CO direct esterification to dimethyl oxalate and dimethyl carbonate: the key functional motifs for catalytic selectivity

• Published in: Nanoscale Vol. 12; no. 39; pp. 2131 - 214
• Main Authors: Wang, Zhi-Qiao, Sun, Jing, Xu, Zhong-Ning, Guo, Guo-Cong
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 15.10.2020
• Subjects: Carbon monoxide; Chemical synthesis; Esterification; Selectivity; Valence
• ISSN: 2040-3364; 2040-3372
• DOI: 10.1039/d0nr03008b

The direct esterification of CO involves processes using CO as the starting material and ester chemicals as products. Dimethyl oxalate (DMO) and dimethyl carbonate (DMC) are two different products of the direct CO esterification reaction. However, the effective control of the reaction pathway and direct synthesis of DMO and DMC are challenging. In this review, we summarize the recent research progress on the direct esterification of CO to DMO/DMC and reveal the functional motifs responsible for the catalytic selectivity. Firstly, we discuss the microstructure of catalysts for the direct esterification of CO to DMO and DMC, including the valence state and the aggregate state of Pd. Then, the influence of characteristics of the support on the selectivity is analyzed. Importantly, the aggregate state of the active component, Pd is deemed as a vital functional motif for catalytic selectivity. The isolated Pd is conducive for the formation of DMC, while the aggregated Pd is beneficial for the formation of DMO. This review will provide rational guidance for the direct esterification of CO to DMO and DMC. The key functional motifs for the selectivity have been discussed in detail in this review. The isolated Pd is conducive for dimethyl carbonate (DMC), while the aggregated Pd is beneficial for dimethyl oxalate (DMO).