Record Details

Nerve Agent Degradation Using Polyoxoniobates

ScholarsArchive at Oregon State University

Field Value
Title Nerve Agent Degradation Using Polyoxoniobates
Names Kinnan, Mark K. (creator)
Creasy, William R. (creator)
Fullmer, Lauren B. (creator)
Schreuder-Gibson, Heidi L. (creator)
Nyman, May (creator)
Date Issued 2014-05 (iso8601)
Note This is an author's peer-reviewed final manuscript, as accepted by the publisher. The published article is copyrighted by Wiley-VCH and can be found at: http://onlinelibrary.wiley.com/doi/10.1002/ejic.201400016/full.
Abstract Polyoxoniobates are exceptional amongst polyoxometalates in that
they can potentially perform base catalysis in water, a process in
which a proton is bonded to an oxo ligand, and a hydroxyl is
released. Catalytic decomposition of chemical warfare agents such
as organofluorophosphates that were used recently in the infamous
civilian attacks in Syria is one opportunity to employ this process.
Upon evaluation of the polyoxoniobate Lindqvist ion, [Nb₆O₁₉]⁸⁻
fast neutralization kinetics was discovered for the breakdown of the
nerve agent simulant diisopropyl fluorophosphate (DFP). Further
testing of the polyoxoniobates against nerve agents Sarin (GB), and
Soman (GD) was also performed. It was determined that different
Lindqvist countercations (Li, K, or Cs) affect the rate of decomposition of the organophosphate
compounds in both aqueous media (homogeneous reaction), and
in the solid-state (heterogeneous reaction). Small-angle X-ray
scattering of solutions of the Li, K, and Cs [Nb₆O₁₉]⁸⁻ salts at
concentrations which the experiments were performed revealed
distinct differences that could be linked to their relative reaction
rates. This study represents the first demonstration of exploiting
the unique alkaline reactivity of polyoxoniobates for nerve agent
decontamination.
Genre Article
Topic Polyoxometalates
Identifier Kinnan, M. K., Creasy, W. R., Fullmer, L. B., Schreuder-Gibson, H. L. and Nyman, M. (2014), Nerve Agent Degradation with Polyoxoniobates. European Journal of Inorganic Chemistry, 2014: 2361–2367. doi: 10.1002/ejic.201400016

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