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In trans-[Ir(C6F5){P(C6F5)(C6H5)2}2(CO)], the Ir-P and Ir-C distances are comparable to those of the triphenylphosphine analogue. F
F interactions appear to dominate the configuration, resulting in virtually eclipsed C6F5(Ir) and C6F5(P) rings.
F interactions appear to dominate the configuration, resulting in virtually eclipsed C6F5(Ir) and C6F5(P) rings.
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