Variational Approach to Electron Transfer in Bridged Diruthenium Complexes

Verfasser / Beitragende:
[Elena Vollmer, Mattias Kordel, Thorsten Koslowski]
Ort, Verlag, Jahr:
2004
Enthalten in:
Zeitschrift für Physikalische Chemie/International journal of research in physical chemistry and chemical physics, 218/5/2004(2004-05-01), 611-622
Format:
Artikel (online)
ID: 378903772
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245 0 0 |a Variational Approach to Electron Transfer in Bridged Diruthenium Complexes  |h [Elektronische Daten]  |c [Elena Vollmer, Mattias Kordel, Thorsten Koslowski] 
520 3 |a In this work, we address the energetics of electron transfer in bridged diruthenium complexes from a theoretical and numerical perspective. The electronic structure of the bridged complexes is described by a tight-binding Hamiltonian, which is extended by an on-site spin pairing energy. The coupling of the system to a polarizable solvent is taken into account by a nonretarded reaction field. The resulting nonlinear Hamiltonian is solved within the Hartree-Fock mean-field approximation, and the emerging potential energy surface is analysed using Marcus´ theory of electron transfer reactions. For the systems studied here, the charge transfer rate depends on the chemical nature of the bridge rather than the intermetal distance. We discuss the special nature of the Creutz-Taube cation, which is on the border of charge delocalization. 
540 |a © 2004 Oldenbourg Wissenschaftsverlag GmbH 
690 7 |a Thermodynamics & statistical physics  |2 nationallicence 
690 7 |a Laboratory techniques, experiments  |2 nationallicence 
690 7 |a Physical chemistry  |2 nationallicence 
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