Covalent-Frameworked 2D Crown Ether with Chemical Multifunctionality

被引:10
|
作者
Kim, Jinseok [1 ,2 ]
Kim, Sungin [1 ,2 ,3 ]
Park, Jinwook [1 ,2 ]
Kang, Sungsu [1 ,2 ,3 ]
Seo, Dong Joo [1 ,2 ]
Park, Namjun [1 ,2 ]
Lee, Siyoung [1 ,2 ]
Kim, Jae Jun [1 ,2 ]
Lee, Won Bo [1 ,2 ]
Park, Jungwon [1 ,2 ,3 ,4 ,5 ]
Lee, Jong-Chan [1 ,2 ]
机构
[1] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea
[2] Seoul Natl Univ, Inst Chem Proc, Seoul 08826, South Korea
[3] Inst Basic Sci IBS, Ctr Nanoparticle Res, Seoul 08826, South Korea
[4] Seoul Natl Univ, Inst Engn Res, Coll Engn, Seoul 08826, South Korea
[5] Seoul Natl Univ, Adv Inst Convergence Technol, Seoul 16229, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
Catalyst activity - Chemical modification - Chemical stability - Crown ethers - Ethers - Ligands - Molar ratio - Physicochemical properties;
D O I
10.1021/jacs.3c11182
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Here, we present the synthesis and characterization of a novel 2D crystalline framework, named C2O, which mainly consists of carbon and oxygen in a 2:1 molar ratio and features crown ether holes in its skeletal structure. The covalent-frameworked 2D crown ether can be synthesized on a gram-scale and exhibits fine chemical stability in various environments, including acid, base, and different organic solvents. The C2O efficiently activates KI through the strong coordination of K+ with crown ether holes in a rigid framework, which enhances the nucleophilicity of I- and significantly improves its catalytic activity for CO2 fixation with epoxides. The presence of C2O with KI results in remarkable increases in CO2 conversion from 5.7% to 99.9% and from 2.9% to 74.2% for epichlorohydrin and allyl glycidyl ether, respectively. Moreover, C2O possesses both electrophilic and nucleophilic sites at the edge of its framework, allowing for the customization of physicochemical properties by a diverse range of chemical modifications. Specifically, incorporating allyl glycidyl ether (AGE) as an electrophile or ethoxyethylamine (EEA) as a nucleophile into C2O enables the synthesis of C2O-AGE or C2O-EEA, respectively. These modified frameworks exhibit improved conversions of 97.2% and 99.9% for CO2 fixation with allyl glycidyl ether, outperforming unmodified C2O showing a conversion of 74.2%. This newly developed scalable, durable, and customizable covalent framework holds tremendous potential for the design and preparation of outstanding materials with versatile functionalities, rendering them highly attractive for a wide range of applications.
引用
收藏
页码:4532 / 4541
页数:10
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