(4)Cu(2)](2)(L)}(ClO(4))(4) (3: L = dpppda; 4: L = dppeda). Analogous reactions of 1 or [(η(5)-C(5)Me(5))(2)Mo(2)(μ(3)-S)(4)Cu(2)(MeCN)(2)](PF(6))(2) (2) with two N,P mixed ligands, N,N-bi(diphenylphosphanylmethyl)-2-aminopyridine (bdppmapy) and N-diphenylphosphanylmethyl-4-aminopyridine (dppmapy), afforded two monocyclic clusters {[(η(5)-C(5)Me(5))(2)Mo(2)(μ(3)-S)(4)Cu(2)](2)(L)(2)}X(4) (5: L = bdppmapy, X = ClO(4); 6: L = dppmapy, X = PF(6)). Compounds 3-6 were fully characterized by elemental analysis, IR spectra, UV-vis spectra, (1)H and (31)P{(1)H} NMR spectra, ESI-MS and single-crystal X-ray crystallography. In the tetracations of 3-6, two cubane-like [Mo(2)(μ(3)-S)(4)Cu(2)] cores are linked either by one dpppda or dppeda bridge to form a bicyclic structure or by a pair of bdppmapy or dppmapy bridges to afford a monocyclic structure. The third-order nonlinear optical (NLO) properties of 1 and 3-6 in MeCN were also investigated by femtosecond degenerate four-wave mixing (DFWM) technique with a 50 fs pulse width at 800 nm. Compounds 3-6 exhibited enhanced third-order NLO performances relative to that of 1. This journal is © The Royal Society of Chemistry 2011

Does dinitrogen hydrogenation follow different mechanisms for [(eta5-C5Me4H)2Zr]2(mu2,eta2,eta2-N2) and {[PhP(CH2SiMe2NSiMe2CH2)PPh]Zr}2(mu2,eta2,eta2-N2) complexes? A computational study.

Science.gov (United States)

Bobadova-Parvanova, Petia; Wang, Qingfang; Quinonero-Santiago, David; Morokuma, Keiji; Musaev, Djamaladdin G

2006-09-06

The mechanisms of dinitrogen hydrogenation by two different complexes--[(eta(5)-C(5)Me(4)H)(2)Zr](2)(mu(2),eta(2),eta(2)-N(2)), synthesized by Chirik and co-workers [Nature 2004, 427, 527], and {[P(2)N(2)]Zr}(2)(mu(2),eta(2),eta(2)-N(2)), where P(2)N(2) = PhP(CH(2)SiMe(2)NSiMe(2)CH(2))(2)PPh, synthesized by Fryzuk and co-workers [Science 1997, 275, 1445]--are compared with density functional theory calculations. The former complex is experimentally known to be capable of adding more than one H(2) molecule to the side-on coordinated N(2) molecule, while the latter does not add more than one H(2). We have shown that the observed difference in the reactivity of these dizirconium complexes is caused by the fact that the former ligand environment is more rigid than the latter. As a result, the addition of the first H(2) molecule leads to two different products: a non-H-bridged intermediate for the Chirik-type complex and a H-bridged intermediate for the Fryzuk-type complex. The non-H-bridged intermediate requires a smaller energy barrier for the second H(2) addition than the H-bridged intermediate. We have also examined the effect of different numbers of methyl substituents in [(eta(5)-C(5)Me(n)H(5)(-)(n))(2)Zr](2)(mu(2),eta(2),eta(2)-N(2)) for n = 0, 4, and 5 (n = 5 is hypothetical) and [(eta(5)-C(5)H(2)-1,2,4-Me(3))(eta(5)-C(5)Me(5))(2)Zr](2)(mu(2),eta(2),eta(2)-N(2)) and have shown that all complexes of this type would follow a similar H(2) addition mechanism. We have also performed an extensive analysis on the factors (side-on coordination of N(2) to two Zr centers, availability of the frontier orbitals with appropriate symmetry, and inflexibility of the catalyst ligand environment) that are required for successful hydrogenation of the coordinated dinitrogen.

Crystal structures of (Z-5-[2-(benzo[b]thiophen-2-yl-1-(3,5-dimethoxyphenylethenyl]-1H-tetrazole and (Z-5-[2-(benzo[b]thiophen-3-yl-1-(3,4,5-trimethoxyphenylethenyl]-1H-tetrazole

Directory of Open Access Journals (Sweden)

Narsimha Reddy Penthala

2016-05-01

Full Text Available (Z-5-[2-(Benzo[b]thiophen-2-yl-1-(3,5-dimethoxyphenylethenyl]-1H-tetrazole methanol monosolvate, C19H16N4O2S·CH3OH, (I, was prepared by the reaction of (Z-3-(benzo[b]thiophen-2-yl-2-(3,5-dimethoxyphenylacrylonitrile with tributyltin azide via a [3 + 2]cycloaddition azide condensation reaction. The structurally related compound (Z-5-[2-(benzo[b]thiophen-3-yl-1-(3,4,5-trimethoxyphenylethenyl]-1H-tetrazole, C20H18N4O3S, (II, was prepared by the reaction of (Z-3-(benzo[b]thiophen-3-yl-2-(3,4,5-trimethoxyphenylacrylonitrile with tributyltin azide. Crystals of (I have two molecules in the asymmetric unit (Z′ = 2, whereas crystals of (II have Z′ = 1. The benzothiophene rings in (I and (II are almost planar, with r.m.s deviations from the mean plane of 0.0084 and 0.0037 Å in (I and 0.0084 Å in (II. The tetrazole rings of (I and (II make dihedral angles with the mean planes of the benzothiophene rings of 88.81 (13 and 88.92 (13° in (I, and 60.94 (6° in (II. The dimethoxyphenyl and trimethoxyphenyl rings make dihedral angles with the benzothiophene rings of 23.91 (8 and 24.99 (8° in (I and 84.47 (3° in (II. In both structures, molecules are linked into hydrogen-bonded chains. In (I, these chains involve both tetrazole and methanol, and are parallel to the b axis. In (II, molecules are linked into chains parallel to the a axis by N—H...N hydrogen bonds between adjacent tetrazole rings.

2-Amino-5-bromopyridinium hydrogen succinate

Directory of Open Access Journals (Sweden)

Hoong-Kun Fun

2010-03-01

Full Text Available In the title compound, C5H6BrN2+·C4H5O4−, the pyridine N atom of the 2-amino-5-bromopyridine molecule is protonated. The protonated N atom and the amino group are linked via N—H...O hydrogen bonds to the carboxylate O atoms of the singly deprotonated succinate anion. The hydrogen succinate anions are linked via O—H...O hydrogen bonds. A weak intermolecular C—H...O hydrogen bond is also observed.

2-Fluoro-5-(4-fluorophenylpyridine

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Fazal Elahi

2012-07-01

Full Text Available In the title compound, C11H7F2N, the fluorobenzene and the 2-fluoropyridine rings are oriented at a dihedral angle of 37.93 (5°. In the crystal, only van der Waals interactions occur.

5 CFR 1320.2 - Effect.

Science.gov (United States)

2010-01-01

... 5 Administrative Personnel 3 2010-01-01 2010-01-01 false Effect. 1320.2 Section 1320.2... PUBLIC § 1320.2 Effect. (a) Except as provided in paragraph (b) of this section, this part takes effect on October 1, 1995. (b)(1) In the case of a collection of information for which there is in effect on...

Lifting business process diagrams to 2.5 dimensions

Science.gov (United States)

Effinger, Philip; Spielmann, Johannes

2010-01-01

In this work, we describe our visualization approach for business processes using 2.5 dimensional techniques (2.5D). The idea of 2.5D is to add the concept of layering to a two dimensional (2D) visualization. The layers are arranged in a three-dimensional display space. For the modeling of the business processes, we use the Business Process Modeling Notation (BPMN). The benefit of connecting BPMN with a 2.5D visualization is not only to obtain a more abstract view on the business process models but also to develop layering criteria that eventually increase readability of the BPMN model compared to 2D. We present a 2.5D Navigator for BPMN models that offers different perspectives for visualization. Therefore we also develop BPMN specific perspectives. The 2.5D Navigator combines the 2.5D approach with perspectives and allows free navigation in the three dimensional display space. We also demonstrate our tool and libraries used for implementation of the visualizations. The underlying general framework for 2.5D visualizations is explored and presented in a fashion that it can easily be used for different applications. Finally, an evaluation of our navigation tool demonstrates that we can achieve satisfying and aesthetic displays of diagrams stating BPMN models in 2.5D-visualizations.

Fragrance material review on 1-(2,5,5-trimethylcycloheptyl)ethan-1-one.

Science.gov (United States)

Scognamiglio, J; Letizia, C S; Api, A M

2013-12-01

A toxicologic and dermatologic review of 1-(2,5,5-trimethylcycloheptyl)ethan-1-one when used as a fragrance ingredient is presented. 1-(2,5,5-Trimethylcycloheptyl)ethan-1-one is a member of the fragrance structural group Alkyl Cyclic Ketones. These fragrances can be described as being composed of an alkyl, R1, and various substituted and bicyclic saturated or unsaturated cyclic hydrocarbons, R2, in which one of the rings may include up to 12 carbons. Alternatively, R2 may be a carbon bridge of C2-C4 carbon chain length between the ketone and cyclic hydrocarbon. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for 1-(2,5,5-trimethylcycloheptyl)ethan-1-one were evaluated then summarized and includes physical properties, skin irritation, mucous membrane (eye) irritation, and skin sensitization data. A safety assessment of the entire Alkyl Cyclic Ketones will be published simultaneously with this document; please refer to Belsito et al. (Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M., Fryer, A.D., Greim, H., Miyachi, Y., Saurat, J.H., Sipes, I.G., 2013. A toxicologic and dermatologic assessment of alkyl cyclic ketones when used as fragrance ingredients. (submitted for publication)) for an overall assessment of the safe use of this material and all Alkyl Cyclic Ketones in fragrances. Copyright © 2013. Published by Elsevier Ltd.

2-[(4-Bromophenyliminomethyl]-5-pentadecylphenol

Directory of Open Access Journals (Sweden)

Basavaraj Padmashali

2012-08-01

Full Text Available 2-[(4-Bromophenyliminomethyl]-5-pentadecylphenol has been synthesized by reaction of 2-hydroxy-4-pentadecylbenzaldehyde with 4-bromoaniline in 1,4-dioxane and its IR, ¹H-NMR, ¹³C-NMR and MS spectroscopic data are presented.

Synthesis of fused 1,2,4-dithiazines and 1,2,3,5-trithiazepines.

