Abstract
The complexes trans-[RhX(CO)PPh3)2] (1, X = Cl, Br, I) react with CO to form [RhX(CO)2(PPh3)2] (2), and not to form cis-[RhX(CO)(PPh3)2]. Complexes 2 contain equivalent axial carbonyl ligands. It is proposed that a series of dicarbonyl complexes, including 2, is formed during decarbonylation reactions catalyzed by 1.
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