Fabricating Multivariate Metal–Organic Frameworks by Metal Site Reduction as Green Catalyst for CO2 Conversion

IF 7.3 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Xiaojiao Hou, Xing Gao, Xu Zhai, Wenxiu He, Yuanlin Fu, Bingbing Chen, Junyi Chen, Yu Fu
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引用次数: 0

Abstract

Multivariate metal–organic frameworks (MTV-MOFs) have the potential to incorporate multiple metal active sites into a single framework, and the synergistic effect between the constituent metals endow porous materials with significant properties for specifically targeted applications. In this work, a novel reduction engineering strategy is described to extend the system of MTV-MOFs, producing multimetallic MTV-MOFs with a more diverse and desired combination of metal elements. This strategy is based on precisely modulating the valence states of specific metal nodes within bimetallic MOFs to accomplish the synthesis of multimetallic MTV-MOFs with the incorporation of more types metal combinations previously inaccessible with traditional one-pot methods. The resulting multimetallic MTV-MOF, CuICuIIZn-DOBDC, which features ternary active sites of CuI, CuII, and ZnII ions, as well as a high density of uncoordinated hydroxyl groups, constructs a noble-metal free heterogeneous catalyst with multiple synergistic catalytic effects. Notably, CuICuIIZn-DOBDC can effectively catalyze the green cyclization of propargylic amines with CO2 under room temperature and atmospheric pressure, without the need for co-catalysts or solvents. Most importantly, this work provides new ideas for extending the scope and tunability of multimetallic MTV-MOFs to incorporate more types of metal ion combinations, while also providing a new pathway for green conversion of CO2.

Abstract Image

用金属位还原法制备多元金属-有机骨架作为CO2转化绿色催化剂
多元金属有机框架(MTV-MOFs)具有将多个金属活性位点整合到单一框架中的潜力,并且组成金属之间的协同效应赋予多孔材料具有特定目标应用的显著性能。在本工作中,描述了一种新的还原工程策略来扩展mtv - mof系统,生产具有更多样化和所需金属元素组合的多金属mtv - mof。该策略是基于精确调制双金属mof内特定金属节点的价态,以实现多金属mft - mof的合成,并结合传统一锅法无法实现的更多类型的金属组合。得到的多金属MTV-MOF, CuICuIIZn-DOBDC,具有CuI、CuII和ZnII离子的三元活性位点,以及高密度的不配位羟基,构建了具有多重协同催化作用的无贵金属多相催化剂。值得注意的是,CuICuIIZn-DOBDC可以在室温常压下,在不需要助催化剂和溶剂的情况下,有效地催化丙炔胺与CO2的绿色环化反应。最重要的是,这项工作为扩展多金属mtv - mof的范围和可调性提供了新的思路,以纳入更多类型的金属离子组合,同时也为CO2的绿色转化提供了新的途径。
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来源期刊
ACS Sustainable Chemistry & Engineering
ACS Sustainable Chemistry & Engineering CHEMISTRY, MULTIDISCIPLINARY-ENGINEERING, CHEMICAL
CiteScore
13.80
自引率
4.80%
发文量
1470
审稿时长
1.7 months
期刊介绍: ACS Sustainable Chemistry & Engineering is a prestigious weekly peer-reviewed scientific journal published by the American Chemical Society. Dedicated to advancing the principles of green chemistry and green engineering, it covers a wide array of research topics including green chemistry, green engineering, biomass, alternative energy, and life cycle assessment. The journal welcomes submissions in various formats, including Letters, Articles, Features, and Perspectives (Reviews), that address the challenges of sustainability in the chemical enterprise and contribute to the advancement of sustainable practices. Join us in shaping the future of sustainable chemistry and engineering.
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