Science.gov (United States)

Koyioni, Maria; Manoli, Maria; Koutentis, Panayiotis A

2014-10-17

Reacting (Z)-N-(4-chloro-5H-1,2,3-dithiazol-5-ylidene)-1H-pyrazol-5-amines 5 with Et2NH and then with concd H2SO4 gives 5H-pyrazolo[3,4-e][1,2,4]dithiazine-3-carbonitriles 7 in good yields (74-85%) and 6H-pyrazolo[3,4-f][1,2,3,5]trithiazepine-4-carbonitriles 9 as minor products (0-6%). Furthermore, the 1,3-dimethylpyrazole analogue 5a was transformed into the dithiazine 7a in two discrete steps, allowing the isolation of a disulfide intermediate (Z)-2-[(diethylamino)disulfan-yl]-2-[(1H-pyrazol-5-yl)imino]acetonitrile (8a). The one-pot, two-step reaction also worked with electron-rich hydroxy- and methoxy-substituted anilines. Thermolysis of the pyrazolo[3,4-e][1,2,4]dithiazines 7 gave the ring-contracted 1H-pyrazolo[3,4-d]thiazole-5-carbonitriles 6 (94-100%). With active sulfur, 1,3-dimethyl-5H-pyrazolo[3,4-e][1,2,4]dithiazine-3-carbonitrile (7a) gave 1,3-dimethyl-6H-pyrazolo[3,4-f][1,2,3,5]trithiazepine-4-carbonitrile (9a), but on prolonged reaction times, it gave 5,7-dimethyl-5H-[1,2,3]dithiazolo[4,5-b]pyrazolo[3,4-e][1,4]thiazine (13). Finally, in the absence of acid, heating a solution of (Z)-2-[(diethylamino)disulfanyl]-2-[(1,3-dimethyl-1H-pyrazol-5-yl)imino]acetonitrile (8a) gave 4,6,10,12-tetramethyl-6H-pyrazolo[3,4-f]pyrazolo[3',4':4,5]pyrimido[6,1-d][1,2,3,5]trithiazepine-8,12b(10H)-dicarbonitrile (19) (67%).

UV Light-Driven Photodegradation of Methylene Blue by Using Mn0.5Zn0.5Fe2O4/SiO2 Nanocomposites

Science.gov (United States)

Indrayana, I. P. T.; Julian, T.; Suharyadi, E.

2018-04-01

The photodegradation activity of nanocomposites for 20 ppm methylene blue solution has been investigated in this work. Nanocomposites Mn0.5Zn0.5Fe2O4/SiO2 have been synthesized using coprecipitation method. The X-ray diffraction (XRD) pattern confirmed the formation of three phases in sample Mn0.5Zn0.5Fe2O4/SiO2 i.e., Mn0.5Zn0.5Fe2O4, Zn(OH)2, and SiO2. The appearance of SiO2 phase showed that the encapsulation process has been carried out. The calculated particles size of Mn0.5Zn0.5Fe2O4/SiO2 is greater than Mn0.5Zn0.5Fe2O4. Bonding analysis via vibrational spectra for Mn0.5Zn0.5Fe2O4/SiO2 confirmed the formation of bonds Me-O-Si stretching (2854.65 cm-1) and Si-O-Si asymmetric stretching (1026.13 cm-1). The optical gap energy of Mn0.5Zn0.5Fe2O4/SiO2 was smaller (2.70 eV) than Mn0.5Zn0.5Fe2O4 (3.04 eV) due to smaller lattice dislocation and microstrain that affect their electronic structure. The Mn0.5Zn0.5Fe2O4/SiO2 showed high photodegradation ability due to smaller optical gap energy and the appearance of SiO2 ligand that can easily attract dye molecules. The Mn0.5Zn0.5Fe2O4/SiO2 also showed high degradation activity even without UV light radiation. The result showed that photodegradation reaction doesn’t follow pseudo-first order kinetics.

5 CFR 1215.2 - Definitions.

Science.gov (United States)

2010-01-01

... 5 Administrative Personnel 3 2010-01-01 2010-01-01 false Definitions. 1215.2 Section 1215.2 Administrative Personnel MERIT SYSTEMS PROTECTION BOARD ORGANIZATION AND PROCEDURES DEBT MANAGEMENT Salary Offset... the debt and authorizes the payment of his/her current pay. (h) Salary offset. An administrative...

Crystal structure of ferroelectric Bi{sub 2}VO{sub 5.5}

Energy Technology Data Exchange (ETDEWEB)

Sooryanarayana, K.; Guru Row, T.N.; Varma, K.B.R. [Indian Inst. of Science, Bangalore (India)

1997-12-01

The structure of the {alpha}-phase of bismuth vanadate Bi{sub 2}VO{sub 5.5} has been determined using single crystal X-ray diffraction data in the space group Aba2. The refinement involves a well defined disorder at the vanadium site, which incorporates the features of the superlattice structure with vanadium tetrahedra and oxygen-deficient octahedra that is displaced about the twofold axis.

Platinum complexes of 5,6-Dihydroacenaphtho[5,6-cd]-1,2-dichalcogenoles

OpenAIRE

Benson, Callum G. M.; Schofield, Catherine M.; Randall, Rebecca A. M.; Wakefield, Lucy; Knight, Fergus R.; Slawin, Alexandra M. Z.; Woollins, J. Derek

2013-01-01

Six bis(phosphane) platinum complexes bearing dichalcogen acenaphthene ligands have been prepared by metathesis from cis-[PtCl2(PR3)(2)] (R-3 = Ph-3, Ph2Me, PhMe2) and the dilithium salts of the parent 5,6-dihydroacenaphtho[5,6-cd]-1,2-dichalcogenoles (AcenapE(2), L1 E = S, L2 E = Se). For their synthesis, the appropriate disulfide or diselenide species was treated with super hydride [LiBEt3H] to afford the dilithium salt by in situ reduction of the AcenapE(2) E-E bond. Further reaction, by m...

The oxidation of 2,2,5-three methyl-6-spiro cyclo hexane di hydro pyranol-5(X CI)

International Nuclear Information System (INIS)

Nikitin, V.I.

1961-01-01

In this chapter of book author as a result of oxidation of 2,2,5-three methyl-6-spiro cyclo hexane di hydro pyranol-5 evolved acetone, cyclopentanone, formic acid, acetic acid, oxalic acid, α-oxi isobutyric acid and adipinic acids

CBe5Hn((n-4)) (n = 2-5): Hydrogen-Stabilized CBe5 Pentagons Containing Planar or Quasi-Planar Pentacoordinate Carbons.

Science.gov (United States)

Guo, Jin-Chang; Ren, Guang-Ming; Miao, Chang-Qing; Tian, Wen-Juan; Wu, Yan-Bo; Wang, Xiaotai

2015-12-31

The diagonal relationship between beryllium and aluminum and the isoelectronic relationship between BeH unit and Al atom were utilized to design a new series ppC- or quasi-ppC-containing species C5v CBe5H5(+), Cs CBe5H4, C2v CBe5H3(-), and C2v CBe5H2(2-) by replacing the Al atoms in previously reported global minima planar pentacoordinate carbon (ppC) species D5h CAl5(+), C2v CAl4Be, C2v CAl3Be2(-), and C2v CAl2Be3(2-) with BeH units. The three-center two-electron (3c-2e) bonds formed between Be and bridging H atoms were crucial for the stabilization of these ppC species. The natural bond orbital (NBO) and adaptive natural density partitioning (AdNDP) analyses revealed that the central ppCs or quasi-ppCs possess the stable eight electron-shell structures. The AdNDP analyses also disclosed that these species are all 6σ+2π double-aromatic in nature. The aromaticity was proved by the calculated negative nucleus-independent chemical shifts (NICS) values. DFT and high-level CCSD(T) calculations revealed that these ppC- or quasi-ppC species are the global minimum or competitive low-lying local minimum (Cs CBe5H4) on their potential energy surfaces. The Born-Oppenheimer molecular dynamic (BOMD) simulations revealed that the H atoms in C2v CBe5H3(-) and C2v CBe5H2(2-) can easily rotate around the CBe5 cores and the structure of quasi-planar C5v CBe5H5(+) will become the planar structure at room temperature; however, these interesting dynamic behaviors did not indicate the kinetic instability as the basic ppC structures were maintained during the simulations. Therefore, it would be potentially possible to realize these interesting ppC- or quasi-ppc-species in future experiments.

Short range structural models of the glass transition temperatures and densities of 0.5Na2S + 0.5[xGeS2 + (1 - x)PS5/2] mixed glass former glasses.

Science.gov (United States)

Bischoff, Christian; Schuller, Katherine; Martin, Steve W

2014-04-03

The 0.5Na2S + 0.5[xGeS2 + (1 - x)PS5/2] mixed glass former (MGF) glass system exhibits a nonlinear and nonadditive negative change in the Na(+) ion conductivity as one glass former, PS5/2, is exchanged for the other, GeS2. This behavior, known as the mixed glass former effect (MGFE), is also manifest in a negative deviation from the linear interpolation of the glass transition temperatures (T(g)) of the binary end-member glasses, x = 0 and x = 1. Interestingly, the composition dependence of the densities of these ternary MGF glasses reveals a slightly positive MGFE deviation from a linear interpolation of the densities of the binary end-member glasses, x = 0 and x = 1. From our previous studies of the structures of these glasses using IR, Raman, and NMR spectroscopies, we find that a disproportionation reaction occurs between PS7/2(4-) and GeS3(2-) units into PS4(3-) and GeS5/2(1-) units. This disproportionation combined with the formation of Ge4S10(4-) anions from GeS5/2(1-) groups leads to the negative MGFE in T(g). A best-fit model of the T(g)s of these glasses was developed to quantify the amount of GeS5/2(1-) units that form Ge4S10(4-) molecular anions in the ternary glasses (∼ 5-10%). This refined structural model was used to develop a short-range structural model of the molar volumes, which shows that the slight densification of the ternary glasses is due to the improved packing efficiency of the germanium sulfide species.

Synthesis and Characterization of Yttria-Stabilized Zirconia Nanoparticles Doped with Ytterbium and Gadolinium: ZrO2 9.5Y2O3 5.6Yb2O3 5.2Gd2O3

Science.gov (United States)

Bahamirian, M.; Hadavi, S. M. M.; Rahimipour, M. R.; Farvizi, M.; Keyvani, A.

2018-06-01

Defect cluster thermal barrier coatings (TBCs) are attractive alternatives to Yttria-stabilized zirconia (YSZ) in advanced applications. In this study, YSZ nanoparticles doped with ytterbium and gadolinium (ZrO2 9.5Y2O3 5.6Yb2O3 5.2Gd2O3 (ZGYbY)) were synthesized through a chemical co-precipitation and calcination method, and characterized by in situ high-temperature X-ray diffraction analysis in the temperature range of 25 °C to 1000 °C (HTK-XRD), thermogravimetric analysis, differential thermal analysis, Fourier transform infrared spectroscopy, Raman spectroscopy, and field emission scanning electron microscopy (FE-SEM). Precise cell parameters of t-prime phase and the best zirconia phase for TBC applications were calculated by Cohen's and Rietveld refinement methods. Optimum crystallization temperature of the precursor powder was found to be 1000 °C. Furthermore, FE-SEM results for the calcined ZGYbY powders indicated orderly particles of uniform shape and size with a small tendency toward agglomeration. Average lattice thermal expansion coefficient in the temperature range of 25 °C to 1000 °C was determined to be 31.71 × 10-6 K-1.

Synthesis and Characterization of Yttria-Stabilized Zirconia Nanoparticles Doped with Ytterbium and Gadolinium: ZrO2 9.5Y2O3 5.6Yb2O3 5.2Gd2O3

Science.gov (United States)

Bahamirian, M.; Hadavi, S. M. M.; Rahimipour, M. R.; Farvizi, M.; Keyvani, A.

