Effect of exchanged cations upon the electron spin resonance hyperfine splitting of chlorine dioxide adsorbed on X-type zeolites

1977 ◽  
Vol 81 (7) ◽  
pp. 669-673 ◽  
Author(s):  
H. Sugihara ◽  
K. Shimokoshi ◽  
I. Yasumori
1976 ◽  
Vol 54 (19) ◽  
pp. 3110-3113 ◽  
Author(s):  
R. Catterall ◽  
J. Slater ◽  
W. A. Seddon ◽  
J. W. Fletcher

The band maxima of transient optical absorption spectra observed by pulse radiolysis in ethylamine (EA)/tetrahydrofuran (THF) mixtures containing sodium tetraphenylboron are correlated with electron spin resonance (esr) hyperfine splitting constants obtained in potassium/EA/THF solutions. The data suggest that the optical spectra can be attributed to the same 'monomeric' species as observed by esr in alkali metal solutions.


Clay Minerals ◽  
1990 ◽  
Vol 25 (3) ◽  
pp. 303-311 ◽  
Author(s):  
A. U. Gehring ◽  
R. Karthein

AbstractElectron spin resonance (ESR) spectroscopy and calorimetric methods were used to characterize conversion processes in multimineral samples from the Northampton ironstone (NIS) at temperatures between 25°C and 800°C. The beginning of the thermal conversion processes can be determined by the formation of asymmetric ESR spectra with g ≈ 2 at 250°C. The breakdown of the berthierine structure between 250°C and 520°C is indicated by the disappearance of the hyperfine splitting in the Mn2+ spectrum and the formation of magnetite. The decomposition of siderite and calcite was found by calorimetric methods at 580°C and 700°C, respectively. The hematite formation between 550°C and 800°C is explained by the decomposition of siderite but also by the oxidation of previously formed magnetite. The occurrence of hematite as the dominant ferric oxide at 800°C signifies the end of the conversion process of the major mineral phases in the NIS samples.


1970 ◽  
Vol 48 (5) ◽  
pp. 805-817 ◽  
Author(s):  
C. A. McDowell ◽  
H. Nakajima ◽  
P. Raghunathan

Preferentially oriented NO2 and NF2 in inert matrices have been studied in some detail by electron spin resonance methods at 4.2 °K. Methods are discussed which may optimize the degree of preferential orientation of the paramagnetic species in appropriate matrices. The results demonstrate that while neon is the best host matrix for orienting NO2, argon is to be preferred for NF2. The g-values and hyperfine splitting data have been accurately determined and are compared with earlier values. Motional processes are suggested to explain the spectra obtained for NF2 in an argon matrix in the temperature range 4–30 °K.


1970 ◽  
Vol 48 (13) ◽  
pp. 1996-1999 ◽  
Author(s):  
J. T. Cooper

The electron spin resonance spectra of several substituted pyrene cations, produced by oxidation with boron trifluoride in sulfur dioxide, are reported. The spectra are analyzed and the splitting constants given. With 4-chloropyrene, hyperfine splitting is observed due to the chlorine atom, for the first time in such a species. Molecular orbital calculations (Hückel and McLachlan) are presented for three of the compounds studied.


1978 ◽  
Vol 56 (2) ◽  
pp. 164-169 ◽  
Author(s):  
James Anthony Howard ◽  
John Charles Tait

The epr spectra of three intermediate copper(II) complexes formed by oxidation of bis[N,N-dialkyl(dithiocarbamato-S,S′)] copper(II) by alkyl hydroperoxides and alkylperoxy radicals are reported. Isotropic and anisotropic spectra of the complexes formed from alkylperoxy radicals enriched with 17O are consistent with the following structures: [Cu(S2CNR2)(OS2CNR2)] (I), [Cu(OS2CNR2)2] (II), and [Cu(OS2CNR2)(O2S2CNR2)] (III). The isotropic 17O hyperfine interaction of I is 19.2 G while the anisotropic spectrum of II indicates that the two oxygen nuclei are equivalent. The anisotropic 17O hyperfine splitting constants are consistent with a structure for these complexes in which the S—O bond(s) is directed out of the plane of the complex and not coordinated to the copper.


1972 ◽  
Vol 50 (12) ◽  
pp. 1825-1830 ◽  
Author(s):  
G. Bigam ◽  
John Hooz ◽  
Siegfried Linke ◽  
R. E. D. McClung ◽  
Melvyn W. Mosher ◽  
...  

Several ferrocenylalkyl- and aryl ketyls were generated and their e.s.r. spectra were recorded. Pentadeuterio-benzoylferrocene and benzoyl perdeuterioferrocene were synthesized. Analysis of the e.s.r. spectra of their corresponding ketyls enabled the determination of the hyperfine splitting constants of benzoylferrocene ketyl, and allowed an assignment of the electron densities at various positions in the molecule.A comparison of the magnitudes of the g-values for the ketyls derived from benzophenone (2.0034), benzoylferrocene (2.0062), and 2,2-dimethylpropanoylferrocene (2.0126), combined with the proton hyperfine splittings, gave some insight into the nature of the interaction of the free electron with the ferrocene system.


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