Electron paramagnetic resonance studies of the E′ centers in alpha-quartz

2008 ◽  
Vol 86 (7) ◽  
pp. 871-881 ◽  
Author(s):  
B D Perlson ◽  
J A Weil

Room-temperature electron paramagnetic resonance (EPR) studies (at ca. 9.85 GHz) of γ- and x-irradiated alpha-quartz are reported and discussed. The previously described E′2 center has been proved to be associated with hydrogen, and this center’s primary silicon-29 hyperfine coupling matrix has now been accurately determined, as were its hydrogen hyperfine coupling and electronic Zeeman splitting (g) matrices. The paramagnetic center is believed to arise from attack on a diamagnetic oxygen-anion vacancy V(O0) (E center) effectively by an electron and a proton arising from atomic hydrogen produced in the irradiation process. A second very similar center, called E′2(II) herein, was discovered and its parameter matrices too have been obtained by EPR, and it was modelled as described herein. It is proposed that the proton in E′2 resides on an oxygen anion adjacent to the vacancy species. Comparison is made of the spin-Hamiltonian parameter matrices and the choice of best symmetry-related sites expressing them, for the various centers E′1–E′4. PACS Nos.: 76.30.–v,61.72.Hh, 76.30.Mi, 42.70.Ce, 61.80.–x, 61.72.–y

2017 ◽  
Vol 231 (4) ◽  
Author(s):  
Andrey A. Kuzhelev ◽  
Victor M. Tormyshev ◽  
Olga Yu. Rogozhnikova ◽  
Dmitry V. Trukhin ◽  
Tatiana I. Troitskaya ◽  
...  

AbstractTriarylmethyl (TAM) radicals are widely used in electron paramagnetic resonance (EPR) spectroscopy as spin labels and in EPR imaging as spin probes for


2004 ◽  
Vol 59 (1-2) ◽  
pp. 103-104 ◽  
Author(s):  
Biray Aşik ◽  
Mehmet Birey

The electron paramagnetic resonance of γ -Irradiated single crystals of dimethyl malonic acid [(CH3)2C(COOH)2] has been studied for different orientations of the crystal in a magnetic field. The radicals produced by gamma irradiation have been investigated between 123 and 300 K. The spectra were found to be temperature independent, and radiation damage centres were attributed to [(CH3)2C(COOH)2]+ radicals. The g factor and hyperfine coupling constants were found to be almost isotropic with average values g = 2.0036, a(COOH)2 = 0.5 mT, a(CH3)2 = 2.1 mT, respectively, and spin density ρ = 91% of the [(CH3)2C(COOH)2]+ radical.


2021 ◽  
Author(s):  
Piotr Garbacz ◽  
Juha Vaara

A chirality-sensitive effect induced by antisymmetric hyperfine coupling, which lifts the intrinsic insensitivity of electron paramagnetic resonance spectroscopy to molecular chirality, is described.


1987 ◽  
Vol 243 (1) ◽  
pp. 235-239 ◽  
Author(s):  
P M A Gadsby ◽  
C Greenwood ◽  
A Coddington ◽  
A J Thomson ◽  
C Godfrey

Formate dehydrogenase from Pseudomonas aeruginosa contains molybdenum, a [4Fe-4S] cluster and cytochrome b. This paper reports the detection of molybdenum as Mo(V) by e.p.r. spectroscopy. In order to generate Mo(V) signals, addition of amounts of excess formate varying between 10- and 50-fold over enzyme, followed by 200-fold excess of sodium dithionite, were used. Two Mo(V) species were observed. One, the major component, has g1 = 2.012, g2 = 1.985 and g3 = 1.968, appeared at low concentrations of formate and increased linearly in intensity with increasing concentrations of formate up to 25-fold excess over the enzyme. At higher formate concentration this signal disappeared. The appearance and disappearance of this Mo(V) signal seems to parallel the state of reduction of the [4Fe-4S] clusters. A second, minor, Mo(V) species with g-values g1 = 1.996, g2 = 1.981 and g3 = 1.941 appears at a constant level during the formate-dithionite titration. No evidence has been obtained for nuclear hyperfine coupling to protons. The major Mo(V) species has unusual e.p.r. signals compared with other molybdenum-containing enzymes, except for that observed in the formate dehydrogenase from Methanobacterium formicicum [Barber, Siegel, Schauer, May & Ferry (1983) J. Biol. Chem. 258, 10839-10845]. The present work suggests that the enzyme is acting as a CO2 reductase, with dithionite as an electron donor to a [4Fe-4S] cluster, which in turn donates electrons to molybdenum, producing a Mo(V) species with CO2 bound to the metal.


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