The anodic and cathodic behaviour of the rhenium(V) complexes nBu4N[ReOCl3(HOPhSal)], nBu4N[ReOCl2(OPhSal)], [ReOCl(OPhSal)(MeOH)] and [ReOCl(OPhSal)(PMe2Ph)] in acetonitrile was studied using platinum and mercury electrodes. Cyclic voltammetry and controlled potential coulometry were the main electroanalytical techniques employed. The nature of the electrolysis products as well as the mechanisms of the electrode oxidation and reduction processes were investigated. In particular a complex of rhenium(VI) containing the group ReO4+ and complexes of rhenium(IV) with ReO2+ core were electrochemically synthesized. They were characterized by elemental analysis, IR spectroscopy, magnetic susceptibility and conductivity measurements.
Electrochemistry of rhenium(V) complexes with N-(2-hydroxyphenyl)salicylideneiminate as schiff base ligand / Seeber, Renato; Gian Antonio, Mazzocchin; Fiorenzo, Refosco; Ulderico, Mazzi; Francesco, Tisato. - In: POLYHEDRON. - ISSN 0277-5387. - STAMPA. - 6:(1987), pp. 1647-1652. [10.1016/S0277-5387(00)80765-2]
Electrochemistry of rhenium(V) complexes with N-(2-hydroxyphenyl)salicylideneiminate as schiff base ligand
SEEBER, Renato;
1987
Abstract
The anodic and cathodic behaviour of the rhenium(V) complexes nBu4N[ReOCl3(HOPhSal)], nBu4N[ReOCl2(OPhSal)], [ReOCl(OPhSal)(MeOH)] and [ReOCl(OPhSal)(PMe2Ph)] in acetonitrile was studied using platinum and mercury electrodes. Cyclic voltammetry and controlled potential coulometry were the main electroanalytical techniques employed. The nature of the electrolysis products as well as the mechanisms of the electrode oxidation and reduction processes were investigated. In particular a complex of rhenium(VI) containing the group ReO4+ and complexes of rhenium(IV) with ReO2+ core were electrochemically synthesized. They were characterized by elemental analysis, IR spectroscopy, magnetic susceptibility and conductivity measurements.Pubblicazioni consigliate
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris