Systematic study on the hydrogen abstraction reactions from oxygenated compounds by H and HO2

IF 1.6 4区 化学 Q4 CHEMISTRY, PHYSICAL International Journal of Chemical Kinetics Pub Date : 2024-11-04 DOI:10.1002/kin.21761
Hiroki Oppata, Daisuke Shimokuri, Akira Miyoshi
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Abstract

To extend the rule-based approach for hydrogen abstraction reactions from oxygenated compounds, a systematic investigation was performed to examine the reactivity of gas-phase hydrogen abstraction reactions from alkyl groups (methyl and ethyl groups) bound to oxygen atoms in five types of oxygenated compounds (alcohols, ethers, formate esters, acetate esters, and carbonate esters) by H atoms and HO2 radicals comprehensively considering rotational conformers. Quantum chemical calculations were conducted at the CBS-QB3 level for stationary points. Rate constants were determined employing conventional transition state theory (TST). For hydrogen abstraction reactions by H, the rotational conformer distribution partition function was employed to approximate partition functions, owing to the similarity in vibrational energy-level structures among conformers. In hydrogen abstraction reactions by HO2, the vibrational structures of transition-state (TS) conformers varied significantly due to the hydrogen bonding, leading to an inappropriate evaluation of rate constants when using the lowest-energy conformer as a representative. Therefore, the rate constants were calculated by the multi-structural TST. It was revealed that the differences in functional groups containing O atoms mainly affect the bond dissociation energies of the C–H bonds and the activation energies of hydrogen abstraction reactions only when the C atoms are adjacent to the O atoms. Additionally, it was found that hydrogen bonds formed in the TSs show minor effect on rate parameters for the overall rate constants, apart from the reduction of the pre-exponential factors for the H-abstraction reactions from the methylene position of ethyl groups. The comparison with the rate constants from previous studies showed reasonable results, indicating that the rate constants in this study, which thoroughly consider rotational conformers, can be the current best estimates.

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H和HO2对含氧化合物吸氢反应的系统研究
为了扩展基于规则的含氧化合物吸氢反应方法,系统研究了5种含氧化合物(醇类、醚类、甲酸酯类、乙酸酯类和碳酸酯类)中烃基(甲基和乙基)与氧原子结合的气相吸氢反应的H原子和HO2自由基的反应活性,并综合考虑了旋转构象。在CBS-QB3水平上对稳态点进行量子化学计算。采用传统的过渡态理论(TST)确定速率常数。对于H吸氢反应,由于各构象的振动能级结构相似,采用旋转构象分布配分函数来近似配分函数。在HO2吸氢反应中,由于氢键的作用,过渡态(TS)构象的振动结构发生了很大的变化,导致以能量最低的构象为代表计算速率常数的方法不正确。因此,采用多结构TST计算速率常数。结果表明,含O官能团的差异主要影响C - h键的键解离能和吸氢反应的活化能,只有当C原子与O原子相邻时才有影响。此外,除了从乙基亚甲基位置提取h的指数前因子降低外,TSs中形成的氢键对总速率常数的速率参数影响较小。与以往研究的速率常数比较,结果合理,表明本研究中充分考虑了旋转构象的速率常数是目前最好的估计。
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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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