Benchmark calculations with correlated molecular wave functions. IV. The classical barrier height of the H+H2→H2+H reaction

作者：Kirk A. Peterson, David E. Woon, Thom H. Dunning · 发表于：The Journal of Chemical Physics · 年份：1994 · DOI：10.1063/1.466884 · 被引用次数：1833 · 研究领域：Advanced Chemical Physics Studies、Spectroscopy and Quantum Chemical Studies、Quantum, superfluid, helium dynamics

Using systematic sequences of correlation consistent Gaussian basis sets from double to sextuple zeta quality, the classical barrier height of the H+H2 exchange reaction has been calculated by multireference configuration interaction (MRCI) methods. The MRCI calculations for collinear H3 have also been calibrated against large basis set full CI (FCI) results, which demonstrate that the MRCI treatment leads to energies less than 1 μhartree (≤0.001 kcal/mol) above the FCI energies. The dependence of both the H2 and H3 total energies on the basis set is found to be very regular, and this behavior has been used to extrapolate to the complete basis set (CBS) limits. The resulting estimate of the H–H–H CBS limit yields a classical barrier height, relative to exact H+H2, of 9.60±0.02 kcal/mol; the best directly calculated value for the barrier is equal to 9.62 kcal/mol. These results are in excellent agreement with recent quantum Monte Carlo calculations.