Beck Ian T, Mitchell Erica C, Hill Annabelle Webb, Turney Justin M, Rotavera Brandon, Schaefer Henry F
Department of Chemistry, University of Georgia, 302 East Campus Road, Athens, Georgia 30602, United States.
Center for Computational Quantum Chemistry, University of Georgia, 1004 Cedar Street, Athens, Georgia 30602, United States.
J Phys Chem A. 2024 Dec 19;128(50):10906-10920. doi: 10.1021/acs.jpca.4c04391. Epub 2024 Dec 6.
Vacuum-ultraviolet (VUV) absorption spectroscopy enables electronic transitions that offer the unambiguous identification of molecules. As target molecules become more complex, multifunctional species present a great challenge to both experimental and computational spectroscopy. This research reports both experimental and theoretical studies of oxiranes. Computationally, the nuclear ensemble approach has been used to accurately predict experimental spectra for a variety of molecules. However, this approach incurs great computational cost, as ensembles generally consist of thousands of geometries. The present study aims to drastically reduce the ensemble by evaluating the significance of the conformers to the predicted spectra. This approach was applied to 11 substituted oxiranes using the Conformer Rotamer Ensemble Sampling Tool (CREST) of Grimme to generate an ensemble of unique conformers determined by their Boltzmann populations. Five TD-DFT functionals (BMK, CAM-B3LYP, M06-2X, MN15, ωB97X-D) and EOM-CCSD were used to simulate the spectrum of each substituted oxirane ensemble. Computed spectra were then compared to the experiment using both qualitative and quantitative metrics. Based on these metrics, it was observed that certain conformers may not be necessary to characterize this set of oxiranes despite the temperature (323 K) of the experiment. A single conformer can then be used with TD-DFT and EOM-CCSD to replicate the experimental spectra of these medium-sized combustion species.
真空紫外(VUV)吸收光谱能够实现电子跃迁,从而明确鉴定分子。随着目标分子变得更加复杂,多功能物种对实验光谱学和计算光谱学都构成了巨大挑战。本研究报告了环氧乙烷的实验和理论研究。在计算方面,核系综方法已被用于准确预测各种分子的实验光谱。然而,这种方法计算成本高昂,因为系综通常由数千种几何结构组成。本研究旨在通过评估构象异构体对预测光谱的重要性来大幅减少系综。使用Grimme的构象异构体旋转异构体系综采样工具(CREST)将该方法应用于11种取代环氧乙烷,以生成由其玻尔兹曼分布确定的独特构象异构体系综。使用五种TD-DFT泛函(BMK、CAM-B3LYP、M06-2X、MN15、ωB97X-D)和EOM-CCSD来模拟每个取代环氧乙烷系综的光谱。然后使用定性和定量指标将计算光谱与实验进行比较。基于这些指标,观察到尽管实验温度为323 K,但某些构象异构体可能对于表征这组环氧乙烷并非必要。然后可以使用单个构象异构体与TD-DFT和EOM-CCSD一起复制这些中等大小燃烧物种的实验光谱。