2018-03-01

Defect cluster thermal barrier coatings (TBCs) are attractive alternatives to Yttria-stabilized zirconia (YSZ) in advanced applications. In this study, YSZ nanoparticles doped with ytterbium and gadolinium (ZrO2 9.5Y2O3 5.6Yb2O3 5.2Gd2O3 (ZGYbY)) were synthesized through a chemical co-precipitation and calcination method, and characterized by in situ high-temperature X-ray diffraction analysis in the temperature range of 25 °C to 1000 °C (HTK-XRD), thermogravimetric analysis, differential thermal analysis, Fourier transform infrared spectroscopy, Raman spectroscopy, and field emission scanning electron microscopy (FE-SEM). Precise cell parameters of t-prime phase and the best zirconia phase for TBC applications were calculated by Cohen's and Rietveld refinement methods. Optimum crystallization temperature of the precursor powder was found to be 1000 °C. Furthermore, FE-SEM results for the calcined ZGYbY powders indicated orderly particles of uniform shape and size with a small tendency toward agglomeration. Average lattice thermal expansion coefficient in the temperature range of 25 °C to 1000 °C was determined to be 31.71 × 10-6 K-1.

2-Hydroxy-5-nitrobenzaldehyde

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Şamil Işık

2009-12-01

Full Text Available The title compound, C7H5NO4, is essentially planar, with a maximum deviation from the mean plane of 0.0116 (11 Å for the hydroxy O atom. The molecular and crystal structure are stabilized by intra- and intermolecular interactions. An intramolecular O—H...O hydrogen bond generates a six-membered ring, producing an S(6 ring motif. The C—H...O interactions result in the formation of C(5 chains and R22(8 rings forming an approximately planar network parallel to (10overline{1}. These planes are interconnected through π–π interactions [centroid–centroid distance 3.582 (2 Å].

Micropore Formation of [Zn2(Oxac) (Taz)2]·(H2O)2.5 via CO2 Adsorption.

Science.gov (United States)

Zubir, Moondra; Hamasaki, Atom; Iiyama, Taku; Ohta, Akira; Ohki, Hiroshi; Ozeki, Sumio

2017-01-24

As-synthesized [Zn 2 (Oxac) (Taz) 2 ]·(H 2 O) 2.5 , referred to as ZOTW 2.5 , was prepared from aqueous methanol solutions of Zn 5 (CO 3 ) 2 (OH) 6 and two kinds of ligands of 1,2,4-triazole (Taz) and oxalic acid (Oxac) at 453 K for 12 h. The crystal structure was determined by the Rietveld method. As-synthesized ZOTW 2.5 was pretreated at 383 K and 1 mPa for t pt h, ZOTW x (t pt h). ZOTW x (≥3h) showed a type I adsorption isotherm for N 2 at 77 K having a saturation amount (V s ) of 180 mg/g, but that pretreated shortly showed only 1/10 in V s . CO 2 was adsorbed at 303 K in sigmoid on nonporous ZOTW x (≤2h) and in Langmuir-type on ZOTW x (≥3h) to reach the adsorption amount of 120 mg/g at 700 Torr. N 2 adsorption on ZOTW x (≤2h)deCO 2 , degassed after CO 2 adsorption on ZOTW x (≤2h), was promoted 5-fold from 180 mg/g on ZOTW x (t pt h) and ZOTW x (≥3h)deCO 2 up to ca. 1000 mg/g. The interaction of CO 2 and H 2 O molecules in micropores may lead to a new route for micropore formation.

(+-{1,2-Bis[(2R,5R-2,5-diethylphospholan-1-yl]ethane-κ2P,P′}(η4-cycloocta-1,5-dienerhodium(I tetrafluoridoborate

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Stefan Schulz

2010-11-01

Full Text Available The title compound, [Rh(C8H12(C18H36P2]BF4, exhibits a rhodium(I complex cation with a bidentate bisphosphine ligand and a bidentate η2,η2-coordinated cycloocta-1,5-diene ligand. The ligands form a slightly distorted square-planar coordination environment for the Rh(I atom. An intramolecular P–Rh–P bite angle of 83.91 (2° is observed. The dihedral angle between the P—Rh—P and the X—Rh—X planes (X is the centroid of a double bond is 14.0 (1°. The BF4 anion is disordered over two positions in a 0.515 (7:0.485 (7 ratio.

Comparisons of urban and rural PM10−2.5 and PM2.5 mass concentrations and semi-volatile fractions in northeastern Colorado

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N. Clements

2016-06-01

Full Text Available Coarse (PM10−2.5 and fine (PM2.5 particulate matter in the atmosphere adversely affect human health and influence climate. While PM2.5 is relatively well studied, less is known about the sources and fate of PM10−2.5. The Colorado Coarse Rural-Urban Sources and Health (CCRUSH study measured PM10−2.5 and PM2.5 mass concentrations, as well as the fraction of semi-volatile material (SVM in each size regime (SVM2.5, SVM10−2.5, from 2009 to early 2012 in Denver and comparatively rural Greeley, Colorado. Agricultural operations east of Greeley appear to have contributed to the peak PM10−2.5 concentrations there, but concentrations were generally lower in Greeley than in Denver. Traffic-influenced sites in Denver had PM10−2.5 concentrations that averaged from 14.6 to 19.7 µg m−3 and mean PM10−2.5 ∕ PM10 ratios of 0.56 to 0.70, higher than at residential sites in Denver or Greeley. PM10−2.5 concentrations were more temporally variable than PM2.5 concentrations. Concentrations of the two pollutants were not correlated. Spatial correlations of daily averaged PM10−2.5 concentrations ranged from 0.59 to 0.62 for pairs of sites in Denver and from 0.47 to 0.70 between Denver and Greeley. Compared to PM10−2.5, concentrations of PM2.5 were more correlated across sites within Denver and less correlated between Denver and Greeley. PM10−2.5 concentrations were highest during the summer and early fall, while PM2.5 and SVM2.5 concentrations peaked in winter during periodic multi-day inversions. SVM10−2.5 concentrations were low at all sites. Diurnal peaks in PM10−2.5 and PM2.5 concentrations corresponded to morning and afternoon peaks of traffic activity, and were enhanced by boundary layer dynamics. SVM2.5 concentrations peaked around noon on both weekdays and weekends. PM10−2.5 concentrations at sites located near highways generally increased with wind speeds above about 3 m s−1. Little wind speed dependence was

7,8,15,16-tetraoxa-dispiro[5.2.5.2]hexadecane-3-carboxylic acid derivatives and their antimalarial activity

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BOGDAN SOLAJA

2004-11-01

Full Text Available Several C2 symmetrical mixed tetraoxanes were prepared starting from a gemdihydroperoxide and a ketone. The obtained tetraoxanes showed pronounced antimalarial activity against P. falciparum chloroquine resistant W2 and chloroquine susceptible D6 strains, with N-(2-dimethylaminoethyl-7,8,15,16-tetraoxa-dispiro[5.2.5.2] hexadecane-3-carboxamide being as active as artemisinin.

Polycrystalline V2O5/Na0.33V2O5 electrode material for Li+ ion redox supercapacitor

International Nuclear Information System (INIS)

Manikandan, Ramu; Justin Raj, C.; Rajesh, Murugesan; Kim, Byung Chul; Park, Sang Yeup; Cho, Bo-Bae; Yu, Kook Hyun

2017-01-01

Highlights: • Different polycrystalline V 2 O 5 /Na 0.33 V 2 O 5 nanostructures were synthesized via simple co-precipitation technique. • The various molar ratios of NaOH precipitator determine the morphology, structural and electrochemical properties of V/Na. • The equimolar ratio of reactant and precipitator shows the formation of ∼96% of pure crystalline phase of V 2 O 5 . • Li + ions intercalation and deintercalation process enhanced the specific capacitance. - Abstract: This work essentially offers a new kind of V 2 O 5 /Na 0.33 V 2 O 5 as electrochemical active material for the development of Li + ion redox supercapacitors. Here, polycrystalline mixed phase of V 2 O 5 /Na 0.33 V 2 O 5 (V/Na) nanostructures are synthesized via simple co-precipitation technique. The various molar ratio of precipitator (NaOH) in the synthesis process displays different nanostructures of V/Na. The structural and morphological properties of V/Na samples are studied using physico-chemical analysis methods. The electrochemical properties of V/Na nanostructured samples are performed using cyclic voltammetry, galvanostatic charge/discharge test and electrochemical impedance spectroscopy techniques in 1 M LiClO 4 aqueous electrolyte. The sample V/Na synthesized using equimolar ratio of vanadium salt and precipitator displayed nanopellet morphology, which exhibited the highest capacitance value of 334 Fg −1 at 1 Ag −1 discharge current density. Moreover, these polycrystalline V/Na nanostructured electrodes show excellent electrochemical properties with comparable stability after 1000 charge/discharge cycles.

Raman, FTIR, thermal and optical properties of TeO2-Nb2O5-B2O3-V2O5 quaternary glass system

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Swapna

2017-07-01

Full Text Available A series of quaternary glass systems with the composition 79TeO2-(20−xNb2O5-xB2O3-1V2O5 was prepared using the melt quench technique. Such studies as optical absorption, Raman, FTIR spectroscopy, EPR and DSC were carried out on the glass system. The physical properties, such as density (ρ and molar volume (VM, were determined. The Urbach energy (ΔE, optical band gap (Eopt, optical basicity (Λ, refractive index (n and electron polarizability (α of the glasses were determined from optical absorption data. Spin-Hamiltonian parameters of VO2+ ions were calculated from the EPR data. With the gradual substitution of B2O3 at the expense of Nb2O5, the density and optical band gap of the glasses decreased, and the electronic polarizability increased. EPR spectra revealed that VO2+ occupies an octahedral site with tetrahedral compression. Spin-Hamiltonian parameters g|| and g⊥ increased as B2O3 content increased in the glass. The glass transition temperature (Tg also decreased as the B2O3 content in the glass increased.

The creep of UO2 fuel doped with Nb2O5

International Nuclear Information System (INIS)

Sawbridge, P.T.; Reynolds, G.L.; Burton, B.

1981-01-01

The creep of UO 2 containing small additions of Nb 2 O 5 has been investigated in the stress range 0.5-90 MN/m 2 at temperatures between 1422 and 1573 K. The functional dependence of the creep rate of five dopant concentrations up to 0.8 mol% Nb 2 O 5 has been examined and it was established that in all the materials the secondary creep rate could be represented by the equation epsilonkT = Asigmasup(n) exp(-Q/RT), where epsilon is the steady state creep rate per hour, Q the activation energy and A and n are constants for each material. It was observed that Nb 2 O 5 additions can cause a dramatic increase in the steady state creep rate as long as the niobium ion is maintainde in the Nb 5+ valence state. Material containing 0.4 mol% Nb 2 O 5 creeps three orders of magnitude faster than the pure material. Analysis of the results in terms of grain size compensated viscosity suggest that, like pure UO 2 , the creep rate of Nb 2 O 5 doped fuel is diffusion-controlled and proportional to the reciprocal square of the grain size. A model is developed which suggests that the increase in creep rate results from suppression of the U 5+ ion concentration by the addition of Nb 5+ ions, which modifies the crystal defect structure and hence the uranium ion diffusion coefficient. (orig.)

1-Methoxy-3-o-tolylbicyclo[2.2.2]oct-5-ene-2,2-dicarbonitrile

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Orhan Büyükgüngör

2009-09-01

Full Text Available In the title compound, C18H18N2O, the cyclohexene and cyclohexane rings of the bicyclo[2.2.2]oct-5-ene unit adopt distorted boat conformations. In the crystal, molecules exist as C—H...N hydrogen-bonded centrosymmetric R22(14 dimers, which are further linked by C—H...π interactions.

