Electrocatalytic properties of a novel ruthenium(ii) terpyridine-based complex towards CO2 reduction

The electrocatalytic properties of Ru complexes are of great technological interest given their potential application in reactions such water splitting and CO2 reduction. In this work, a novel terpyridine-based Ru(ii) complex, [RuCl(trpy)(acpy)], trpy = 2,2 ':6 ',2 ''-terpyridine, acpy(-) = 2-pyridylacetate was synthesized and its spectroscopic, electrochemical and catalytic properties were explored in detail. In dry acetonitrile, the complex exhibits two reduction peaks at -1.95 V and -2.20 V vs. Fc/Fc(+), attributed to consecutive 1 e(-) reduction. Under CO2 atmosphere, a catalytic wave is observed (E-onset = 2.1 V vs. Fc/Fc(+)), with CO as the main reduction product. Bulk electrolysis reveals a turnover number (TON) of 12 (k(obs) = 1.5 s(-1)). In the presence of 1% water, an improvement in the catalytic activity is observed (TONCO = 21 and k(obs) = 2.0 s(-1)) and, additionally, formate was also detected (TONHCOO = 7). Spectroelectrochemical experiments allowed the identification of a metallocarboxylate (Ru-COO-) intermediate under anhydrous conditions, while in water, the partial labilization of the acpy(-) ligand was observed in the course of the catalytic cycle. The experimental data was combined with DFT calculations, allowing the proposal of a catalytic cycle. The results establish important relationships between selectivity, ligand structure and reaction conditions.

Automated summary

A novel terpyridine-based Ru(ii) complex was synthesized and its spectroscopic, electrochemical, and catalytic properties were investigated. The complex exhibited two reduction peaks in dry acetonitrile, attributed to consecutive 1 e(-) reduction. Under CO2 atmosphere, a catalytic wave was observed, with CO as the main reduction product. The presence of water improved the catalytic activity and formate production was detected.