| dc.contributor.author | Lloyd, Nicholas C. | |
| dc.contributor.author | Nicholson, Brian K. | |
| dc.contributor.author | Wilkins, Alistair L. | |
| dc.contributor.author | Thomson, Ralph A. | |
| dc.date.accessioned | 2010-10-20T21:08:37Z | |
| dc.date.available | 2010-10-20T21:08:37Z | |
| dc.date.issued | 2002 | |
| dc.identifier.citation | Lloyd, 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.uri | http://hdl.handle.net/10289/4709 | |
| dc.description.abstract | Organo-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.mimetype | application/pdf | |
| dc.language.iso | en | |
| dc.publisher | New Zealand Institute of Chemistry | en_NZ |
| dc.relation.uri | http://nzic.org.nz/CiNZ/CiNZ.html | en_NZ |
| dc.rights | This article has been published in the journal: Chemistry in New Zealand. Used with permission. | en_NZ |
| dc.subject | chemistry | en_NZ |
| dc.title | Novel six-coordinate Aryl- and Alkyltin complexes | en_NZ |
| dc.type | Journal Article | en_NZ |