Subject electron spin resonance

Transient concentrations of Ag(II) were detected spectrophotometrically, and by electron spin resonance. The thermal decomposition of Ag(II) perchlorate, the subject of a separate studytakes place by... 

Despite their short half-lives, it is possible to detect free radicals in biological tissues by the addition of nonradicals such as nitrones or nitroso compounds, which act as spin traps by forming relatively stable free radicals on reaction with the endogenous radical species. Utilizing the technique of electron spin resonance (e.s.r.) spectroscopy, we have demonstrated ROM generation by human rheumatoid synovium when subjected to cycles of hypoxia/normoxia in vitro. Using 3,5-dibromo-4-nitroso-benzenesulphonate (DBNBS) as a spin trap, a... 

The chapter Electron Spin Resonance in Catalysis by Lunsford was prompted by the extensive activity in this field since the publication of an article on a similar subject in Volume 12 of this serial publication. This chapter is limited to paramagnetic species that are reasonably well defined by means of their spectra. It contains applications of ESR technique to the study of adsorbed atoms and molecules, and also to the evaluation of surface effects. The application of ESR to the determination of the state of transition metal ions in catalytic reactions is also discussed. 

The title Spectroscopy in Catalysis is attractively compact but not quite precise. The book also introduces microscopy, diffraction and temperature programmed reaction methods, as these are important tools in the characterization of catalysts. As to applications, I have limited myself to supported metals, oxides, sulfides and metal single crystals. Zeolites, as well as techniques such as nuclear magnetic resonance and electron spin resonance have been left out, mainly because the author has little personal experience with these subjects. Catalysis in the year 2000 would not be what it is without surface science. Hence, techniques that are applicable to study the surfaces of single crystals or metal foils used to model catalytic surfaces, have been included. 

In order to investigate the active sites of these proteins, laccases I and III were subjected to ESR (electron spin resonance) spectroscopic analysis. The ESR spectra shown in Figure 5 indicate clear differences in peaks 2 and 6 which support the concept that the copper atoms in laccases I and III have different conformations in each molecule. Furthermore, immunological similarity between laccases I and III was also investigated. Antibody specific for laccase III was prepared from rabbit serum by conventional methods. When applied to Ouchterlony diffusion plates containing laccase I, no precipitation lines developed (Figure 6). This result showed that there were no conserved epitopes on the surfaces laccases I and III. 

Thanks to the extensive literature on Aujj and the related smaller gold cluster compounds, plus some new results and reanalysis of older results to be presented here, it is now possible to paint a fairly consistent physical picture of the AU55 cluster system. To this end, the results of several microscopic techniques, such as Extended X-ray Absorption Fine Structure (EXAFS) [39,40,41], Mossbauer Effect Spectroscopy (MES) [24, 25, 42,43,44,45,46], Secondary Ion Mass Spectrometry (SIMS) [35, 36], Photoemission Spectroscopy (XPS and UPS) [47,48,49], nuclear magnetic resonance (NMR) [29, 50, 51], and electron spin resonance (ESR) [17, 52, 53, 54] will be combined with the results of several macroscopic techniques, such as Specific Heat (Cv) [25, 54, 55, 56,49], Differential Scanning Calorimetry (DSC) [57], Thermo-gravimetric Analysis (TGA) [58], UV-visible absorption spectroscopy [40, 57,17, 59, 60], AC and DC Electrical Conductivity [29,61,62, 63,30] and Magnetic Susceptibility [64, 53]. This is the first metal cluster system that has been subjected to such a comprehensive examination. 

An electron spin resonance study (4-300 K) of [Cu(l-Me-ttaH)6]-[BF4]2 reveals that the two crystallographically inequivalent Cu(II) sites are subject to different Jahn-Teller effects arising from differences in the symmetries of the two sites (220a). 

The data on electron spin resonance (ESR), electron-nuclear double resonance (ENDOR), and general triple resonance spectroscopy for 2,5-dihydro-l,2,3,5-thiatriazole-5-yl radicals was reviewed by Holm and Larsen <1996CHEC-II(4)733>. There are no new data on this subject. 

