共价键
对映选择合成
材料科学
电化学发光
离子液体
亚胺
离子键合
共价有机骨架
组合化学
猝灭(荧光)
分析物
手性(物理)
光化学
对映体
电子受体
对映体过量
接受者
电子供体
化学
生物传感器
电子
多金属氧酸盐
作者
Ru Zhang,Lewei Wang,Runde Suo,Chuanfu Zhu,Datong Wu,Wenrong Cai,J. C. Li,Yong Kong
标识
DOI:10.1002/adom.202503001
摘要
Abstract The fabrication of chiral covalent organic frameworks (CCOFs) with electrochemiluminescence (ECL) properties tailored for enantioselective sensing remains challenging. This study employs a post‐synthetic modification strategy to synthesize ionic CCOFs with pronounced ECL behavior. First, an achiral covalent organic framework is constructed via imine condensation. Subsequently, the imidazolyl group in the COF is covalently functionalized with optically pure, chlorine‐substituted chiral reagents, forming an imidazolium moiety. Within this engineered architecture, the imidazolium and pyrenyl units serve as the electron acceptor and donor components, respectively. The obtained ionic CCOFs exhibit strong ECL activity. When applied as chiral sensors, the achieved ECL‐active CCOFs demonstrate a consistent recognition pattern: ( S )‐CCOFs exhibit deeper ECL quenching toward ( S )‐analytes. The ECL intensity ratios between the ( R )‐ and ( S )‐analytes range from 1.6–13.1. Moreover, a robust correlation is observed between analyte concentration (or enantiomeric composition) and ECL intensity.
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