Isolated, cationic bis(cyclooctene)−Ir(I) complexes stabilized by acetonitrile or acetone solvent molecules were obtained and reacted with simple alkylphosphines, leading to selective displacement of the cyclooctene ligand. With the bulky t Bu 3 P, facile intramolecular C−H activation is observed, giving cyclometalated, solvent-stabilized bis(phosphine)−Ir(III) species and leading to the isolation of the first 14-electron alkyl−Ir(III) complex.
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Dorta et al. (2003) studied this question.
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