Investigation of dioxygen activation by copper(ii)–iminate/aminate complexes. Issue 45 (6th November 2018)

• Record Type: Journal Article
• Authors: Papanikolaou, Michael G.; Hadjithoma, Sofia; Chatzikypraiou, Dimitra S.; Papaioannou, Dionysios; Drouza, Chryssoula; Tsipis, Athanassios C.; Miras, Haralampos N.; Keramidas, Anastasios D.; Kabanos, Themistoklis A.
• Is Part Of: Dalton transactions. Volume 47:Issue 45(2018)
• Page Start: 16242
• Page End: 16254
• Publication Date: 2018-11-06
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c8dt03137a
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Cu II amidate/iminate complexes activate dioxygen by a ligated to Cu II, –HCN– moiety. Abstract : The activation of dioxygen by metal ions is critical in chemical and bio-chemical processes. A scientific challenge is the elucidation of the activation site of dioxygen in some copper metalloproteins, which is either the metal center or the substrate. In an effort to address this challenge, we prepared a series of new copper(ii ) complexes (1 ·2H2 O, 2 ·CH3 OH, 3 ) with bio-inspired amidate ligands and investigated their activity towards dioxygen activation. The secondary amine group ligated to copper(ii ) of the complex1 ·2H2 O in methyl alcohol is oxidized (2e − ) by air dioxygen in a stepwise fashion to an imine group, affording complex2 . The copper(ii ) complex2 in methyl alcohol induces the 4e − oxidation by air dioxygen of the imine functionality ligated to copper(ii ) to an azinate group, resulting in the isolation of a dinuclear azinate copper(ii ) compound (4 ). Experimental and computational studies, including X-band c. w. EPR, UV-vis and ESI-MS spectroscopy and density functional theory computations, indicate a direct attack of the dioxygen on the –HCN– group ligated to copper(ii ), and a possible mechanism of the oxidation of the –HCN– functionality ligated to copper(ii ) to an azinate group is provided. This unprecedented activation of dioxygen by a copper substrate paves the way for further exploration of the O2 activation mechanisms in enzymes and the development of effective catalysts in O2 -involved green organic synthesis.