聚苯乙烯
共价键
马来酰亚胺
化学
连接器
催化作用
肽
组合化学
钴
辅因子
水溶液
单层
高分子化学
聚合物
有机化学
酶
生物化学
计算机科学
操作系统
作者
Dong Wang,Aaron A. Ingram,Julian Luka,Maochao Mao,Leon Ahrens,Marian Bienstein,Thomas P. Spaniol,Ulrich Schwaneberg,Jun Okuda
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-01-22
卷期号:63 (13): e202317419-e202317419
被引量:6
标识
DOI:10.1002/anie.202317419
摘要
A typical component of polymer waste is polystyrene (PS) used in numerous applications, but degraded only slowly in the environment due to its hydrophobic properties. To increase the reactivity of polystyrene, polar groups need to be introduced. Here, biohybrid catalysts based on the engineered anchor peptide LCI_F16C are presented, which are capable of attaching to polystyrene microparticles and hydroxylating benzylic C-H bonds in polystyrene microparticles using commercially available oxone as oxidant. LCI peptides achieve a dense surface coverage of PS through monolayer formation within minutes in aqueous solutions at ambient temperature. The catalytically active cobalt cofactor Co-L1 or Co-L2 with a modified NNNN macrocyclic TACD ligand (TACD=1,4,7,10-tetraazacyclododecane) is covalently bound to the anchor peptide LCI through a maleimide linker. Compared to the free cofactors, a 12- to 15-fold improvement in catalytic activity using biohybrid catalysts based on LCI_F16C was observed.
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