Light-driven electron transfer in a modular assembly of a ruthenium(II) polypyridine sensitiser and a manganese(II) terpyridine unit separated by a redox active linkage. DFT analysis - 03/03/17
, Shyamal Das b , Rajaa Farran b , Christian Herrero a , Annamaria Quaranta b , Reza Fallahpour c , Stefano Protti d , Marie-France Charlot a , Ally Aukauloo a, b , Winfried Leibl b, ⁎ Bienvenido a EM-consulte, la referencia de los profesionales de la salud.
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Abstract |
A series of ruthenium polypyridine-based complexes covalently bound to a terpyridine coordinating site for MnII ion coordination has been developed. A redox active unit separates the photoactive unit and the manganese complex. Introducing ester groups on the bipyridine skeleton allows modulation of redox properties of the chromophore. Intramolecular electron transfer from the MnII to the photogenerated RuIII was studied by time-resolved transient absorption and EPR. Photophysical studies support the participation of the imidazole unit in the electron transfer process from the Mn(II) complex and Ru(III) in the case of ester containing chromophores. DFT calculations were performed and used to rationalize the photophysical behavior of the complexes, in particular the effect of coordination of the MnII ion to the terpyridine cavity as well as the influence of the electron withdrawing groups on the Ru chromophore.
El texto completo de este artículo está disponible en PDF.Keywords : Artificial photosynthesis, Molecular assemblies, Light-induced electron transfer, Density functional calculations, Ruthenium, Manganese
Esquema
Vol 20 - N° 3
P. 323-332 - mars 2017 Regresar al número
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