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Oxidative addition of hydrosilanes, a hydrogermane, and a hydrostannane to the ((cyclopentadienylalkyl)phosphane)cobalt(I) chelate 1 results in the formation of cyclopentadienylhydridocobalt(III) complexes having a tethered phosphorus ligand and silyl ( rac - 4 − rac - 8 ), germyl ( rac - 10 ), and stannyl substituents ( rac - 11 ). The pseudo-four-coordinate complexes are chiral. The X-ray structures of 5 and 7 have been determined. Variable-temperature NMR spectra indicate racemization in solution due to reversible dissociation of the phosphorus ligand. The barrier of this process has been estimated to be in the range of 13−16 kcal/mol.
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Li et al. (2003) studied this question.
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