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dc.contributor.authorLi, Yang
dc.contributor.authorHua, Guo-Xiong
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorWoollins, J. Derek
dc.date.accessioned2012-07-25T14:31:01Z
dc.date.available2012-07-25T14:31:01Z
dc.date.issued2009-02-23
dc.identifier.citationLi , Y , Hua , G-X , Slawin , A M Z & Woollins , J D 2009 , ' The X-ray crystal structures of primary aryl substituted selenoamides ' , Molecules , vol. 14 , no. 2 , pp. 884-892 . https://doi.org/10.3390/molecules14020884en
dc.identifier.issn1420-3049
dc.identifier.otherPURE: 4637840
dc.identifier.otherPURE UUID: a351bb01-168e-46f9-84f6-31081ee17287
dc.identifier.otherWOS: 000263823400023
dc.identifier.otherScopus: 61449101376
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861509
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779273
dc.identifier.urihttps://hdl.handle.net/10023/3020
dc.descriptionThe authors are grateful to the University of St Andrews and the Engineering and Physical Science Research Council (EPSRC, U.K.) for financial support.en
dc.description.abstractThe X-ray structures of 12 primary selenoamides are reported. Metric parameters are provided, together with an illustration of the range of hydrogen bonding motifs.
dc.format.extent9
dc.language.isoeng
dc.relation.ispartofMoleculesen
dc.rights© 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).en
dc.subjectWoollins reagenten
dc.subjectPrimary selenoamidesen
dc.subjectX-ray structuresen
dc.subjectPhosphorus-selenium Heterocyclesen
dc.subjectPhotodynamic therapyen
dc.subjectComplexesen
dc.subjectDerivativesen
dc.subject(PHP(SE)(MU-SE))(2)en
dc.subjectSelenoacrylamidesen
dc.subjectDehydrogenaseen
dc.subjectSensitizersen
dc.subjectCynamidesen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleThe X-ray crystal structures of primary aryl substituted selenoamidesen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.3390/molecules14020884
dc.description.statusPeer revieweden


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