Dipolar Relaxation of 7Li by Hindered Rotators NDxH3−x in Lithimn Hydrazinium Sulfate.

dc.contributor.authorParker, Robert S.
dc.contributor.authorSchmidt, V. Hugo
dc.date.accessioned2015-02-12T22:22:30Z
dc.date.available2015-02-12T22:22:30Z
dc.date.issued1972-04
dc.description.abstractWhen a hindered rotation does not change the spatial charge distribution but merely permutes the locations of nuclear magnetic moments, the resulting spin-lattice relaxation of a nearby fixed nucleus is likely to be dipolar even if this nucleus has a quadrupole moment. The dipolar relaxation rate is props rtional to the average of γ2I(I + 1) for the rotating nuclei and accordingly varies linearly with percentage of deuteration. For 7Li in LiN2H5SO4 at 14 MHz the peak is 1.8 sec− at 185°K, while in 81% deuterated LiN2D5SO4 it is 4.2 times smaller, as predicted. The ND2 group deuterons also have a peak at this temperature, and all three curves show activation energy of about 0.19 eV, as found previously for protons and deuterons within rotating NH3 and ND3 groups.en_US
dc.identifier.citationParker, Robert S, and V Hugo Schmidt. “Dipolar Relaxation of 7Li by Hindered Rotators NDxH3−x in Lithimn Hydrazinium Sulfate.� Journal of Magnetic Resonance (1969) 6, no. 4 (April 1972): 507–515. doi:10.1016/0022-2364(72)90160-6.en_US
dc.identifier.issn1090-7807
dc.identifier.urihttps://scholarworks.montana.edu/handle/1/8842
dc.subjectElectromagneticsen_US
dc.titleDipolar Relaxation of 7Li by Hindered Rotators NDxH3−x in Lithimn Hydrazinium Sulfate.en_US
dc.typeArticleen_US
mus.citation.extentfirstpage507en_US
mus.citation.extentlastpage515en_US
mus.citation.issue4en_US
mus.citation.journaltitleJournal of Magnetic Resonanceen_US
mus.citation.volume6en_US
mus.identifier.categoryPhysics & Mathematicsen_US
mus.identifier.doi10.1016/0022-2364(72)90160-6en_US
mus.relation.collegeCollege of Letters & Science
mus.relation.collegeCollege of Letters & Scienceen_US
mus.relation.departmentPhysics.en_US
mus.relation.universityMontana State University - Bozemanen_US

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