Issue 6, 1983

Cationic metal nitrosyl complexes. Part 5. Synthesis of dinitrosylmolybdenum compounds

Abstract

The reaction of [Mo(NO)2L2Cl2][L = MeCN, PhCN, CH2[double bond, length half m-dash]CHCN, pyridine (py), or PPh3; L2= 2,2′-bipyridine (bipy) or 1,2-bis(diphenylphosphino)ethane (dppe)] in 1,2-dimethoxyethane (dme) affords monocationic [Mo(NO)2L2Cl(dme)]+ and dicationic [Mo(NO)2L2(dme)2]2+ species. The mechanism of chloride abstraction has been investigated by i.r., n.m.r., and u.v.–visible spectroscopy, conductimetry, and potentiometry. The dme solvates, when treated with nitries or bipy, yield a series of cationic dinitrosylmolybdenum complexes. Some of the dicationic complexes catalyse the polymerisation of norbornadiene. The characterization of all new complexes is described.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1983, 1143-1148

Cationic metal nitrosyl complexes. Part 5. Synthesis of dinitrosylmolybdenum compounds

D. Ballivet-Tkatchenko and C. Bremard, J. Chem. Soc., Dalton Trans., 1983, 1143 DOI: 10.1039/DT9830001143

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