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dc.contributor.authorKilin, D.en
dc.contributor.authorZenkevich, E.en
dc.contributor.authorBorczyskowski, C. vonen
dc.coverage.spatialNew Jerseyen
dc.date.accessioned2017-05-27T13:04:50Z
dc.date.available2017-05-27T13:04:50Z
dc.date.issued2015
dc.identifier.citationKilin, D. Dynamics of photoinduced electron transfer in multiporphyrin nanoassemblies / D. Kilin, E. Zenkevich, C. von Borczyskowski // Proceedings of the International Conference "Nanomeeting-2015". Physics, Chemistry and Applications of Nanostructures. Reviews and Short Notes (May 26-29, 2015) / Eds. V. E. Borisenko [et. al]. – New Jersey : World Scientific Publishing Co., 2015. – P. 12-15.en
dc.identifier.urihttps://rep.bntu.by/handle/data/30193
dc.description.abstractIn self-assembled nanoscale porphyrin triads based on Zn-octaethylporphyrin chemical dimer (donor, D) and dipyridyl substituted porphyrin free base (acceptor, A), fluorescence quenching of D (down to 1.7-10 ps) and A (by ~1.3-1.6 times) subunits is strongly dependent on the solvent polarity (toluene-acetone mixtures) and temperature (77-350 K). The obtained experimental findings are analyzed using the reduced density matrix formalism in the frame of Haken-Strobl-Reineker approach taking into account the energy transfer, charge separation, and the dephasing of coherence between the excited electronic states of the triad.en
dc.language.isoenen
dc.publisherWorld Scientific Publishing Co.en
dc.titleDynamics of photoinduced electron transfer in multiporphyrin nanoassembliesen
dc.typeWorking Paperru
dc.identifier.doi10.1142/9789814696524_0002


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