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

Photocatalytic CO 2 reduction reaction has been developed as an effective strategy to convert CO 2 into reusable chemicals. However, the reduction products of this reaction are often of low utilization value. Herein, we effectively connect photocatalytic CO 2 reduction and amino carbonylation reacti...

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Published inNature communications Vol. 13; no. 1; pp. 2964 - 12
Main Authors Xia, Yuan-Sheng, Tang, Meizhong, Zhang, Lei, Liu, Jiang, Jiang, Cheng, Gao, Guang-Kuo, Dong, Long-Zhang, Xie, Lan-Gui, Lan, Ya-Qian
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Published London Nature Publishing Group UK 26.05.2022
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Abstract Photocatalytic CO 2 reduction reaction has been developed as an effective strategy to convert CO 2 into reusable chemicals. However, the reduction products of this reaction are often of low utilization value. Herein, we effectively connect photocatalytic CO 2 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 CO 2 -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 13 C isotopically labeled organic molecules. This work represents an important and feasible pathway for the subsequent separation and application of CO 2 photoreduction product. A Ni-based MOF catalyst is reported to facilitate the photocatalytic reduction of CO2 to CO, a low-value product. In tandem, the as-produced CO is used as a reactant in the Pd-catalyzed carbonylation of aryl halides and other fine organic chemicals.
AbstractList 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.A Ni-based MOF catalyst is reported to facilitate the photocatalytic reduction of CO2 to CO, a low-value product. In tandem, the as-produced CO is used as a reactant in the Pd-catalyzed carbonylation of aryl halides and other fine organic chemicals.
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.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.
Photocatalytic CO 2 reduction reaction has been developed as an effective strategy to convert CO 2 into reusable chemicals. However, the reduction products of this reaction are often of low utilization value. Herein, we effectively connect photocatalytic CO 2 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 CO 2 -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 13 C isotopically labeled organic molecules. This work represents an important and feasible pathway for the subsequent separation and application of CO 2 photoreduction product.
Photocatalytic CO 2 reduction reaction has been developed as an effective strategy to convert CO 2 into reusable chemicals. However, the reduction products of this reaction are often of low utilization value. Herein, we effectively connect photocatalytic CO 2 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 CO 2 -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 13 C isotopically labeled organic molecules. This work represents an important and feasible pathway for the subsequent separation and application of CO 2 photoreduction product. A Ni-based MOF catalyst is reported to facilitate the photocatalytic reduction of CO2 to CO, a low-value product. In tandem, the as-produced CO is used as a reactant in the Pd-catalyzed carbonylation of aryl halides and other fine organic chemicals.
A Ni-based MOF catalyst is reported to facilitate the photocatalytic reduction of CO2 to CO, a low-value product. In tandem, the as-produced CO is used as a reactant in the Pd-catalyzed carbonylation of aryl halides and other fine organic chemicals.
ArticleNumber 2964
Author Lan, Ya-Qian
Jiang, Cheng
Dong, Long-Zhang
Tang, Meizhong
Liu, Jiang
Gao, Guang-Kuo
Xia, Yuan-Sheng
Xie, Lan-Gui
Zhang, Lei
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Snippet Photocatalytic CO 2 reduction reaction has been developed as an effective strategy to convert CO 2 into reusable chemicals. However, the reduction products of...
Photocatalytic CO2 reduction reaction has been developed as an effective strategy to convert CO2 into reusable chemicals. However, the reduction products of...
A Ni-based MOF catalyst is reported to facilitate the photocatalytic reduction of CO2 to CO, a low-value product. In tandem, the as-produced CO is used as a...
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SubjectTerms 639/301/299/890
639/638/549
639/638/77/890
639/638/911
Aromatic compounds
Carbon dioxide
Carbon monoxide
Carbonyls
Catalysts
Chemical reduction
Chemical synthesis
Chemicals
DEET
Fine chemicals
Halides
Humanities and Social Sciences
Iodides
multidisciplinary
Organic chemicals
Organic chemistry
Photocatalysis
Photoreduction
Science
Science (multidisciplinary)
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Title Tandem utilization of CO2 photoreduction products for the carbonylation of aryl iodides
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Volume 13
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