McGraw Michael L, Reilly Liam T, Clarke Ryan W, Cavallo Luigi, Falivene Laura, Chen Eugene Y-X
Department of Chemistry, Colorado State University, Fort Collins, CO 80523-1872, USA.
King Abdullah University of Science and Technology (KAUST), Physical Sciences and Engineering Division, KAUST Catalysis Center, Thuwal, 23955-6900, Saudi Arabia.
Angew Chem Int Ed Engl. 2022 Apr 4;61(15):e202116303. doi: 10.1002/anie.202116303. Epub 2022 Feb 19.
In typical cyclic polymer synthesis via ring-closure, chain growth and cyclization events are competing with each other, thus affording cyclic polymers with uncontrolled molecular weight or ring size and high dispersity. Here we uncover a mechanism by which Lewis pair polymerization (LPP) operates on polar vinyl monomers that allows the control of where and when cyclization takes place, thereby achieving spatial and temporal control to afford precision cyclic vinyl polymers or block copolymers with predictable molecular weight and low dispersity (≈1.03). A combined experimental and theoretical study demonstrates that cyclization occurs only after all monomers have been consumed (when) via conjugate addition of the propagating chain end to the specific site of the initiating chain end (where), allowing the cyclic polymer formation steps to be regulated and executed with precision in space and time.
在通过闭环进行的典型环状聚合物合成中,链增长和环化过程相互竞争,从而得到分子量、环尺寸不受控制且分散度高的环状聚合物。在此,我们揭示了一种路易斯对聚合(LPP)作用于极性乙烯基单体的机制,该机制能够控制环化发生的位置和时间,从而实现空间和时间上的控制,以得到具有可预测分子量和低分散度(≈1.03)的精确环状乙烯基聚合物或嵌段共聚物。一项结合实验和理论的研究表明,环化仅在所有单体被消耗后(时间)通过增长链端对引发链端特定位点的共轭加成(位置)发生,从而使环状聚合物的形成步骤能够在空间和时间上精确地调控和执行。