Protolytic Reactions of 3,6-DI-tert-Butyl-2-Hydroxyphenoxyl with Nitrogen Bases

Masalimov, A. S.; Tur, A. A.; Nikolskiy, S. N.

dc.contributor.author	Masalimov, A. S.
dc.contributor.author	Tur, A. A.
dc.contributor.author	Nikolskiy, S. N.
dc.date.accessioned	2018-04-17T06:40:58Z
dc.date.available	2018-04-17T06:40:58Z
dc.date.issued	2016-03
dc.identifier.citation	Masalimov A. S.Protolytic Reactions of 3,6-DI-tert-Butyl-2-Hydroxyphenoxyl with Nitrogen Bases/A. S. Masalimov, A. A. Tur, S. N. Nikolskiy//Theoretical and Experimental Chemistry.-2016.-№1(52).-pp 57–65	ru_RU
dc.identifier.issn	0040-5760
dc.identifier.uri	http://rep.ksu.kz/handle/data/2586
dc.description.abstract	Stable phenoxyl radicals were used as spin probes for the EPR spectral determination of the kinetic basicity of amines, nitrogen heterocycles, alkaloids, and of rate constants for rapid intermolecular proton exchange with various NH-acids in nonaqueous media. An analysis was carried out on the effect of the solvation properties of the medium on the EPR spectral parameters of the components of acid–base reactions required for spectral kinetic investigations.	ru_RU
dc.language.iso	en	ru_RU
dc.publisher	Springer US	ru_RU
dc.relation.ispartofseries	Theoretical and Experimental Chemistry;№1(52)
dc.subject	phenoxyl radical	ru_RU
dc.subject	protolytic reactions	ru_RU
dc.subject	nitrogen bases	ru_RU
dc.subject	EPR spectra	ru_RU
dc.title	Protolytic Reactions of 3,6-DI-tert-Butyl-2-Hydroxyphenoxyl with Nitrogen Bases	ru_RU
dc.type	Article	ru_RU