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Advanced Search Results For "Pirnazarova N"

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 "Pirnazarova N"
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The semiquinone ion radical in the oxidation of 2.6-di-tert-butyl-4-aminoalkylphenols

Publication Type:Periodical

Source(s):Russian Chemical Bulletin; January 1968, Vol. 17 Issue: 1 p53-56, 4p

Abstract:1.In the oxidation of four different 2,6-dialkyl-4-aminoalkyIphenols by molecular oxygen in aqueous alcohol alkaline solution, 2,6-dialkyl-1,4-benzosemiquinone, the EPR spectrum of which represents a triplet with splitting of 1.4 Oe and intensity ratio...

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The semiquinone ion radical in the oxidation of 2.6-di-tert-butyl-4-aminoalkylphenols.

Publication Type:Academic Journal

Source(s):Bulletin of the Academy of Sciences of The USSR, Division of Chemical Science; 1968, Vol. 17 Issue 1, p53-56, 4p

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Ionization potentials of phenothiazine derivatives and their correlation with the pharmacological effect

Publication Type:Periodical

Source(s):Russian Chemical Bulletin; September 1973, Vol. 22 Issue: 9 p2050-2053, 4p

Abstract:1.The ionization potentials (I) of some phenothiazine derivatives (PTD) were calculated from the optical spectra of the charge-transfer complexes.2.The obtained values were compared with the indices that characterize the cholinolytic and antiarrhythmic...

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Crystal structure and Hirshfeld surface analysis of 3-methyl-4-oxo- N -phenyl-3,4-di-hydro-quinazoline-2-carbo-thio-amide.

Publication Type:Academic Journal

Source(s):Acta crystallographica. Section E, Crystallographic communications [Acta Crystallogr E Crystallogr Commun] 2022 Jan 01; Vol. 78 (Pt 1), pp. 47-50. Date of Electronic Publication: 2022 Jan 01 (Print Publication: 2022).

Abstract:The asymmetric unit of the title compound, C 16 H 13 N 3 OS, comprises two mol-ecules ( A and B ) with similar conformations that differ mainly in the orientation of the phenyl group relative to the rest of the mol-ecule, as expressed by the C thio-ami...

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