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Si–Cl bonds undergo facile, rarely observed oxidative addition to (C8H14)Ir(PMe3)3Cl (1) to yield, when MeSiCl3 is used, the crystallographically characterized mer-Ir(PMe3)3(Cl)2(SiMeCl2), exhibiting a short Ir–Si bond; reaction of (1) and of other electron-rich IrI complexes with Me3SiCl yields Ir–H complexes, probably arising from a rare silyl β-hydride elimination process.
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Zlota et al. (1989) studied this question.
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