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IR induced cis⇆trans isomerization of 2-naphthol:: Catalytic role of hydrogen-bond in the photoinduced isomerization
被引:14
作者:
Ebata, T
[1
]
Kouyama, K
[1
]
Mikami, N
[1
]
机构:
[1] Tohoku Univ, Dept Chem, Grad Sch Sci, Sendai, Miyagi 9808578, Japan
关键词:
EXCITED-STATE;
GAS-PHASE;
ROTATIONAL ISOMERS;
PROTON-TRANSFER;
CLUSTERS;
SPECTROSCOPY;
WATER;
SPECTRA;
PHENOL;
EXCITATION;
D O I:
10.1063/1.1596831
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:
An infrared laser induced cis<---->trans isomerization has been investigated for 2-naphthol and its hydrogen(H)-bonded cluster with NH3 in the S-1 electronic state by UV-IR double resonance excitation in a supersonic jet. A specific isomer was pumped to a X-H (X=O, C or N) stretching vibration in S-1 by a sequential UV-IR two-photon excitation, and the resultant product species were analyzed by dispersing their fluorescence. It was found that the IR excitation induces the isomerization for the H-bonded cluster with the excitation less than 3000 cm(-1), while no isomerization was found to occur for bare 2NpOH even with an input energy of 3610 cm(-1). The substantial reduction of the isomerization barrier height represents evidence of the catalytic nature of H-bonding in the conformational isomerization. It was also found that the isomerization efficiency is very high at low IR frequency and exhibits a marked IR frequency dependence. (C) 2003 American Institute of Physics.
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页码:2947 / 2950
页数:4
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