@article {1119,
	title = {Determining the geometry of strongly hydrogen-bonded silanols in a layered hydrous silicate by solid-state nuclear magnetic resonance},
	journal = {Journal of Chemical Physics},
	volume = {122},
	number = {5},
	year = {2005},
	note = {ISI Document Delivery No.: 895RGTimes Cited: 7Cited Reference Count: 45},
	month = {Feb},
	pages = {10},
	type = {Article},
	abstract = {High-resolution solid-state NMR spectroscopy is exploited to obtain structural constraints involving strongly hydrogen-bonded silanols in octosilicate, a prominent member of the layered hydrous sodium silicates. Proton-silicon cross-polarization dynamics reveals that octosilicate contains two types of Q(3) silicons present in hydrogen-bonded -Si-O-H...O-Si- and -Si-O{\textendash}type sites which can only be distinguished by their different abilities to cross polarize and the different mobilities of neighboring hydrous species. The theoretical analysis of the oscillating components of the polarization transfer buildup curves suggests that the model of heteronuclear pairs is an adequate description of the quantum spin system within hydrogen-bonded -Si-O-H...O-Si- fragments. We also show that dipolar modulated, slow speed magic-angle Si-29 NMR spectrum provides unique geometric information on strongly hydrogen-bonded silanols. The dipolar modulated spinning sidebands contain all the information necessary to determine the internuclear Si...H distances as well as the magnitude and orientation of the principal elements of the Si-29 chemical shielding tensor in the molecular frame. The data provide definite proof of the intralayer character of strongly hydrogen-bonded silanol groups in a bridging, albeit not symmetric, position between neighboring tetrahedra. The approach developed in this work may be useful to obtain structural information on related layered alkali metal silicates, silica gels as well as on other classes of microporous materials. (C) 2005 American Institute of Physics.},
	keywords = {DYNAMICS, MAGADIITE, MAS, NMR CROSS-POLARIZATION, RESOLUTION, ROTATING SOLIDS, SIDE-BAND, SPECTRA, SPECTROSCOPY, SPIN-EXCHANGE},
	isbn = {0021-9606},
	url = {<Go to ISI>://000226880100042},
	author = {Gardiennet, C. and Marica, F. and Fyfe, C. A. and Tekely, P.}
}
@article {993,
	title = {Recent developments in solid-state magic-angle spinning, nuclear magnetic resonance of fully and significantly isotopically labelled peptides and proteins},
	journal = {Philosophical Transactions of the Royal Society of London Series B-Biological Sciences},
	volume = {359},
	number = {1446},
	year = {2004},
	note = {ISI Document Delivery No.: 834XSTimes Cited: 7Cited Reference Count: 125},
	month = {Jun},
	pages = {997-1008},
	type = {Review},
	abstract = {In recent years, a large number of solid-state nuclear magnetic resonance (NMR) techniques have been developed and applied to the study of fully or significantly isotopically labelled (C-13, N-15 or C-13/N-15) biomolecules. In the past few years, the first structures of C-13/N-15-labelled peptides, Gly-Ile and Met-Leu-Phe, and a protein, Src-homology 3 domain, were solved using magic-angle spinning NMR, without recourse to any structural information obtained from other methods. This progress has been made possible by the development of NMR experiments to assign solid-state spectra and experiments to extract distance and orientational information. Another key aspect to the success of solid-state NMR is the advances made in sample preparation. These improvements will be reviewed in this contribution. Future prospects for the application of solid-state NMR to interesting biological questions will also briefly be discussed.},
	keywords = {assignment strategies, CHEMICAL-SHIFT ANISOTROPIES, CROSS-POLARIZATION, DIPOLAR-CORRELATION SPECTROSCOPY, DISTANCE, HIGH-FIELD, magic-angle spinning, MAS NMR, MEASUREMENTS, MEMBRANE-PROTEIN, NMR-SPECTROSCOPY, peptide and protein labelling, RESOLUTION, ROTATING SOLIDS, SH3 DOMAIN, SOLID-STATE NMR, SPECTRIN, structural parameters},
	isbn = {0962-8436},
	url = {<Go to ISI>://000222444800010},
	author = {Straus, S. K.}
}
@article {2807,
	title = {SOLID-STATE DOUBLE-RESONANCE NMR EXPERIMENTS INVOLVING QUADRUPOLAR AND SPIN 1/2 NUCLEI},
	journal = {Journal of Physical Chemistry},
	volume = {97},
	number = {51},
	year = {1993},
	note = {ISI Document Delivery No.: MP905Times Cited: 101Cited Reference Count: 58},
	month = {Dec},
	pages = {13484-13495},
	type = {Article},
	abstract = {In this work we describe coherence-transfer and dipolar-dephasing double-resonance NMR experiments that demonstrate spatial proximity of quadrupolar and spin 1/2 nuclei (other than protons) in solids. These experiments exploit heteronuclear dipolar couplings, whose magnitudes are proportional to the inverse third power of the internuclear distance and are therefore extremely sensitive to the separation of the coupled spins. Coherence transfer through cross-polarization is observed in both directions between Al-27 (I = 5/2) and P-31 (I = 1/2) nuclei in the inorganic aluminophosphate framework systems VPI-5 and AlPO4-8, and an experimental investigation of the parameters controlling the efficiency of the transfer is presented. Dipolar-dephasing difference experiments, rotational-echo double-resonance (REDOR), and transferred-echo double-resonance (TEDOR) experiments under magic-angle spinning conditions are also demonstrated. Two-dimensional extensions of the cross-polarization and TEDOR experiments reveal the dipolar couplings between specific pairs of Al-27 and P-31 nuclei in two-dimensional correlation spectra, directly mapping connectivities from distinct sites with resolved NMR resonances.},
	keywords = {CROSS-POLARIZATION NMR, DOUBLE-ROTOR, MAGIC ANGLE, MAGNETIC-RESONANCE, MAS-NMR, MOLECULAR-SIEVE VPI-5, RESOLUTION, ROTATING SOLIDS, SPECTRA, SPECTROSCOPY},
	isbn = {0022-3654},
	url = {<Go to ISI>://A1993MP90500012},
	author = {Fyfe, C. A. and Mueller, K. T. and Grondey, H. and Wongmoon, K. C.}
}
