Scalable carbon dioxide electroreduction coupled to carbonylation chemistry

被引:64
作者
Jensen, Mikkel T. [1 ]
Ronne, Magnus H. [1 ]
Ravn, Anne K. [1 ]
Juhl, Rene W. [1 ]
Nielsen, Dennis U. [1 ]
Hu, Xin-Ming [1 ]
Pedersen, Steen U. [1 ]
Daasbjerg, Kim [1 ]
Skrydstrup, Troels [1 ]
机构
[1] Aarhus Univ, Dept Chem, Interdisciplinary Nanosci Ctr, Carbon Dioxide Activat Ctr CADIAC, Gustav Wieds Vej 14, DK-8000 Aarhus C, Denmark
来源
NATURE COMMUNICATIONS | 2017年 / 8卷
基金
新加坡国家研究基金会;
关键词
ELECTROCHEMICAL REDUCTION; CO2-TO-CO CONVERSION; CO2; ELECTROREDUCTION; ORGANIC FRAMEWORKS; ARYL BROMIDES; EX-SITU; CATALYSIS; PORPHYRINS; IMMOBILIZATION; POLYMERIZATION;
D O I
10.1038/s41467-017-00559-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Significant efforts have been devoted over the last few years to develop efficient molecular electrocatalysts for the electrochemical reduction of carbon dioxide to carbon monoxide, the latter being an industrially important feedstock for the synthesis of bulk and fine chemicals. Whereas these efforts primarily focus on this formal oxygen abstraction step, there are no reports on the exploitation of the chemistry for scalable applications in carbonylation reactions. Here we describe the design and application of an inexpensive and user-friendly electrochemical set-up combined with the two-chamber technology for performing Pd-catalysed carbonylation reactions including amino-and alkoxycarbonylations, as well as carbonylative Sonogashira and Suzuki couplings with near stoichiometric carbon monoxide. The combined two-reaction process allows for milligram to gram synthesis of pharmaceutically relevant compounds. Moreover, this technology can be adapted to the use of atmospheric carbon dioxide.
引用
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页数:8
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