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通过锇催化实现共轭微孔聚合物的骨架羰基化以进行富含胺的功能化

Skeleton Carbonylation of Conjugated Microporous Polymers by Osmium Catalysis for Amine-Rich Functionalization.

作者信息

Ko Ju Hong, Lee Sang Moon, Kim Hae Jin, Ko Yoon-Joo, Son Seung Uk

机构信息

Department of Chemistry, Sungkyunkwan University, Suwon 16419, Korea.

Korea Basic Science Institute, Daejeon 34133, Korea.

出版信息

ACS Macro Lett. 2018 Nov 20;7(11):1353-1358. doi: 10.1021/acsmacrolett.8b00617. Epub 2018 Oct 26.

DOI:10.1021/acsmacrolett.8b00617
PMID:35651242
Abstract

This work introduces a new efficient method for the postsynthetic modification of conjugated microporous polymers (CMPs). Osmium catalysis of hollow CMP (H-CMP) in the presence of NaClO resulted in the conversion of alkynes in the skeleton of CMPs to dicarbonyl groups to form H-CMP-DC. Through controlling the reaction time, the carbonylation degree of H-CMP could be managed, maintaining hollow morphology. We verified the benefits of carbonyl groups in H-CMP-DC in the removal of Cr(VI) from water. Imination of H-CMP-DC resulted in amine-rich H-CMP (H-CMP-A), which showed enhanced adsorption performance toward Cr(VI) in water with up to 73 mg/g, compared with the H-CMP and H-CMP-DC. The H-CMP-A could be recycled at least five times, maintaining its original adsorption ability.

摘要

这项工作介绍了一种用于共轭微孔聚合物(CMPs)后合成修饰的新型高效方法。在NaClO存在下,锇催化中空CMP(H-CMP),使CMP骨架中的炔烃转化为二羰基基团,形成H-CMP-DC。通过控制反应时间,可以控制H-CMP的羰基化程度,同时保持中空形态。我们验证了H-CMP-DC中羰基基团在从水中去除Cr(VI)方面的优势。H-CMP-DC的亚胺化产生了富含胺的H-CMP(H-CMP-A),与H-CMP和H-CMP-DC相比,其对水中Cr(VI)的吸附性能增强,高达73 mg/g。H-CMP-A可以至少循环使用五次,保持其原始吸附能力。

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