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Tandem utilization of CO2 photoreduction products for the carbonylation of aryl iodides.


ABSTRACT: Photocatalytic CO2 reduction reaction has been developed as an effective strategy to convert CO2 into reusable chemicals. However, the reduction products of this reaction are often of low utilization value. Herein, we effectively connect photocatalytic CO2 reduction and amino carbonylation reactions in series to reconvert inexpensive photoreduction product CO into value-added and easily isolated fine chemicals. In this tandem transformation system, we synthesize an efficient photocatalyst, NNU-55-Ni, which is transformed into nanosheets (NNU-55-Ni-NS) in situ to improve the photocatalytic CO2-to-CO activity significantly. After that, CO serving as reactant is further reconverted into organic molecules through the coupled carbonylation reactions. Especially in the carbonylation reaction of diethyltoluamide synthesis, CO conversion reaches up to 85%. Meanwhile, this tandem transformation also provides a simple and low-cost method for the 13C isotopically labeled organic molecules. This work represents an important and feasible pathway for the subsequent separation and application of CO2 photoreduction product.

SUBMITTER: Xia YS 

PROVIDER: S-EPMC9135707 | biostudies-literature | 2022 May

REPOSITORIES: biostudies-literature

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Tandem utilization of CO<sub>2</sub> photoreduction products for the carbonylation of aryl iodides.

Xia Yuan-Sheng YS   Tang Meizhong M   Zhang Lei L   Liu Jiang J   Jiang Cheng C   Gao Guang-Kuo GK   Dong Long-Zhang LZ   Xie Lan-Gui LG   Lan Ya-Qian YQ  

Nature communications 20220526 1


Photocatalytic CO<sub>2</sub> reduction reaction has been developed as an effective strategy to convert CO<sub>2</sub> into reusable chemicals. However, the reduction products of this reaction are often of low utilization value. Herein, we effectively connect photocatalytic CO<sub>2</sub> reduction and amino carbonylation reactions in series to reconvert inexpensive photoreduction product CO into value-added and easily isolated fine chemicals. In this tandem transformation system, we synthesize  ...[more]

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