Kinetics and mechanism of the CN + NCO → NCN + CO reaction studied by experiment and theory

Shiang Yang Tzeng, Po Hsueh Chen, Niann-Shiah Wang, L. C. Lee, Z. F. Xu, Ming-Chang Lin

研究成果: Article同行評審

5 引文 斯高帕斯(Scopus)


The rate coefficients for the CN + NCO → NCN + CO reaction have been measured by a laser-photolysis/ laser-induced fluorescence technique in the temperature range of 254-353 K and the He pressures of 123-566 Torr. The CN radical was produced from the photolysis of BrCN at 193 nm, and the NCO radical from the CN + O2 reaction. The NCN radical was monitored by laser-induced fluorescence with a dye laser at 329.01 nm. The rate constants derived from kinetic modeling, with a negative temperature dependence but no pressure effect, can be expressed by k = (2.15 ± 0.70) × 10 -11 exp[(155 ± 92)/T]cm3 molecule-1 s-1, where the quoted errors are two standard deviations. The reaction mechanism and rate constant have also been theoretically predicted for the temperature range of 200-3000 K at He pressures ranging from 10-4 Torr to 1000 atm based on dual channel Rice-Ramsperger-Kassel-Marcus (RRKM) calculations with the potential energy surface evaluated at the G2M and CCSD(T) levels. The rate constant calculated by variational RRKM theory agrees reasonably with experimental data.

頁(從 - 到)6314-6325
期刊Journal of Physical Chemistry A
出版狀態Published - 4 6月 2009


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