The use of differential transverse relaxation to detect mobile species in solids

Delayed acquisition of the proton NMR in selected organic molecular solids ( l-alanine, durene, ethyl fumarate, and p-hydroxybenzoic acid) is shown to allow the observation of mobile species in the presence of relatively rigid bulk molecules. The mobility is found to be thermally activated. The comb...

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Published inSolid state nuclear magnetic resonance Vol. 6; no. 1; pp. 63 - 71
Main Authors Gerstein, B.C., Hu, Jian Zhi, Zhou, Jinuan, Ye, Chaohui, Solum, Mark, Pugmire, Ronald, Grant, David M.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Inc 01.02.1996
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Summary:Delayed acquisition of the proton NMR in selected organic molecular solids ( l-alanine, durene, ethyl fumarate, and p-hydroxybenzoic acid) is shown to allow the observation of mobile species in the presence of relatively rigid bulk molecules. The mobility is found to be thermally activated. The combination of the thermally activated motion and magic-angle spinning leads to a fraction of these species moving nearly isotropically on the time scale of the inverse of the homonuclear dipolar splitting. In the case of ethyl fumarate and alanine, there exist populations with differing values of T 1 and T 1ϱ. This indicates the co-existence of relatively rigid and relatively mobile molecules in the same sample. The intensities under delayed acquisition cannot always be trusted to yield quantitative information. Comparison of spectra taken under delayed acquisition and under the CRAMPS (B.C. Gerstein, R.G. Pembleton, R.C. Wilson and L.M. Ryan, J. Chem. Phys., 66 (1977) 361) technique is made.
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ISSN:0926-2040
1527-3326
DOI:10.1016/0926-2040(95)01211-7