The mechanism of silicon-hydrogen and carbon-hydrogen bond activation by iridium(III): Production of a silylene complex and the first direct observation of Ir(III)/Ir(V) C-H bond oxidative addition and reductive elimination
Journal Article
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· Journal of the American Chemical Society
The complexes Cp*(PMe{sub 3})Ir(Me)OTf (Me = CH{sub 3}, OTf = OSO{sub 2}CF{sub 3}) (1) and Cp*(PMe{sub 3})Ir(Me)(CH{sub 2}Cl{sub 2})[BAr{sub f}] (BAr{sub f}{sup {minus}} = [(3,5-(CF{sub 3}){sub 2}C{sub 6}H{sub 3}){sub 4}B]{sup {minus}}) (2), which contain iridium in oxidation state +3, were recently shown to undergo C-H activation reactions with alkanes under mild thermal conditions. The authors report a series of observations, including the first conversion of Ir(III) precursors to an isolable, structurally characterized Ir(V) aryl-hydride and a spectroscopically observable Ir(V) alkyl-hydride, that lends convincing experimental support to the Ir(III) {r{underscore}arrow} Ir(V) {r{underscore}arrow} Ir(III) mechanism. The complex Cp*(PMe{sub 3})Ir(Me)OTf (1) reacts rapidly with alkanes (H-CR{sub 3}) to produce 1 equiv of methane (CH{sub 4}) and rearranged products derived from Cp*(PMe{sub 3})Ir(CR{sub 3})OTf, which form as a consequence of the {beta}-hydride elimination pathway. When 1 is added to silanes (H-SiR{sub 3}, R = Me, Ph), products of a structural rearrangement type unobserved in C-H activation reactions are isolated along with 1 equiv of methane. These products, Cp*(PMe{sub 3})Ir(SiR{sub 2}OTf)(R), are presumably derived from a 1,2-migration in Cp*(PMe{sub 3})Ir(SiR{sub 3})OTf, wherein one of the groups initially bound to silicon migrates to iridium (eq 1).
- Research Organization:
- Univ. of California, Berkeley, CA (US); Lawrence Berkeley National Lab., CA (US)
- Sponsoring Organization:
- US Department of Energy; National Science Foundation
- DOE Contract Number:
- AC03-76SF00098
- OSTI ID:
- 20017337
- Journal Information:
- Journal of the American Chemical Society, Journal Name: Journal of the American Chemical Society Journal Issue: 8 Vol. 122; ISSN JACSAT; ISSN 0002-7863
- Country of Publication:
- United States
- Language:
- English
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