(E-1-(2-Bromophenyl-3-(2,5-dimethoxyphenylprop-2-en-1-one

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Jerry P. Jasinski

2010-08-01

Full Text Available The title compound, C17H15BrO3, is a chalcone with the 2-bromophenyl and 2,5-dimethoxyphenyl rings bonded at opposite ends of a propene group. The dihedral angle between the mean planes of the ortho-bromo and ortho,meta-dimethoxy-substituted benzene rings is 77.3 (1°. The dihedral angles between the mean plane of the prop-2-ene-1-one group and the mean planes of the 2-bromophenyl and 2,5-dimethoxyphenyl rings are 58.6 (1 and 30.7 (4°, respectively. Weak C—H...O, C—H...Br and π–π stacking intermolecular interactions [centroid–centroid distance = 3.650 (2 Å] are present in the structure.

Reactions of 5,5\\'-dithiobis(2-nitrobenzoate) with CysB5(23)β and ...

African Journals Online (AJOL)

The reactivities of the sulphydryl groups of duck minor hemoglobin have been studied for a comparison with those of duck major hemoglobin. Boyer titration with p-hydroxymercuri(II)benzoic acid (pMB) gave four reactive sulphydryl groups per (tetramer) molecule. Titration with 5,5'- dithiobis(2-nitrobenzoic acid) (DTNB) also ...

Crystal structure of tetraaqua(5,5′-dimethyl-2,2′-bipyridyl-κ2N,N′iron(II sulfate

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Yamine Belamri

2014-12-01

Full Text Available In the title compound, [Fe(C12H12N2(H2O4]SO4, the central FeII ion is coordinated by two N atoms from the 5,5′-dimethyl-2,2′-bipyridine ligand and four water O atoms in a distorted octahedral geometry. The Fe—O coordination bond lengths vary from 2.080 (3 to 2.110 (3 Å, while the two Fe—N coordination bonds have practically identical lengths [2.175 (3 and 2.177 (3 Å]. The chelating N—Fe—N angle of 75.6 (1° shows the largest deviation from an ideal octahedral geometry; the other coordination angles deviate from ideal values by 0.1 (1 to 9.1 (1°. O—H...O hydrogen bonding between the four aqua ligands of the cationic complex and four O-atom acceptors of the anion leads to the formation of layers parallel to the ab plane. Neighbouring layers further interact by means of C—H...O and π–π interactions involving the laterally positioned bipyridine rings. The perpendicular distance between π–π interacting rings is 3.365 (2 Å, with a centroid–centroid distance of 3.702 (3 Å.

2-Amino-5-bromopyridinium trifluoroacetate

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Madhukar Hemamalini

2010-04-01

Full Text Available In the title compound, C5H6BrN2+·C2F3O2−, the F atoms of the anion are disordered over two sets of sites, with occupancies of 0.59 (2:0.41 (2. In the crystal structure, the anions and cations are linked into a two-dimensional network parallel to (100 by N—H...O and C—H...O hydrogen bonds. Within this network, the N—H...O hydrogen bonds generate R22(8 ring motifs.

Crystal structures of ZnCl2·2.5H2O, ZnCl2·3H2O and ZnCl2·4.5H2O

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Erik Hennings

2014-12-01

Full Text Available The formation of different complexes in aqueous solutions is an important step in understanding the behavior of zinc chloride in water. The structure of concentrated ZnCl2 solutions is governed by coordination competition of Cl− and H2O around Zn2+. According to the solid–liquid phase diagram, the title compounds were crystallized below room temperature. The structure of ZnCl2·2.5H2O contains Zn2+ both in a tetrahedral coordination with Cl− and in an octahedral environment defined by five water molecules and one Cl− shared with the [ZnCl4]2− unit. Thus, these two different types of Zn2+ cations form isolated units with composition [Zn2Cl4(H2O5] (pentaaqua-μ-chlorido-trichloridodizinc. The trihydrate {hexaaquazinc tetrachloridozinc, [Zn(H2O6][ZnCl4]}, consists of three different Zn2+ cations, one of which is tetrahedrally coordinated by four Cl− anions. The two other Zn2+ cations are each located on an inversion centre and are octahedrally surrounded by water molecules. The [ZnCl4] tetrahedra and [Zn(H2O6] octahedra are arranged in alternating rows parallel to [001]. The structure of the 4.5-hydrate {hexaaquazinc tetrachloridozinc trihydrate, [Zn(H2O6][ZnCl4]·3H2O}, consists of isolated octahedral [Zn(H2O6] and tetrahedral [ZnCl4] units, as well as additional lattice water molecules. O—H...O hydrogen bonds between the water molecules as donor and ZnCl4 tetrahedra and water molecules as acceptor groups leads to the formation of a three-dimensional network in each of the three structures.

Kinetics of the reactions H+C2H4->C2H5, H+C2H5->2CH3 and CH3+C2H5->products studies by pulse radiolysis combined with infrared diode laser spectroscopy

DEFF Research Database (Denmark)

Sillesen, A.; Ratajczak, E.; Pagsberg, P.

1993-01-01

Formation of methyl radicals via the consecutive reactions H+C2H4+M-->C2H5+M (1) and H+C2H5-->CH3+CH3 (2a) was initiated by pulse radiolysis of 10-100 mbar H-2 in the presence of ethylene. The kinetics of CH3 Were studied by monitoring the transient infrared absorption at the Q(3, 3) line of the ...

Bis(2,3,5,6-tetra-2-pyridylpyrazine-κ3N2,N1,N6iron(II bis(dicyanamidate 4.5-hydrate

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R. Cortés

2010-03-01

Full Text Available In the title compound, [Fe(C24H16N62][N(CN2]2·4.5H2O, the central iron(II ion is hexacoordinated by six N atoms of two tridentate 2,3,5,6-tetra-2-pyridylpyrazine (tppz ligands. Two dicyanamide anions [dca or N(CN2−] act as counter-ions, and 4.5 water molecules act as solvation agents. The structure contains isolated cationic iron(II–tppz complexes and the final neutrality is obtained with the two dicyanamide anions. One of the dicyanamide anions and a water molecule are disordered with an occupancy ratio of 0.614 (8:0.386 (8. O—H...O, O—H...N and C—H...O hydrogen bonds involving dca, water and tppz molecules are observed.

Synthesis and electroluminescence properties of a new aluminium complex [5-choloro-8-hydroxyquinoline] bis [2,2'bipyridine] Aluminium Al(Bpy)2(5-Clq)

Science.gov (United States)

Kumar, Rahul; Bhargava, Parag; Srivastava, Ritu; Singh, Punita

2015-11-01

We have synthesized a new aluminium complex, [5-choloro-8-hydroxyquinoline] bis[2,2'bipyridine] Aluminium Al(Bpy)2(5-Clq) and characterized it for structural, thermal and photoluminescence properties. The prepared material was characterized by Fourier -transformed infra-red spectroscopy (FTIR), thermal gravimetric analysis (TGA) and photoluminescence. The prepared material showed thermal stability up to 240 °C. The photoluminescence spectrum of Al(Bpy)2(5-Clq) in toluene solution showed peak at 515 nm. This material was used as an emissive layer in organic light emitting diodes (OLEDs). The fundamental structure of device is ITO/F4-TCNQ(1 nm)/α-NPD(35 nm)/Al(Bpy)2(5-Clq) (35 nm)/BCP(6 nm)/Alq3(28 nm)/LiF(1 nm)/Al(150 nm). The device emits an yellowish green light (CIE coordinates, x = 0.32, y = 0.52) with maximum luminescence 314 Cd/m2 at 18 V. The maximum current efficiency of OLED was 0.09 Cd/A and maximum power efficiency was 0.03 lm/W at 9 V respectively.

Molecular CsF 5 and CsF 2 +

KAUST Repository

Rogachev, Andrey Yu.; Miao, Mao-sheng; Merino, Gabriel; Hoffmann, Roald

2015-01-01

D5h star-like CsF5, formally isoelectronic with known XeF5− ion, is computed to be a local minimum on the potential energy surface of CsF5, surrounded by reasonably large activation energies for its exothermic decomposition to CsF+2 F2, or to CsF3 (three isomeric forms)+F2, or for rearrangement to a significantly more stable isomer, a classical Cs+ complex of F5−. Similarly the CsF2+ ion is computed to be metastable in two isomeric forms. In the more symmetrical structures of these molecules there is definite involvement in bonding of the formally core 5p levels of Cs.

Molecular CsF 5 and CsF 2 +

KAUST Repository

Rogachev, Andrey Yu.

2015-06-03

D5h star-like CsF5, formally isoelectronic with known XeF5− ion, is computed to be a local minimum on the potential energy surface of CsF5, surrounded by reasonably large activation energies for its exothermic decomposition to CsF+2 F2, or to CsF3 (three isomeric forms)+F2, or for rearrangement to a significantly more stable isomer, a classical Cs+ complex of F5−. Similarly the CsF2+ ion is computed to be metastable in two isomeric forms. In the more symmetrical structures of these molecules there is definite involvement in bonding of the formally core 5p levels of Cs.

Mööblifirmade trump a la carte-teenuses / Heli Lehtsaar

Index Scriptorium Estoniae

Lehtsaar, Heli, 1976-

2008-01-01

Mööblitootjad on muutuvas majandusolukorras hakanud seeriatootmise asemel pöörama rohkem tähelepanu eritellimustele. Vt. samas: Aktiivne müük ja likviidne käibevara aitavad madalseisu ajal elus püsida. Ain Alvela. Edule pürgiv mööblitootja peab moevooludega kaasa sörkima

N′-(3,5-Dibromo-2-hydroxybenzylidene-2-methylbenzohydrazide

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Chun-Bao Tang

2010-12-01

Full Text Available The asymmetric unit of the title compound, C15H12Br2N2O2, contains two independent molecules in which the dihedral angles between the benzene rings are 49.5 (7 and 66.4 (7°. Intramolecular O—H...N hydrogen bonds generate S(6 ring motifs in each molecule. In the crystal, molecules are linked through intermolecular N—H...O hydrogen bonds, forming chains along the b axis.

The quinternary thiophosphate Cs0.5Ag0.5Nb2PS10

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Sojeong Park

2010-07-01

Full Text Available The quinternary thiophosphate Cs0.5Ag0.5Nb2PS10, cesium silver tris(disulfido[tetrathiophosphato(V]diniobate(IV, has been prepared from the elements using a CsCl flux. The crystal structure is made up of ∞1[Nb2PS10] chains expanding along [010]. These chains are built up from bicapped trigonal-prismatic [Nb2S12] units and tetrahedral [PS4] groups and are linked through a linear S—Ag—S bridge, forming a two-dimensional layer. These layers then stack on top of each other, completing the three-dimensional structure with an undulating van der Waals gap. The disordered Cs+ ions reside on sites with half-occupation in the voids of this arrangement. Short [2.8843 (5 Å] and long [3.7316 (4 Å] Nb—Nb distances alternate along the chains, and anionic S22− and S2− species are observed. The charge balance of the compound can be represented by the formula [Cs+]0.5[Ag+]0.5[Nb4+]2[PS43−][S22−]3.

