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Impressum
(c) 2002 BMO

"Ultrafast electron transfer, recombination and spin dynamics"
P. Gilch, F. Pöllinger-Dammer, U.E. Steiner, M.E. Michel-Beyerle ME
Chem. Phys. Lett. 275 (1997) 339


Abstract:
The quenching of excited singlet methylene blue ((MB+)-M-1*) by N,N-dimethylaminomethylferrocene (FcN) in acetonitrile at room temperature has been studied using femtosecond pump-probe absorption spectroscopy. At high FcN concentration static quenching via an intermolecular electron transfer mechanism constitutes the predominating decay channel for (MB+)-M-1* The time constants of the large amplitude components for the forward electron transfer from FcN donor to (MB+)-M-1* and the subsequent recombination process recovering the ground states have been determined to be 390 fs and 1 ps, respectively. Thus, the majority of radical pairs has recombined before paramagnetic relaxation induces spin mixing giving rise to triplet-phased radical pairs. These can escape geminate recombination as the system does not offer low-lying local triplet states to be occupied in the recombination process.

This publication has not been written at BMO

BMO authors (in alphabetic order):
Peter Gilch


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Letzte Änderung: 2016-09-14 13:34