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Photolysis of n-butyl nitrite and isoamyl nitrite at 355 nm: A time-resolved Fourier transform infrared emission spectroscopy and ab initio study
被引:9
|作者:
Ji, Min
Zhen, Junfeng
Zhang, Qun
[1
]
Chen, Yang
机构:
[1] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
基金:
中国国家自然科学基金;
关键词:
ab initio calculations;
density functional theory;
Fourier transform spectra;
infrared spectra;
organic compounds;
photodissociation;
reaction kinetics theory;
spectrochemical analysis;
time resolved spectra;
ultraviolet spectra;
vibrational modes;
OVERTONE PHOTOFRAGMENT SPECTROSCOPY;
PHOTODISSOCIATION DYNAMICS;
STATE DISTRIBUTIONS;
ENERGY-DISTRIBUTION;
ABSORPTION-SPECTRUM;
OH FRAGMENT;
S-2;
STATE;
CH3ONO;
HONO;
ALIGNMENT;
D O I:
10.1063/1.3129806
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:
We report on the photodissociation dynamics study of n-butyl nitrite and isoamyl nitrite by means of time-resolved Fourier transform infrared (TR-FTIR) emission spectroscopy. The obtained TR-FTIR emission spectra of the nascent NO fragments produced in the 355 nm laser photolysis of the two alkyl nitrite species showed an almost identical rotational temperature and vibrational distributions of NO. In addition, a close resemblance between the two species was also found in the measured temporal profiles of the IR emission of NO and the recorded UV absorption spectra. The experimental results are consistent with our ab initio calculations using the time-dependent density functional theory at the B3LYP/6-311G(d,p) level, which indicate that the substitution of one of the two gamma-H atoms in n-C4H9ONO with a methyl group to form (CH3)(2)C3H5ONO has only a minor effect on the photodissociation dynamics of the two molecules.
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