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影响钴氢化物形成动力学的反应参数:对基准析氢催化剂的意义。

Reaction Parameters Influencing Cobalt Hydride Formation Kinetics: Implications for Benchmarking H(2)-Evolution Catalysts.

机构信息

Department of Chemistry, University of North Carolina , Chapel Hill, North Carolina 27599-3290, United States.

出版信息

J Am Chem Soc. 2017 Jan 11;139(1):239-244. doi: 10.1021/jacs.6b10148. Epub 2016 Dec 20.

Abstract

The need for benchmarking hydrogen evolution catalysts has increasingly been recognized. The influence of acid choice on activity is often reduced to the overpotential for catalysis. Through the study of a stable cobalt hydride complex, we demonstrate the influence of acid choice, beyond pK, on the kinetics of hydride formation. A linear free energy relationship between acid pK and second-order rate constants is observed for weaker acids. For stronger acids, however, further increases in pK do not correlate to increases in rate constants. Further, steric bulk around the acidic proton is shown to influence rate constants dramatically. Together, these observations reveal the complex factors dictating catalyst performance.

摘要

基准测试析氢催化剂的需求日益受到重视。通常情况下,人们会将酸的选择对活性的影响简化为催化的过电位。通过对稳定的钴氢化物配合物的研究,我们证明了酸的选择(超出 pK 值)对氢化物形成动力学的影响。观察到酸的 pK 值与二级速率常数之间存在线性自由能关系,适用于较弱的酸。然而,对于更强的酸,pK 值的进一步增加与速率常数的增加并不相关。此外,酸性质子周围的空间位阻对速率常数有显著影响。综上所述,这些观察结果揭示了决定催化剂性能的复杂因素。

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