School of Materials Science and Engineering, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Sun Yat-Sen University, Guangzhou 510006, China.
Department of Polymeric Materials, School of Materials Science and Engineering, Tongji University, Shanghai 201804, China.
ACS Macro Lett. 2023 Jun 20;12(6):794-800. doi: 10.1021/acsmacrolett.3c00284. Epub 2023 May 25.
Ring-opening metathesis polymerization (ROMP) in an aqueous medium provides an important environmentally friendly platform for the preparation of water-soluble polymeric materials. However, it is challenging to keep high synthetic efficacy and good control over molecular weight and distribution due to the inevitable catalyst decomposition in an aqueous medium. To meet this challenge, we propose a facile monomer emulsified aqueous ROMP (ME-ROMP) by injecting a tiny amount of a CHCl solution of the Grubbs' third-generation catalyst (G3) into the aqueous solution of norbornene (NB) monomers without deoxygenation. Driven by the minimization of interfacial tension, the water-soluble monomers could serve as surfactants with hydrophobic NB moieties inserted into the CHCl droplets of G3, leading to the significantly suppressed catalyst decomposition and accelerated polymerization. The ME-ROMP is confirmed to be living with an ultrafast polymerization rate, near quantitative initiation and monomer conversion, for the highly efficient and ultrafast synthesis of well-defined water-soluble polynorbornenes with various compositions and architectures.
开环易位聚合(ROMP)在水相介质中为制备水溶性聚合材料提供了一个重要的环保平台。然而,由于催化剂在水相介质中不可避免的分解,保持高的合成效率和对分子量及分布的良好控制具有挑战性。为了应对这一挑战,我们提出了一种简便的单体乳化水相 ROMP(ME-ROMP)方法,即将少量的 Grubbs 第三代催化剂(G3)的 CHCl 溶液注入到没有脱氧的降冰片烯(NB)单体的水溶液中。在界面张力最小化的驱动下,水溶性单体可以作为表面活性剂,具有疏水性的 NB 部分插入到 G3 的 CHCl 液滴中,从而显著抑制了催化剂的分解并加速了聚合。ME-ROMP 被证实是活的,具有超快的聚合速率、接近定量的引发和单体转化率,可高效、快速地合成具有各种组成和结构的水溶性高定义的聚降冰片烯。