催化作用
对偶(语法数字)
聚碳酸酯
化学
动能
高分子化学
材料科学
组合化学
有机化学
物理
量子力学
艺术
文学类
作者
Zhiyu Chen,Guan‐Wen Yang,Tianhao Wu,Zizhao Qian,Guang‐Peng Wu
标识
DOI:10.1021/acs.macromol.4c02912
摘要
Biomimetic catalysis is extensively used in chemical synthesis targeting to achieve satisfactory reactivities. However, artificial catalysts possessing outstanding sequence controllability over macromolecular structures that could be precisely achieved in nature remain scarce, especially in the preparation of complex macromolecules featuring kinetically trapped structures. Herein, we report a dual biomimetic catalyst design for precise sequence regulation in kinetically controlled CO2/epoxide copolymerization. The as-synthesized dissymmetric organoboron catalysts possess dissymmetric catalysis microenvironments, which differentiate the transfer rates of polymer alkoxy anions between the two boron centers, thus enabling precise sequence regulation. Consequently, a high −ABB–/–AB– ratio of 92% was achieved, up to 3.3 times that of analogous symmetric catalysts (Nat. Synth. 2022, 1, 892–901). Detailed mechanistic studies reveal that dual kinetic modulations are responsible for sequence regulation. This catalyst design tactic should inspire effective catalyst designs for precise chemical transformations.
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