催化作用
锆
星团(航天器)
化学
位阻效应
苯甲醇
环己烷
纳米晶
金属有机骨架
化学工程
无机化学
材料科学
有机化学
纳米技术
吸附
计算机科学
工程类
程序设计语言
作者
Jikson Pulparayil Mathew,Carlotta Seno,Mohit Jaiswal,Charlotte Simms,Nico Reichholf,Dietger Van den Eynden,Tatjana N. Parac‐Vogt,Jonathan De Roo
标识
DOI:10.1002/smsc.202400369
摘要
Oxo clusters are a unique link between oxide nanocrystals and Metal‐Organic Frameworks (MOFs), representing the limit of downscaling each of the respective crystals. Herein, the superior catalytic activity of clusters, compared to zirconium MOF UiO‐66 and nanocrystals is shown. Focus is on esterification reactions given their general importance in consumer products and the challenge of converting large substrates. Oxo clusters have a higher surface‐to‐volume ratio than nanocrystals, rendering them more active. For large substrates, for example, oleic acid, MOF UiO‐66 has negligible catalytic activity while clusters provide almost quantitative conversion, a fact we ascribe to limited diffusion of large substrates through the MOF pores. Clusters do not suffer from limited mass transfer and we also obtain high conversion in solvent‐free reactions with sterically hindered alcohols (hexanol, 2‐ethyl hexanol, benzyl alcohol, and neopentyl alcohol). The cluster catalyst can be recovered and shows identical activity when reused. The structural integrity of the cluster is confirmed using X‐ray total scattering and pair distribution function analysis. Moreover, when homogeneous zirconium alkoxides are used as catalysts, the same oxo cluster is retrieved, showing that oxo clusters are the active catalytic species, even in previously assumed homogeneously catalyzed reactions.
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