Stabilisation of Copper(I) by an Azoimine Ligand: Redox Properties and Reactions of Bis(phenylazoacetaldoximato)bis(phenylacetaldoxime)dicopper(I)

DOI: 10.1039/DT9850000159

Source and publish data:

Journal of the Chemical Society, Dalton Transactions p. 159 - 162 (1985)

Update date:2022-08-05

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Authors:

Pal, Samudranil

Bandyopadhyay, Debkumar

Datta, Dipankar

Chakravorty, Animesh

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Article abstract of DOI:10.1039/DT9850000159

The high preference of phenylazoacetaldoxime, MeC(=NOH)N=NPh (HL), for copper(I) is rationalised in terms of electronic and steric factors.The complex (1) undergoes a one-electron oxidation at ca. 0.8 V vs. saturated calomel electrode to an unstable Cu(II)Cu(I) species.Tertiary phosphines displace HL from (1) affording . (2a) reacts with HCl to form <4> and with HClO4 to give the complex .All complexes having the chelated CuL or Cu(HL) fragment are shown to have a characteristic low-energy metal-to-ligand charge-transfer transition (700-900 nm).

Full text of DOI:10.1039/DT9850000159

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