定向外电场辅助下的氧化亚氮脱氧反应

IF 2.3 3区 化学 Q3 CHEMISTRY, PHYSICAL International Journal of Quantum Chemistry Pub Date : 2024-04-27 DOI:10.1002/qua.27384
Ming-Xia Zhang, Jun Li, Hao Lei, Jia-Hui Chen, Peng-Yang Sun, Meng-Ting Yao, Lin Liu, Jia Guo
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引用次数: 0

摘要

由于一氧化二氮具有高稳定性和潜在的臭氧消耗性,温室气体一氧化二氮的转化备受关注。本文以定向外电场(OEEF)为催化策略,对氧化亚氮与硅烷的脱氧反应提出了新的见解。当使用定向外电场时,由于它是沿着正的 NO/OSi 键轴定向的,因此脱氧反应的反应障碍大大降低。特别是在场强为 300 × 10-4 a.u. 时,与无场时相比,差异高达 22.4/18.3 kcal mol-1。此外,一旦 SiH4 中的 H 原子被甲基取代,就会出现两种反应模式,其中当 N2O 捕获附着在 Si 原子上的 H 原子,而不是附着在 C 原子上时,脱氧过程更容易。此外,还考虑了脱氧反应的溶剂效应,但得到的影响较弱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Deoxygenation reactions of nitrous oxide assisted by oriented external electric field

Due largely to the high stability and the potential ozone-depleting, the transformation of greenhouse gas nitrous oxide has gained much attentions. In present paper, a new insight into the deoxygenation of nitrous oxide with silane was reported by using oriented external electric field (OEEF) as a catalytic strategy. When the OEEF was employed, the reaction barrier of deoxygenation was marvelously decreased as it was oriented along the positive NO/OSi bond-axis. Especially the field strength is 300 × 10−4 a.u., the differences are up to 22.4/18.3 kcal mol−1 as compared with that of nonfield. In addition, once the H atom in SiH4 was replaced by methyl, two reaction modes were obtained, in which the deoxygenation process was easier when the N2O captured the H atom attached to the Si atom, not attached to the C atom. Further, the solvent effects of deoxygenation reaction were also considered, but with a weak influence were obtained.

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来源期刊
International Journal of Quantum Chemistry
International Journal of Quantum Chemistry 化学-数学跨学科应用
CiteScore
4.70
自引率
4.50%
发文量
185
审稿时长
2 months
期刊介绍: Since its first formulation quantum chemistry has provided the conceptual and terminological framework necessary to understand atoms, molecules and the condensed matter. Over the past decades synergistic advances in the methodological developments, software and hardware have transformed quantum chemistry in a truly interdisciplinary science that has expanded beyond its traditional core of molecular sciences to fields as diverse as chemistry and catalysis, biophysics, nanotechnology and material science.
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