{"title":"Bench-Stable Low-Valent Chromium Catalysts for Hydrogenation of CO2, Bicarbonate, and Inorganic Carbonates to Formate","authors":"Tushar Singh, Akash Gutal, Anitta Regina, Amitava Banerjee, Manikandan Paranjothy, Subrata Chakraborty","doi":"10.1021/acscatal.4c04492","DOIUrl":null,"url":null,"abstract":"Catalytic hydrogenation of the potent greenhouse gas carbon dioxide to obtain value-added products represents a much sought after methodology in academia and industry. Hydrogenation of CO<sub>2</sub> to formic acid catalyzed by molecular complexes is a highly desirable protocol because of the industrial importance of formic acid and its potential application as a renewable hydrogen storage material. Herein we disclose that the bench-stable, low-valent phosphine-tethered chromium carbonyl complex Cr(DPPP)(CO)<sub>4</sub> (<b>C-3</b>) (DPPP = 1,3-bis(diphenylphosphino)propane) catalyzed efficient hydrogenation of CO<sub>2</sub> to formate giving a maximum turnover number (TON) of 259,000 at 130 °C in THF/H<sub>2</sub>O mixture after 24 h at the expense of 40 bar (CO<sub>2</sub>:H<sub>2</sub> = 10:30) pressure. Biologically relevant sodium bicarbonate and inorganic carbonates were also tested for hydrogenation to sodium formate, furnishing decent yields of the desired products. Mechanistic investigation along with theoretical studies revealed that the reaction proceeded via the formation of a metallacarboxylate intermediate, which was further converted to a formato complex via an anionic hydrido carbonyl intermediate.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":null,"pages":null},"PeriodicalIF":11.3000,"publicationDate":"2024-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.4c04492","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Catalytic hydrogenation of the potent greenhouse gas carbon dioxide to obtain value-added products represents a much sought after methodology in academia and industry. Hydrogenation of CO2 to formic acid catalyzed by molecular complexes is a highly desirable protocol because of the industrial importance of formic acid and its potential application as a renewable hydrogen storage material. Herein we disclose that the bench-stable, low-valent phosphine-tethered chromium carbonyl complex Cr(DPPP)(CO)4 (C-3) (DPPP = 1,3-bis(diphenylphosphino)propane) catalyzed efficient hydrogenation of CO2 to formate giving a maximum turnover number (TON) of 259,000 at 130 °C in THF/H2O mixture after 24 h at the expense of 40 bar (CO2:H2 = 10:30) pressure. Biologically relevant sodium bicarbonate and inorganic carbonates were also tested for hydrogenation to sodium formate, furnishing decent yields of the desired products. Mechanistic investigation along with theoretical studies revealed that the reaction proceeded via the formation of a metallacarboxylate intermediate, which was further converted to a formato complex via an anionic hydrido carbonyl intermediate.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.