MECHANISM OF ELECTROPHILIC CLEAVAGE OF THE PT-C (ALKYL) BOND IN TRANS-[PT(PET3)2(YC6H4)(CH3)] COMPLEXES

被引:29
作者
ROMEO, R
MINNITI, D
LANZA, S
机构
[1] Istituto di Chimica Fisica, Università di Messina, 98100 Messina, Via dei Verdi
关键词
D O I
10.1016/S0022-328X(00)94333-X
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Protonolysis of the complexes trans-[Pt(PEt3)2(R)(Me)] (R = C6H5 ; m-MeC6H4 ; o-MeC6H4 ; m-FC6H4 ; p-FC6H4 ; m-CF3C6H4 and C6F5) by hydrogen chloride in methanol/water ( 90 10 v/v) selectively cleaves the alkyl group yielding trans-[Pt(PEt3)2(R)Cl] and methane. A kinetic study of these reactions suggests that the primary step involves a proton transfer to the carbonmetal σ-bond with release of CH4 in a three-center transition state. © 1979.
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收藏
页码:C36 / C38
页数:3
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