Simultaneous hypercrosslinking and functionalization of polyHIPEs for use as coarse powder catalyst supports

被引:13
作者
Barkan-Ozturk, Hande [1 ]
Menner, Angelika [1 ]
Bismarck, Alexander [1 ,2 ]
Woodward, Robert T. [1 ]
机构
[1] Univ Vienna, Fac Chem, Inst Mat Chem & Res, Polymer & Composite Engn PaCE Grp, Wahringer Str 42, A-1090 Vienna, Austria
[2] Imperial Coll London, Dept Chem Engn, South Kensington Campus, London SW7 2AZ, England
关键词
Emulsion templating; polyHIPEs; Hierarchical porous polymers; Hypercrosslinking; Heterogeneous catalyst support; Suzuki-Miyaura reaction; MICROPOROUS ORGANIC POLYMERS; MIYAURA COUPLING REACTIONS; INTERNAL PHASE EMULSIONS; SURFACE-AREA; RECYCLABLE CATALYST; LINKED POLYSTYRENE; NETWORK POLYMERS; PALLADIUM; POLYMERIZATION; MONOLITHS;
D O I
10.1016/j.ces.2022.118151
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Porous polymers offer desirable properties for heterogeneous catalysis, such as excellent stability, high active site density, and reusability. However, their synthesis is often complicated, requiring expensive reagents and laborious synthetic processes. We produce organophosphorus functionalized polyHIPEs by the polymerization of particle and surfactant stabilized water-in-styrene/divinylbenzene high internal phase emulsion templates, followed by post-functionalization using low-cost hypercrosslinking strate-gies. Three hypercrosslinking approaches were investigated, including knitting with an external crosslin-ker, solvent stitching and Scholl coupling reaction. Each approach's ability to simultaneously create micro/mesoporosity and incorporate organophosphorus moieties into the polyHIPE structure as catalyst anchor sites were assessed, introducing surface areas of up to 410 m2/g and phosphorus concentrations of up to 7.4 wt%. After Pd-loading, the polyHIPEs displayed outstanding catalytic performance in a Suzuki-Miyaura coupling reaction, reaching turnover frequencies of 5722 h-1. The coarse powder form of the polyHIPEs allowed for simple catalyst recovery from the reaction mixture for reuse. (c) 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页数:10
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