(Carbonato-κ2 O,O′)bis­(5,5′-dimethyl-2,2′-bipyridyl-κ2 N,N′)cobalt(III) bromide trihydrate

Science.gov (United States)

Arun Kumar, Kannan; Meera, Parthsarathi; Amutha Selvi, Madhavan; Dayalan, Arunachalam

2012-01-01

In the title complex, [Co(CO3)(C12H12N2)2]Br·3H2O, the CoIII cation has a distorted octa­hedral coordination environment. It is chelated by four N atoms of two different 5,5′-dimethyl-2,2′-bipyridyl (dmbpy) ligands in axial and equatorial positions, and by two O atoms of a carbonate anion completing the equatorial positions. Although the water mol­ecules are disordered and their H atoms were not located, there are typical O⋯O distances between 2.8 and 3.0 Å, indicating O—H⋯O hydrogen bonding. The crystal packing is consolidated by C—H⋯O and C—H⋯Br hydrogen bonds, as well as π–π stacking inter­actions between adjacent pyridine rings of the dmbpy ligands, with centroid–centroid distances of 3.694 (3) and 3.7053 (3) Å. PMID:22589773

Vibrational spectroscopic analysis of 2-chloro-5-(2,5-dimethoxy-benzylidene)-1,3-diethyl-dihydro-pyrimidine-4,6(1H,5H)-dione

Science.gov (United States)

Soliman, H. S.; Eid, Kh. M.; Ali, H. A. M.; Atef, S. M.; El-Mansy, M. A. M.

2012-11-01

In the present work, a combined experimental and computational study for the optimized molecular structural parameters, FT-IR spectra, thermo-chemical parameters, total dipole moment and HOMO-LUMO energy gap for 2-chloro-5-(2,5-dimethoxy-benzylidene)-1,3-diethyl-dihydro-pyrimidine-4,6(1H,5H)-dione have been investigated using B3LYP/6-311G basis set. Our calculated results have showed that the investigated compound possesses a dipole moment of 4.9 Debye and HOMO-LUMO energy gap of 3 eV which indicate high recommendations for photovoltaic devices fabrication.

TAE+ 5.2 - TRANSPORTABLE APPLICATIONS ENVIRONMENT PLUS, VERSION 5.2 (DEC RISC ULTRIX VERSION)

Science.gov (United States)

TAE SUPPORT OFFICE

1994-01-01

programs to display and control the user interfaces. Since the WPTs access the workbench-generated resource files during each execution, details such as color, font, location, and object type remain independent from the application code, allowing changes to the user interface without recompiling and relinking. In addition to WPTs, TAE Plus can control interaction of objects from the interpreted TAE Command Language. TCL provides a means for the more experienced developer to quickly prototype an application's use of TAE Plus interaction objects and add programming logic without the overhead of compiling or linking. TAE Plus requires MIT's X Window System and the Open Software Foundation's Motif. The HP 9000 Series 700/800 version of TAE 5.2 requires Version 11 Release 5 of the X Window System. All other machine versions of TAE 5.2 require Version 11, Release 4 of the X Window System. The Workbench and WPTs are written in C++ and the remaining code is written in C. TAE Plus is available by license for an unlimited time period. The licensed program product includes the TAE Plus source code and one set of supporting documentation. Additional documentation may be purchased separately at the price indicated below. The amount of disk space required to load the TAE Plus tar format tape is between 35Mb and 67Mb depending on the machine version. The recommended minimum memory is 12Mb. Each TAE Plus platform delivery tape includes pre-built libraries and executable binary code for that particular machine, as well as source code, so users do not have to do an installation. Users wishing to recompile the source will need both a C compiler and either GNU's C++ Version 1.39 or later, or a C++ compiler based on AT&T 2.0 cfront. TAE Plus was developed in 1989 and version 5.2 was released in 1993. TAE Plus 5.2 is available on media suitable for five different machine platforms: (1) IBM RS/6000 series workstations running AIX (.25 inch tape cartridge in UNIX tar format), (2) DEC RISC

5 CFR 1201.2 - Original jurisdiction.

Science.gov (United States)

2010-01-01

... 5 Administrative Personnel 3 2010-01-01 2010-01-01 false Original jurisdiction. 1201.2 Section 1201.2 Administrative Personnel MERIT SYSTEMS PROTECTION BOARD ORGANIZATION AND PROCEDURES PRACTICES AND PROCEDURES Jurisdiction and Definitions § 1201.2 Original jurisdiction. The Board's original...

Mööbel suvekodusse / Aili Ermel

Index Scriptorium Estoniae

Ermel, Aili

2008-01-01

2008. a. Milano messil "Salone Internazionale del Mobile" oli mööblit, mis projekteeritud ekstra õuele, aga oli ka sellist, mis sobib suvel õue ja talvel tuppa. Mööbel firmalt Cappellini, Gervason (disainer Paola Navone), Horm (disainer Mario Bellini), Zanotta (disainerid Gae Aulenti, Prospero Rasulo, Emaf Progetti, Roberto Barbieri), EMU (disainer Patricia Urquiola), Moroso (disainerid Nipa Doshi, Jonhatan Levien, Edward Van Vliet), Cassina (Tokujin Yoshioka) ja RODA. 14 värv. ill

Stress corrosion of the alloy U-7.5 Nb-2.5 Zr

International Nuclear Information System (INIS)

Lepoutre, D.; Nomine, A.M.; Miannay, D.

1983-09-01

Oxide formed on U-7.5 Nb-2.5 Zr at room temperature during stress corrosion cracking in oxygen is identical to the natural oxide of the alloy. It is formed by UO 2 with Nb and Zr and is associated with an increased Nb content at the interface. This oxide would be responsible for cracking [fr

Glass formation and properties of glasses in V/sub 2/O/sub 5/-B/sub 2/O/sub 3/-P/sub 2/O/sub 5/ system

Energy Technology Data Exchange (ETDEWEB)

Sedmale, G P; Vajvad, Ya A; Arkhipova, S E; Laukmanis, L A

1987-01-01

The glass formation in the system V/sub 2/O/sub 5/-B/sub 2/O/sub 3/-P/sub 2/O/sub 5/ and the properties of the obtained glasses have been studied by methods including that of the mathematical design and the treatment of the obtained data on ECM. The glass formation region is limited by the molar content of V/sub 2/O/sub 5/ 30-80%, B/sub 2/O/sub 3/ 0-45%, P/sub 2/O/sub 5/ 20-65%. The chemical stability data show that at the molar content of V/sub 2/O/sub 5/ 45-50% the transfer of vanadium from the state of the modificator to the glass-forming agent takes place. For the studied glasses the electron mechanism of conductivity is the dominating one.

Synthesis and Transformations of di-endo-3-Aminobicyclo-[2.2.2]oct-5-ene-2-carboxylic Acid Derivatives

Directory of Open Access Journals (Sweden)

Márta Palkó

2011-09-01

Full Text Available all-endo-3-amino-5-hydroxybicyclo[2.2.2]octane-2-carboxylic acid (13 and all-endo-5-amino-6-(hydroxymethylbicyclo[2.2.2]octan-2-ol (10 were prepared via dihydro-1,3-oxazine or g-lactone intermediates by the stereoselective functionalization of an N-protected derivative of endo-3-aminobicyclo[2.2.2]oct-5-ene-2-carboxylic acid (2. Ring closure of b-amino ester 4 resulted in tricyclic pyrimidinones 15 and 16. The structures, stereochemistry and relative configurations of the synthesized compounds were determined by IR and NMR.

Natural 4-Hydroxy-2,5-dimethyl-3(2H)-furanone (Furaneol®)

OpenAIRE

Wilfried Schwab

2013-01-01

4-Hydroxy-2,5-dimethyl-3(2H)-furanone (HDMF, furaneol®) and its methyl ether 2,5-dimethyl-4-methoxy-3(2H)-furanone (DMMF) are import aroma chemicals and are considered key flavor compounds in many fruit. Due to their attractive sensory properties they are highly appreciated by the food industry. In fruits 2,5-dimethyl-3(2H)-furanones are synthesized by a series of enzymatic steps whereas HDMF is also a product of the Maillard reaction. Numerous methods for the synthetic preparation of these c...

Glass formation in AgI:Ag2O:V2O5 and AgI:Ag2O:(V2O5+B2O3) systems

International Nuclear Information System (INIS)

Kaushik, R.; Hariharan, K.

1988-01-01

Transport properties of glasses in the system AgI:Ag 2 O: V 2 O 5 and AgI:Ag 2 O: (V 2 O 5 +B 2 O 3 ) have ben investigated. It was found that, at high AgI concentrations, the addition of another glass former (B 2 O 3 ) did not improve the conduction characteristics of the pure vanadate glasses, the best conducting composition of which had ambient temperature, ionic conductivity comparable to that of conventional liquid electrolytes. The highest conducting composition was used as an electrolyte in the study of silver solid state cells. The discharge characteristics of different cells fabricated with the glassy electrolyte, have been compared with those having the best conducting polycrystalline ompositions as electrolytes. 11 refs.; 4 figs.; 1 table

Luminescent properties of Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F oxyfluorides

Energy Technology Data Exchange (ETDEWEB)

Park, Sangmoon, E-mail: spark@silla.ac.kr [Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of)

2012-04-15

Effective orange Sm{sup 3+}-doped Sr{sub 2.5}Ba{sub 0.5}AlO{sub 4}F phosphors excited at 254 and 408 nm excitation were prepared by the solid-state method. The excitation and emission spectra of Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F and Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4-{alpha}}F{sub 1-{delta}} (x=0.001{approx}0.1) based on photoluminescence spectroscopy are investigated. The defects in anion-deficient Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4-{alpha}}F{sub 1-{delta}} (x=0.001, 0.01) are monitored by broad-band photoluminescence emission centered near 480 nm along with the orange emission transitions of Sm{sup 3+}. CIE values and relative luminescent intensities of Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F and Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4-{alpha}}F{sub 1-{delta}} by changing the Sm{sup 3+} content (x=0.001{approx}0.1) are discussed. - Highlights: Black-Right-Pointing-Pointer Under the excitation of 408 nm competent orange emitting Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F phosphor is initiated. Black-Right-Pointing-Pointer Sm{sup 3+}-activated oxyfluoride phosphor is quite effective to prepare white-emitting light for near-UV LED applications. Black-Right-Pointing-Pointer Defects could be visibly created in the Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}Al O{sub 4}F host lattices when Sm{sup 3+} ions are doped less than 5 mol %. Black-Right-Pointing-Pointer The gradual substitution of Sm{sup 3+} contents in oxyfluoride hosts is amenable to change CIE values and desired emitting intensity.

trans-Bis(5,5-diphenylhydantoinato-κN3bis(propane-1,2-diamine-κ2N,N′nickel(II

Directory of Open Access Journals (Sweden)

Xiaojiao Li

2008-12-01

Full Text Available The asymmetric unit of the title complex, [Ni(pht2(pn2] (pht is 5,5-diphenylhydantoinate and pn is propane-1,2-diamine or [Ni(C15H11N2O22(C3H10N22], contains one-half [Ni(pht2(pn2] molecule. The NiII atom is situated on a crystallographic center of inversion and shows a distorted octahedral coordination geometry. A three-dimensional network structure is assembled by inter- and intramolecular N—H...O=C interactions.

