(η5-Cyclopentadienyl)(halo or acido) (substituted 1-methylthio-χS-ethylene-2-thiolato)cobalt(III):: Formation, stereoisomers, and isomerization

被引:9
作者
Harada, T [1 ]
Takayama, C [1 ]
Kajitani, M [1 ]
Sugiyama, T [1 ]
Akiyama, T [1 ]
Sugimori, A [1 ]
机构
[1] Sophia Univ, Dept Chem, Chiyoda Ku, Tokyo 1028554, Japan
关键词
D O I
10.1246/bcsj.71.2645
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The addition of protic acids to (eta(5)-cyclopentadienyl)(1-methylenethio)-HC, HS-ethylene-2-thiolato)cobalt(III) complexes (2) causes a Co-C bond cleavage in the three-membered cobaltathiirane ring to give (eta(5)-cyclopentadienyl)(halo or acido)(1-methylthio-HS-ethylene-2-thiolato)cobalt(III) complexes (3). In the crystalline state, these complexes have either syn- or anti-configuration with respect to halo (or acido) and the methyl or substituted methyl group attached to S. In some cases, complexes 3 exist in equilibria between syn- and anti-stereoisomeric forms in solutions. In solutions, an exchange of the coordinated anions occurs very easily.
引用
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页码:2645 / 2653
页数:9
相关论文
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