Iridapyrrole complexes via formal 3+2 cycloaddition of iridium alkenyls to acetonitrile

被引:43
作者
Alvarado, Y
Daff, PJ
Perez, PJ
Poveda, ML
SanchezDelgado, R
Carmona, E
机构
[1] UNIV SEVILLA, CSIC, DEPT QUIM INORGAN, INST CIENCIA MAT, E-41071 SEVILLE, SPAIN
[2] INST VENEZOLANO INVEST CIENT, CARACAS 1020A, VENEZUELA
[3] UNIV HUELVA, DEPT QUIM & CIENCIA MAT, E-21819 HUELVA, SPAIN
关键词
D O I
10.1021/om950957o
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Under appropriate conditions, the bis(ethylene) derivative Tp*Ir(C2H4)(2) (TP* = hydrotris(3,5-dimethyl-1-pyrazolyl)borate) reacts with MeCN to provide the Ir(III) complex Tp*Ir(CH=CH2)(C2H5)(NCMe) (1). In the presence of catalytic amounts of water, 1 undergoes intramolecular coupling of the vinyl and acetonitrile ligands, with formation of a compound (2a) that contains a delocalized, five-membered iridapyrrole ring. This unusual cycloaddition reaction can be extended to other related alkenyl complexes of iridium.
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页码:2192 / 2194
页数:3
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