2-[(2,4,4,6,6-Pentachloro-1,3,5,2λ5,4λ5,6λ5-triazatriphosphinin-2-ylazanidyl]pyridinium

Directory of Open Access Journals (Sweden)

Safaa A. Ahmed

2012-02-01

Full Text Available The title compound, C5H5Cl5N5P3, crystallizes as a zwitterion in which the pyridine N atom is protonated. An S(6 ring motif is formed via an intramolecular C—H...N hydrogen bond. The triazatriphosphinine ring adopts an envelope conformation, with one N atom displaced by 0.145 (1 Å from the other atoms. In the crystal, N—H...N and C—H...N hydrogen bonds link the molecules into centrosymmetric dimers containing one R22(7 ring motif and two R22(8 ring motifs.

10 CFR 960.5-2-8 - Surface characteristics.

Science.gov (United States)

2010-01-01

... 10 Energy 4 2010-01-01 2010-01-01 false Surface characteristics. 960.5-2-8 Section 960.5-2-8... Closure § 960.5-2-8 Surface characteristics. (a) Qualifying condition. The site shall be located such that, considering the surface characteristics and conditions of the site and surrounding area, including surface...

Autroadiographic characterization of 125I-labeled 2,5-dimethoxy-4-iodophenylisopropylamine (DOI): A phenylisopropylamine derivative labeling both 5HT2 and 5HT1c receptors

International Nuclear Information System (INIS)

Appel, N.M.; Mitchell, W.M.; Garlick, R.K.; Glennon, R.A.; Titeler, M.; De Souza, E.B.

1990-01-01

The best-characterized 5HT 2 radioligands, such as [ 3 H]ketanserin and [ 3 H]spiperone, are antagonists that label both high- and low-affinity states of this receptor. Recently, the radiolabeled phenylisopropylamine hallucinogens DOB and DOI, which are agonists at 5HT 2 receptors, have been demonstrated to label selectively the high-affinity state of brain 5HT 2 receptors. In the present study, the authors determined optimum conditions for autoradiographic visualization of [ 125 I]DOI binding and characterized its pharmacology and guanine nucleotide sensitivity under those conditions. In slide-mounted tissue sections (rat forebrain; two 10 μm sections/slide), (±)[ 125 I]DOI binding was saturable, of high affinity (K D ∼4nM) and displayed a pharmacological profile [R(-)DOI > spiperone > DOB > (±)DOI > ketanserin > S(+)DOI > 5HT > DOM] comparable to that seen in homogenate assays. Consistent with coupling of 5HT 2 receptors to a guanine nucleotide regulatory protein, [ 125 I]DOI binding was inhibited by guanine nucleotides but not by ATP. In autoradiograms, high densities of [ 125 I]DOI binding sites were present in frontal cortex, olfactory tubercle, claustrum, caudate/putamen and mamillary nuclei with lower densities in trigeminal and solitary nuclei. The highest density of [ 125 l]DOI binding was observed in choroid plexus; these binding sites displayed a pharmacological profile characteristic of 5HT 1C receptors. These data suggest that [ 125 I]DOI labels both 5HT 2 and 5HT 1C receptors

Synthesis, stability range and characterization of Pr2Cu2O5

Science.gov (United States)

Fernández-Sanjulián, Javier; Morán, Emilio; Ángel Alario-Franco, Miguel

2010-03-01

A novel Pr2Cu2O5 phase has been prepared under high-pressure and high-temperature conditions (P ∼6 GPa and T ∼1673 K) in a Belt-type apparatus and characterized by X-ray diffraction and electron microscopy. The crystal structure appears to be an orthorhombic "oxygen-deficient perovskite" (M.T. Anderson, J.T. Vaughey, and K.R. Poeppelmeier, Structural similarities among oxygen-deficient perovskites, Chem. Mater. 5 (1993), pp. 151-165) isostructural with La2Cu2O5 (J.F. Bringley, B.A. Scott, S.J. La Placa, R.F. Boheme, T.M. Shaw, M.W. McElfresh, S.S. Trail, and D.E. Cox, Synthesis of the defect perovskite series LaCuO 3-δ with copper valence varying from 2+to 3+, Nature 347 (1990), pp. 263-265) and Nd2Cu2O5 (B.-H. Chen, D. Walker, E. Suard, B.A. Scott, B. Mercey, M. Hervieu, and B. Raveau, High pressure synthesis of NdCuO3-δ perovskites (0≤δ≤0.5). Inorg. Chem. 34 (1995), pp. 2077-2083).

Ca{sub 2}Cr{sub 0.5}Ga{sub 1.5}O{sub 5}—An extremely redox-stable brownmillerite phase

Energy Technology Data Exchange (ETDEWEB)

Luo, Kun; Amano Patino, Midori; Hayward, Michael A., E-mail: michael.hayward@chem.ox.ac.uk

2015-02-15

Investigation of the Ca{sub 2}Cr{sub x}Ga{sub 2−x}O{sub 5} compositional series reveals a maximum chromium solubility of 25%. The most chromium rich composition, Ca{sub 2}Cr{sub 0.5}Ga{sub 1.5}O{sub 5}, adopts a brownmillerite-type anion deficient perovskite structure described in space group Pnma (a=5.368 Å, b=14.547 Å, c=5.593 Å). Neutron powder diffraction data reveals rigorous B-site cation order, with all of the tetrahedral coordination sites occupied exclusively by gallium and the octahedral coordination sites occupied by gallium or chromium. Annealing studies reveals Ca{sub 2}Cr{sub 0.5}Ga{sub 1.5}O{sub 5} is stable in both oxidizing (100% O{sub 2}) and reducing (5% H{sub 2} in N{sub 2}) conditions up to 800 °C, suggesting it could find application as a stable host lattice for fuel cell electrodes or electrolytes with suitable doping to enhance catalytic behaviour and/or anionic conductivity. - Graphical abstract: Ca{sub 2}Cr{sub 0.5}Ga{sub 1.5}O{sub 5}, adopts a brownmillerite-type anion deficient perovskite structure yet it is stable in both oxidizing (100% O{sub 2}) and reducing (5% H{sub 2} in N{sub 2}) conditions up to 800 °C. - Highlights: • Anion deficient oxide stable to both oxidation and reduction up to 800 °C. • Cation-ordered brownmillerite structure determined by powder neutron diffraction. • Low solubility of Cr{sup 3+} in framework due to spherical d{sup 3} electron configuration.

The influence of PM2.5 coal power plant emissions on environment PM2.5 in Jilin Province, China

Science.gov (United States)

Sun, Ye; Li, Zhi; Zhang, Dan; Zhang, He; Zhang, Huafei

2018-02-01

In recent years, in the Northeast of China, the heating period comes with large range of haze weather. All the units of coal power plants in Jilin Province have completed the cogeneration reformation; they provide local city heat energy. Many people believe that coal power plants heating caused the heavy haze. In is paper, by compared concentration of PM2.5 in environment in heating period and non heating period, meanwhile the capacity of local coal power plants, conclude that the PM2.5 emission of coal power plants not directly cause the heavy haze in Changchun and Jilin in the end of October and early November. In addition, the water-soluble iron composition of PM2.5 coal power plant emissions is compared with environment, which further proves that the heating supply in coal power plants is not the cause of high concentration of PM2.5 in Jilin province.

Cs2.5H0.5PWO40/SiO2 as addition self-humidifying composite membrane for proton exchange membrane fuel cells

International Nuclear Information System (INIS)

Wang, L.; Yi, B.L.; Zhang, H.M.; Xing, D.M.

2007-01-01

In this paper, we first reported a novel self-humidifying composite membrane for the proton exchange membrane fuel cell (PEMFC). Cs 2.5 H 0.5 PWO 40 /SiO 2 catalyst particles were dispersed uniformly into the Nafion (registered) resin, and then Cs 2.5 H 0.5 PWO 40 -SiO 2 /Nafion composite membrane was prepared using solution-cast method. Compared with the H 3 PWO 40 (PTA) , the Cs 2.5 H 0.5 PWO 40 /SiO 2 was steady due to the substitute of H + with Cs + and the interaction between the Cs 2.5 H 0.5 PWO 40 and SiO 2 . And compared with the performance of the fuel cell with commercial Nafion (registered) NRE-212 membrane, the cell performance with the self-humidifying composite membrane was obviously improved under both humidified and dry conditions at 60 and 80 o C. The best performance under dry condition was obtained at 60 o C. The self-humidifying composite membrane could minimize membrane conductivity loss under dry conditions due to the presence of catalyst and hydrophilic Cs 2.5 H 0.5 PWO 40 /SiO 2 particles

Theoretical Stark broadening parameters for spectral lines arising from the 2p5ns, 2p5np and 2p5nd electronic configurations of Mg III

Science.gov (United States)

Colón, C.; Moreno-Díaz, C.; Alonso-Medina, A.

2013-10-01

In the present work we report theoretical Stark widths and shifts calculated using the Griem semi-empirical approach, corresponding to 237 spectral lines of Mg III. Data are presented for an electron density of 1017 cm-3 and temperatures T = 0.5-10.0 (104K). The matrix elements used in these calculations have been determined from 23 configurations of Mg III: 2s22p6, 2s22p53p, 2s22p54p, 2s22p54f and 2s22p55f for even parity and 2s22p5ns (n = 3-6), 2s22p5nd (n = 3-9), 2s22p55g and 2s2p6np (n = 3-8) for odd parity. For the intermediate coupling (IC) calculations, we use the standard method of least-squares fitting from experimental energy levels by means of the Cowan computer code. Also, in order to test the matrix elements used in our calculations, we present calculated values of 70 transition probabilities of Mg III spectral lines and 14 calculated values of radiative lifetimes of Mg III levels. There is good agreement between our calculations and experimental radiative lifetimes. Spectral lines of Mg III are relevant in astrophysics and also play an important role in the spectral analysis of laboratory plasma. Theoretical trends of the Stark broadening parameter versus the temperature for relevant lines are presented. No values of Stark parameters can be found in the bibliography.

NEW METABOLITES OF THE DRUG 5-AMINOSALICYLIC ACID .2. N-FORMYL-5-AMINOSALICYLIC ACID

DEFF Research Database (Denmark)

Tjornelund, J.; Hansen, S. H.; Cornett, Claus

1991-01-01

1. A new metabolite of the drug 5-aminosalicylic acid (5-ASA) has been found in urine from pigs and in plasma of humans. The metabolite has been isolated from pig urine using an XAD-2 column and purified using preparative h.p.l.c. 2. The metabolite has been identified as N-formyl-5-ASA (5-formami...

5 CFR 10.2 - Accountability systems.

Science.gov (United States)

2010-01-01

... 5 Administrative Personnel 1 2010-01-01 2010-01-01 false Accountability systems. 10.2 Section 10.2 Administrative Personnel OFFICE OF PERSONNEL MANAGEMENT CIVIL SERVICE RULES AGENCY ACCOUNTABILITY SYSTEMS; OPM AUTHORITY TO REVIEW PERSONNEL MANAGEMENT PROGRAMS (RULE X) § 10.2 Accountability systems. The Director of...

PM 2.5 Nonattainment Areas

Data.gov (United States)

U.S. Environmental Protection Agency — This data layer identifies areas in the U.S. where air pollution levels have not met the National Ambient Air Quality Standards (NAAQS) for PM 2.5 and have been...

