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速率控制程度:中间体和过渡态的能量对速率的控制程度。

Degree of rate control: how much the energies of intermediates and transition states control rates.

作者信息

Stegelmann Carsten, Andreasen Anders, Campbell Charles T

机构信息

Department of Chemistry and Applied Engineering Science, Aalborg University, Niels Bohrs Vej 8 6700 Esbjerg, Denmark.

出版信息

J Am Chem Soc. 2009 Jun 17;131(23):8077-82. doi: 10.1021/ja9000097.

Abstract

For many decades, the concept of a "rate-determining step" has been of central importance in understanding chemical kinetics in multistep reaction mechanisms and using that understanding to advantage. Yet a rigorous method for identifying the rate-determining step in a reaction mechanism was only recently introduced, via the "degree of rate control" of elementary steps. By extending that idea, we argue that even more useful than identifying the rate-determining step is identifying the rate-controlling transition states and the rate-controlling intermediates. These identify a few distinct chemical species whose relative energies we could adjust to achieve a faster or slower net reaction rate. Their relative energies could be adjusted by a variety of practical approaches, such as adding or modifying a catalyst, modifying the solvent, or simply modifying a reactant's molecular structure to affect electronic or steric control on the relative energies of the key species. Since these key species are the ones whose relative energies most strongly influence the net reaction rate, they also identify the species whose energetics must be most accurately measured or calculated to achieve an accurate kinetic model for any reaction mechanism. Thus, it is very important to identify these rate-controlling transition states and rate-controlling intermediates for both applied and basic research. Here, we present a method for doing that.

摘要

几十年来,“速率决定步骤”的概念在理解多步反应机理中的化学动力学并利用这种理解发挥优势方面一直至关重要。然而,一种用于确定反应机理中速率决定步骤的严格方法直到最近才通过基元步骤的“速率控制程度”被引入。通过扩展这一概念,我们认为,识别速率控制过渡态和速率控制中间体比识别速率决定步骤更有用。这些识别出一些不同的化学物种,我们可以调整它们的相对能量以实现更快或更慢的净反应速率。它们的相对能量可以通过多种实际方法进行调整,例如添加或改性催化剂、改性溶剂,或者简单地改性反应物的分子结构以影响对关键物种相对能量的电子或空间控制。由于这些关键物种是其相对能量对净反应速率影响最强烈的物种,它们也识别出为任何反应机理建立准确动力学模型时其能量必须最准确测量或计算的物种。因此,识别这些速率控制过渡态和速率控制中间体对于应用研究和基础研究都非常重要。在此,我们提出一种实现此目的的方法。

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