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Equilibrating metal-oxide cluster ensembles for oxidation reactions using oxygen in water

Abstract

Although many enzymes can readily and selectively use oxygen in water—the most familiar and attractive of all oxidants and solvents, respectively—the design of synthetic catalysts for selective water-based oxidation processes utilizing molecular oxygen1,2,3,4 remains a daunting task5,6. Particularly problematic is the fact that oxidation of substrates by O2 involves radical chemistry, which is intrinsically non-selective and difficult to control. In addition, metallo-organic catalysts are inherently susceptible to degradation5 by oxygen-based radicals, while their transition-metal-ion active sites often react with water to give insoluble, and thus inactive, oxides or hydroxides7. Furthermore, pH control is often required to avoid acid or base degradation of organic substrates or products. Unlike metallo-organic catalysts, polyoxometalate anions are oxidatively stable and are reversible oxidants8,9 for use with O2 (refs 8,9,10). Here we show how thermodynamically controlled self-assembly of an equilibrated ensemble of polyoxometalates, with the heteropolytungstate anion11,12 [AIVVW11O40]6- as its main component, imparts both stability in water and internal pH-management. Designed to operate at near-neutral pH, this system facilitates a two-step O2-based process for the selective delignification of wood (lignocellulose) fibres. By directly monitoring the central Al atom, we show that equilibration reactions typical of polyoxometalate anions13,14 keep the pH of the system near 7 during both process steps.

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Figure 1: Proposed two-step process for conversion of lignin in wood to CO2 and H2O. (Wood is a composite of lignin and cellulose15.) The structures of polyoxometalates (POMs) α-[AlVVW11O40]6- and α-[AlVIVW11O40]7- (α-1 and α-2) are shown in polyhedral notation.
Figure 2: Stepwise synthesis of kinetically stable pure 1, and equilibration to give a thermodynamically stable reaction medium.
Figure 3: Oxidation of lignin in wood-pulp fibres to CO2 and H2O.
Figure 4: NMR analysis of the solution used in the 10-cycle experiment in Fig. 3.

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Acknowledgements

I.A.W. is a visiting scientist at the Department of Chemistry, Emory University, but based at the Forest Products Laboratory. We thank W. E. Bowerman, H. Zeng, S. Ralph and L. L. Landucci for technical assistance; we also acknowledge the contributions of R. H. Atalla, M. J. Birchmeier, C. G. Hill Jr, C. J. Houtman, S. E. Reichel and E. L. Springer. This work was supported by the DOE, NSF and member companies of the USDA Forest Service, Polyoxometalate Bleaching Consortium.

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Correspondence to Craig L. Hill.

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Weinstock, I., Barbuzzi, E., Wemple, M. et al. Equilibrating metal-oxide cluster ensembles for oxidation reactions using oxygen in water. Nature 414, 191–195 (2001). https://doi.org/10.1038/35102545

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