Department of Chemistry, KU Leuven (University of Leuven), Celestijnenlaan 200 F, 3001 Heverlee, Belgium.
IMEC, Kapeldreef 75, 3001 Leuven, Belgium.
Molecules. 2023 Apr 22;28(9):3649. doi: 10.3390/molecules28093649.
The availability of thermochemical properties allows for the prediction of the equilibrium compositions of chemical reactions. The accurate prediction of these can be crucial for the design of new chemical synthesis routes. However, for new processes, these data are generally not completely available. A solution is the use of thermochemistry calculated from first-principles methods such as Density Functional Theory (DFT). Before this can be used reliably, it needs to be systematically benchmarked. Although various studies have examined the accuracy of DFT from an energetic point of view, few studies have considered its accuracy in predicting the temperature-dependent equilibrium composition. In this work, we collected 117 molecules for which experimental thermochemical data were available. From these, we constructed 2648 reactions. These experimentally constructed reactions were then benchmarked against DFT for 6 exchange-correlation functionals and 3 quality of basis sets. We show that, in reactions that do not show temperature dependence in the equilibrium composition below 1000 K, over 90% are predicted correctly. Temperature-dependent equilibrium compositions typically demonstrate correct qualitative behavior. Lastly, we show that the errors are equally caused by errors in the vibrational spectrum and the DFT electronic ground state energy.
热化学性质的可用性使得可以预测化学反应的平衡组成。这些的准确预测对于新的化学合成路线的设计可能至关重要。然而,对于新的工艺,通常无法完全获得这些数据。一种解决方案是使用从头算方法(例如密度泛函理论(DFT))计算的热化学数据。在可以可靠地使用之前,需要对其进行系统的基准测试。尽管已经有许多研究从能量角度研究了 DFT 的准确性,但很少有研究考虑其在预测与温度相关的平衡组成方面的准确性。在这项工作中,我们收集了 117 种具有实验热化学数据的分子。从中,我们构建了 2648 个反应。然后,我们针对 6 种交换相关泛函和 3 种基组质量对这些实验构建的反应进行了基准测试。我们表明,在平衡组成中没有温度依赖性的反应中,超过 90%的反应是正确预测的。与温度相关的平衡组成通常表现出正确的定性行为。最后,我们表明误差同样是由振动光谱和 DFT 电子基态能量的误差引起的。