Design of polymer nanofiber systems for the immobilization of homogeneous catalysts -: Preparation and leaching studies

被引:40
作者
Stasiak, Michael
Roeben, Caren
Rosenberger, Nadine
Schleth, Florian
Studer, Armido
Greiner, Andreas
Wendorff, Joachim H.
机构
[1] Univ Marburg, Dept Chem, D-35032 Marburg, Germany
[2] Univ Munster, Inst Organ Chem, D-48149 Munster, Germany
关键词
nanofibers; controlled radical polymerization; catalytic activity; FREE-RADICAL POLYMERIZATION; ORGANIC-SYNTHESIS; HOST SYSTEMS; FIBERS;
D O I
10.1016/j.polymer.2007.07.006
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this paper a novel general concept for the immobilization of catalysts is presented. It will be shown that catalysts covalently bound to low-molecular weight polystyrene (M-n > 4000 g/mol) can be immobilized into high molecular weight polystyrene nanofibers using the electro-spinning process. The immobilized catalyst-oligostyrene conjugates are well dispersed within the fibers as shown by DSC and X-ray studies. In DMSO, the oligostyrene tails of the catalysts suppress the leaching of the catalysts out of the fibers into the solution for thermodynamic reasons. Leaching studies are conducted using naphthalene-conjugated oligostyrenes using fluorescence spectroscopy. The naphthalene-polystyrene conjugates with defined molecular weight are readily prepared using nitroxide-mediated radical polymerization (NMP). As a model catalyst system, proline-poly styrene conjugates are synthesized by NMP to study catalyst leaching out of the polystyrene nanofibers used as a catalyst matrix. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5208 / 5218
页数:11
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