Spectroscopic and catalytic properties of SBA-15 molecular sieves functionalized with acidic and basic moieties

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• 作者：D. Srinivas ; P. Ratnasamy
• 关键词：Organo-functionalization of SBA-15 ; Immobilization of Mn complexes ; Functionalization with acidic and basic moieties ; Solid acid– ; base catalysts ; CO₂ utilization ; Cyclic carbonates synthesis ; Epoxidation ; Aerial oxidation of terpenes
• 刊名：Microporous and Mesoporous Materials
• 出版年：2007
• 期刊代码：78_13871811
• 类别：ch
• 出版时间：15 September 2007
• 卷：105
• 期：1-2
• 页码：170-180
• 文件大小：409 K

摘要

SBA-15, grafted with Lewis acidic Ti⁴⁺ ions and basic amines (imidazole, guanine or adenine) exhibited high catalytic activity in the cycloaddition of CO₂ to epoxides yielding selectively cyclic carbonate precursors of polycarbonates. In the second class of materials, the surface of SBA-15 was grafted with thiol or sulfonic acid functionalities. Mn(Salen)Cl was, then, covalently bound to these acidic groups. The resulting catalysts show enhanced chemo-, regio- and stereo-selective catalytic activity in the epoxidation of terpenes such as R-(+)-limonene, α-pinene and Δ-carene with molecular oxygen. The acid–base properties of these modified SBA-15 materials were investigated by temperature-programmed desorption and diffuse-reflectance infrared Fourier transform spectroscopy. Ammonia and pyridine were used as probe molecules for acidic sites and CO₂ for basic sites. Acidic Ti sites activated epoxides and the grafted basic amines activated CO₂. The simultaneous presence of both acidic and basic sites on amine/adenine-functionalized Ti-SBA-15 enabled synergistic enhancement in catalytic activity in the cycloaddition reaction of CO₂ to epoxides. When Mn(Salen)Cl was immobilized on thiol or sulfonic acid-functionalized SBA-15, the oxidation state of Mn decreased from +3 to +2. The organo-acidic functional groups (thiol or sulfonic acid) axially coordinated to Mn ions modified the electronic structure of Mn ions enhancing the activity and selectivity of Mn(Salen) complexes in aerial oxidation reactions.