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关于氢原子与灭火剂2-H七氟丙烷和CF3Br之间两个反应的密度泛函理论(DFT)和从头算计算。

DFT and ab initio calculations on two reactions between hydrogen atoms and the fire suppressants 2-H heptafluoropropane and CF3Br.

作者信息

Lee Edmond P F, Dyke John M, Chow Wan-Ki, Chau Foo-Tim, Mok Daniel K W

机构信息

Department of Building Services Engineering, The Hong Kong Polytechnic University, Hung Hom, Hong Kong.

Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Hong Kong.

出版信息

J Comput Chem. 2007 Jul 15;28(9):1582-1592. doi: 10.1002/jcc.20695.

Abstract

Reaction enthalpies and barrier heights of the reactions CF3Br+H-->CF3+HBr {reaction (1)} and CF3CHFCF3+H-->CF3CFCF3+H2 {reaction (2)} have been calculated at the near state-of-the-art ab initio level, and also by employing the B3LYP, BH&HLYP, BB1K, MPW1K, MPWB1K and TPSS1KCIS functionals. In addition, the integrated molecular orbital+molecular orbital (IMOMO) method has been used to study reaction (2). The ab initio benchmark values of the reaction enthalpy (298 K) and barrier height (0 K) of reaction (2) are reported for the first time {-(0.7+/-0.7) and 13.3+/-0.5 kcal/mole respectively}. When density functional theory (DFT) results are compared with ab initio benchmarks for both reactions (1) and (2), the MPWB1K functional is found to have the best performance of the six functionals used. The IMOMO method with the RCCSD/aug-cc-pVTZ and/or RCCSD(T)/aug-cc-pVTZ levels, as the high levels of calculation on the model system, gives reaction enthalpies and barrier heights of reaction (2), which agree with ab initio benchmark values to within 1 kcal/mole. Computed key geometrical parameters and imaginary vibrational frequencies of the transition state structures of reactions (1) and (2) obtained at different levels of calculation are compared. The magnitudes of the computed imaginary vibrational frequencies of the transition states of both reactions considered are found to be very sensitive to the levels of calculation used to obtain them. The heat of formation (298 K) of CF3CFCF3 calculated at the near state-of-the-art level has a value of -(318+/-3) kcal/mole.

摘要

在接近最新的从头算水平下,以及通过使用B3LYP、BH&HLYP、BB1K、MPW1K、MPWB1K和TPSS1KCIS泛函,计算了反应CF3Br + H→CF3 + HBr{反应(1)}和CF3CHFCF3 + H→CF3CFCF3 + H2{反应(2)}的反应焓和势垒高度。此外,采用集成分子轨道+分子轨道(IMOMO)方法研究反应(2)。首次报道了反应(2)的反应焓(298 K)和势垒高度(0 K)的从头算基准值{分别为-(0.7±0.7)和13.3±0.5 kcal/mol}。当将密度泛函理论(DFT)结果与反应(1)和(2)的从头算基准进行比较时,发现MPWB1K泛函在所使用的六种泛函中具有最佳性能。以RCCSD/aug-cc-pVTZ和/或RCCSD(T)/aug-cc-pVTZ水平作为模型体系的高水平计算方法的IMOMO方法,给出了反应(2)的反应焓和势垒高度,其与从头算基准值的偏差在1 kcal/mol以内。比较了在不同计算水平下得到的反应(1)和(2)过渡态结构的计算关键几何参数和虚振动频率。发现所考虑的两个反应过渡态的计算虚振动频率大小对用于获得它们的计算水平非常敏感。在接近最新水平下计算得到的CF3CFCF3的生成热(298 K)值为-(318±3) kcal/mol。

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