烷烃ch活化机理:5/6效应、单因素补偿效应、最强反应物、最早过渡态。希洛夫反应的谜题

IF 5.062
Elisey S. Rudakov
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引用次数: 5

摘要

综述了作者在水介质和酸性介质中烷烃活化动力学和机理的研究成果,包括理论和实验方法。介绍了“CH活化的直接动力学研究”、“可见和隐试剂预活化”、“最强反应物和最早过渡态”(ETS)、“5/6效应”( - c5h10 / - c6h12对中CH键分裂速率恒定的比率)、“单因素补偿效应”(SCE)和“精细补偿温度”等新概念。补偿效应(CE)在现实中是存在的,但有必要排除影响因素,例如从速率常数到5/6效应,以观察其最纯粹的形式。以5/6-CE组合为例,SCE是研究ch活化机理的新工具。结果表明,水溶液(PtII、MnO4−、HMnO4、HOCl、HOONO、HVO2 - RuIV、OH、SO4−)和硫酸(PdII、HgII、CrO3、MnIII、CoIII、NO2+、OH+、1-adamantyl阳离子、C14H11+、СН2OH+、SO3H+)中各试剂的温度随温度变化呈(5/6)关系。影响(5/6)值的唯一因素是C5和C6环的构象应变差,在一系列一型反应中,构象应变差随试剂活性的增加而减小。揭示了四种机制:h原子被阴离子(I−)、不带电(I0)和阳离子(I+)氧中心的“o -反应物”抽离,以及亲电阳离子碱加合物(II+)的CH键双功能结合。发现了这些基团的各种SCE线(熵变与焓变)。它们汇聚成一个“SCE极”(ETS的第一个例子)。讨论了这些机理的特点、PtII、PdII、HgII酸配合物作为试剂的差异以及希洛夫反应物PtIICl3(H2O)与水中OH自由基惊人的相似性。在各种过程中产生能谱的一般原因可能是粒子间相互作用热力学中的补偿效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mechanisms of alkane CH-activation: The 5/6 effect, single-factor compensation effect, strongest reactant and earliest transition state. A puzzle of Shilov reaction

Mechanisms of alkane CH-activation: The 5/6 effect, single-factor compensation effect, strongest reactant and earliest transition state. A puzzle of Shilov reaction

The results on the investigation of alkane activation kinetics and mechanisms in aqueous and acidic media, including theoretical and experimental approaches to the problem, proposed by the author are summarized. The new concepts are introduced: a “direct kinetic study of CH activation”, “visible and hidden reagent preactivation”, the “strongest reactant and earliest transition state” (ETS), the “5/6 effect” (the ratio of CH bonds splitting constant rates in the с-C5H10/с-C6H12 couple), “single-factor compensation effect” (SCE), and a “refined compensation temperature”. The compensation effect (CE) exists in reality, but it is necessary to exclude the influence side factors, for example, to go from rate constants to the 5/6 effect to observe its purest form. The 5/6-CE combination as an example SCE is a new instrument for studying CH-activation mechanisms. Temperature dependences of (5/6) values for the reagents in aqueous solution (PtII, MnO4, HMnO4, HOCl, HOONO, HVO2 – RuIV, OH, SO4) and sulfuric acid (PdII, HgII, CrO3, MnIII, CoIII, NO2+, OH+, 1-adamantyl cation, C14H11+, СН2OH+, SO3H+) are found. The only influencing factor on the (5/6) value is conformational strain difference in the C5 and C6 rings, which in a series of one-type reactions decreases with increasing the reagent activity. Four mechanisms are revealed: H-atom abstraction by anionic (I), uncharged (I0) and cationic (I+) oxygen-centered “O-reactants”, and a bifunctional incorporation into CH bond of electrophilic cation – base adduct (II+). Various SCE lines (the entropy change versus enthalpy changing) for these groups are found. They converge in a “SCE pole” (the first example of ETS). Features of these mechanisms, differences of PtII, PdII, HgII acidocomplexes as the reagents and a surprising similarity between the Shilov reactant PtIICl3(H2O) and OH radicals in the water are discussed. The probable general cause of CEs in various processes is compensation effects in thermodynamics of interparticle interactions.

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2.8 months
期刊介绍: The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.
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