Department of Polymer Science and Engineering and State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai 200240, P. R. China.
ACS Appl Mater Interfaces. 2011 Mar;3(3):898-909. doi: 10.1021/am101258k. Epub 2011 Mar 7.
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.
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。