Preparation and functionalization of (vinyl)polystyrene polyHIPE® -: Short routes to binding functional groups through a dimethylene spacer

被引:57
作者
Mercier, A
Deleuze, H [1 ]
Mondain-Monval, O
机构
[1] Univ Bordeaux 1, Chim Organ & Organomet Lab, CNRS, UMR 5802, F-33405 Talence, France
[2] Ctr Rech Paul Pascal, CNRS, UPR 8641, F-33600 Pessac, France
关键词
pendant vinyl groups; (vinyl)polystyrene polyHIPE (R); batch method; continuous flow method;
D O I
10.1016/S1381-5148(00)00040-7
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This paper describes the preparation and post-functionalization of an emulsion-derived polymeric foam, called polyHIPE(R), bearing pendant vinyl functionalities. The large pores and large channels of polyHIPE allow liquids and solvents to be driven through the molded monolith at very low pressure. In the presence of a free-radical initiator, compounds such as HBr and thiols underwent an anti-Markovnikov addition to the residual vinyl groups. Other reactions such as hydroboration with BH3 followed by hydrolysis with H2O2 have also been investigated. In this paper, a comparison between two ways of functionalization has been made: a 'batch' method, corresponding to diffusion of reactants through the pores of small cubes of polymers, and a 'continuous flow' method, forcing reactants to flow through the interconnected porous structure by applied low pressure. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:67 / 79
页数:13
相关论文
共 38 条
[1]   APPLICATION OF FUNCTIONALIZED POLYMERS IN ORGANIC-SYNTHESIS [J].
AKELAH, A ;
SHERRINGTON, DC .
CHEMICAL REVIEWS, 1981, 81 (06) :557-587
[2]  
AKELAH A, 1990, FUNCTIONALIZED POLYM
[3]   High internal phase emulsions (HIPEs) containing divinylbenzene and 4-vinylbenzyl chloride and the morphology of the resulting PolyHIPE materials [J].
Barbetta, A ;
Cameron, NR ;
Cooper, SJ .
CHEMICAL COMMUNICATIONS, 2000, (03) :221-222
[4]  
Barby D., 1982, European Patent, Patent No. [0060138, 0,060,138]
[5]  
BARTHOLIN M, 1981, MAKROMOL CHEM, V182, P2075
[6]   Hydroboration. VII. Directive effects in the hydroboration of olefins [J].
Brown, Herbert C. ;
Zweifel, George .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1960, 82 (17) :4708-4712
[7]   Synthesis and characterization of poly(aryl ether sulfone) PolyHIPE materials [J].
Cameron, NR ;
Sherrington, DC .
MACROMOLECULES, 1997, 30 (19) :5860-5869
[8]   Chemical modification of monolithic poly(styrene-divinylbenzene) PolyHIPE(R) materials [J].
Cameron, NR ;
Sherrington, DC ;
Ando, I ;
Kurosu, H .
JOURNAL OF MATERIALS CHEMISTRY, 1996, 6 (05) :719-726
[9]   RADICAL CHAIN REDUCTION OF ALKYL-HALIDES, DIALKYL SULFIDES AND O-ALKYL S-METHYL DITHIOCARBONATES TO ALKANES BY TRIALKYLSILANES [J].
COLE, SJ ;
KIRWAN, JN ;
ROBERTS, BP ;
WILLIS, CR .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1991, (01) :103-112
[10]   CHEMICAL MODIFICATION OF POLYSTYRENE RESINS - APPROACHES TO THE BINDING OF REACTIVE FUNCTIONALITIES TO POLYSTYRENE RESINS THROUGH A DIMETHYLENE SPACER [J].
DARLING, GD ;
FRECHET, JMJ .
JOURNAL OF ORGANIC CHEMISTRY, 1986, 51 (12) :2270-2276