Spectroelectrochemical Properties and Catalytic Activity in Cyclohexane Oxidation of the Hybrid Zr/Hf-Phthalocyaninate-Capped Nickel(II) and Iron(II) tris-Pyridineoximates and Their Precursors

Autor: Maria-Andreea Lungan, Svetlana A. Belova, Dumitru Samohvalov, Denisa Darvasiová, Armando J. L. Pombeiro, Vladimir B. Arion, Semyon V. Dudkin, Yan Z. Voloshin, Corina-Mihaela Manta, Peter Rapta, Samuel M. Meier-Menches, Michal Malček, Luísa M. D. R. S. Martins, Daniel Gherca
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Models
Molecular

Indoles
Clathrochelate
Pyridines
Pharmaceutical Science
Isoindoles
phthalocyanines
DFT calculations
01 natural sciences
zirconium(IV)
Analytical Chemistry
law.invention
chemistry.chemical_compound
clathrochelates
law
Coordination Complexes
Nickel
Drug Discovery
Oximes
Electron paramagnetic resonance
Density Functional Theory
iron(II)
homogeneous catalysis
3. Good health
Chemistry (miscellaneous)
Molecular Medicine
Oxidation-Reduction
nickel(II)
Cyclohexane
Iron
chemistry.chemical_element
hafnium(IV)
010402 general chemistry
Redox
Catalysis
Article
lcsh:QD241-441
Transition metal
lcsh:Organic chemistry
Cyclohexanes
Polymer chemistry
Physical and Theoretical Chemistry
Zirconium
oxidation reactions
010405 organic chemistry
Organic Chemistry
Electron Spin Resonance Spectroscopy
spectroelectrochemistry
0104 chemical sciences
chemistry
Hafnium
Zdroj: Molecules, Vol 26, Iss 336, p 336 (2021)
Molecules
Volume 26
Issue 2
ISSN: 1420-3049
Popis: The in situ spectroelectrochemical cyclic voltammetric studies of the antimony-monocapped nickel(II) and iron(II) tris-pyridineoximates with a labile triethylantimony cross-linking group and Zr(IV)/Hf(IV) phthalocyaninate complexes were performed in order to understand the nature of the redox events in the molecules of heterodinuclear zirconium(IV) and hafnium(IV) phthalocyaninate-capped derivatives. Electronic structures of their 1e-oxidized and 1e-electron-reduced forms were experimentally studied by electron paramagnetic resonance (EPR) spectroscopy and UV&minus
vis&minus
near-IR spectroelectrochemical experiments and supported by density functional theory (DFT) calculations. The investigated hybrid molecular systems that combine a transition metal (pseudo)clathrochelate and a Zr/Hf-phthalocyaninate moiety exhibit quite rich redox activity both in the cathodic and in the anodic region. These binuclear compounds and their precursors were tested as potential catalysts in oxidation reactions of cyclohexane and the results are discussed.
Databáze: OpenAIRE