Photochemical Z→E isomerization of a hemithioindigo/hemistilbene ω-amino acid

被引:31
作者
Cordes, Thorben
Heinz, Bjoern
Regner, Nadia
Hoppmann, Christian
Schrader, Tobias E.
Summerer, Wolfram
Rueck-Braun, Karola
Zinth, Wolfgang
机构
[1] Univ Munich, Dept Phys, Lehrstuhl BioMol Opt, D-80538 Munich, Germany
[2] Munich Ctr Integrated Prot Sci CIPS, Munich, Germany
[3] Tech Univ Berlin, Inst Chem, D-10623 Berlin, Germany
关键词
isomerization; photochemistry; photochromism; time-resolved spectroscopy; ultrafast spectroscopy;
D O I
10.1002/cphc.200700223
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The molecule HTI, which combines hemithioindigo and hemistilbene molecular parts, allows reversible switching between two isomeric states. Photochromic behaviour of the HTI molecule is observed by irradiation with UV/Vis light. The photochemical reaction, a Z/E isomerization around the central double bond connecting the two molecular parts, is investigated by transient absorption and emission spectroscopy. For a special HTI molecule, namely, an omega-amino acid, the Z --> E isomerization process occurs on a timescale of 30 ps. In the course of the reaction fast processes on the 1-10 ps timescale are observed which point to motions of the molecule on the potential-energy surface of the excited state. The combination of transient absorption experiments in the visible spectral range with time-resolved fluorescence and infrared measurements reveal a photochemical pathway with three intermediate states. Together with a theoretical modelling procedure the experiments point to a sequential reaction scheme and give indications of the nature of the involved intermediates.
引用
收藏
页码:1713 / 1721
页数:9
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