Binuclear Intermediates in Oxidation Reactions: [(Me3SiCC)Me2(bipy)Pt-PtMe2(bipy)]+ in the Oxidation of PtIIMe2(bipy) (bipy=2,2′-Bipyridine) by IPh(CCSiMe3)(OTf) (OTf = Triflate)

被引：36

作者：

Canty, Allan J. ^{[1
]}

Gardiner, Michael G. ^{[1
]}

Jones, Roderick C. ^{[1
]}

Rodemann, Thomas ^{[2
]}

Sharma, Manab ^{[1
]}

机构：

[1] Univ Tasmania, Sch Chem, Hobart, Tas 7001, Australia

[2] Univ Tasmania, Cent Sci Lab, Hobart, Tas 7001, Australia

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 2009年 / 131卷 / 21期

基金：

澳大利亚研究理事会;

关键词：

PT-PT COMPLEXES; 2-HYDROXYPYRIDINATO BRIDGING LIGANDS; H BOND ACTIVATION; DINUCLEAR COMPLEXES; ORGANOMETALLIC CHEMISTRY; DIMETHYLPLATINUM(II) COMPLEXES; ADDITION-REACTIONS; PLATINUM(III); REACTIVITY; PALLADIUM;

D O I：

10.1021/ja902799u

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A study of the reaction of PtMe2(bipy) with IPh(C CSiMe3)(OTf) at low temperature in acetone, leading to detection of the Pt-Pt-bonded cation [Pt2Me4(C CSiMe3)(bipy)(2)](+), an intermediate in the oxidation of Pt-II to Pt-IV, is reported. The cation is assessed as Pt-III-Pt-III <-> Pt-IV-Pt-II, and at the other extreme may be regarded as a cationic alkynylplatinum(IV) center, "[(PtMe2)-Me-IV(C CSiMe3)(bipy)](+)", stabilized by "(PtMe2)-Me-II(bipy)" as a donor ligand. The detection and isolation of the [Pt2Me4(C CSiMe3)(bipy)(2)](+) cation provides a number of insights into the mechanisms of oxidation reactions.

引用

页码：7236 / +

页数：3

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