Oxidatively induced alkyne rotation in dicobalt complexes: structural tests of molecular orbital theory

The complexes [Co2(CO)2(µ-RC2R)(µ-dppm)2]1(R = Me, Ph or CO2Me; dppm = Ph2PCH2PPh2) undergo reversible one-electron oxidation at a platinum-bead electrode in CH2Cl2; chemical oxidation of 1 with the ferrocenium ion or with iodine gives stable salts of the monocations 1+. The X-ray structures of 1(R = Me and Ph) show the alkyne bridge to be orthogonal to a cobalt–cobalt bond which is also bridged by the two dppm ligands. The overall structure of 1+(R = Me), as its [PF6]– salt, is similar but with the alkyne bridge rotated by 12° about an axis perpendicular to the shortened metal–metal bond. The structural changes observed provide direct experimental support for previous bonding studies of the structural preferences of hydrocarbon-bridged M2(CO)6 complexes.