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Magnetic electron paramagnetic

Other magnetic measurements of catalysts include electron paramagnetic resonance and magnetic susceptibility. Although those are not as common as NMR, they can be used to look at the properties of paramagnetic and ferromagnetic samples. Examples of these applications can be found in the literature [87. [Pg.1794]

The reaction of bis(benzene)vanadium [12129-72-5] with TCNE affords an insoluble amorphous black soHd that exhibits field-dependent magnetization and hysteresis at room temperature, an organic-based magnet (12). The anion radical is quite stable in the soHd state. It is paramagnetic, and its intense electron paramagnetic resonance (epr) spectmm has nine principal lines with the intensity ratios expected for four equivalent N nuclei (13) and may be used as an internal reference in epr work (see Magnetic spin resonance). [Pg.403]

Nuclear Magnetic Resonance 2.1.1.3.A Electron Paramagnetic Resonance 2.1.1.4 Thermal/Mechanical Energy Interaction... [Pg.246]

Nuclear magnetic resonance spectroscopy of the solutes in clathrates and low temperature specific heat measurements are thought to be particularly promising methods for providing more detailed information on the rotational freedom of the solute molecules and their interaction with the host lattice. The absence of electron paramagnetic resonance of the oxygen molecule in a hydroquinone clathrate has already been explained on the basis of weak orientational effects by Meyer, O Brien, and van Vleck.18... [Pg.34]

Local Structure of the Eu2+ Impurity. From the experimental perspective, the doping of lanthanide ions into solid state materials can be probed by different instrumental technics such as nuclear magnetic resonance (NMR),44 extended X-ray absorption fine structure (EXAFS),45,46 or electron paramagnetic resonance (EPR),47 which instead of giving a direct clue of the local geometry offers only data that can be corroborated to it. From the theoretical point of view,... [Pg.2]

In general, several spectroscopic techniques have been applied to the study of NO, removal. X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR), nuclear magnetic resonance (NMR), extended X-ray absorption fine structure (EXAFS) and X-ray absorption near-edge structure (XANES) are currently used to determine the surface composition of the catalysts, with the aim to identify the cationic active sites, as well as their coordinative environment. [Pg.98]

G. Palmer, Electron paramagnetic resonance of metalloproteins, in Physical Methods in Bioinorganic Chemistry, Spectroscopy and Magnetism, ed. L. Que, Jr, University Science Books, Sausalito, CA, 2000. [Pg.164]

Bramley, R. and Strach, S.J. 1983. Electron paramagnetic resonance spectroscopy at zero magnetic field. Chemical Reviews 83 49-82. [Pg.232]

Foumel, A., Gambarelli, S., Guigliarelli, B., More, C., Asso, M., Chouteau, G., Hille, R., and Bertrand, P. 1998. Magnetic interactions between a 4Fe-4S l+ cluster and a flavin mononucleotide radical in the enzyme trimethylamine dehydrogenase a high-field electron paramagnetic resonance study. Journal of Chemical Physics 109 10905-10913. [Pg.233]

Hagen, W.R. 1981. Dislocation strain broadening as a source of anisotropic linewidth and asymmetrical lineshape in the electron paramagnetic resonance spectrum of metal-loproteins and related systems. Journal of Magnetic Resonance 44 447-469. [Pg.234]

Venable, J.H. 1967. Electron paramagnetic resonance spectroscopy of protein single crystals II. Computational methods. In Magnetic Resonance in Biological Systems, eds. A. Ehrenberg, B.G. Malmstrom and T. Vanngard Elmsford. New York Pergamon Press, 373-381. [Pg.239]


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See also in sourсe #XX -- [ Pg.706 , Pg.710 , Pg.711 ]




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