Huang Hao-Yi, Ren Bai-Hao, Xie Min, Huang Yu-Ting, Li Kun, Cai Zhongzheng, Lu Xiao-Bing, Zhu Jian-Bo
National Engineering Laboratory of Eco-Friendly Polymeric Materials (Sichuan) College of Chemistry, Sichuan University, 29 Wangjiang Rd, Chengdu, 610064, P. R. China.
State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian, 116024, P. R. China.
Angew Chem Int Ed Engl. 2025 Feb 10;64(7):e202419494. doi: 10.1002/anie.202419494. Epub 2025 Jan 7.
Polyhydroxyalkanoates (PHAs) have attracted broad interest as promising sustainable materials to address plastic pollution and resource scarcity. However, the chemical synthesis of stereoregular PHAs via ring-opening polymerization (ROP) has long been an elusive endeavor. In this contribution, we exploited a robust spiro-salen yttrium complex (Y3) as the catalyst to successfully prepare syndiotactic PHAs with diverse pendent groups. Simply altering the ratio of enantiomeric catalysts allowed to access of PHAs with diverse syndiotacticity (P=0.5-0.99, from sticky oil to tough materials), delivering tunable thermal properties (glass transition temperature, T from -52 to 70 °C and melting transition temperature, T from 38 to 223 °C). A combined experimental and computational study suggested a polymeric exchange mechanism could boost the polymerization activity and control the syndioselectivity.
聚羟基脂肪酸酯(PHAs)作为解决塑料污染和资源短缺问题的可持续材料,已引起广泛关注。然而,通过开环聚合(ROP)化学合成立构规整的PHAs长期以来一直是一项难以实现的努力。在本研究中,我们利用一种强大的螺环-双水杨醛亚胺钇配合物(Y3)作为催化剂,成功制备了具有不同侧基的间同立构PHAs。简单地改变对映体催化剂的比例,就可以获得具有不同间同立构规整度(P = 0.5 - 0.99,从粘性油到坚韧材料)的PHAs,其热性能可调(玻璃化转变温度,T从 -52到70°C,熔点转变温度,T从38到223°C)。实验和计算相结合的研究表明,一种聚合物交换机制可以提高聚合活性并控制间同选择性。