Hydrogen-bonded complexes of ethynethiol and hydrogen cyanide trapped in low-temperature argon matrices

被引:0
|
作者
Miyazaki, Jun [1 ]
Hatayama, Takahiro [2 ]
Akai, Nobuyuki [2 ]
Nakata, Munetaka [2 ]
机构
[1] Hokuriku Univ, Fac Pharmaceut Sci, Ho 3,Kanagawa Machi, Kanazawa, Ishikawa 9201181, Japan
[2] Tokyo Univ Agr & Technol, Grad Sch BASE Bioapplicat & Syst Engn, 2-24-16 Naka Cho, Koganei, Tokyo 1848588, Japan
关键词
Matrix-isolation; Hydrogen-bonded complexes; Photochemistry; Thiazole; Infrared spectroscopy; OFT calculations; ISOLATION INFRARED-SPECTROSCOPY; FUNCTIONAL-THEORY CALCULATIONS; MOLECULE; IR;
D O I
10.1016/j.molstruc.2018.08.028
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
Hydrogen bonding is one of the exciting and interesting research themes because it plays important roles in biomolecules, plant cells, and so on. Here we report hydrogen-bonded complexes among the photodecomposition products of thiazole, being studied by a joint use of infrared (IR) spectroscopy and density-functional-theory (DFT) calculations. Three types of hydrogen-bonded complexes of ethynethiol (HS-C CH) and hydrogen cyanide (HC N), which are photodecomposed by two cleavages of the NC-SC and CN-CC single bonds of thiazole in argon matrices, have been identified by comparison of the observed IR spectra with the corresponding calculated spectral patterns. In addition, another complex with weak interaction between S atom and HCF N, which are photoproduced by cleavages of the three single bonds of thiazole, is detected by comparison with the wavenumbers previously reported in literature. The reaction mechanisms to form these complexes are discussed based on the analysis of IR spectra and the DFT calculations. (C) 2018 Elsevier B.V. All rights reserved.
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页码:900 / 905
页数:6
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