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
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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