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甲醇在CH伸缩基频区域的亚多普勒红外光谱与扭转-转动能量流形

Sub-Doppler Infrared Spectra and Torsion-Rotation Energy Manifold of Methanol in the CH-Stretch Fundamental Region.

作者信息

Xu LH, Wang X, Cronin TJ, Perry DS, Fraser GT, Pine AS

机构信息

Department of Physical Sciences, University of New Brunswick, Saint John, New Brunswick, E2L 4L5, Canada

出版信息

J Mol Spectrosc. 1997 Sep;185(1):158-72. doi: 10.1006/jmsp.1997.7367.

DOI:10.1006/jmsp.1997.7367
PMID:9344807
Abstract

The infrared spectrum of jet-cooled methanol in the CH-stretch fundamental region has been investigated by two sub-Doppler laser techniques: optothermally detected molecular-beam electric resonance and direct-absorption slit-jet spectroscopy. With the aid of microwave-infrared double resonance and ground state combination differences, 27 subbands in the frequency range 2967 to 3027 cm-1 have been assigned to the nu2 fundamental. Perturbation systems in the K' = 0 E, -1 E, and -2 E symmetry subbands have been analyzed to yield matrix elements of 0.013, 0.041, and 0.75 cm-1, respectively. The A-E torsional tunneling splitting for J = 0 of the nu2 vibration of -3.26 cm-1 is of opposite sign and a factor of three smaller in magnitude than the ground state value of +9.12 cm-1. Copyright 1997 Academic Press. Copyright 1997Academic Press

摘要

利用两种亚多普勒激光技术,对喷射冷却甲醇在C-H伸缩基频区域的红外光谱进行了研究:光热检测分子束磁共振和直接吸收狭缝射流光谱法。借助微波-红外双共振和基态组合差,在2967至3027 cm-1频率范围内的27个亚带已被指定为ν2基频。对K' = 0 E、-1 E和-2 E对称亚带中的微扰系统进行了分析,分别得到了0.013、0.041和0.75 cm-1的矩阵元。ν2振动J = 0时的A-E扭转隧道分裂为-3.26 cm-1,其符号与基态值+9.12 cm-1相反,大小为基态值的三分之一。版权所有1997年学术出版社。版权所有1997年学术出版社

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