Reaction Dynamics of a Molecular Switch Unveiled by Coherent Two-Dimensional Electronic Spectroscopy

被引:57
作者
Kullmann, Martin [1 ]
Ruetzel, Stefan [1 ]
Buback, Johannes [1 ]
Nuernberger, Patrick [1 ]
Brixner, Tobias [1 ]
机构
[1] Univ Wurzburg, Inst Phys & Theoret Chem, D-97074 Wurzburg, Germany
关键词
2D IR SPECTROSCOPY; INFRARED-SPECTROSCOPY; FEMTOSECOND SPECTROSCOPY; 2D-IR SPECTROSCOPY; PULSE-SHAPER; HYDROGEN-BOND; SPIROPYRAN; EXCHANGE; SPECTRA; TIME;
D O I
10.1021/ja2032037
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Coherent two-dimensional electronic spectroscopy is usually employed on molecular species with fixed geometric configuration. Here we present two-dimensional Fourier-transform electronic spectra of dissolved 6,8-dnitro-1',3',3'-trimethylspiro[2H-1-benzopyran-2,2'-indoline] (6,8-dinitro-BIPS), a photochromic system present in two ring-open forms differing in the cis/trans configuration of a double bond, which both undergo a photoinduced ring closure. The two-dimensional spectra, recorded with 20 fs pump pulses centered at 605 nm and a supercontinuum probe covering the complete visible spectral range, allow for a detailed analysis of the photophysics and photochemistry of the two isomers and directly reveal that cis/trans isomerization among them does not play a major role. This experiment demonstrates the potential of two-dimensional electronic spectroscopy for reactive processes.
引用
收藏
页码:13074 / 13080
页数:7
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