Issue 33, 2007

Silylenediamido [(CH3)2Si(NTs)22−; Ts = p-CH3C6H4SO2] complexes of iridium: synthesis, structures and facile Si–N bond cleavage

Abstract

The N,N′-bis(sulfonyl)diaminosilane TsdmsinH2 (TsdmsinH2 = (CH3)2Si(NHTs)2, Ts = p-CH3C6H4SO2) reacted with [Cp*IrCl2]2 (Cp* = η5-C5(CH3)5) in the presence of a base to give the coordinatively unsaturated (silylenediamido)iridium complex [Cp*Ir(Tsdmsin)] (2), which was further converted to the 18e adducts [Cp*Ir(Tsdmsin)L] (L = P(C6H5)3 (3a), P(OC2H5)3, CO); the reactions of 2 and 3a with water led to the formation of the imido-bridged dinuclear complex [Cp*Ir(µ2-NTs)2IrCp*] and the bis(amido) complex [Cp*Ir(NHTs)2{P(C6H5)3}], respectively.

Graphical abstract: Silylenediamido [(CH3)2Si(NTs)22−; Ts = p-CH3C6H4SO2] complexes of iridium: synthesis, structures and facile Si–N bond cleavage

Supplementary files

Article information

Article type
Communication
Submitted
29 Jun 2007
Accepted
02 Jul 2007
First published
17 Jul 2007

Dalton Trans., 2007, 3606-3608

Silylenediamido [(CH3)2Si(NTs)22−; Ts = p-CH3C6H4SO2] complexes of iridium: synthesis, structures and facile Si–N bond cleavage

K. Ishiwata, S. Kuwata and T. Ikariya, Dalton Trans., 2007, 3606 DOI: 10.1039/B709930B

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