Abstract
Reaction of the organometallic aqua ion [Cp*Ir(H(2)O)(3)](2+) with tert-butyl(trimethylsilyl)amine in acetone yielded a novel trinuclear (µ(3)-oxido)(µ(3)-imido)pentamethylcyclopentadienyliridium(iii) complex, [(Cp*Ir)(3)(O)(N(t)Bu)](2+). Single crystal structure analyses show the complex can be isolated both in the double salt ((t)BuNH(3))[(Cp*Ir)(3)(O)(N(t)Bu)](CF(3)SO(3))(3) (1) and in the simple triflate [(Cp*Ir)(3)(O)(N(t)Bu)](CF(3)SO(3))(2) (2). The double salt is stabilized by hydrogen bonding between the tert-butylammonium ion and the three triflate anions. It is the first time that a trinuclear (µ(3)-oxido)(µ(3)-imido) transition metal complex has been structurally characterized.
Original language | English |
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Journal | Dalton Transactions (Print Edition) |
Volume | 40 |
Issue number | 16 |
Pages (from-to) | 4212-6 |
Number of pages | 5 |
ISSN | 1477-9226 |
DOIs | |
Publication status | Published - 28 Apr 2011 |