Syntheses of selected .epsilon.-(2- or 9-anthryl)alkanoic acids and certain esters - carbon-13 spin-lattice relaxation time measurements of methyl 5-(2-anthryl)pentanoate and methyl 7-(2-anthryl)heptanoate

1981 ◽  
Vol 46 (3) ◽  
pp. 626-629 ◽  
Author(s):  
Palanisamy Arjunan ◽  
Nagaraj Shymasundar ◽  
K. Darrell Berlin ◽  
Dada Najjar ◽  
Mark G. Rockley
Keyword(s):  
Relaxation Time ◽  
Lattice Relaxation ◽  
Lattice Relaxation Time ◽  
Spin Lattice Relaxation ◽  
Spin Lattice Relaxation Time ◽  
Spin Lattice ◽  
Alkanoic Acids

NUCLEAR SPIN-LATTICE RELAXATION TIME IN TIN

1978 ◽  
Vol 39 (C6) ◽  
pp. C6-1215-C6-1216
Author(s):  
H. Ahola ◽  
G.J. Ehnholm ◽  
S.T. Islander ◽  
B. Rantala
Keyword(s):  
Relaxation Time ◽  
Nuclear Spin ◽  
Lattice Relaxation ◽  
Lattice Relaxation Time ◽  
Spin Lattice Relaxation ◽  
Spin Lattice Relaxation Time ◽  
Spin Lattice ◽  
Nuclear Spin Lattice Relaxation

Pressure dependence of iodine nuclear relaxation in rubidium iodide

1978 ◽  
Vol 56 (10) ◽  
pp. 1386-1389
Author(s):  
Marie D'Iorio ◽  
Robin L. Armstrong
Keyword(s):  
Relaxation Time ◽  
Lattice Relaxation ◽  
Low Pressure ◽  
Lattice Relaxation Time ◽  
Lattice Defects ◽  
Spin Lattice Relaxation ◽  
Polymorphic Phase Transition ◽  
Spin Lattice Relaxation Time ◽  
Spin Lattice ◽  
Pressure Phase

The pressure-induced polymorphic phase transition at about 4 k bar in rubidium iodide was studied using nuclear magnetic resonance. The signature of the structural transition is a loss of echo intensity which presumably is due to an increase in the number of lattice defects as a result of the transition. The ratio of the spin–spin relaxation times of the iodine nuclei in the two phases is in agreement with the ratio predicted by a second moment calculation. The actual experimental values, however, are considerably smaller than the theoretical predictions signifying the migration of lattice defects. Estimates of the iodine spin–lattice relaxation time at atmospheric pressure indicate the necessity to include both an anharmonic Raman contribution and a covalency factor. The change in spin–lattice relaxation time with pressure as measured in the low pressure phase is dominated by the change in the lattice parameter. At the critical pressure the spin–lattice relaxation time decreases by a fractional amount which is approximately equal to the fractional volume change characterizing the transition. The pressure derivative of the spin–lattice relaxation time in the high pressure phase is nearly equal to that in the low pressure phase.

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