Abstract
Abstract - A series of dirhodium tetracarboxylate complexes, containing triphenylphosphine as axial ligand was investigated by electronic and Raman spectroscopy, aiming to detect the influence of electronic effects of the carboxylate substituents on the v1[v(RhRh)] and v2[v(RhO)] Modes. When pairs of complexes with similar molecular weights are compared, as in the case of the cyclopentanecarboxylate and trifluoroacetate complexes, the striking difference in the inductive character of the two species results in substantial shifts of the v1 and v2 modes as a consequence of variations in the corresponding force constants rather than a simple mass effect as previously observed for non-substituted rhodium-carboxylates.