五元环酰胺或内酰胺直接和水介导的同分异构反应动力学

IF 1.5 4区 化学 Q4 CHEMISTRY, PHYSICAL International Journal of Chemical Kinetics Pub Date : 2024-03-26 DOI:10.1002/kin.21722
Judith Würmel, John M. Simmie
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引用次数: 0

摘要

作为亚胺酸-酰胺类氢原子转移或同分异构反应系列研究的一部分,我们报告了一组 24 个五元环状化合物在低温(50-300 K)和高温(500-1500 K)下的速率常数。这些速率常数既适用于高温下的直接反应,也适用于在低温下通过额外水分子促进氢转移反应的反应。在后一种情况下,我们发现在低至 50 K 的温度下,反应前复合物的反应速率可以在 1 毫秒的时间尺度上迅速变化,并且由量子力学效应主导,这是由小曲率和定量反应态隧道法评估得出的。此外,我们还展示了这些未知物种的热化学数据,如形成焓、熵、等压热容和焓函数,这些物种涵盖了从吡咯烷酮到氧化四唑的一系列化合物。
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Kinetics of direct and water-mediated tautomerization reactions of five-membered cyclic amides or lactams

As part of a series of studies of hydrogen-atom transfer or tautomerization reactions of imidic acid–amide species, H O C N O C N H ${\rm H\bond O\dbond C\bond N\bond} \rightleftharpoons {\rm O\dbond C\bond N\bond H}$ , we report the rate constants for a set of 24 five-membered cyclic compounds at low, 50–300 K, and high, 500–1500 K, temperatures. These rate constants are for both the high temperature direct reaction and for that mediated by an additional water molecule which facilitates the hydrogen transfer reaction at low temperatures. In the latter case we show that the rate of reaction from a pre-reaction complex can be rapid at temperatures down to 50 K on a 1 ms timescale and is dominated by quantum mechanical effects as evaluated by small-curvature and quantised-reaction-states tunnelling. In addition, we present thermochemical data such as enthalpies of formation, entropies, isobaric heat capacities and enthalpy functions for these largely unknown species which span a range of compounds from pyrolidinone to oxo-tetrazoles.

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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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