Investigations of the influence of two pyridyl-mesoionic carbene constitutional isomers on the electrochemical and spectroelectrochemical properties of group 6 metal carbonyl complexes

Abstract

Metal complexes of mesoionic carbenes (MICs) of the triazolylidene type and their derivatives have gained increasing attention in the fields of electrocatalysis and photochemistry. The redox activity of these metal complexes is critical for their applications in both the aforementioned fields. Easy accessibility and modular synthesis open a wide field for the design of ligands, such as bidentate ligands. The combination of an MIC with a pyridyl unit in a bidentate ligand setup increases the π acceptor properties of the ligands while retaining their strong σ donor properties. The analogy with the well-established 2,2′-bipyridine ligand allows conclusions to be drawn about the influence of the mesoionic carbene (MIC) moiety in tetracarbonyl group 6 complexes in cyclic voltammetry and (spectro)electrochemistry (SEC). However, the effects of the different connectivity in pyridyl-MIC ligands remain underexplored. Based on our previous studies, we present a thorough investigation of the influence of the two different pyridyl-MIC constitutional isomers on the electrochemical and the UV-vis-NIR/IR/EPR spectroelectrochemical properties of group 6 carbonyl complexes. Moreover, the presented complexes were investigated for the electrochemical conversion of CO2 using two different working electrodes, providing a fundamental understanding of the influence of the electrode material in the precatalytic activation.