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Facile Proton Conduction via Ordered Water Molecules in a Phosphonate Metal−Organic Framework
Author(s) -
Jared M. Taylor,
Roger K. Mah,
Igor Moudrakovski,
Christopher I. Ratcliffe,
Ramanathan Vaidhyanathan,
George K. H. Shimizu
Publication year - 2010
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja107035w
Subject(s) - chemistry , phosphonate , molecule , proton , arrhenius plot , crystallography , metal , solid state nuclear magnetic resonance , deuterium , nuclear magnetic resonance spectroscopy , arrhenius equation , zirconium , activation energy , stereochemistry , inorganic chemistry , nuclear magnetic resonance , organic chemistry , physics , quantum mechanics
A new phosphonate metal-organic framework (MOF) with a layered motif but not that of the classical hybrid inorganic-organic solid is presented. Zn(3)(L)(H(2)O)(2)·2H(2)O (L = [1,3,5-benzenetriphosphonate](6-)), henceforth denoted as PCMOF-3, contains a polar interlayer lined with Zn-ligated water molecules and phosphonate oxygen atoms. These groups serve to anchor free water molecules into ordered chains, as observed by X-ray crystallography. The potential for proton conduction via the well-defined interlayer was studied by (2)H solid-state NMR spectroscopy and AC impedance spectroscopy. The proton conductivity in H(2) was measured as 3.5 × 10(-5) S cm(-1) at 25 °C and 98% relative humidity. More interestingly, an Arrhenius plot gave a low activation energy of 0.17 eV for proton transfer, corroborating the solid-state NMR data that showed exchange between all deuterium sites in the D(2)O analogue of PCMOF-3, even at -20 °C.

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