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Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene Full article

Journal Molecules
, E-ISSN: 1420-3049
Output data Year: 2021, Volume: 26, Number: 3, Article number : 526, Pages count : DOI: 10.3390/molecules26030526
Tags perfluorinated tetrathiacalix[4]arene; perfluoro-m-xylene; dioxadithiacalix[4]arenes; tetraoxadithiacalix[6]arene; thiourea; 2; 5-difluoro-4; 6-bis(trifluoromethyl)benzene-1; 3-dithiol; X-ray analyses
Authors Kovtonyuk Vladimir N. 1 , Gatilov Yuri V. 1 , Nikul'shin Pavel V. 1 , Bredikhin Roman A. 1
Affiliations
1 (Данные Web of science) SB RAS, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Academician Lavrentjev Ave, Novosibirsk 630090, Russia

Abstract: Perfluorinated tetrathiacalix[4]arene was obtained by heating perfluoro-m-xylene with thiourea or 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol at 90 degrees C. Interaction of perfluoro-m-xylene with resorcinol or orcinol under mild conditions and subsequent heating of the mixture with 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol leads to polyfluorinated dioxadithiacalix[4]arenes. Triphenyl and pentaphenyl ethers formed by the interaction of perfluoro-m-xylene with resorcinol under heating with thiourea gives polyfluorinated oxathiacalixarenes containing six and five aromatic nuclei, respectively.
Cite: Kovtonyuk V.N. , Gatilov Y.V. , Nikul'shin P.V. , Bredikhin R.A.
Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene
Molecules. 2021. V.26. N3. 526 . DOI: 10.3390/molecules26030526 WOS Scopus РИНЦ OpenAlex
Files: Full text from publisher
Dates:
Published online: Jan 20, 2021
Identifiers:
Web of science: WOS:000615460700001
Scopus: 2-s2.0-85100480243
Elibrary: 46745294
OpenAlex: W3122502936
Citing:
DB Citing
Web of science 3
Scopus 3
Elibrary 1
OpenAlex 3
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