A 2,2'-bipyridine-containing covalent organic framework bearing rhenium(i) tricarbonyl moieties for CO 2 reduction

• Published in: Dalton transactions : an international journal of inorganic chemistry Vol. 47; no. 48; pp. 17450 - 17460
• Main Authors: Popov, Damir A, Luna, John M, Orchanian, Nicholas M, Haiges, Ralf, Downes, Courtney A, Marinescu, Smaranda C
• Format: Journal Article
• Language: English
• Published: England Royal Society of Chemistry (RSC) 11.12.2018
• ISSN: 1477-9226; 1477-9234
• DOI: 10.1039/C8DT00125A

The reduction of CO2 into higher energy products such as carbon-based fuels and feedstocks is an attractive strategy for mitigating the continuous rise in CO2 emissions associated with the growing global energy demand. Rhenium tricarbonyl complexes bearing 2,2'-bipyridine (2,2'-bpy) ligands are well-established molecular electrocatalysts for the selective reduction of CO2 to CO. Construction of efficient devices for this electrochemical process requires the immobilization of electrocatalysts to electrode surfaces. To integrate Re(2,2'-bpy)(CO)3 fragments into a covalent organic framework (COF), Re(5,5'-diamine-2,2'-bpy)(CO)3Cl (1) was synthesized and electrochemically investigated. Complex 1 is an active and selective electrocatalyst for the reduction of CO2 to CO with excellent faradaic efficiency (99%). The presence of the amine substituents leads to a destabilization of the π* orbital of the 5,5'-diamine-2,2'-bpy ligand with respect to the metal center. Therefore, 1 requires more negative potentials (-2.47 V vs. Fc+/0) to reach the doubly reduced catalytically active species. DFT studies were conducted to understand the electronic structure of 1, and support the destabilizing effect of the amine substituents. The Re-2,2'-bpy fragments were successfully integrated into a COF containing 2,2'-bpy moieties (COF-2,2'-bpy) via a post-metallation synthetic route to generate COF-2,2'-bpy-Re. A composite of COF-2,2'-bpy-Re, carbon black, and polyvinylidene fluoride (PVDF) was readily immobilized onto glassy carbon electrodes and electrocatalytic CO2 reduction to CO was observed at -2.8 V vs. Fc0/+, with a faradaic efficiency of 81% for CO production.