Discrimination of nuclear spin isomers exploiting the excited state dynamics of a quinodimethane derivative

被引:8
作者
Obaid, Rana [1 ,2 ]
Kinzel, Daniel [1 ]
Oppel, Markus [1 ]
Gonzalez, Leticia [1 ]
机构
[1] Univ Wien, Inst Theoret Chem, A-1090 Vienna, Austria
[2] Al Quds Univ, Fac Pharm, Abu Dis, Israel
关键词
INTRAMOLECULAR VIBRATIONAL REDISTRIBUTION; SCHRODINGER-EQUATION; LASER-PULSES; FLUORESCENCE; CONVERSION; MODEL; 9-(N-CARBAZOLYL)-ANTHRACENE; SIMULATIONS; TRANSITIONS; SEPARATION;
D O I
10.1063/1.4899178
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
Despite the concept of nuclear spin isomers (NSIs) exists since the early days of quantum mechanics, only few approaches have been suggested to separate different NSIs. Here, a method is proposed to discriminate different NSIs of a quinodimethane derivative using its electronic excited state dynamics. After electronic excitation by a laser field with femtosecond time duration, a difference in the behavior of several quantum mechanical operators can be observed. A pump-probe experimental approach for separating these different NSIs is then proposed. (C) 2014 AIP Publishing LLC.
引用
收藏
页数:7
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