Karton Amir
School of Molecular Sciences , The University of Western Australia , Perth , WA 6009 , Australia.
J Phys Chem A. 2019 Aug 8;123(31):6720-6732. doi: 10.1021/acs.jpca.9b04611. Epub 2019 Jul 30.
The ability to accurately calculate reaction barrier heights is of central importance to many areas of chemistry. We report an extensive study examining the basis set convergence of post-CCSD(T) contributions (up to CCSDT(Q)) for a diverse set of 28 reaction barrier heights. In contrast to previous studies, we focus here on larger transition structures (TSs) involving 4-7 non-hydrogen atoms. The set of reaction barrier heights includes pericyclic, bipolar cycloaddition, cycloreversion, and multiple-proton transfer reactions. We find that in most cases post-CCSD(T) contributions converge rapidly toward the basis set limit, such that even double-ζ and truncated double-ζ basis sets provide useful estimates of the T-(T) and (Q) contributions, respectively. In addition, we find that due to the tendency of these small basis sets to systematically underestimate the T-(T) and (Q) components, scaling is an effective approach for improving performance. For example, scaling the T-(T)/cc-pVDZ contribution by 1.25 results in an RMSD of merely 0.4 kJ mol relative to basis set limit reference values from W3lite-F12 theory. Similarly, calculating the (Q) contribution with a cc-pVDZ basis set without d functions and scaling by 1.6 results in an RMSD of 0.5 kJ mol. We also examine the magnitude of post-CCSD(T) contributions for a wide range of TSs. We find that for pericyclic, bipolar cycloaddition, and multiple-proton transfer reactions there is an effective cancellation between the T-(T) and (Q) components (i.e., they have opposite signs and are of similar magnitude), such that overall post-CCSD(T) contributions to the reaction barrier heights are below ∼1 kJ mol (in absolute value). However, for the barrier heights of cycloreversion reactions, the T-(T) and (Q) components are both negative and large and consequentially post-CCSD(T) contributions reduce the reaction barrier heights by significant amounts ranging between 4.1 and 6.7 kJ mol.
准确计算反应势垒高度的能力在化学的许多领域都至关重要。我们报告了一项广泛的研究,考察了28种不同反应势垒高度的后CCSD(T)贡献(直至CCSDT(Q))的基组收敛情况。与之前的研究不同,我们在此关注涉及4 - 7个非氢原子的较大过渡结构(TSs)。反应势垒高度的集合包括周环反应、双极环加成反应、环化反转反应和多质子转移反应。我们发现,在大多数情况下,后CCSD(T)贡献迅速收敛到基组极限,以至于即使是双ζ和截断双ζ基组也分别为T-(T)和(Q)贡献提供了有用的估计。此外,我们发现由于这些小基组倾向于系统地低估T-(T)和(Q)分量,缩放是提高性能的有效方法。例如,将T-(T)/cc-pVDZ贡献缩放1.25,相对于W3lite-F12理论的基组极限参考值,均方根偏差(RMSD)仅为0.4 kJ/mol。同样,使用没有d函数的cc-pVDZ基组计算(Q)贡献并缩放1.6,RMSD为0.5 kJ/mol。我们还研究了广泛的TSs的后CCSD(T)贡献的大小。我们发现,对于周环反应、双极环加成反应和多质子转移反应,T-(T)和(Q)分量之间存在有效的抵消(即它们具有相反的符号且大小相似),因此后CCSD(T)对反应势垒高度的总体贡献低于约1 kJ/mol(绝对值)。然而,对于环化反转反应的势垒高度,T-(T)和(Q)分量均为负且较大,因此后CCSD(T)贡献使反应势垒高度显著降低,降低幅度在4.1至6.7 kJ/mol之间。