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伦敦分散力对大型有机分子异构化反应的影响:密度泛函基准研究。

Effects of London dispersion on the isomerization reactions of large organic molecules: a density functional benchmark study.

机构信息

Theoretische Organische Chemie, Organisch-Chemisches Institut der Universität Münster, Corrensstrasse 40, D-48149 Münster, Germany.

出版信息

Phys Chem Chem Phys. 2010 Jul 14;12(26):6940-8. doi: 10.1039/c003951a. Epub 2010 May 11.

Abstract

A benchmark set of 24 isomerization reactions of large organic molecules (consisting of 24 to 81 atoms) is presented (termed ISOL). The molecules are much larger than what is typically considered in thermochemical tests. To obtain reference isomerization energies, complete basis set (CBS) extrapolations at the (SCS)-MP2 level have been computed that are augmented by perturbative third-order corrections (SCS-MP3 and MP2.5 methods). Based on these carefully examined reference data, a diverse set of common density functionals varying from GGA to double-hybrid functional level with and without dispersion correction (DFT-D) is tested. Double-hybrid and the PBE0 hybrid functionals are found to be the methods of choice for the type of main group thermochemistry examined here. For all isomerizations with an average reaction energy of 22.7 kcal mol(-1) (in a range between 0.5 and 74.5 kcal mol(-1)), PBE0-D, B2PLYP-D and B2GP-PLYP-D yield mean absolute deviations of 2.5, 4.1 and 2.9 kcal mol(-1). Most importantly it is found that the use of a dispersion correction is essential if such large molecules are considered. For all DFT methods the MAD is lowered very significantly by 1.4-5.0 kcal mol(-1) when DFT-D is used. Intramolecular (mainly medium-range) London dispersion interactions account in some cases for more than 50% (41 kcal mol(-1)) of the isomerization energy even though the size of the systems remains unchanged. This study also demonstrates for the first time clearly that typical DFT errors are larger than expected (about 5 kcal mol(-1)) and that chemical accuracy (about 1 kcal mol(-1)) even for these electronically well-behaved molecules is currently not reached by DFT. We propose this new test set as a difficult challenge for electronic structure methods that claim to be routinely applicable to large molecules. We also suggest to use a distance range resolved dispersion energy as a diagnostic for problematic cases in DFT.

摘要

本文呈现了一组由 24 个大分子(由 24 到 81 个原子组成)的异构化反应基准集(称为 ISOL)。这些分子比通常在热化学测试中考虑的要大得多。为了获得参考异构化能,在 SCS-MP2 水平上进行了完整基组(CBS)外推,并用微扰三阶修正(SCS-MP3 和 MP2.5 方法)进行了修正。基于这些经过仔细检查的参考数据,测试了一系列不同的常用密度泛函,从 GGA 到双杂交功能水平,以及是否带有色散校正(DFT-D)。双杂交和 PBE0 杂化函数被发现是这里研究的主族热化学类型的首选方法。对于平均反应能为 22.7 kcal/mol(在 0.5 到 74.5 kcal/mol 之间)的所有异构化反应,PBE0-D、B2PLYP-D 和 B2GP-PLYP-D 的平均绝对偏差分别为 2.5、4.1 和 2.9 kcal/mol。最重要的是,如果考虑到如此大的分子,发现使用色散校正至关重要。对于所有 DFT 方法,当使用 DFT-D 时,平均绝对偏差(MAD)都显著降低了 1.4-5.0 kcal/mol。在某些情况下,即使系统大小保持不变,分子内(主要是中程)伦敦色散相互作用也占异构化能的 50%以上(41 kcal/mol)。本研究还首次清楚地表明,典型的 DFT 误差比预期的要大(约 5 kcal/mol),即使对于这些电子性能良好的分子,化学精度(约 1 kcal/mol)目前也无法通过 DFT 达到。我们建议将这个新的测试集作为对声称能够常规应用于大分子的电子结构方法的一个困难挑战。我们还建议使用距离分辨的色散能作为 DFT 中出现问题的情况的诊断。

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