Infrared spectroscopy of rovibrational transitions of methyl radicals (CH3, CD3) in solid parahydrogen

被引:12
作者
Hoshina, Hiromichi [2 ]
Fushitani, Mizuho [2 ]
Momose, Takamasa [1 ,2 ]
机构
[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
[2] Kyoto Univ, Div Chem, Grad Sch Sci, Kyoto 6068502, Japan
基金
加拿大自然科学与工程研究理事会;
关键词
Spectroscopy; Infrared; Solid parahydrogen; Matrix isolation; Methyl radical; Group theory; Crystal field; HIGH-RESOLUTION SPECTROSCOPY; MATRIX-ISOLATION SPECTROSCOPY; TUNNELING CHEMICAL-REACTIONS; DIODE-LASER SPECTROSCOPY; NU-2; BAND; K; MOLECULES; METHANE; SPECTRUM; CRYSTAL;
D O I
10.1016/j.jms.2011.04.014
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The v(3) and v(4) vibrational transitions of CH3 and CD3 isolated in solid parahydrogen were studied by high-resolution infrared spectroscopy. The radicals were produced by in situ UV photolysis of methyl iodides trapped in solid parahydrogen. The observed spectra showed clear rotational fine structures, which were subjected to further splitting due to the electrostatic field of solid parahydrogen. The molecular constants and crystal field parameters of the radicals in solid parahydrogen were determined by analyzing the spectral structures of the v(3) and 54 transitions of CD3 by the crystal field theory. The rotational constants of the CD3 radical were found to be only a few percent smaller than those in the gas phase. The determined crystal field parameters indicated significant quantum effects in the intermolecular interactions between the radicals and hydrogen molecules in solid parahydrogen. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:164 / 172
页数:9
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