Li Yiwen, Dong Xue-Hui, Guo Kai, Wang Zhao, Chen Ziran, Wesdemiotis Chrys, Quirk Roderic P, Zhang Wen-Bin, Cheng Stephen Z D
Department of Polymer Science, College of Polymer Science and Polymer Engineering, ‡Department of Chemistry, The University of Akron, Akron, Ohio 44325-3909, United States.
Department of Polymer Science, College of Polymer Science and Polymer Engineering, Department of Chemistry, The University of Akron, Akron, Ohio 44325-3909, United States.
ACS Macro Lett. 2012 Jul 17;1(7):834-839. doi: 10.1021/mz300196x. Epub 2012 Jun 19.
A series of shape amphiphiles based on functionalized polyhedral oligomeric silsesquioxane (POSS) head tethered with two polymeric tails of symmetric or asymmetric compositions was designed and synthesized using sequential "grafting-from" and "click" surface functionalization. The monofunctionalization of octavinylPOSS was performed using thiol-ene chemistry to afford a dihydroxyl-functionalized POSS that was further derived into precisely defined homo- and heterobifunctional macroinitiators. Polymer tails, such as polycaprolactone and polystyrene, could then be grown from these POSS-based macroinitiators with controlled molecular weight via ring-opening polymerization and atom transfer radical polymerization (ATRP). The vinyl groups on POSS were found to be compatible with ATRP conditions. These macromolecular precursors were further modified by thiol-ene chemistry to install surface functionalities onto the POSS cage. The polymer chain composition and POSS surface chemistry can thus be tuned separately in a modular and efficient way.
基于功能化多面体低聚倍半硅氧烷(POSS)头部连接有对称或不对称组成的两条聚合物尾巴的一系列形状两亲物,通过连续的“接枝自”和“点击”表面功能化设计并合成。使用硫醇-烯化学对八乙烯基POSS进行单功能化,得到二羟基功能化的POSS,其进一步衍生为精确确定的均双功能和异双功能大分子引发剂。然后,诸如聚己内酯和聚苯乙烯之类的聚合物尾巴可以通过开环聚合和原子转移自由基聚合(ATRP)从这些基于POSS的大分子引发剂上以可控分子量生长。发现POSS上的乙烯基与ATRP条件兼容。这些大分子前体通过硫醇-烯化学进一步修饰,以在POSS笼上安装表面功能。因此,可以以模块化和高效的方式分别调节聚合物链组成和POSS表面化学。