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pubmed-article:12932473pubmed:abstractTextSpin-state selection in solid-state NMR is demonstrated, using similar pulse sequences as used in liquid-state NMR. The different transitions of all three carbon resonances in fully 13C-labeled L-alanine are separated in different spectra. By selecting spin-states, the contribution of the J-coupling to the linewidth is removed, leading to a considerable enhancement in resolution. The spin-state-selective technique is demonstrated for magic-angle spinning frequencies from 6 to 35kHz. Other experimental conditions affecting the sensitivity of the experiments are discussed. Sensitivity losses due to the introduction of the spin-state-selective filter are shown to be acceptable. Finally, spin-state selection was used to experimentally confirm the differential broadening expected for the two transitions of the CH3 resonance.lld:pubmed
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pubmed-article:12932473pubmed:authorpubmed-author:EmsleyLyndonLlld:pubmed
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pubmed-article:12932473pubmed:year2003lld:pubmed
pubmed-article:12932473pubmed:articleTitleSpin-state selection in solid-state NMR.lld:pubmed
pubmed-article:12932473pubmed:affiliationLaboratoire de Chimie (UMR-5532 CNRS/ENS), Laboratoire de Recherche Conventionné du CEA (23V), Ecole Normale Supérieure de Lyon, 46 Allée d'Italie, 69364 Lyon, France.lld:pubmed
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