Freeze drying synthesis of LiNi0.5Mn0.5O2 cathode materials

International Nuclear Information System (INIS)

Shlyakhtin, O.A.; Yoon, Young Soo; Choi, Sun Hee; Oh, Young-Jei

2004-01-01

The influence of several processing conditions on the phase formation and electrochemical performance of LiNi 0.5 Mn 0.5 O 2 powders, obtained by freeze drying method, is studied. Thermal processing in pellets at maximum heating rate promotes better crystallographic ordering of hexagonal LiNi 0.5 Mn 0.5 O 2 and maximum capacity values irrespectively of chemical composition of the precursor. Instead, intense mechanical processing of precursors exerts considerable negative effect on the electrochemical performance. Cathode materials containing superstoichiometric amount of lithium (Li 1.3 Mn 0.5 Ni 0.5 O 2+δ ) demonstrate reversible capacity values up to 190 mAh/g between 2.5 and 4.6 V

Phase change behaviors of Zn-doped Ge2Sb2Te5 films

International Nuclear Information System (INIS)

Wang Guoxiang; Nie Qiuhua; Shen Xiang; Fu Jing; Xu Tiefeng; Dai Shixun; Wang, R. P.; Wu Liangcai

2012-01-01

Zn-doped Ge 2 Sb 2 Te 5 phase-change materials have been investigated for phase change memory applications. Zn 15.16 (Ge 2 Sb 2 Te 5 ) 84.84 phase change film exhibits a higher crystallization temperature (∼258 °C), wider band gap (∼0.78 eV), better data retention of 10 years at 167.5 °C, higher crystalline resistance, and faster crystallization speed compared with the conventional Ge 2 Sb 2 Te 5 . The proper Zn atom added into Ge 2 Sb 2 Te 5 serves as a center for suppression of the face-centered-cubic (fcc) phase to hexagonal close-packed (hcp) phase transition, and fcc phase has high thermal stability partially due to the bond recombination among Zn, Sb, and Te atoms.

CATALYTIC KINETIC RESOLUTION OF 5-ALKOXY-2(5H)-FURANONES

OpenAIRE

FABER, WS; Kok, Johan C; DELANGE, B; FERINGA, BL; Faber, Wijnand S.; Lange, Ben de; Feringa, Bernard

1994-01-01

The kinetic resolution of racemic 5-alkoxy-2(5H)-furanones, using a chiral aminoalcohol catalyzed 1-4-addition of arylthiols, was examined. Using various butenolides it was shown that a gamma-alkoxy substituent appears to be essential to reach high enantioselectivities whereas electron-donating substituents in the arylthiols also increase the selectivity. Cinchona alkaloids are the preferred catalysts for the kinetic resolution, with quinine and quinidine leading to the most efficient and sel...

Synthesis of homogeneous Ca0.5Sr0.5FeO2.5+δ compound using a mirror furnace method

International Nuclear Information System (INIS)

Mahboub, M.S.; Zeroual, S.; Boudjada, A.

2012-01-01

Graphical abstract: X-ray diffraction pattern indexing of Ca 0.5 Sr 0.5 FeO 2.5+δ powder sample obtained by mirror furnace method after thermal treatment. Highlights: ► A homogenous compound Ca 0.5 Sr 0.5 FeO 2.5+δ has been synthesized for the first time by a mirror furnace method. ► Ca 0.5 Sr 0.5 FeO 2.5+δ powder sample is perfectly homogenous, confirmed by X-ray diffraction, Raman spectroscopy and EDS technique. ► The thermal treatment of Ca 0.5 Sr 0.5 FeO 2.5+δ powder sample can increase their average grain sizes. -- Abstract: A new synthesis method using melting zone technique via the double mirror furnace around 1600 °C is used to obtain homogenous brownmillerite compounds Ca 1−x Sr x FeO 2.5+δ in the range 0.3 ≤ x ≤ 0.7. These compounds play important role in understanding the mystery of the oxygen diffusion in the perovskite-related oxides. We have successfully solved the miscibility gap problem by synthesizing a good quality of homogenous powder samples of Ca 0.5 Sr 0.5 FeO 2.5+δ compound. Our result was confirmed by X-rays diffraction, Raman spectroscopy and energy dispersive spectroscopy analysis. Thermal treatment was also applied until 800 °C under vacuum to confirm again the homogeneity of powder samples, improve its quality and show that no decomposition or return to form Ca- and Sr-enriched microdomains takes place as a result of phase separation.

(Gd1−xErx)5Si2Ge2 compounds

Indian Academy of Sciences (India)

Gd metal (3 N) by arc melting, and then annealed at 1523 K (3 h). The phase, microstructure, Curie ... The temperature of magnetic transition decreases linearly from 281 K to 177 K with the increase of Er content from x = 0–0·2. ... Gd5Si2Ge2 serial compounds, different rare earth elements substituted for Gd in Gd5(Six ...

A study on the delayed hydride cracking mechanism in cold worked Zr-2.5Nb, heat treated Zr-2.5Nb and zircaloy-2 pressure tubes

Energy Technology Data Exchange (ETDEWEB)

Choi, Kwang Sik

1992-02-15

Cold worked Zr-2.5Nb, heat treated Zr-2.5Nb and Zircaloy-2 pressure tubes were hydrided to the hydrogen concentration of 68 ppm, 49 ppm and 242-411 ppm, respectively, and compact tension specimens were machined from the hydrided materials. The crack growth rate by delayed hydride cracking was measured by potential drop method at various temperatures on the above mentioned three types of specimens. The activation energy obtained were 43 KJ/mol for cold worked Zr-2.5Nb and 37 KJ/mol for heat treated Zr-2.5Nb, which were in good agreements with that of Coleman (1977), while they were lower than the activation energy of 65.5 KJ/mol obtained by Simpson-puls (1979) and 71.5 KJ/mol by Ambler (1984). The DHC growth rate in Zircaloy-2 were about one fifth of that of Zr-2.5Nb, which is due to the texture and material strength effects. Striations which indicate stepwise DHC growth were observed at fracture surface by scanning electron microscope and unsymmetric crack tunnellings were also observed, which seems to be due to the difference in hydrogen diffusion rate caused by the difference in stress fields between inner and outer surface. The comparison of test results with the DHC growth rate calculated by Simpson-puls model showed good agreement at high temperatures, whereas at the lower temperatures the crack growth rates were 2.5 times higher than the calculated values.

A study on the delayed hydride cracking mechanism in cold worked Zr-2.5Nb, heat treated Zr-2.5Nb and zircaloy-2 pressure tubes

International Nuclear Information System (INIS)

Choi, Kwang Sik

1992-02-01

Cold worked Zr-2.5Nb, heat treated Zr-2.5Nb and Zircaloy-2 pressure tubes were hydrided to the hydrogen concentration of 68 ppm, 49 ppm and 242-411 ppm, respectively, and compact tension specimens were machined from the hydrided materials. The crack growth rate by delayed hydride cracking was measured by potential drop method at various temperatures on the above mentioned three types of specimens. The activation energy obtained were 43 KJ/mol for cold worked Zr-2.5Nb and 37 KJ/mol for heat treated Zr-2.5Nb, which were in good agreements with that of Coleman (1977), while they were lower than the activation energy of 65.5 KJ/mol obtained by Simpson-puls (1979) and 71.5 KJ/mol by Ambler (1984). The DHC growth rate in Zircaloy-2 were about one fifth of that of Zr-2.5Nb, which is due to the texture and material strength effects. Striations which indicate stepwise DHC growth were observed at fracture surface by scanning electron microscope and unsymmetric crack tunnellings were also observed, which seems to be due to the difference in hydrogen diffusion rate caused by the difference in stress fields between inner and outer surface. The comparison of test results with the DHC growth rate calculated by Simpson-puls model showed good agreement at high temperatures, whereas at the lower temperatures the crack growth rates were 2.5 times higher than the calculated values

Dr Jekyll and Mr Hyde: a strange case of 5-ethynyl-2 '-deoxyuridine and 5-ethynyl-2 '- deoxycytidine

Czech Academy of Sciences Publication Activity Database

Ligasová, A.; Liboska, Radek; Friedecký, D.; Mičová, K.; Adam, T.; Oždian, T.; Rosenberg, Ivan; Koberna, K.

2016-01-01

Roč. 6, č. 1 (2016), č. článku 150172. ISSN 2046-2441 R&D Projects: GA MZd NV15-31604A Institutional support: RVO:61388963 Keywords : cytidine deaminase * dCMP deaminase * 5-ethynyl-2 '-deoxyuridine * 5-ethynyl-2 '-deoxycytidine * DNA replication Subject RIV: EB - Genetics ; Molecular Biology Impact factor: 3.481, year: 2016 http://rsob.royalsocietypublishing.org/content/6/1/150172

10 CFR 960.5-2-10 - Hydrology.

Science.gov (United States)

2010-01-01

... 10 Energy 4 2010-01-01 2010-01-01 false Hydrology. 960.5-2-10 Section 960.5-2-10 Energy DEPARTMENT OF ENERGY GENERAL GUIDELINES FOR THE PRELIMINARY SCREENING OF POTENTIAL SITES FOR A NUCLEAR WASTE... Hydrology. (a) Qualifying condition. The site shall be located such that the geohydrologic setting of the...

Differentiation of 5-hydroxytryptamine2 receptor subtypes using 125I-R-(-)2,5-dimethoxy-4-iodo-phenylisopropylamine and 3H-ketanserin

International Nuclear Information System (INIS)

McKenna, D.J.; Peroutka, S.J.

1989-01-01

The radioligand binding characteristics of 125I-R-(-)4-iodo-2,5-dimethoxyphenylisopropylamine [125I-R-(-)DOI] and 3H-ketanserin were compared in rat and bovine cortical membranes. In rat cortex, 125I-R-(-)DOI labels a relatively low density of binding sites (Bmax = 2.5 +/- 0.2 pmol/gm tissue) with high affinity (KD = 0.63 +/- 0.09 nM). In bovine cortex, specific binding of 125I-R-(-)DOI represents less than 20% of total binding at radioligand concentrations above 0.6 nM, and, therefore, the data cannot be analyzed adequately by Scatchard transformation. By contrast, 3H-ketanserin displays saturable, specific high-affinity binding in both rat cortex (KD = 1.0 +/- 0.1 nM; Bmax = 11 +/- 0.4 pmol/gm tissue) and bovine cortex (KD = 1.2 +/- 0.2 nM; Bmax = 5.3 +/- 0.4 pmol/gm tissue). Ki values for 30 drugs were determined for 125I-R-(-)DOI-labeled sites in rat cortex and 3H-ketanserin-labeled sites in bovine cortex. 5-Hydroxytryptamine (5-HT) displays 250-fold higher selectivity for the 125I-R-(-)DOI-labeled sites (Ki = 3.0 +/- 0.7 nM) than for the 3H-ketanserin-labeled sites (Ki = 750 +/- 50 nM). Structural congeners of R-(-)DOI display 80- to 160-fold higher affinity for the 125I-R-(-)DOI binding site than for the 3H-ketanserin-labeled binding site. d-LSD and putative 5-HT2 antagonists are approximately equipotent at both sites. Significant correlations were found between drug affinities for 125I-R-(-)DOI-labeled sites in rat cortex and putative 5-HT2A sites labeled previously by 77Br-R-(-)DOB (r = 0.93, p less than 0.01), putative 5-HT2B sites labeled by 3H-ketanserin in bovine cortex (r = 0.63, p less than 0.01), and 5-HT1C binding sites that have been characterized by other investigators (r = 0.78, p less than 0.01). No significant correlations were found between drug affinities for 125I-R-(-)DOI-labeled sites in rat cortex and 5-HT1A, 5-HT1B, 5-HT1D, or 5-HT3 sites, as determined by previous investigators

Conversion of 2-deoxy-D-ribose into 2-amino-5-(2-deoxy-beta-D-ribofuranosyl)pyridine, 2'-deoxypseudouridine, and other C-(2'-deoxyribonucleosides).

