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一种用于评估催化循环的动力学-量子力学联合模型:应用于交叉偶联反应和Heck反应。

A combined kinetic-quantum mechanical model for assessment of catalytic cycles: application to cross-coupling and Heck reactions.

作者信息

Kozuch Sebastian, Shaik Sason

机构信息

Department of Organic Chemistry and The Lise Meitner-Minerva Center for Computational Quantum Chemistry, Givat Ram Campus, Jerusalem 91904, Israel.

出版信息

J Am Chem Soc. 2006 Mar 15;128(10):3355-65. doi: 10.1021/ja0559146.

Abstract

The efficiency of catalytic cycles is measured by their turnover frequency (TOF). The degree of TOF control determines which states contribute most to the rate of the cycle, and thus indicates the steps that have the highest impact on the cycle. A kinetic model developed by Christiansen (Christiansen, J. A. Adv. Catal. 1953, 5, 311) for catalytic cycles is implemented here in a form that utilizes state energies. This enables one to assess the efficiency of quantum mechanically computed catalytic cycles like the palladium-catalyzed cross-coupling and Heck reactions, to test alternative hypotheses, and to make some predictions. This implementation can also account for effects such as Sabatier's volcano curve for heterogeneous catalysis. The model leads to a dependence of the TOF for any cycle on the "corrected" energy span quantity, deltaE, whose precise expression depends on the location of the summit and trough of the cycle in the step sequence of the cycle. Thus, knowing the highest energy transition state, the most abundant reaction intermediate, and the reaction energy enables one to make quick predictions about relative efficiency of cycles. At the same time, the degree of TOF control determines which states contribute most to the rate of reaction, and thus indicates the values to be included in the calculation of the energetic span and the steps that may be tinkered with to improve the cycle.

摘要

催化循环的效率通过其周转频率(TOF)来衡量。TOF的控制程度决定了哪些状态对循环速率的贡献最大,从而表明了对循环影响最大的步骤。克里斯蒂安森(Christiansen, J. A. Adv. Catal. 1953, 5, 311)为催化循环建立的动力学模型在此以利用状态能量的形式实现。这使得人们能够评估量子力学计算的催化循环(如钯催化的交叉偶联反应和赫克反应)的效率,检验替代假设,并做出一些预测。这种实现方式还可以考虑诸如多相催化的萨巴蒂尔火山曲线等效应。该模型导致任何循环的TOF依赖于“校正”后的能量跨度量δE,其精确表达式取决于循环在其步骤序列中的峰顶和谷底的位置。因此,知道最高能量的过渡态、最丰富的反应中间体和反应能量,就能快速预测循环的相对效率。同时,TOF的控制程度决定了哪些状态对反应速率的贡献最大,从而表明在能量跨度计算中应包含的值以及为改善循环可能需要调整的步骤。

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