Heteronuclear double-quantum MAS NMR spectroscopy in dipolar solids

Citation
K. Saalwachter et al., Heteronuclear double-quantum MAS NMR spectroscopy in dipolar solids, J MAGN RES, 139(2), 1999, pp. 287-301
Citations number
38
Categorie Soggetti
Chemistry & Analysis","Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF MAGNETIC RESONANCE
ISSN journal
10907807 → ACNP
Volume
139
Issue
2
Year of publication
1999
Pages
287 - 301
Database
ISI
SICI code
1090-7807(199908)139:2<287:HDMNSI>2.0.ZU;2-G
Abstract
A new pulse sequence for high-resolution solid-state heteronuclear double-q uantum MAS NMR spectroscopy of dipolar-coupled spin-1/2 nuclei is introduce d. It is based on the five-pulse sequence known from solution-state NMR, wh ich is here applied synchronously to both spin species. The heteronuclear d ouble-quantum (HeDQ) spinning-sideband patterns produced by this experiment are shown to be sensitive to the heteronuclear distance, as well as the re lative orientations of the chemical-shift and dipolar tensors. In particula r, it is shown that the HeDQ patterns exhibit an enhanced sensitivity to th e chemical shielding tensors as compared with the single-quantum spinning-s ideband patterns. The detection of HeDQ patterns via the I and S spins is d iscussed. The isolated C-13-H-1 spin pair in deuterated ammonium formate wi th C-13 in natural abundance was chosen as a model system, and the perturbi ng influence of dipolar couplings to surrounding protons on the C-13-H-1 DQ coherence is discussed. The pulse sequence can also be used as a heteronuc lear double-quantum filter, hence providing information about heteronuclear couplings, and thus allowing the differentiation of quaternary and CH, bon ded carbons. The elucidation of C-13-H-1 dipolar proximities is presented f or a sample of bisphenol A polycarbonate with C-13 in natural abundance, re corded with a broadband version of the synchronized five-pulse sequence. (C ) 1999 Academic Press.