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当TPAP被限制在混合氟化硅基质中时,其在超临界二氧化碳中进行氧化催化的活性依据。

The grounds for the activity of TPAP in oxidation catalysis in supercritical carbon dioxide when confined in hybrid fluorinated silica matrices.

作者信息

Fidalgo Alexandra, Ciriminna Rosaria, Ilharco Laura M, Campestrini Sandro, Carraro Massimo, Pagliaro Mario

机构信息

Centro de Química-Física Molecular, Instituto Superior Técnico, Complexo I, Av. Rovisco Pais 1, 1049-001, Lisboa, Portugal.

出版信息

Phys Chem Chem Phys. 2008 Apr 21;10(15):2026-32. doi: 10.1039/b716405j. Epub 2008 Jan 31.

Abstract

Fluorinated organo-silica gels doped with tetra-n-propylammonium perruthenate (TPAP) are excellent catalysts for the aerobic oxidative dehydrogenation of alcohols in supercritical CO2 (scCO2). Their activity and stability are subtly dictated by structure, depending on the degree of fluorination and on the length of the fluoroalkyl chain linked to the silica network. Such dependence reflects the hydrophilic-hydrophobic balance (HHB) of the matrix, as evaluated by diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy. The remarkable correlation between the materials' HHB and reactivity provides a finding of general validity for reaction-controlled mechanisms, which opens the route to the synthesis of second generation sol-gel entrapped catalysts for the production of fine chemicals in scCO2.

摘要

掺杂四正丙基铵高钌酸盐(TPAP)的氟化有机硅胶是超临界二氧化碳(scCO2)中醇类有氧氧化脱氢反应的优良催化剂。它们的活性和稳定性受结构的微妙影响,这取决于氟化程度以及与二氧化硅网络相连的氟代烷基链的长度。通过漫反射红外傅里叶变换(DRIFT)光谱评估,这种依赖性反映了基质的亲水-疏水平衡(HHB)。材料的HHB与反应性之间的显著相关性为反应控制机制提供了具有普遍有效性的发现,这为合成用于在scCO2中生产精细化学品的第二代溶胶-凝胶包封催化剂开辟了道路。

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