Abstract
The redox properties of mononuclear dicarbonyl and carbonylphosphine rhodium (I) complexes (CO)(L)Rh(RC(O)CHC(O)R’) with chelate β-diketonate ligands (L = CO, PPh3; R, R’ = Me, Ph; CF3, C4H3S) were studied by electrochemical methods at platinum, glassed carbon and dropping mercury electrodes in acetonitrile. Schemes of their redox reactions were established
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