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Probing molecular geometry of solids by nuclear magnetic resonance spin exchange at the n=0 rotational resonance condition

Tekely, P., Gardiennet, C., Potrzebowski, M.J., Sebald, A., Reichert, D. and Luz, Z. (2002) Probing molecular geometry of solids by nuclear magnetic resonance spin exchange at the n=0 rotational resonance condition. Journal of Chemical Physics, 116 (17). pp. 7607-7616. ISSN 0021-9606

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Abstract

Exploration of the molecular geometry in rotating powder solids on the basis of magnetization exchange between spins with identical isotropic chemical shifts but differing chemical shielding tensor orientations is demonstrated experimentally. For this we take advantage of the potential of the ODESSA (one-dimensional exchange spectroscopy by sidebands alternation) experiment for the accurate measurement of spin exchange rate constants. We also report the observation of oscillatory behavior of the rotor-driven magnetization exchange at this so-called n = 0 rotational-resonance condition which, in contrast to n = 1,2,3, rotational-resonance conditions, takes place at nearly arbitrary magic-angle spinning frequencies. The sensitivity of the longitudinal exchange decays to the relevant physical parameters of the spin system under conditions of rotor-driven and proton-driven magnetization exchange is discussed theoretically and demonstrated experimentally. Several 13C and 31P spin-exchange measurements have been performed on a series of model compounds covering a broad range of internuclear distances between carboxyl carbon atoms, and on a series of phosphorylated amino acids with different internuclear distances between phosphorus sites. The capacity of the ODESSA experiment for an unambiguous recognition of distinct internuclear distances is demonstrated. Potential applications of such measurements involve the exploration of intermolecular distances and the determination of the mutual orientation of neighboring molecular fragments in polycrystalline and noncrystalline solids. ©2002 American Institute of Physics.

Item Type: Article
Institution: The University of York
Academic Units: The University of York > Chemistry (York)
Depositing User: York RAE Import
Date Deposited: 11 Jun 2009 11:55
Last Modified: 11 Jun 2009 11:55
Published Version: http://dx.doi.org/10.1063/1.1465416
Status: Published
Publisher: American Institute of Physics
Identification Number: 10.1063/1.1465416
URI: http://eprints.whiterose.ac.uk/id/eprint/6503

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