Science.gov (United States)

Reese, Colin B; Wu, Qinpei

2003-09-21

The synthesis of 2-amino-5-(2-deoxy-beta-D-ribofuranosyl)pyridine 2a, 2-amino-5-(2-deoxy-alpha-D-ribofuranosyl)-pyridine 23, 2-amino-5-(2-deoxy-beta-D-ribofuranosyl)-3-methylpyridine 2b, 2-amino-5-(2-deoxy-alpha-D-ribofuranosyl)-3-methylpyridine 29 and 5-(2-deoxy-beta-D-ribofuranosyl)-2,4-dioxopyrimidine [2'-deoxypseudouridine] 30a is described. These C-nucleosides are prepared either from 2-deoxy-3,5-O-(1,1,3,3-tetraisopropyldisiloxan-1,3-diyl)-D-ribofuranose 15 or from 2-deoxy-3,5-O-(1,1,3,3-tetraisopropyldisiloxan-1,3-diyl)-D-ribono-1,4-lactone 16, which are themselves prepared from 2-deoxy-D-ribose 13. The sugar derivatives are first allowed to react with the appropriate 5-lithio-pyridine or 5-lithio-pyrimidine derivatives, which are prepared from 5-bromo-2-(dibenzylamino)pyridine 12a, 5-bromo-2-[bis(4-methoxybenzyl)amino]pyridine 12b, 5-bromo-2-dibenzylamino-3-methylpyridine 25 and 5-bromo-2,4-bis(4-methoxybenzyloxy)pyrimidine 33. The products from the reactions between the lithio-derivatives and the lactol 15 are cyclized under Mitsunobu conditions; the products from the reactions between the lithio-derivatives and the lactone 16 are first reduced with L-Selectride before cyclization, also under Mitsunobu conditions. In all cases, the beta-anomers of the protected C-nucleosides are the predominant products. Finally, the separation of the alpha- and beta-anomers and the removal of all of the protecting groups are described.

Synthesis and crystal structures of two α-bromoamides, (2'R,1S,2S)-N(2-bromopropanoyl)-2-amino-1-phenylpropane-1,3-diol and (2'S,5S,6S)-N(2-bromopropanoyl)-5-amino-6-phenyl-2-oxo-1,3,2-dioxathiane

International Nuclear Information System (INIS)

English, R.B.; Liddell, R.J.; Whiteley, C.G.

1987-01-01

One pair of diastereomeric bromoamides, (2'R,1S,2S)- and (2'S,1S,2S)-N(2-bromopropanoyl)-2-amino-1-phenylpropane-1,3-diol have been synthesized from ethyl 2-bromopropionate and an optically active amino-diol. The crystal structures of both were determined from single-crystal X-ray analyses. Both compounds are orthorhombic with space group P2 1 2 1 2 1 with Z = 4 in a unit cell of dimensions a 22,124(5),b 12,812(5), and c 4,886(5)A and a 15,510(5), b 9,707(5), and c 9,457(5)A. The proton chemical shifts of the groups attached to the asymmetric centre C(2'), and consequently, the identification of the configuration of the molecules, were resolved with the help of high-resolution nuclear magnetic resonance

Hydrazinium lanthanide oxalates: synthesis, structure and thermal reactivity of N_2H_5[Ln_2(C_2O_4)_4(N_2H_5)].4H_2O, Ln = Ce, Nd

International Nuclear Information System (INIS)

De Almeida, Lucie; Grandjean, Stephane; Abraham, Francis; Rivenet, Murielle; Patisson, Fabrice

2014-01-01

New hydrazinium lanthanide oxalates N_2H_5[Ln_2(C_2O_4)_4(N_2H_5)].4H_2O, Ln = Ce (Ce-H_yO_x) and Nd (Nd- H_yO_x), were synthesized by hydrothermal reaction at 150 C between lanthanide nitrate, oxalic acid and hydrazine solutions. The structure of the Nd compound was determined from single-crystal X-ray diffraction data, space group P2_1/c with a = 16.315(4), b = 12.127(3), c = 11.430(2) Angstroms, β = 116.638(4) degrees, V = 2021.4(7) Angstroems"3, Z = 4, and R1 = 0.0313 for 4231 independent reflections. Two distinct neodymium polyhedra are formed, NdO_9 and NdO_8N, an oxygen of one monodentate oxalate in the former being replaced by a nitrogen atom of a coordinated hydrazinium ion in the latter. The infrared absorption band at 1005 cm"-"1 confirms the coordination of N_2H_5"+ to the metal. These polyhedra are connected through μ"2 and μ"3 oxalate ions to form an anionic three-dimensional neodymium-oxalate arrangement. A non-coordinated charge-compensating hydrazinium ion occupies, with water molecules, the resulting tunnels. The N-N stretching frequencies of the infrared spectra demonstrate the existence of the two types of hydrazine ions. Thermal reactivity of these hydrazinium oxalates and of the mixed isotypic Ce/Nd (CeNd-H_yO_x) oxalate were studied by using thermogravimetric and differential thermal analyses coupled with gas analyzers, and high temperature X-ray diffraction. Under air, fine particles of CeO_2 and Ce_0_._5Nd_0_._5O_1_._7_5 are formed at low temperature from Ce-H_yO_x and CeNd-H_yO_x, respectively, thanks to a decomposition/oxidation process. Under argon flow, dioxy-mono-cyanamides Ln_2O_2CN_2 are formed. (authors)

Ethyl 2-{4-[(1,5-dibenzyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3-ylmethyl]-1H-1,2,3-triazol-1-yl}acetate

Directory of Open Access Journals (Sweden)

Hind Jabli

2010-01-01

Full Text Available The reaction of 1,5-dibenzyl-3-propargyl-1,5-benzodiazepine-2,4-dione with ethyl azidoacetate in the presence of copper sulfate pentahydrate and sodium ascorbate leads to the formation of the title regioisomer, C30H29N5O4, which features a phenylene ring fused with a seven-membered diazepinyl ring. The latter ring adopts a boat conformation (with the methyltriazolylacetate-bearing C atom as the prow and the fused-ring C atoms as the stern. The benzyl groups connected to the diazepinyl ring jprotrude from the sides; the methyltriazolylacetate substituent occupies an axial position.

Chlorine activation by N2O5: simultaneous, in situ detection of ClNO2 and N2O5 by chemical ionization mass spectrometry

Directory of Open Access Journals (Sweden)

J. A. Thornton

2009-05-01

Full Text Available We report a new method for the simultaneous in situ detection of nitryl chloride (ClNO2 and dinitrogen pentoxide (N2O5 using chemical ionization mass spectrometry (CIMS. The technique relies on the formation and detection of iodide ion-molecule clusters, I(ClNO2− and I(N2O5−. The novel N2O5 detection scheme is direct. It does not suffer from high and variable chemical interferences, which are associated with the typical method of nitrate anion detection. We address the role of water vapor, CDC electric field strength, and instrument zero determinations, which influence the overall sensitivity and detection limit of this method. For both species, the method demonstrates high sensitivity (>1 Hz/pptv, precision (~10% for 100 pptv in 1 s, and accuracy (~20%, the latter ultimately determined by the nitrogen dioxide (NO2 cylinder calibration standard and characterization of inlet effects. For the typically low background signals (S/N ratios of 2 for 1 pptv in 60 s averages, but uncertainty associated with the instrumental zero currently leads to an ultimate detection limit of ~5 pptv for both species. We validate our approach for the simultaneous in situ measurement of ClNO2 and N2O5 while on board the R/V Knorr as part of the ICEALOT 2008 Field Campaign.

{2-[Bis(2,4-di-tert-butylphenoxyphosphanyloxy-κP]-3,5-di-tert-butylphenyl-κC1}[(1,2,5,6-η-cycloocta-1,5-diene]rhodium(I toluene monosolvate

Directory of Open Access Journals (Sweden)

Detlef Selent

2012-02-01

Full Text Available The reaction of (η3-allyl[(1,2,5,6-η-cycloocta-1,5-diene]rhodium(I with tris(2,4-di-tert-butylphenylphosphite in toluene produces the title compound, [Rh(C42H62O3P(C8H12]·C7H8, by spontaneous metallation at one of the nonsubstituted phenyl ortho-C atoms of the phosphite molecule. The coordination geometry at the RhI ion is distorted square-planar. The toluene solvent molecule is disordered over two different orientations, with site-occupation factors of 0.810 (2 and 0.190 (2.

The synthesis of 5'-[14C1] and 3a, 4-[13C2] labelled panadiplon (U-78875; 3-(5'-cyclopropyl-1,2,4-oxadiazol-3-yl)-5-(1-methylethyl)-imidazo-[1,5a]-quinoxalin-4(5H)-one)

International Nuclear Information System (INIS)

Ackland, M.J.; Howard, M.R.; Dring, L.G.

1993-01-01

5'-[ 14 C 1 ]Panadiplon was prepared in 3 steps starting from [ 14 C 1 ]cyclopropane carboxylic acid and 3-(5'-cyano-1,2,4-oxadiazol-3-yl)-5-(1-methylethyl)-imidazo-[1,5a] -quinoxalin-4(5H)-one. 3a, 4-[ 13 C 2 ]Panadiplon was prepared in two steps from 13 C 2 -oxalic acid and N-1-(1-methylethyl)-o-phenylenediamine. The position of labelling was confirmed by the appearance of two coupled resonances (J C-C =80.59 Hz) at 121.95 and 154.39 ppm in the assigned 13 C-NMR spectrum. (Author)

Asymmetric 1,3-Dipolar Cycloadditions to 5-(R)-Menthyloxy-2(5H)-Furanone

NARCIS (Netherlands)

Rispens, Minze T.; Keller, Erik; Lange, Ben de; Zijlstra, Robert W.J.; Feringa, Bernard

Various diazo compounds, nitrile oxides, nitrones and azomethine ylides were examined in 1,3-dipolar cycloadditions to enantiomerically pure 5-(R)-menthyloxy-2(5H)-furanone 1a. Pyrazoline 9 was obtained in 100% c.y. as a mixture of 2 diastereoisomers in ratios up to 72 : 28, whereas pyrazoline 16

2-[(4-Bromophenylimino)methyl]-5-pentadecylphenol

OpenAIRE

Basavaraj Padmashali; Patchanita Thamyongkit; Amorn Petsom; Gadada Naganagowda

2012-01-01

2-[(4-Bromophenylimino)methyl]-5-pentadecylphenol has been synthesized by reaction of 2-hydroxy-4-pentadecylbenzaldehyde with 4-bromoaniline in 1,4-dioxane and its IR, ¹H-NMR, ¹³C-NMR and MS spectroscopic data are presented.