Composition dependence of low-frequency excitations in lithium silicophosphate glasses by nuclear magnetic resonance and electrical conductivity

1997 ◽  
Vol 55 (22) ◽  
pp. 14836-14846 ◽  
Author(s):  
J. Dieckhöfer ◽  
O. Kanert ◽  
R. Küchler ◽  
A. Volmari ◽  
H. Jain
2003 ◽  
Vol 802 ◽  
Author(s):  
N. J. Curro ◽  
L. Morales

Nuclear Magnetic Resonance studies of Ga stabilized δ-Pu reveal detailed information about the local distortions surrounding the Ga impurities as well as provides information about the local spin fluctuations experienced by the Ga nuclei. The Ga NMR spectrum is inhomogeneously broadened by a distribution of local electric field gradients (EFGs), which indicates that the Ga experiences local distortions from cubic symmetry. The Knight shift and spin lattice relaxation rate indicate that the Ga is dominantly coupled to the Fermi surface via core polarization, and is inconsistent with magnetic order or low frequency spin correlations.


1984 ◽  
Vol 62 (3) ◽  
pp. 621-627 ◽  
Author(s):  
Tim Allman ◽  
Ram G. Goel

Cationic complexes of the type [Hg(phosphine)n](ClO4)2 (n = 2, 3, 4) (phosphine = P(t-Bu)3, PCy3, P(4-Me2NC6H4)3, P(4-MeOC6H4)3, P(4-MeC6H4)3, P(3-MeC6H4)3, P(2-MeC6H4)3, P(4-FC6H4)3, P(4-ClC6H4)3) have been prepared and studied by vibrational spectroscopy in the perchlorate and low frequency regions, as well as by 31P and 199Hg nmr. The skeletal Hg—P frequencies have been assigned in both solution and the solid state. It was found that 1J(Hg—P) decreases with increasing phosphine basicity and that it is also dependent upon sample concentration and temperature.


1986 ◽  
Vol 5 (2) ◽  
pp. 89-96 ◽  
Author(s):  
Masuo MURO ◽  
Akira NAGATA ◽  
Chiseko SAKUMA ◽  
Toshio MORITANI ◽  
MaSae YONA ◽  
...  

1971 ◽  
Vol 49 (8) ◽  
pp. 1151-1160 ◽  
Author(s):  
P. R. Heckley ◽  
D. G. Holah ◽  
D. Brown

Reactions between niobium(V), tantalum(V), and protactinium(V) chlorides and bromides and sodium N,N-diethyldithiocarbamate (Nadtc) have been examined in non-aqueous, non-oxygenated organic solvents. Complexes obtained are of the types Mdtc4X, Mdtc3X2, Mdtc3S, Mdtc2X3, and Mdtc2X3.nC6H6 (n = 0.7–1.0); not all complexes have been isolated for each metal. Within each group the niobium(V) and tantalum(V) complexes are isostructural; possible structures are discussed in the light of results from infrared (i.r.) and nuclear magnetic resonance (n.m.r.) spectra, molecular weight, and electrical conductivity measurements.


2003 ◽  
Vol 118 (24) ◽  
pp. 11129-11138 ◽  
Author(s):  
Peter A. Beckmann ◽  
Carolyn A. Buser ◽  
Kathleen Gullifer ◽  
Frank B. Mallory ◽  
Clelia W. Mallory ◽  
...  

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