Simonovsky Felix I, Porter Stephen C, Ratner Buddy D
Department of Bioengineering, University of Washington, P.O. Box 351720, Seattle, WA 98195-1720, USA.
J Biomater Sci Polym Ed. 2005;16(2):267-84. doi: 10.1163/1568562053115462.
A series of linear and branched functionalized high-molecular-weight segmented poly (ether urethane)s and poly(ether urethane urea)s were prepared by chain-extending isocyanate pre-polymers based on poly(tetramethylene oxide) with molecular weight 1000 and 4,4'-diphenylmethane diisocyanate. Different functional groups were incorporated within the polymer backbone or on side-chains by using several chain extenders during the synthesis: glycerol, 2,2-bis (hydroxymethyl) propionic acid, 1H, 1H,2H,3H,3H-perfluoroundecane-1,2-diol, 1H,1H,8H,8H-dodecanefluoro-1,8-octanediol, 1,3-diamino-2-hydroxypropane and 3,5-diaminobenzoic acid, using the method of gradual approach to stoichiometry. In some cases, pendant functional groups were used as reactive sites for the further attachment of side groups. Polymers were characterized using 1H-NMR and FT-IR spectroscopies and GPC in conjunction with chemical structural confirmation by a model compound comparison study of 4,4'-diphenylmethane diisocyanate or trifluoro-p-tolyl isocyanate reacted with 1,3-diamino-2-hydroxypropane and 1,4-butanediol.
通过用分子量为1000的聚四氢呋喃和4,4'-二苯基甲烷二异氰酸酯扩链异氰酸酯预聚物,制备了一系列线性和支化的功能化高分子量嵌段聚(醚脲)和聚(醚脲脲)。在合成过程中,通过使用几种扩链剂将不同的官能团引入聚合物主链或侧链:甘油、2,2-双(羟甲基)丙酸、1H,1H,2H,3H,3H-全氟十一烷-1,2-二醇、1H,1H,8H,8H-十二氟-1,8-辛二醇、1,3-二氨基-2-羟基丙烷和3,5-二氨基苯甲酸,采用逐步接近化学计量的方法。在某些情况下,侧基官能团用作进一步连接侧基的反应位点。通过1H-NMR和FT-IR光谱以及GPC对聚合物进行了表征,并通过4,4'-二苯基甲烷二异氰酸酯或三氟对甲苯基异氰酸酯与1,3-二氨基-2-羟基丙烷和1,4-丁二醇反应的模型化合物比较研究进行了化学结构确认。