Whereas the Nuclear Quadrupole Resonance (NQR) spectra of organic halides formed the subject of a chapter in the previous volume of this series1—from now on referred to as I— the Electron Spin Resonance (ESR) spectra of halogenated organic radicals were not discussed in any of the previous volumes. The major part of this present chapter is therefore devoted to ESR spectra while the section on NQR spectra is an update of I. 

Tt is well known that the presence of precipitated polymer can influence the course of polymerization. In bulk acrylonitrile polymerization the effects are most dramatic and have been the subject of many studies. The literature on this subject has been reviewed by Bamford et al. (4) by Thomas (29), and by Peebles (23). Under conditions where the system becomes heterogeneous owing to precipitation of small particles of polymer, a protracted acceleration period is observed at the start of polymerization, and the final rate is found to depend on the 0.8 power of the concentration of free radical initiator. Unusual post-polymerization effects are observed in photoinitiated polymerization of acrylonitrile, owing to the presence of trapped radicals which can be detected by electron spin resonance. None of the detailed mechanisms proposed to... 

To illustrate the technique we will consider a few examples of free radicals which have been prepared in the rotating cryostat. In particular phenyl and acetyl radicals and methyl-substituted allyl radicals are of interest as they have not been trapped previously or identified with certainty. Since electron spin resonance has been used extensively to detect and identify the free radicals, account of the results will inevitably involve some description and analysis of their spectra, but we wish to focus the main discussion on the conclusions that can be drawn about structure and reactivity of the radicals. For information about the principles of e.s.r. and the interpretation of the spectra of free radicals the reader is referred to review articles and books on the subject (Symons, 1963 Norman and Gilbert, 1967 Maki, 1967 Horsfield, 1967 Carrington and McLachlan, 1967 Ayscough, 1967 Carrington and Luckhurst, 1968). 

These tubes were then subjected to gamma radiation at 0.5 megaroentgen per hour for 87.2 hours. An attempted electron spin resonance determination of the radical content yielded no evidence of the presence of radicals. 

Accident dosimetry using biological systems in which the quantification of chromosome aberrations or the ratios between different blood proteins can give an indication of exposure, is hampered by the individual characteristics of the victim (i.e. general health, diet etc.), and by the complexity of the techniques. These problems can be avoided by adopting a more physical approach, and both chemiluminescence and thermoluminescence of possible dosimeters, for example, have been found to be useful. The drawbacks here concern the solubility with chemiluminescence, the amount of sample required for thermoluminescence, and the impossibility of taking repeated measurements with either system. In contrast, electron spin resonance (ESR) spectroscopy is not subject to these constraints. Measurement is made directly on the sample, very small amounts of material can be used, and repeated measurements are possible... 

Secondly there are direct techniques, notably electron spin resonance spectroscopy (ESR), in which the free radicals produced by the fracture of covalent bonds are directly observed, both in respect of their chemical nature and their number. Much of this review is orncemed with the results of ESR studies and this technique is therefore treated at some length below. One little used technique for the direct assessment of free radicals produced by n chanical means is that of Pazonyi et al and Salloum and Eckert They dropped various polymers in an ethanolic solution of diphenyl picryl hydrazyl, a chemical indicator, and determined the free radical concentration in the cut surfaces by colorimetrie measurements of the colour change. This method is subject to soixm uncertainty on account of possible side reactions. 

Metal- and proton-exchanged zeolites have been recently attracted much attention because of their selective catalytic activity to efficiently reduce nitrogen monoxide (NO) by hydrocarbon in an 02-rich atmosphere [1]. The formation of nitrogen dioxide (NO2) from NO and O2 has been suggested as an important step in the selective reduction [2, 3] NO2 is one of rare stable paramagnetic gaseous molecules and has been subjected to electron spin resonance (ESR) studies [4-7]. The ESR parameters and their relation/to the electronic structure have been well established [4] and NO2 can be used as a "spin probe" for the study of molecular dynamics at the gas-solid interface by ESR. 

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