(η5-cyclopentadienyl)[η2-bis(tert-butylsulfonyl)acetylene]-(carbonyl)cobalt -: An electrophilic reagent to yield CpCo-stabilized cyclobutadiene derivatives

被引:13
作者
Benisch, C
Gleiter, R
Staeb, TH
Nuber, B
Oeser, T
Pritzkow, H
Rominger, F
机构
[1] Univ Heidelberg, Inst Organ Chem, D-69120 Heidelberg, Germany
[2] Univ Heidelberg, Inst Anorgan Chem, D-69120 Heidelberg, Germany
关键词
cyclobutadiene complexes; alkynes; cobalt complexes; cyclization;
D O I
10.1016/S0022-328X(01)01364-X
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Various substituted (R=H, CH3, SiMe3, CO2Me, COCH3, EtMe,) (R-eta(5)-cyclopentadienyl)[eta(2)-bis(tert-butylsulfonyl)acetylene](carbonyl)cobalt complexes (8-13) proved to be very reactive towards alkynes under rather mild conditions. Dithiaacetylenes reacted at room temperature, dialkyl- and diarylalkynes had to be heated to 80-90 degreesC to yield the corresponding R-CpCo-stabilized cyclobutadiene complexes 18-37 and 39-42. X-ray investigations on 24-26, 30, 36 and 39-41 showed almost equal C-C bond lengths in the cyclobutadiene rings. (C) 2002 Published by Elsevier Science B.V.
引用
收藏
页码:102 / 112
页数:11
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