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Stabilizing Single Sites on Solid Supports: Robust Grafted Ti(IV)-Calixarene Olefin Epoxidation Catalysts via Surface Polymerization and Cross-Linking

机译:稳定固相支持物上的单个位点:通过表面聚合和交联的稳健接枝的Ti(IV)-ar芳烃烯烃环氧化催化剂

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摘要

This manuscript develops a surface polymerization and cross-linking approach for the stabilization of single-site catalysts on solid surfaces, which is demonstrated here for grafted Ti(IV)-calixarene Lewis acids on silica. Our approach relies on cationic polymerization that is initiated by an adsorbed B(C_6F_5)_3 and uses styrene as the monomer and diisopropenylbenzene as the cross-linking agent. The mildness of this polymerization method is demonstrated by its lack of blocking micropores and only slight consumption of mesopore internal surface area on the basis of N2 physisorption data at 77 K, both of which are in contrast to previously reported surface-polymerization approaches. Catalysis of samples before and after polymerization and cross-linking was investigated with a probe reaction consisting of the epoxidation of 1-octene with tert-butyl hydroperoxide as oxidant, which is known to be catalyzed by Lewis-acid sites, and a comparison of catalyst hydrolytic stability was performed. Added water in the latter was used as a a trigger to induce site aggregation, as a stress test to determine the effectiveness of site protection by our polymerization approach. Consistent with the N2 physisorption data, catalysis data demonstrate that surface polymerization does not block small-molecule reactant and product access to Lewis-acid sites on the surface, since the conversion remains essentially unchanged before and after surface polymerization and cross-linking. DR UV–vis, TGA, and catalysis data reveal that the grafted Ti(IV)-calixarene sites on silica maintain their catalytic activity even after being treated with corrosive protic stress-test solution. In sharp contrast, grafted sites without the polymer layer leach nearly all of their calixarene and Ti contents during similar stress testing, resulting in the near complete loss of catalytic activity. We hypothesize that the surface polymer acts as a nanoreactor gatekeeper, which prevents the large Ti(IV)-calixarene site from leaching and keeps surface complexes as single sites grafted on the silica surface, by blocking access for the migration of sites from the surface to bulk solution.
机译:该手稿开发了一种表面聚合和交联方法,用于稳定固体表面上的单中心催化剂,在此证明了在硅胶上接枝Ti(IV)-杯芳烃路易斯酸的方法。我们的方法依赖于阳离子聚合反应,该反应由吸附的B(C_6F_5)_3引发,并使用苯乙烯作为单体,使用二异丙烯基苯作为交联剂。该聚合方法的温和性是基于77 K的N2物理吸附数据,没有封闭的微孔而仅消耗了中孔内表面积的少量,这与以前报道的表面聚合方法形成了鲜明的对比。用探针反应研究了样品在聚合和交联之前和之后的催化作用,该探针反应包括1-辛烯与叔丁基过氧化氢作为氧化剂的环氧化反应,已知该反应是由路易斯酸位催化的,并比较了催化剂进行水解稳定性。后者中添加的水被用作引发位点聚集的触发物,作为压力测试以确定通过我们的聚合方法进行位点保护的有效性。与N 2的物理吸附数据一致,催化数据表明表面聚合不会阻止小分子反应物和产物进入表面上的路易斯酸位点,因为在表面聚合和交联之前和之后转化率基本上保持不变。 DR UV-vis,TGA和催化数据表明,即使在经过腐蚀质子应力测试溶液处理后,二氧化硅上的接枝Ti(IV)-杯芳烃部位仍保持其催化活性。与之形成鲜明对比的是,在类似的应力测试中,没有聚合物层的接枝位点几乎浸出了所有杯芳烃和Ti含量,导致催化活性几乎完全丧失。我们假设表面聚合物充当纳米反应器的守门员,它阻止了大的Ti(IV)-杯芳烃位点的浸出,并通过阻止位点从表面迁移到二氧化硅表面而将表面复合物保持为接枝到二氧化硅表面的单个位点。批量解决方案。

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