Redox properties of ruthenium(III/II)–edta complexes with o-phenylenediamine and o-benzoquinone diimine ligands
Author:
Publisher
Elsevier BV
Subject
Electrochemistry
Reference33 articles.
1. Changing the electrochemical behavior of catechols by means of their conversion into the corresponding ruthenium(III)–dioxolene complexes
2. Transition metal complexes of o-benzoquinone, o-semiquinone, and catecholate ligands
3. The ground and excited state electronic structures of ruthenium quinones and related species
4. Trends in metal–ligand orbital mixing in generic series of ruthenium N-donor ligand complexes—effect on electronic spectra and redox properties
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1. Electrochemistry of Ru(edta) complexes relevant to small molecule transformations: Catalytic implications and challenges;Coordination Chemistry Reviews;2021-06
2. Electropolymerization using binuclear nickel(ii) Schiff base complexes bearing N4O4donors as supramolecular building blocks;RSC Advances;2015
3. [Ru(bpy) 2 (bqdiBr 2 )](PF 6 ) 2 bearing a 3,6-dibromo-1,2-benzoquinone diimine ligand (bqdiBr 2 = Br-C 6 H 2 (NH) 2 -Br): Synthesis and its cross coupling reactions with organostannanes and organoboronic acids;Inorganica Chimica Acta;2014-09
4. Cyclometalated platinum(II) complexes bearing o-phenylenediamine derivatives: Synthesis and electrochemical behavior;Journal of Organometallic Chemistry;2011-03
5. Ruthenium complexes with non-innocent ligands: Electron distribution and implications for catalysis;Coordination Chemistry Reviews;2010-02
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