Experimental Detection of Branching at a Conical Intersection in a Highly Fluorescent Molecule

被引:57
作者
Brazard, Johanna [1 ]
Bizimana, Laurie A. [1 ]
Gellen, Tobias [1 ]
Carbery, William P. [1 ]
Turner, Daniel B. [1 ]
机构
[1] NYU, Dept Chem, New York, NY 10003 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2016年 / 7卷 / 01期
基金
美国国家科学基金会;
关键词
WAVE-PACKET MOTION; ABSORPTION-SPECTRA; NUCLEAR MOTION; CRESYL VIOLET; DYNAMICS; SPECTROSCOPY; STATE; PHOTOISOMERIZATION; PHOTOCHEMISTRY; ISOMERIZATION;
D O I
10.1021/acs.jpclett.5b02476
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
Conical intersections are molecular configurations at which adiabatic potential-energy surfaces touch. They are predicted to be ubiquitous, yet condensed-phase experiments have focused on the few systems with clear spectroscopic signatures of negligible fluorescence, high photoactivity, or femtosecond electronic kinetics. Although rare, these signatures have become diagnostic for conical intersections. Here we detect a coherent surface-crossing event nearly two picoseconds after optical excitation in a highly fluorescent molecule that has no photoactivity and nanosecond electronic kinetics. Time frequency analysis of high-sensitivity measurements acquired using sub-8 fs pulses reveals phase shifts of the signal due to branching of the wavepacket through a conical intersection. The time frequency analysis methodology demonstrated here on a model compound will enable studies of conical intersections in molecules that do not exhibit their diagnostic signatures. Improving the ability to detect conical intersections will enrich the understanding of their mechanistic role in molecular photochemistry.
引用
收藏
页码:14 / 19
页数:6
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