The unexpected reactivity of Zeise's anion in strong basic medium discloses new substitution patterns at the platinum centre

被引：26

作者：

Benedetti, M

Fanizzi, FP

Maresca, L

Natile, G

机构：

[1] Univ Lecce, Dipartimento Sci & Tecnol Biol & Ambientali, I-73100 Lecce, Italy

[2] Univ Bari, Dipartimento Farm Chim, I-70125 Bari, Italy

来源：

CHEMICAL COMMUNICATIONS | 2006年 / 10期

关键词：

D O I：

10.1039/b516818j

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Zeise's anion in strongly basic hydroxylated solvents undergoes unprecedented nucleophilic addition of OR- (R = H, Me, Et) to the eta(2)-ethene giving trans-[PtCl2(eta(1)-C2H4OR)(OR)](2-) which readily reacts with bidentate nitrogen donors N-N to give Cl 2 and OR- substitution and formation of [PtCl(CH2CH2OR)(N-N)]. Protonolysis of this stable organometallic species offers a versatile route to cationic [PtCl(eta(C2H4)-C-2)(N-N)](+) complexes.

引用

收藏

页码：1118 / 1120

页数：3

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