Citation: Huihua GONG, Tianhua CUI, Li JI, Liyuan ZHANG, Xueli ZHENG, Haiyan FU, Hua CHEN, Jiawei MAO, Ruixiang LI. Efficient hydrogenation of CO2 realized by Ru-NNN complex[J]. Chinese Journal of Inorganic Chemistry, ;2026, 42(5): 1085-1095. doi: 10.11862/CJIC.20250321 shu

Efficient hydrogenation of CO2 realized by Ru-NNN complex

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  • To develop highly stable and active Ru complex catalysts for CO2 hydrogenation, we synthesized Ru complexes bearing rigid pincer-type tridentate NNN (pyrazole-pyridine-pyrazole) ligands and weakly coordinated triphenylphosphine (PPh3) ligands. The NNN ligands can strongly chelate with the Ru metal center, contributing to the overall robustness of the catalytic system. Meanwhile, PPh3 can easily dissociate to form vacant coordination sites, thereby enhancing catalytic activity. As a result, the Ru(Ⅱ)-NNN complex [Ru(L-NNN)Cl(PPh3)2]Cl (1, L-NNN=2,6-bis(5-methyl-1H-pyrazol-3-yl)pyridine) was not only quite stable, but also showed high activity for CO2 hydrogenation to formate, achieving a TON of up to 150 000. In the mechanism study, based on the results of in-situ NMR, in-situ HPLC-HRMS spectra, and density functional theory calculations, it is speculated that the active intermediates with empty coordination sites are highly active species in CO2 hydrogenation.
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