2026-04-14T03:11:23Zhttps://recercat.cat/oai/request

oai:recercat.cat:2072/3058632026-01-15T14:12:31Zcom_2072_300912com_2072_4427col_2072_301309

00925njm 22002777a 4500 dc Matheu, Roc author Ertem, Mehmed .Z. author Benet-Buchholz, Jordi author Coronado, Eugenio author Batista, Victor S. author Sala, Xavier author Llobet, Antoni author 2015 <p> We introduce a new family of complexes with the general formula [Ru<em>ⁿ</em>(tda)(py)₂]<em>^m</em>⁺ (<em>n</em> = 2, <em>m</em> = 0, <strong>1</strong>; <em>n</em> = 3, <em>m</em> = 1, <strong>2</strong>⁺; <em>n</em> = 4, <em>m</em> = 2, <strong>3</strong>²⁺), with tda^2&ndash; being [2,2&prime;:6&prime;,2&Prime;-terpyridine]-6,6&Prime;-dicarboxylate, including complex [Ru^IV(OH)(tda-&kappa;-N³O)(py)₂]⁺, <strong>4H</strong>⁺, which we find to be an impressive water oxidation catalyst, formed by hydroxo coordination to <strong>3</strong>²⁺ under basic conditions. The complexes are synthesized, isolated, and thoroughly characterized by analytical, spectroscopic (UV&ndash;vis, nuclear magnetic resonance, electron paramagnetic resonance), computational, and electrochemical techniques (cyclic voltammetry, differential pulse voltammetry, coulometry), including solid-state monocrystal X-ray diffraction analysis. In oxidation state IV, the Ru center is seven-coordinated and diamagnetic, whereas in oxidation state II, the complex has an unbonded dangling carboxylate and is six-coordinated while still diamagnetic. With oxidation state III, the coordination number is halfway between the coordination of oxidation states II and IV. Species generated in situ have also been characterized by spectroscopic, computational, and electrochemical techniques, together with the related species derived from a different degree of protonation and oxidation states. <strong>4H</strong>⁺ can be generated potentiometrically, or voltammetrically, from <strong>3</strong>²⁺, and both coexist in solution. While complex <strong>3</strong>²⁺ is not catalytically active, the catalytic performance of complex <strong>4H</strong>⁺ is characterized by the foot of the wave analysis, giving an impressive turnover frequency record of 8000 s^&ndash;1 at pH 7.0 and 50 000 s^&ndash;1 at pH 10.0. Density functional theory calculations provide a complete description of the water oxidation catalytic cycle of <strong>4H</strong>⁺, manifesting the key functional role of the dangling carboxylate in lowering the activation free energies that lead to O&ndash;O bond formation.</p> <p> &nbsp;</p> <p> &nbsp;</p> http://hdl.handle.net/2072/305863 https://doi.org/10.1021/jacs.5b06541 Intramolecular proton transfer boosts water oxidation catalyzed by a Ru complex