中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Probe metal binding mode of imine covalent organic frameworks: cycloiridation for (photo)catalytic hydrogen evolution from formate

文献类型:期刊论文

作者Hu, Jiyun4; Mehrabi, Hamed1; Meng, Yin-Shan5; Taylor, Maddison4; Zhan, Jin-Hui2; Yan, Qigeng5; Benamara, Mourad3; Coridan, Robert H.4; Beyzavi, Hudson4
刊名CHEMICAL SCIENCE
出版日期2021-05-11
页码7
ISSN号2041-6520
DOI10.1039/d1sc01692j
英文摘要Metalation of covalent organic frameworks (COFs) is a critical strategy to functionalize COFs for advanced applications yet largely relies on the pre-installed specific metal docking sites in the network, such as porphyrin, salen, 2,2 '-bipyridine, etc. We show in this study that the imine linkage of simple imine-based COFs, one of the most popular COFs, readily chelate transition metal (Ir in this work) via cyclometalation, which has not been explored before. The iridacycle decorated COF exhibited more than 10-fold efficiency enhancement in (photo)catalytic hydrogen evolution from aqueous formate solution than its molecular counterpart under mild conditions. This work will inspire more functional cyclometallated COFs to be explored beyond catalysis considering the large imine COF library and the rich metallacycle chemistry.
WOS关键词IRIDIUM CATALYST ; H-2 EVOLUTION ; FORMIC-ACID ; COMPLEXES ; DEHYDROGENATION ; CO2 ; CYCLOMETALATION ; REDUCTION ; DOCKING ; SITES
资助项目University of Arkansas ; National Natural Science Foundation of China[21875255] ; U.S. Department of Energy (D.O.E.), Office of Science, Office of Basic Energy Sciences[DE-SC-0020301]
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000649002300001
出版者ROYAL SOC CHEMISTRY
资助机构University of Arkansas ; National Natural Science Foundation of China ; U.S. Department of Energy (D.O.E.), Office of Science, Office of Basic Energy Sciences
源URL[http://ir.ipe.ac.cn/handle/122111/48582]  
专题中国科学院过程工程研究所
通讯作者Zhan, Jin-Hui; Beyzavi, Hudson
作者单位1.Univ Arkansas, Mat Sci & Engn Program, Fayetteville, AR 72701 USA
2.Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
3.Univ Arkansas, Inst Nanosci & Engn, Fayetteville, AR 72701 USA
4.Univ Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USA
5.Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China
推荐引用方式
GB/T 7714
Hu, Jiyun,Mehrabi, Hamed,Meng, Yin-Shan,et al. Probe metal binding mode of imine covalent organic frameworks: cycloiridation for (photo)catalytic hydrogen evolution from formate[J]. CHEMICAL SCIENCE,2021:7.
APA Hu, Jiyun.,Mehrabi, Hamed.,Meng, Yin-Shan.,Taylor, Maddison.,Zhan, Jin-Hui.,...&Beyzavi, Hudson.(2021).Probe metal binding mode of imine covalent organic frameworks: cycloiridation for (photo)catalytic hydrogen evolution from formate.CHEMICAL SCIENCE,7.
MLA Hu, Jiyun,et al."Probe metal binding mode of imine covalent organic frameworks: cycloiridation for (photo)catalytic hydrogen evolution from formate".CHEMICAL SCIENCE (2021):7.

入库方式: OAI收割

来源:过程工程研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。