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dc.contributor.authorLloyd, Nicholas C.
dc.contributor.authorNicholson, Brian K.
dc.contributor.authorWilkins, Alistair L.
dc.contributor.authorThomson, Ralph A.
dc.date.accessioned2010-10-20T21:08:37Z
dc.date.available2010-10-20T21:08:37Z
dc.date.issued2002
dc.identifier.citationLloyd, N.C., Nicholson, B.K., Wilkins, A.L. & Thomson, R. (2002). Novel six-coordinate Aryl- and Alkyltin complexes. Chemistry in New Zealand, 66(1), 53-54.en_NZ
dc.identifier.urihttps://hdl.handle.net/10289/4709
dc.description.abstractOrgano-tin compounds have wide applications as pesticides and as intermediates for organic synthesis.¹ They are invariably Sn(IV) derivatives and are generally four-coordinate.² The mixed organo/chioro compounds of the type RnSnCI4-n do however have the ability to expand their coordination numbers to five or six. This depends critically on the substituents - with four organic groups, R₄Sn, there is no tendency at all to coordinate extra ligands, while at the other extreme SnCl₄ readily forms six-coordinate [SnC1₄L₂] complexes since the electronegative halo groups increase the Lewis acidity of the tin centre.en_NZ
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.publisherNew Zealand Institute of Chemistryen_NZ
dc.relation.urihttp://nzic.org.nz/CiNZ/CiNZ.htmlen_NZ
dc.rightsThis article has been published in the journal: Chemistry in New Zealand. Used with permission.en_NZ
dc.subjectchemistryen_NZ
dc.titleNovel six-coordinate Aryl- and Alkyltin complexesen_NZ
dc.typeJournal Articleen_NZ
dc.relation.isPartOfChemistry in New Zealanden_NZ
pubs.begin-page53en_NZ
pubs.editionMarchen_NZ
pubs.elements-id27338
pubs.end-page54en_NZ
pubs.issue.en_NZ
pubs.volume.en_NZ


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