Resonance Femtosecond-Stimulated Raman Spectroscopy without Actinic Excitation Showing Low-Frequency Vibrational Activity in the S2 State of All-Trans β-Carotene

被引:26
|
作者
Quick, Martin [1 ]
Dobryakov, Alexander L. [1 ]
Kovalenko, Sergey A. [1 ]
Ernsting, Nikolaus P. [1 ]
机构
[1] Humboldt Univ, Dept Chem, D-12489 Berlin, Germany
来源
关键词
EXCITED-STATE; INTERNAL-CONVERSION; FEMTOSECOND; DYNAMICS; RELAXATION; ABSORPTION;
D O I
10.1021/acs.jpclett.5b00243
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
Raman scattering with stimulating femtosecond probe pulses (FSR) was used to observe vibrational activity of all-trans beta-carotene in n-hexane. The short-lived excited electronic state S-2 was accessed in two ways: (i) by transient FSR after an actinic pulse to populate the S-2 state, exploiting resonance from an S-x <- S-2 transition, and (ii) by FSR without actinic excitation, using S-2 <-> S-2 resonance exclusively and narrow band Raman/broad-band feintosecond probe pulses only The two approaches have nonlinear optical susceptibilities chi((5)) and chi((3)), respectively. Both methods show low-frequency bands of the S-2 state at 200, 400, and,similar to 600 cm(-1), which are reported for the first time. With (ii) the intensities of lowfrequency vibrational resonances in S-2 are larger compared to those in S-0, implying strong anharmonicities/mode mixing in the excited state. In principle, for short-lived electronic states, the chi((3)) method should allow the best characterization of low-frequency modes.
引用
收藏
页码:1216 / 1220
页数:5
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