Reaction path of UV photolysis of matrix isolated acetyl cyanide:: Formation and identification of ketenes, zwitterion, and keteneimine intermediates

被引:21
作者
Guennoun, Z
Couturier-Tamburelli, I
Combes, S
Aycard, JP
Piétri, N
机构
[1] Univ Aix Marseille 1, Lab Phys Interact Ion & Mol, UMR 6633 Equipe Spectrometries & Dynam Mol, Ctr St Jerome, F-13397 Marseille 20, France
[2] Univ Aix Marseille 1, UMR 6517, Lab Chim Biol & Radicaux Libres, Ctr St Jerome, F-13397 Marseille 20, France
关键词
D O I
10.1021/jp0536854
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
Irradiations at lambda > 180 nm and > 230 nm of CH3COCN (CD3COCN) trapped in an argon matrix at 10 K have been performed and monitored by Fourier transform infrared spectroscopy. For both wavelengths, the first photoreaction product is acetyl isocyanide. At lambda > 180 nm acetonitrile and methyl isocyanide are obtained as final products. They are formed by photolysis of acetyl isocyanide and acetyl cyanide, respectively. Unstable intermediates, such as ketene:HCN and ketene:HNC complexes, H2CNCH zwitterion, and H2C2NH keteneimine, not observed in the gas phase, are trapped and identified at our experimental temperature. The complexes have an L-shaped structure with a hydrogen bond between the oxygen atom of ketene and the hydrogen atom of HCN or HNC. A pathway process is proposed and compared with the ones determined in the ground state by ab initio calculations.
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收藏
页码:11733 / 11741
页数:9
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