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Electron spin resonance and

Quadrupole coupling constants for molecules are usually determined from the hyperfine structure of pure rotational spectra or from electric-beam and magnetic-beam resonance spectroscopies. Nuclear magnetic resonance, electron spin resonance and Mossbauer spectroscopies are also routes to the property. There is a large amount of experimental data for and halogen-substituted molecules. Less data is available for deuterium because the nuclear quadrupole is small. [Pg.278]

This comprehensive review of theoretical models and techniques will be invaluable to theorists and experimentalists in the fields of infrared and Raman spectroscopy, nuclear magnetic resonance, electron spin resonance and flame thermometry. It will also be useful to graduate students of molecular dynamics and spectroscopy. [Pg.301]

Evidence indicates [28,29] that in most cases, for organic materials, the predominant intermediate in radiation chemistry is the free radical. It is only the highly localized concentrations of radicals formed by radiation, compared to those formed by other means, that can make recombination more favored compared with other possible radical reactions involving other species present in the polymer [30]. Also, the mobility of the radicals in solid polymers is much less than that of radicals in the liquid or gas phase with the result that the radical lifetimes in polymers can be very long (i.e., minutes, days, weeks, or longer at room temperature). The fate of long-lived radicals in irradiated polymers has been extensively studied by electron-spin resonance and UV spectroscopy, especially in the case of allyl or polyene radicals [30-32]. [Pg.855]

Hartmann, M., A. Piippl et al. (1996). Ethylene dimerization and butene isomerization in nickel-containing MCM-41 and A1MCM-41 mesoporous molecular sieves An electron spin resonance and gas chromatography study. J. Phys. Chem. 100 9906-9910. [Pg.186]

More advanced scale was proposed by Kamlet and Taft [52], This phenomenological approach is very universal as may be successfully applied to the positions and intensities of maximal absorption in IR, NMR (nuclear magnetic resonance), ESR (electron spin resonance), and UV-VS absorption and fluorescence spectra, and to many other physical or chemical parameters (reaction rates, equilibrium constant, etc.). The scale is quite simple and may be presented as ... [Pg.208]

This means that addition of elemental E to alkali metal polychalcogenide fluxes (200-600°C) will promote the formation of longer chains as potential ligands, when such molten salts are employed as reaction media for the preparation of polychalcogenide complexes. Speciation analysis for polychalcogenides in solution has been performed by a variety of physical methods including UV/vis absorption spectroscopy, Raman spectroscopy, Se, Te and Te NMR, electron spin resonance and electrospray mass spectrometry. [Pg.546]

Let us take 1978 as the starting point. Massoth [51] then published an extensive review of what was known about the structure of HDS catalysts. Characterization was essentially based on techniques such as X-ray diffraction, electron microscopy, photoelectron spectroscopy, electron spin resonance and magnetic methods. Massoth was rather unhappy with the state of affairs in 1978. He was struck by the ...diversity and apparent contradictions of results and interpretations... It almost seems as though everyone is working with a different catalyst . [Pg.267]

A. Shengelaya, S. Reich, Y. Tsabba, and K. A. Muller, Electron spin resonance and magnetic susceptibility suggest superconductivity in Na doped WO3 samples, Eur. Phys. J. B 12(1), 13-15 (1999). [Pg.135]

As indicated in the previous discussion, Mossbauer spectroscopy provides information that when coupled with results using other structural techniques assists in determining the structure of the complex under analysis. The relationships between the various techniques are summarized in Table II. The Mossbauer chemical shift provides information about the 4 electron contribution to the bond between the metal and the ligands in a complex. Similar estimates can be obtained from the results of measurements on the fine structure in the x-ray absorption edge and nuclear magnetic resonance data. The number of unpaired electrons can be evaluated from magnetic susceptibility data, electron spin resonance, and the temperature coeflScient of the Mossbauer quadrupole splitting (Pr). [Pg.59]

M. Rizzotto, V. Moreno, S. Signorella, V. Daier, and L. F. Sala, Electron spin resonance and potentiometric studies of the interaction of Cr(VI) and Cr(V) with D-ribose-5-phosphate and nucleotides, Polyhedron, 19 (2000) 417 123. [Pg.119]

