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一种介孔金属有机框架,用于将铜(II)可持续地释放到还原性水介质中以促进铜催化的叠氮化物-炔烃环加成点击反应。

A mesoporous metal-organic framework used to sustainably release copper(ii) into reducing aqueous media to promote the CuAAC click reaction.

作者信息

Hoffmann Pascal, Lherbet Christian, Fabing Isabelle, Barthélémy Marie-Claire, Borjon-Piron Yann, Laurent Christophe, Vigroux Alain

机构信息

LSPCMIB, Université Toulouse 3 Paul Sabatier, UMR CNRS UPS 5068 118 Route de Narbonne 31062 Toulouse France

Institut de Chimie de Toulouse, Université Toulouse 3 Paul Sabatier, ICT-FR CNRS 2599 118 Route de Narbonne 31062 Toulouse France.

出版信息

RSC Adv. 2022 Sep 22;12(41):26825-26833. doi: 10.1039/d2ra04298c. eCollection 2022 Sep 16.

DOI:10.1039/d2ra04298c
PMID:36320833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9494208/
Abstract

The mesoporous metal-organic framework Cr-MIL-101-NH (MOF1) has been used to encapsulate, by a simple impregnation method, large amounts of copper sulfate. The resulting loaded material, Cu@MOF1, was successfully employed to slowly release copper(ii) into an appropriate reaction medium in which the reducing agent sodium ascorbate reduces copper(ii) to copper(i), thus allowing the well-known copper(i)-catalyzed alkyne-azide cycloaddition (CuAAC) "click" reaction to proceed in the absence of potentially high local copper(i) concentrations. The use of a MOF-based controlled copper release system such as Cu@MOF1 may be relevant for copper(i)-catalyzed reactions having substrates that could be degraded by potentially high local concentrations of copper(i). The copper chelating ligand TBTA (tris(benzyltriazolylmethyl)amine), a very useful ligand for click chemistry, has been successfully attached to the pores of MOF1. The resulting TBTA-functionalized MOF (MOF3) was compared with its non-functionalized version (MOF1). At copper loadings of 3 mmol g, the results revealed that the performances of the two materials are strikingly similar. Upon immersion in methanol/water (95/5) containing sodium ascorbate, both materials slowly released copper encapsulated in their pores and could be recovered and reused efficiently for up to five reaction cycles without reloading with metal ion, while allowing the CuAAC reaction to proceed with excellent conversion rates and yields.

摘要

介孔金属有机框架材料Cr-MIL-101-NH(MOF1)已通过简单的浸渍法用于封装大量硫酸铜。所得的负载材料Cu@MOF1成功用于将铜(II)缓慢释放到合适的反应介质中,在该介质中还原剂抗坏血酸钠将铜(II)还原为铜(I),从而使著名的铜(I)催化的炔烃-叠氮化物环加成(CuAAC)“点击”反应在不存在潜在高局部铜(I)浓度的情况下进行。使用诸如Cu@MOF1之类的基于MOF的可控铜释放系统可能与具有可能被潜在高局部铜(I)浓度降解的底物的铜(I)催化反应相关。铜螯合配体TBTA(三(苄基三唑基甲基)胺)是一种对点击化学非常有用的配体,已成功连接到MOF1的孔中。将所得的TBTA功能化的MOF(MOF3)与其未功能化的版本(MOF1)进行了比较。在铜负载量为3 mmol g时,结果表明这两种材料的性能惊人地相似。将两种材料浸入含有抗坏血酸钠的甲醇/水(95/5)中后,它们都会缓慢释放封装在其孔中的铜,并且可以回收并高效重复使用多达五个反应循环,而无需重新加载金属离子,同时使CuAAC反应以优异的转化率和产率进行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/c0caa8ca6993/d2ra04298c-s3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/165ce5f4b12d/d2ra04298c-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/8b10ea2c3aa2/d2ra04298c-s2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/0c438197452f/d2ra04298c-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/765c1b02b4f7/d2ra04298c-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/a80455fc1e0c/d2ra04298c-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/b6852d2f2229/d2ra04298c-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/c0caa8ca6993/d2ra04298c-s3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/165ce5f4b12d/d2ra04298c-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/8b10ea2c3aa2/d2ra04298c-s2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/0c438197452f/d2ra04298c-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/765c1b02b4f7/d2ra04298c-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/a80455fc1e0c/d2ra04298c-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/b6852d2f2229/d2ra04298c-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af4/9494208/c0caa8ca6993/d2ra04298c-s3.jpg

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