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三(3,3,3-三氟丙基)倍半硅氧烷封端的聚(N-异丙基丙烯酰胺)遥爪聚合物:物理水凝胶的合成与行为。

Hepta(3,3,3-trifluoropropyl) polyhedral oligomeric silsesquioxane-capped poly(N-isopropylacrylamide) telechelics: synthesis and behavior of physical hydrogels.

机构信息

Department of Polymer Science and Engineering and State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai 200240, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2011 Mar;3(3):898-909. doi: 10.1021/am101258k. Epub 2011 Mar 7.

Abstract

Hepta(3,3,3-trifluoropropyl) polyhedral oligomeric silsesquioxane (POSS)-capped poly(N-isopropylacrylamide) (PNIPAAm) telechelics with variable lengths of PNIPAAm midblocks were synthesized by the combination of reversible addition-fragmentation chain transfer polymerization (RAFT) and the copper-catalyzed Huisgen 1,3-cycloaddition (i.e., click chemistry). The POSS-capped trithiocarbonate was synthesized and used as the chain transfer agent for the RAFT polymerization of N-isopropylacrylamide. The organic-inorganic amphiphilic telechelics were characterized by means of nuclear magnetic resonance spectroscopy (NMR) and gel permeation chromatography (GPC). Atomic force microscopy (AFM) shows that all the POSS-capped PNIPAAm telechelics exhibited microphase-separated morphologies, in which the POSS terminal groups were self-assembled into the microdomains and dispersed into the continuous PNIPAAm matrices. The POSS nanodomains could behave as the physical cross-linking sites and as a result the physical hydrogels were formed while these POSS-capped PNIPAAm telechelics were subjected to the solubility tests with water. These physical hydrogels possessed well-defined volume phase transition phenomena and displayed rapid reswelling and deswelling thermoresponsive behavior compared to control PNIPAAm hydrogel.

摘要

具有不同长度的聚(N-异丙基丙烯酰胺)(PNIPAAm)中间嵌段的七(3,3,3-三氟丙基)笼型倍半硅氧烷(POSS)封端的聚(N-异丙基丙烯酰胺)遥爪聚合物是通过可逆加成-断裂链转移聚合(RAFT)和铜催化的 Huisgen 1,3-环加成(即点击化学)的组合合成的。合成了 POSS 封端的三硫代碳酸酯,并将其用作 RAFT 聚合 N-异丙基丙烯酰胺的链转移剂。通过核磁共振波谱(NMR)和凝胶渗透色谱(GPC)对 POSS 封端的两亲性遥爪聚合物进行了表征。原子力显微镜(AFM)表明,所有 POSS 封端的 PNIPAAm 遥爪聚合物都表现出微相分离形态,其中 POSS 端基自组装成微区并分散在连续的 PNIPAAm 基质中。POSS 纳米区可以作为物理交联点,因此当这些 POSS 封端的 PNIPAAm 遥爪聚合物进行与水的溶胀测试时,形成了物理水凝胶。与对照的 PNIPAAm 水凝胶相比,这些物理水凝胶具有明确定义的体积相转变现象,并表现出快速的再溶胀和去溶胀的温度响应行为。

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