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Copper co-ordination chemistry of some quadridentate pyridazine and phthalazine (N4) thioether ligands. Binuclear copper(II) complexes exhibiting two-electron reduction at positive potentials
Journal article

Copper co-ordination chemistry of some quadridentate pyridazine and phthalazine (N4) thioether ligands. Binuclear copper(II) complexes exhibiting two-electron reduction at positive potentials

Tai Chin Woon, Robert McDonald, Sanat K Mandal, Laurence K Thompson, Sean P Connors and Anthony W Addison
Dalton Transactions, (11), pp 2381-2386
1986

Abstract

Binuclear, hydroxo-bridged, copper( II ) complexes of a series of quadridentate pyridazine and phthalazine thioether ligands involving nitrogen donor groups (derived from pyridine, imidazole, benzimidazole) exhibit room-temperature magnetic moments in the range 1.1-1.7 B.M., indicative of antiferromagnetically coupled binuclear copper( II ) centres. Cyclic voltammetry and coulometry on most of these systems indicate reversible or quasi-reversible redox processes, involving two-electron transfer, at positive potentials (0.23-0.49 V vs . a saturated calomel electrode in CH 3 CN or dimethylformamide). Mononuclear copper( II ) derivatives, involving bidentate ligands, also exhibit reduction at positive potentials. Catecholase activity involving 3,5-di-t-butylbenzene1,2-diol has been demonstrated for the hydroxo-bridged complex [Cu 2 (ptpd)(OH)Cl 3 ]·EtOH [ptpd = 3,6-di(2′-pyridylthio)pyridazine], in which a Michaelis-Menten kinetic treatment gave K M = 3.4 × 10 -4 mol dm -3 and a value of k p = 2.1 × 10 -2 s -1 for the dissociation of the catechol-complex intermediate.

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