@article {1461,
	title = {The rotational spectrum and hyperfine structure of arsenic monophosphide, AsP},
	journal = {Journal of Molecular Spectroscopy},
	volume = {238},
	number = {1},
	year = {2006},
	note = {ISI Document Delivery No.: 061MMTimes Cited: 4Cited Reference Count: 40Leung, Flora Cooke, Stephen A. Gerry, Michael C. L.},
	month = {Jul},
	pages = {36-41},
	type = {Article},
	abstract = {Arsenic monophosphide has been prepared by laser ablation of arsenic in the presence of PH3. The J = 2-1 and 1-0 transitions in both the ground and first excited vibrational states have been measured with a cavity pulsed jet Fourier-transform microwave spectrometer. An improved equilibrium internuclear distance (r(e)) has been obtained. Hyperfine structure in the rotational spectrum of AsP has been resolved and has led to the first determinations of the As nuclear quadrupole coupling constant and both nuclear spin-rotation constants. The data enable the electronic structure of AsP to be compared with those of other mixed Group 15 diatomic molecules. (c) 2006 Elsevier Inc. All rights reserved.},
	keywords = {arsenic monophosphide microwave rotational spectrum, BiP, CONSTANTS, DENSITY-FUNCTIONAL THEORY, DISTANCE, ENERGY, equilibrium internuclear, Fourier transform, laser ablation, microwave spectrum, MOLECULES, of arsenic monophosphide, ORDER REGULAR APPROXIMATION, RESONANCE, SPIN-ROTATION, TENSORS},
	isbn = {0022-2852},
	url = {<Go to ISI>://000238876600004},
	author = {Leung, F. and Cooke, S. A. and Gerry, M. C. L.}
}
@article {4549,
	title = {Characterization of Na5P3O10 polymorphs by Na-23 MAS, Na-23 MQMAS, and P-31 MAS NMR spectroscopy},
	journal = {Inorganic Chemistry},
	volume = {38},
	number = {1},
	year = {1999},
	note = {ISI Document Delivery No.: 157MUTimes Cited: 20Cited Reference Count: 42},
	month = {Jan},
	pages = {84-92},
	type = {Article},
	abstract = {The two anhydrous polymorphs of Na5P3O10 have been characterized by Na-23 and P-31 MAS NMR spectroscopy, The Na-23 multiple-quantum (MQ) MAS NMR spectrum of the low-temperature form (phase II) displays three resonances for which the quadrupole coupling parameters and isotropic chemical shifts have been accurately determined from the MAS NMR spectra of the central transition. Thereby, discrepancies between recently reported Na-23 MQMAS spectra of this phase and the crystal structure have been clarified. The Na-23 resonances observed for the low-temperature form are assigned to the crystallographically nonequivalent Na sites in the crystal structure using point-monopole calculations of the electric-field gradient tensors. Three Na-23 resonances have also been observed for the high-temperature form (phase I), with two signals having very similar quadrupolar couplings and isotropic chemical shifts indicating similar coordination environments for the corresponding Na sites, in disagreement with the reported single-crystal structure. Point-monopole calculations of the electric-field gradient tensors based on the crystal structure fail to reproduce the experimental values. The P-31 chemical shielding anisotropies, obtained from P-31 MAS NMR spectra, show that the terminal P atoms of the P3O105- ions have a negative shielding anisotropy parameter (delta(sigma) = delta(iso) - delta(33)) in agreement with similar observations reported for diphosphates. This characteristic feature has been used in the assignment of the three P-31 resonances observed for the hexahydrate Na5P3O10. 6H(2)O.},
	keywords = {2-SPIN SYSTEMS, ANGLE-SPINNING NMR, CHEMICAL SHIELDING, CONDENSED PHOSPHATES, DIPOLAR, NUCLEAR-MAGNETIC-RESONANCE, QUADRUPOLAR NUCLEI, SODIUM TRIPHOSPHATE, SOLID-STATE, SPECTRA, TENSORS},
	isbn = {0020-1669},
	url = {<Go to ISI>://000078066900013},
	author = {Fyfe, C. A. and Altenschildesche, H. M. Z. and Skibsted, J.}
}
