AI Article Synopsis

  • The bioinspired Mn-oxo cubane complex [Mn(4)O(4)L(6)](+) 1b(+) effectively mimics the photosynthetic oxygen-evolving complex and electrochemically oxidizes water at 1.00 V under UV-visible light when used with a proton-conducting membrane.
  • Spectroscopic analyses indicate that 1b(+) is the main electro-active entity in the Nafion system, which correlates with the observed catalytic activity for oxygen production.
  • The catalytic mechanism likely involves the photolytic breakdown of a phosphinate ligand, leading to oxygen formation, with optimal catalytic performance influenced by factors such as applied potential and light wavelength, achieving remarkable turnover rates of over 1000 molecules of

Article Abstract

The bioinspired Mn-oxo cubane complex, [Mn(4)O(4)L(6)](+) 1b(+) (L = (p-MeO-Ph)(2)PO(2)), is a model of the photosynthetic O(2)-evolving complex. It is able to electro-oxidize water at 1.00 V (vs Ag/AgCl) under illumination by UV-visible light when suspended in a proton-conducting membrane (Nafion) coated onto a conducting electrode. Electrochemical measurements, and UV-visible, NMR, and EPR spectroscopies are interpreted to indicate that 1b(+) is the dominant electro-active species in the Nafion, both before and after catalytic cycling, and thus correlates closely with activity. The observation of a possible intermediate and free phosphinate ligand within the Nafion suggests a catalytic mechanism involving photolytic disruption of a phosphinate ligand, followed by O(2) formation, and subsequent reassembly of the cubane structure. Several factors that influence catalytic turnover such as the applied potential, illumination wavelength, and energy have been examined in respect of attaining optimum catalytic activity. Catalytic turnover frequencies of 20-270 molecules O(2) h(-1) catalyst(-1) at an overpotential of 0.38 V plus light (275-750 nm) and turnovers numbers >1000 molecules O(2) catalyst(-1) are observed. The 1b(+)-Nafion system is among the most active and durable molecular water oxidation catalysts known.

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Source
http://dx.doi.org/10.1021/ic9006982DOI Listing

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