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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.isoen_USen
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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