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Electron–nuclear double resonance on copper (II) tetraimidazole

dc.contributor.authorVan Camp, Harlan L.en_US
dc.contributor.authorSands, Richard H.en_US
dc.contributor.authorFee, James A.en_US
dc.date.accessioned2010-05-06T22:47:33Z
dc.date.available2010-05-06T22:47:33Z
dc.date.issued1981-09-01en_US
dc.identifier.citationVan Camp, Harlan L.; Sands, Richard H.; Fee, James A. (1981). "Electron–nuclear double resonance on copper (II) tetraimidazole." The Journal of Chemical Physics 75(5): 2098-2107. <http://hdl.handle.net/2027.42/70838>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/70838
dc.description.abstractWe have investigated the electron–nuclear double resonance (ENDOR) from frozen aqueous solutions of 65Cu++(imidazole)4, 65Cu++ (imidazole–15N)4, and 65Cu++(imidazole–Dn)4, where n = 1, 2, 3, and 4 for selectively deuterated imidazole. We have observed ENDOR associated with the imidazole protons and the two imidazole nitrogens. The selective deuteration has allowed us to attempt identification of the weakly coupled protons responsible for the ENDOR spectrum, and a comparison of the overall line shape of that spectrum taken at two extreme points of the EPR spectrum suggests that some of the imidazole planes are tilted with respect to the plane of the complex. The ENDOR arising from the nitrogen nearest the copper is primarily isotropic with A(g⊥) = 41.6±1.5 MHz and A(g∥) = 39.8±1.5 MHz. The resonance shows little structure and seems consistent with a picture that requires some inequivalence among the various imidazoles. The remote nitrogen ENDOR reveals both hyperfine and quadrupole effects with approximately isotropic A(14N) = 1.79 MHz, Qz′z′?0.360 MHz, and Qx′x′y′x′?0.349 MHz. These values are in agreement with the results of the nuclear modulation effect [J. Chem. Phys. 69, 4921 (1978)]. The values for the quadrupole constants are thought to be accurate within 10% and are the same as are found in free imidazole. It is also demonstrated that, in this instance, ENDOR and the nuclear modulation effect are complementary in that they have each provided different parts of the same hyperfine spectrum.en_US
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dc.publisherThe American Institute of Physicsen_US
dc.rights© The American Institute of Physicsen_US
dc.titleElectron–nuclear double resonance on copper (II) tetraimidazoleen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumBiophysics Research Division, Institute of Science and Technology, The University of Michigan, Ann Arbor, Michigan 48109en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/70838/2/JCPSA6-75-5-2098-1.pdf
dc.identifier.doi10.1063/1.442313en_US
dc.identifier.sourceThe Journal of Chemical Physicsen_US
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dc.owningcollnamePhysics, Department of


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