A Ru-bda Complex with a Dangling Carboxylate Group: Synthesis and Electrochemical Properties

Abolfazl Ghaderian; Jan Holub; Jordi Benet-Buchholz; Antoni Llobet; Carolina Gimbert-Suriñach

doi:10.1021/acs.inorgchem.9b03595

A Ru-bda Complex with a Dangling Carboxylate Group: Synthesis and Electrochemical Properties

Inorg Chem. 2020 Apr 6;59(7):4443-4452. doi: 10.1021/acs.inorgchem.9b03595. Epub 2020 Mar 10.

Authors

Abolfazl Ghaderian^{1

2}, Jan Holub¹, Jordi Benet-Buchholz¹, Antoni Llobet^{1

3}, Carolina Gimbert-Suriñach¹

Affiliations

¹ Institute of Chemical Research of Catalonia (ICIQ), Barcelona Institute of Science and Technology, Av. Països Catalans 16, 43007 Tarragona, Spain.
² Departament de Química Física i Inorgànica, Universitat Rovira i Virgili, Campus Sescelades, C/Marcel·lí Domingo, s/n, 43007 Tarragona, Spain.
³ Universitat Autònoma de Barcelona, Departament de Química, Cerdanyola del Vallès, 08193 Barcelona, Spain.

PMID: 32155060
DOI: 10.1021/acs.inorgchem.9b03595

Abstract

Ruthenium complexes containing the tetradentate 2,2'-bipyridine-6,6'-dicarboxylato (bda^2-) equatorial ligand and ortho-subsituted pyridines in the axial position have been prepared and characterized using spectroscopic, crystallographic and electrochemical techniques. Complexes [Ru(Hbda)(DMSO)(pyC)] (1) and [Ru(bda)(DMSO)(pyA)] (2) (where pyC is 2-pyridinecarboxylate, pyA is pyridine-2-ylmethanol and DMSO is dimethyl sulfoxide) have been isolated in moderate to high yields. The solid state structures of (1-H)^- and 2 reveal the strong chelate effect of the axial pyridine ligand that coordinates in a bidentate fashion leaving the bda^2- equatorial ligand coordinating in a tridentate mode. In solution, compound 2 shows a dynamic equilibrium between different coordination modes of the bda^2- and pyA ligands. This phenomenon does not occur for 1 because the carboxylate binds stronger than the labile alcohol in 2. Cyclic voltammetry analysis of 1 reveals a complex behavior with a pH-independent wave at E_1/2 = 1.12 V that is tentatively associated with the two-electron Ru^IV/II couple. In sharp contrast, complex 2 shows a pH-dependent one-electron wave at E_1/2 = 0.83 V (pH 1), assigned to the proton-coupled electron transfer process of the Ru^III/II couple and a pH-independent wave at E_1/2 = 1.06 V assigned to the Ru^IV/III couple. Compound 2 is used to prepare complex [Ru(bda)(pic)(pyA)] (4). This complex is air sensitive and converts to complex [Ru(bda)(pic)(pyE)] (5) (where pyE is methyl 2-pyridine carboxylate) in the presence of methanol. This oxidation also occurs by applying a positive potential to an aqueous solution of 4, producing the derivative [Ru(bda)(pic)(pyC)] (3). Cyclic voltammetry of 3 shows two pH-independent one-electron oxidation waves at E_1/2 = 0.64 V and E_1/2 = 1.0 V, corresponding to the Ru^III/II and Ru^IV/III couples, respectively. In addition, a water oxidation catalytic wave appears at E_onset ≈ 1.4 V. Foot-of-the-wave analysis of this catalytic wave based on a water nucleophilic attack accounts for a TOF_max = 0.63-0.74 s^-1.