IRIDAPYRROLE COMPLEXES VIA FORMAL 3+2 CYCLOADDITION OF IRIDIUM ALKENYLS TO ACETONITRILE

Citation
Y. Alvarado et al., IRIDAPYRROLE COMPLEXES VIA FORMAL 3+2 CYCLOADDITION OF IRIDIUM ALKENYLS TO ACETONITRILE, Organometallics, 15(9), 1996, pp. 2192-2194
Citations number
50
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
02767333
Volume
15
Issue
9
Year of publication
1996
Pages
2192 - 2194
Database
ISI
SICI code
0276-7333(1996)15:9<2192:ICVF3C>2.0.ZU;2-9
Abstract
Under appropriate conditions, the bis(ethylene) derivative TpIr(C2H4) (2) (TP = hydrotris(3,5-dimethyl-1-pyrazolyl)borate) reacts with MeCN to provide the Ir(III) complex TpIr(CH=CH2)(C2H5)(NCMe) (1). In the presence of catalytic amounts of water, 1 undergoes intramolecular cou pling of the vinyl and acetonitrile ligands, with formation of a compo und (2a) that contains a delocalized, five-membered iridapyrrole ring. This unusual cycloaddition reaction can be extended to other related alkenyl complexes of iridium.