期刊
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
卷 -, 期 32, 页码 3660-3667出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.201800525
关键词
Redox-active ligands; Coordination chemistry; Copper; Electron transfer; Valence tautomerism
资金
- Deutsche Forschungsgemeinschaft (DFG)
- Ministry of Science, Research and the Arts BadenWurttemberg
- Universities of the State of BadenWurttemberg, Germany
Intramolecular electron transfer (IET) processes between the metal and a redox-active ligand in a transition-metal complex are currently intensively studied, as they represent key steps of some redox-catalytic reactions in synthetic chemistry and of some enzymatic redox reactions in biological systems. Using a combination of experimental results and quantum chemical calculations, we herein examine in detail the role of the solvent polarity and seemingly small modifications at the redox-active ligand on IET processes in mononuclear copper complexes with redox-active bisguanidine ligands. A direct and simple correlation between the coordination mode and the electronic structure in these complexes is established, assisting in the fine-tuning of the ligand properties for optimal promotion of IET.
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