The Synthesis of New Functionalized 1,3,5-Triazine-Based Stable bi- and trinitroxides of the 2,5-Dihydroimidazole Series Full article
Journal |
Arkivoc
ISSN: 1551-7004 , E-ISSN: 1551-7012 |
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Output data | Year: 2018, Volume: 2018, Number: 5, Pages: 359-374 Pages count : 16 DOI: 10.24820/ark.5550190.p010.614 | ||||
Tags | 1,3,5-Triazine-based nitroxides, biradicals, triradicals, organic free radicals, 2,5-dihydroimidazoles | ||||
Authors |
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Affiliations |
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Funding (1)
1 | Russian Foundation for Basic Research | 17-53-50043 |
Abstract:
New non-conjugated functionalized 2,5-dihydroimidazole-type bi- and trinitroxyl radicals are described. The synthesis of which was based on a nucleophilic substitution reaction between 2,4,6-trichloro-1,3,5-triazine or 2,4-dichloro-6-methoxy-1,3,5-triazine and spiro-fused 2,5-dihydroimidazole-type monoradicals bearing both a p-hydroxyaryl moiety at the C-4 atom of the heterocycle and a residue at the fourth position of the cyclohexane ring. The model tris-nitroxide with an unsubstituted cyclohexane unit was structurally characterized in the solid state
Cite:
Zaytseva E.V.
, Gatilov Y.V.
, Mazhukin D.G.
The Synthesis of New Functionalized 1,3,5-Triazine-Based Stable bi- and trinitroxides of the 2,5-Dihydroimidazole Series
Arkivoc. 2018. V.2018. N5. P.359-374. DOI: 10.24820/ark.5550190.p010.614 WOS Scopus РИНЦ
The Synthesis of New Functionalized 1,3,5-Triazine-Based Stable bi- and trinitroxides of the 2,5-Dihydroimidazole Series
Arkivoc. 2018. V.2018. N5. P.359-374. DOI: 10.24820/ark.5550190.p010.614 WOS Scopus РИНЦ
Files:
Full text from publisher
Dates:
Published online: | Apr 8, 2018 |
Submitted: | May 4, 2018 |
Accepted: | Jul 16, 2018 |
Published print: | Aug 4, 2018 |
Identifiers:
Web of science | WOS:000456008800030 |
Scopus | 2-s2.0-85054570320 |
Elibrary | 38623369 |
Chemical Abstracts | 2018:2033760 |
Chemical Abstracts (print) | 169:525979 |
OpenAlex | W2889124283 |