Electronic and Geometric Characterization of TICT Formation in Hemithioindigo Photoswitches by Picosecond Infrared Spectroscopy

被引:7
|
作者
Stallhofer, Klara [1 ]
Nuber, Matthias [1 ]
Schueppel, Franziska [2 ]
Thumser, Stefan [2 ]
Iglev, Hristo [1 ]
de Vivie-Riedle, Regina [2 ]
Zinth, Wolfgang [3 ]
Dube, Henry [4 ]
机构
[1] Tech Univ Munich, Phys Dept, Lehrstuhl Laser & Rontgenphys, D-85748 Garching, Germany
[2] Ludwig Maximilians Univ Munchen, Dept Chem, D-81377 Munich, Germany
[3] Ludwig Maximilians Univ Munchen, Lehrstuhl Biomol Opt, D-80538 Munich, Germany
[4] Friedrich Alexander Univ Erlangen Nurnberg, Dept Chem & Pharm, D-91058 Erlangen, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2021年 / 125卷 / 20期
关键词
INTRAMOLECULAR CHARGE-TRANSFER; EXCITED-STATE; FLUORESCENCE; SINGLE; DONOR; VISCOSITY; PHOTOISOMERIZATION; SERIES; ATOMS; TRANS;
D O I
10.1021/acs.jpca.1c02646
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
Deciphering the exact electronic and geometric changes of photoexcited molecules is an important task not only to understand the fundamental atomistic mechanisms but also to rationally design molecular properties and functions. Here, we present a combined experimental and theoretical study of the twisted intramolecular charge transfer (TICT) process in hemithioindigo photoswitches. Using ultrafast transient IR spectroscopy as the main analytical method, a detailed understanding of the extent and direction of charge transfer within the excited molecule is obtained. At the same time, the geometrical distortion is monitored directly via changes of indicative vibrational modes over the time course of the photoreaction. These high-resolution data deliver a detailed molecular movie of the TICT process in this important class of chromophores with picosecond time resolution.
引用
收藏
页码:4390 / 4400
页数:11
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