Electrochem. methods were used to study the redox behavior of the Cu(II) complexes of H2N(CH2)nNH(CH2)mNH(CH2)nNH2 (n, m = 2, 3) in MeCN. Cu(III) complexes persisted in soln. only on the time-scale of the cyclic voltammetry expt., whereas fairly stable Cu(I) complexes were obtained with both the shortest- and longest-chain ligands studied. Electrode potentials for both the Cu(III) → Cu(II) and Cu(II) → Cu(I) redox reactions were compared with those reported for the corresponding complexes with macrocyclic tetraamines.

Oxidation and reduction behavior of copper(II) complexes with open-chain analogs of tetraaza macrocycles

FABBRIZZI, LUIGI;POGGI, ANTONIO;
1984-01-01

Abstract

Electrochem. methods were used to study the redox behavior of the Cu(II) complexes of H2N(CH2)nNH(CH2)mNH(CH2)nNH2 (n, m = 2, 3) in MeCN. Cu(III) complexes persisted in soln. only on the time-scale of the cyclic voltammetry expt., whereas fairly stable Cu(I) complexes were obtained with both the shortest- and longest-chain ligands studied. Electrode potentials for both the Cu(III) → Cu(II) and Cu(II) → Cu(I) redox reactions were compared with those reported for the corresponding complexes with macrocyclic tetraamines.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/454424
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