Chakraborty, Subrata

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.

We present here a phosphine-free, quinoline-based pincer Mn catalyst for α-alkylation of methyl ketones using primary alcohols as alkyl surrogates. The C-C bond formation reaction proceeds via a hydrogen auto-transfer methodology. The sole by-product formed is water, rendering the protocol atom efficient. Electronic structure theory studies corroborated the proposed mechanism.

Herein, we report the hydrogenation of carbon dioxide to sodium formate catalyzed by low-valent molybdenum phosphine complexes. The 1,3-bis(diphenylphosphino)propane (DPPP)-based Mo complex was found to be an efficient catalyst in the presence of NaOH affording formate with a TON of 975 at 130 °C in THF/H2O after 24 h utilizing 40 bar (CO2 : H2 = 10 : 30) pressure. The complex was also active in the hydrogenation of sodium bicarbonate and inorganic carbonates to the corresponding formates. Mechanistic investigation revealed that the reaction proceeded via an intermediate formato complex.