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dc.contributor.authorHua, Guoxiong
dc.contributor.authorWoollins, J. Derek
dc.date.accessioned2014-08-11T14:31:01Z
dc.date.available2014-08-11T14:31:01Z
dc.date.issued2012-07-25
dc.identifier30482328
dc.identifier49becb75-f15d-438d-9b6f-1c452d5eff6c
dc.identifier000307152900027
dc.identifier84863784246
dc.identifier.citationHua , G & Woollins , J D 2012 , ' Sodium phenyldiselenophosphonate salts and Se-alkyl-O-alkylphenyl-phosphonodiselenoates and Se,Se '-dialkyl-O,O '-dialkyl-bis(phenylphosphonodiselenoate)s ' , Polyhedron , vol. 42 , no. 1 , pp. 190-195 . https://doi.org/10.1016/j.poly.2012.05.010en
dc.identifier.issn0277-5387
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779216
dc.identifier.urihttps://hdl.handle.net/10023/5105
dc.descriptionFunding: University of St Andrewsen
dc.description.abstractThe reaction of sodium alkoxides [(RONa)-O-1, R-1 = CH3, CH3CH2, (CH3)(2)CH and CH3CH2CH2] with 2,4-diphenyl-1,3-diselenadiphosphetane-2,4-diselenide [PhP(Se)(mu-Se)](2) (Woollins' reagent, WR) gave the non-symmetric sodium phenyldiselenophosphonate salts 1a-1d, the latter were further treated with haloalkanes [(RX)-X-2, R-2 = alkyl and aryl; X = Br, Cl and I] or dihaloalkanes [Br-(CH2)(n)-Br, n = 1-3 and BrCH2C6H4CH2Br-p] to afford a series of new Se-alkyl O-alkylphenylphosphonodiselenoate esters 2a-2k and Se,Se'-dialkyl-O,O'-dialkyl bis(phenylphosphonodiselenoate) esters 3a-3j in good to excellent yields. Crown Copyright (c) 2012 Published by Elsevier Ltd. All rights reserved.
dc.format.extent6
dc.format.extent581731
dc.language.isoeng
dc.relation.ispartofPolyhedronen
dc.subjectWoollins’ reagenten
dc.subjectPhosphorusen
dc.subjectSeleniumen
dc.subjectSodium phenyldiselenophosphonate salts and Se-alkyl-O-alkylphenyl-phosphonodiselenoates and Se,Se '-dialkyl-O,O '-dialkylen
dc.subjectbis(phenylphosphonodiselenoate) estersen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleSodium phenyldiselenophosphonate salts and Se-alkyl-O-alkylphenyl-phosphonodiselenoates and Se,Se '-dialkyl-O,O '-dialkyl-bis(phenylphosphonodiselenoate)sen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1016/j.poly.2012.05.010
dc.description.statusPeer revieweden


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