Bench-Stable Low-Valent Chromium Catalysts for Hydrogenation of CO2, Bicarbonate, and Inorganic Carbonates to Formate

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2024-09-25 DOI:10.1021/acscatal.4c04492
Tushar Singh, Akash Gutal, Anitta Regina, Amitava Banerjee, Manikandan Paranjothy, Subrata Chakraborty
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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.

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将二氧化碳、碳酸氢盐和无机碳酸盐加氢转化为甲酸酯的台式稳定低价铬催化剂
催化氢化强效温室气体二氧化碳以获得高附加值产品是学术界和工业界孜孜以求的方法。由于甲酸在工业上的重要性及其作为可再生储氢材料的潜在应用,在分子络合物催化下将二氧化碳氢化为甲酸是一种非常理想的方案。在此,我们揭示了稳定的低价膦系铬羰基络合物 Cr(DPPP)(CO)4 (C-3) (DPPP = 1,3-双(二苯基膦)丙烷)催化二氧化碳高效加氢为甲酸的过程,在 130 °C 的 THF/H2O 混合物中,压力为 40 巴(CO2:H2 = 10:30),24 小时后的最大周转次数(TON)为 259,000。此外,还测试了与生物相关的碳酸氢钠和无机碳酸盐加氢生成甲酸钠的过程,结果表明所需产物的产量相当可观。机理研究和理论研究表明,反应是通过形成金属羧酸中间体进行的,而金属羧酸中间体又通过阴离子水合羰基中间体进一步转化为甲酸络合物。
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
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.
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