In terms of coupling flame generation and detection methods, several combinations are common. Generally, shock tubes are coupled with IR and UV absorption and gas chromatography (GC) detectors, while flow reactors are used in tandem with GC, electron spin resonance, and resonance fluorescence detection. [Pg.88]

Graslund, A. Ehrenberg, A. Rupprecht, A. Intemat. Conf. on Electron Spin Resonance and Nuclear Magnetic Resonance in Biology and Medicine and Fifth Internat. Conf. on Magnetic Resonance in Biological Systems, 1972. [Pg.466]

There appear to be only two independent reports in the literature on CD CdTe (which is the only telluride reported in the CD literature). In the first one, the CdTe was deposited with the main purpose of carrying out electron spin resonance and morphological studies of the effect of annealing, while another paper, based apparently on the first, described the deposition, with the main purpose of further use in photovoltaic cells. Therefore only limited detail on the actual deposition or properties of the as-deposited films were given. This is surprising in view of the fact that the first report is the first case of a CD telluride. [Pg.182]

T. M. McKinney, Electroanal. Chem. 10 91 (1977). Electron Spin Resonance and Electrochemistry. ... [Pg.955]

Formation of radical anions 109 and 110 from l,l-dimethyl-2,5-diphenylsilole and 1,1-dimethyl-2,3,4,5-tetraphenylsilole164, which are further reduced to the dianions 111 and 112, respectively, has been shown by electron spin resonance and UV-visible spectrometry (equation 62). [Pg.2010]

Cadet J, Voituriez L, Berger M, Myers LS Jr (1983) Radiation-induced degradation of purine and pyrimidine 2 -deoxyribonudeosides in agueous KBr solutions. Z Naturforsch 38b 1643-1651 Champagne MH, Mullins MW, Colson A-O, Sevilla MD (1991) Electron spin resonance evidence for intra- and intermolecular oo bonding in methionine radicals relative stabilities of S-CI, S-Br, S-N, and S-S three electron bonds. J Phys Chem 95 6487-6493 Chawla OP, Fessenden RW (1975) Electron spin resonance and pulse radiolysis studies of some reactions of S04. J Phys Chem 79 2693-2700... [Pg.97]

Behrens G, Bothe E, Koltzenburg G, Schulte-Frohlinde D (1980) Formation and structure of 1,1-di-alkoxyalkene radical cations in aqueous solution. An in situ electron spin resonance and pulse conductivity study. J Chem Soc Perkin Trans 2 883-889... [Pg.128]

Nelson WH, Sagstuen E, Hole EO, Close DM (1998) Electron spin resonance and electron nuclear double resonance study of X-irradiated deoxyadenosine proton transfer behaviour of primary ionic radicals. Radiat Res 149 75-86... [Pg.325]

Electron spin resonance and electrochemistry Spectroelectrochemistry— transparent electrodes Digital simulation methods in electrochemistry... [Pg.164]

Bayer, C., Martin-Neto, L., Mielniczuk, J., and Ceretta, C. A. (2000). Effect of no-till cropping systems on soil organic matter in a sandy clay loam Acrisol from Southern Brazil monitored by electron spin resonance and nuclear magnetic resonance. Soil Til. Res. 53, 95-104. [Pg.717]


See other pages where Electron spin resonance and is mentioned: [Pg.494]    [Pg.33]    [Pg.438]    [Pg.153]    [Pg.109]    [Pg.315]    [Pg.10]    [Pg.134]    [Pg.53]    [Pg.62]    [Pg.115]    [Pg.166]    [Pg.184]    [Pg.26]    [Pg.8]    [Pg.80]    [Pg.376]    [Pg.87]    [Pg.307]    [Pg.139]    [Pg.964]    [Pg.786]    [Pg.57]    [Pg.387]   
See also in sourсe #XX -- [ Pg.2 , Pg.2 , Pg.407 ]

See also in sourсe #XX -- [ Pg.199 , Pg.200 ]




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