IR-induced interconversions between five conformers of methanol dimers trapped in nitrogen matrix

被引:25
作者
Coussan, S
Loutellier, A
Perchard, JP
Racine, S
Peremans, A
Tadjeddine, A
Zheng, WQ
机构
[1] Univ Paris 06, Lab Spectrochim Mol, CNRS, URA 508, F-75252 Paris 05, France
[2] Univ Paris Sud, LURE, F-91405 Orsay, France
关键词
D O I
10.1016/S0301-0104(97)00233-4
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
Interconversions between five open-chain conformers of methanol dimer trapped in solid nitrogen have been studied through selective excitation of their CH and OH stretching modes. A nearly complete vibrational assignment for three of them is deduced from these irradiation effects and also from thermal conversion observed between 7 and 8 K. Kinetic studies allow us to precise the schemes of conversion and, in favourable cases, to get the quantum yields which are significantly mode dependent. A careful examination of the CO stretching overtone region, around 2050 cm(-1), led to the identification of a simultaneous transition of the CO stretching mode of both molecules, with intensities strongly varying according to the conformer. Such a variation is accounted for in the framework of the theory of the intensities of combination transitions, assuming a dipole-dipole interaction between the two CO bonds. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:279 / 292
页数:14
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