催化作用
化学
金属羰基
金属
合理设计
动能
组合化学
多相催化
动力学
有机化学
贵金属
动力学同位素效应
贵金属
反应机理
范围(计算机科学)
光化学
反应条件
计算化学
铂金
无机化学
催化加氢
标识
DOI:10.1002/slct.202505435
摘要
ABSTRACT Metal catalysts stand in the central position for carbonyl hydrogenation reactions. Comparison of catalyst activities and stabilities on different metal catalysts is ubiquitous and greatly beneficial to the design and screening of metal catalysts. For the sake of finding fundamental distinctions and further intensifying the design and screening process, a integrated and rational comparison from macrokinetics to microkinetics is highly required. In this article, we outline a general method of comparing intrinsic kinetics and avoiding pitfalls on different metal catalysts in carbonyl hydrogenation and then walk through the major aspects of comparison, such as intrinsic initial rates, initial deactivation profiles, apparent kinetics, kinetic isotope effects, reaction mechanism, and microkinetics. Finally, a case study on the integrated and rigorous kinetic comparison in carbonyl hydrogenation reactions over different noble metal catalysts is carried out. Overall, this article is expected not only to highlight the great importance of comprehensive and reasonable catalyst comparison for carbonyl hydrogenation but also to extend the scope of such comparison strategy further to other catalytic reactions and other types of solid catalysts for effective catalyst design and screening.
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