Email this article Synthesis and structure of novel substituted N-sulfinylanilines
- Authors: Veremeichik Y.V.1, Tevs O.A.1, Krivolapov D.B.2, Lodochnikova O.A.2,3, Plemenkov V.V.1,3
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Affiliations:
- Chemical Biological Institute
- Arbuzov Institute of Organic and Physical Chemistry
- Butlerov Chemical Institute
- Issue: Vol 87, No 6 (2017)
- Pages: 1143-1147
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/220145
- DOI: https://doi.org/10.1134/S107036321706007X
- ID: 220145
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Abstract
N-Sulfinylanilines derived from 4-bromoaniline, 3-nitroaniline, and 4,4′-di(ethane-1,2-diyl)dianiline were synthesized. X-ray diffraction analysis of 4-bromo-N-sulfinylaniline, 3-nitro-N-sulfinylaniline, and 4,4′-(ethane-1,2-diyl)di-N-sulfinylaniline was performed. The sulfinyl function in the planar conformation of the Ar-NSO fragment was found to have Z configuration. The nature of intra- and intermolecular structure-forming interactions was established.
About the authors
Ya. V. Veremeichik
Chemical Biological Institute
Email: lod_olga@mail.ru
Russian Federation, Kalinigrad
O. A. Tevs
Chemical Biological Institute
Email: lod_olga@mail.ru
Russian Federation, Kalinigrad
D. B. Krivolapov
Arbuzov Institute of Organic and Physical Chemistry
Email: lod_olga@mail.ru
Russian Federation, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
O. A. Lodochnikova
Arbuzov Institute of Organic and Physical Chemistry; Butlerov Chemical Institute
Author for correspondence.
Email: lod_olga@mail.ru
Russian Federation, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088; Kazan, Tatarstan
V. V. Plemenkov
Chemical Biological Institute; Butlerov Chemical Institute
Email: lod_olga@mail.ru
Russian Federation, Kalinigrad; Kazan, Tatarstan
