LMU München
Fakultät für Physik



(c) 2002 BMO

"Photochromic bis(thiophen-3-yl)maleimides studied with time-resolved spectroscopy"
C. Elsner, T. Cordes, P. Dietrich, M. Zastrow, T. T. Herzog, K. Rück-Braun, W. Zinth
The Journal of Physical Chemistry A, 2009, 113 (6), pp 10331039

The dynamics of the ring closure reaction of three different bis(thiophen-3-yl)maleimides are investigated using ultrafast spectroscopy in the visible range. The structure of the molecules differs with respect to substitution of the thiophene-ring and the maleimide. The experiments reveal reaction kinetics which point to the population of an excited electronic state for several nanoseconds. In the case of completely unsubstituted thiophene rings, a long excited state lifetime (biexponential decay with 3 ns and 15 ns) can be observed. The remaining ultrafast absorption transients of this molecule are due to relaxational processes on the excited electronic potential energy surface. The ring-closure reaction has a small yield (< 1 %) and does not show up in the ultrafast absorption experiments. A dimethyl-substitution of the thiophene-ring results in completely different behaviour: after transients related to relaxation in the ex-cited electronic state, one finds pronounced absorption transients with tau = 16 ps which represent the partial decay of the excited electronic state and the formation of the ring closed isomer. Another fraction of the emitting excited electronic state decays again on the few nanosecond timescale. The experiments suggest that the open isomer of the dimethyl-substituted imides exist in two conformations.

BMO authors (in alphabetic order):
Thorben Cordes
Cord Elsner
Teja Herzog
Wolfgang Zinth

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Letzte Änderung: 2016-09-14 11:34