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Size- and solvent-dependent kinetics for cis-trans isomerization in donor-acceptor systems
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Photochemistry and Molecular Science.
2009 (English)In: Spectrochimica Acta Part A - Molecular and Biomolecular Spectroscopy, ISSN 1386-1425, E-ISSN 1873-3557, Vol. 72, no 5, 1014-1019 p.Article in journal (Refereed) Published
Abstract [en]

We have investigated, using time-resolved and steady-state optical spectroscopy, the cis-trans isomerization dynamics in a series of charge transfer. donor-acceptor compounds. The number of donor (dithiafulvene) and acceptor (p-nitrophenyl) moieties as well as their spatial arrangement around a central ethynylethene core has been varied in a systematic way, All compounds in the series are weakly fluorescent. We show that the fluorescence spectrum red-shifts within a few picoseconds, a shift which occurs concurrently with a blue-shift of the transient absorption spectrum. The kinetics following the initial relaxation are in all cases multi-exponential, and the time constants correlate with molecular size and solvent viscosity. We interpret the data as a result of conformational change where the conjugation through the central double bond is broken upon excitation into the charge-transfer transition, and the time for rotation around this bond is dependent on the molecular interactions between solute and solvent. (C) 2009 Elsevier B.V. All Fights reserved.

Place, publisher, year, edition, pages
2009. Vol. 72, no 5, 1014-1019 p.
Keyword [en]
Charge transfer, Isomerization, Solvent dependence, Time-resolved emission and transient absorption spectroscopy
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:uu:diva-129127DOI: 10.1016/j.saa.2008.12.029ISI: 000264992000017OAI: oai:DiVA.org:uu-129127DiVA: diva2:337696
Available from: 2010-08-09 Created: 2010-08-05 Last updated: 2017-12-12Bibliographically approved

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