Conformational analysis of 2-substituted 1-nitro-and 1-bromo-1-nitroethenes

dc.contributor.author	Ishmaeva E.
dc.contributor.author	Gazizova A.
dc.contributor.author	Vereshchagina Y.
dc.contributor.author	Chachkov D.
dc.contributor.author	Anisimova N.
dc.contributor.author	Makarenko S.
dc.contributor.author	Smirnov A.
dc.contributor.author	Berestovitskaya V.
dc.date.accessioned	2018-09-18T20:18:21Z
dc.date.available	2018-09-18T20:18:21Z
dc.date.issued	2007
dc.identifier.issn	1070-3632
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/138527
dc.description.abstract	Conformational analysis of 2-trichloromethyl(ethoxycarbonyl)-1-nitro-and 2-trichloromethyl-(ethoxycarbonyl)-1-bromo-1-nitroethenes was performed using the dipole moment method, IR spectroscopy, and DFT quantum-chemical calculations (B3LYP/6-31G*). The nitro and ester (or trichloromethyl) groups in the molecules of these compounds were found to occupy trans positions with respect to the double C=C bond, i.e., the nitroalkenes have E, and their bromine-containing analogs, Z configuration; the compounds having an ethoxycarbonyl group are characterized by s-cis orientation of the C=C and C=O bonds. © Nauka/Interperiodica 2007.
dc.relation.ispartofseries	Russian Journal of General Chemistry
dc.title	Conformational analysis of 2-substituted 1-nitro-and 1-bromo-1-nitroethenes
dc.type	Article
dc.relation.ispartofseries-issue	5
dc.relation.ispartofseries-volume	77
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	894
dc.source.id	SCOPUS10703632-2007-77-5-SID34547302845

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