Yavuz Erdem, Cherkasov Nikolay, Degirmenci Volkan
School of Engineering, University of Warwick Coventry CV4 7AL UK
Istanbul Technical University, Department of Chemistry, Faculty of Science 34469 Maslak Istanbul Turkey.
RSC Adv. 2019 Mar 12;9(15):8175-8183. doi: 10.1039/c9ra01053j.
The polyHIPE catalysts based on styrene, vinyl benzyl chloride, and divinylbenzene co-polymerisation were functionalised with carboxylic and tertiary amine groups. Catalyst characterisation showed covalent bonding of the graft polymers. The macroporous and highly interconnected structure of polyHIPEs allows isolation of the acid and base functional groups and allows the presence of these otherwise incompatible functionalities on the same catalyst. The functionalised polyHIPE catalysts were shown to perform two reactions; (i) acid-catalysed acetal hydrolysis and (ii) base-catalysed Knoevenagel condensation in one-pot with 97% yield. The yield obtained is substantially higher than that observed with the homogeneous or resin polymer type catalysts due to the compartmentalisation of the active sites and improved mass transfer through the open porous polyHIPE structure.
基于苯乙烯、乙烯基苄基氯和二乙烯基苯共聚的聚HIPE催化剂用羧基和叔胺基团进行了官能化。催化剂表征显示接枝聚合物的共价键合。聚HIPE的大孔和高度互连结构允许酸和碱官能团的隔离,并允许在同一催化剂上存在这些原本不相容的官能团。官能化的聚HIPE催化剂被证明能进行两种反应:(i)酸催化的缩醛水解和(ii)碱催化的Knoevenagel缩合,一锅法产率为97%。由于活性位点的分隔以及通过开放多孔聚HIPE结构改善了传质,所获得的产率大大高于均相或树脂聚合物型催化剂所观察到的产率。