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dc.contributor.authorSlepukhin, P. A.en
dc.contributor.authorPervova, I. G.en
dc.contributor.authorRezinskikh, Z. G.en
dc.contributor.authorLipunova, G. N.en
dc.contributor.authorGorbatenko, Y. A.en
dc.contributor.authorLipunov, I. N.en
dc.date.accessioned2019-09-20T15:19:12Z-
dc.date.available2019-09-20T15:19:12Z-
dc.date.issued2008-
dc.identifier.citationSlepukhin, P. A. X-ray diffraction investigation of 1-phenyl-3-isopropyl-5-(benzothiazol-2- yl)formazan / P. A. Slepukhin, I. G. Pervova, Z. G. Rezinskikh [et al.] // Crystallography Reports. – 2008. – Vol. 53. – Iss. 1. – P. 88-91.en
dc.identifier.issn1063-7745-
dc.identifier.urihttps://elar.usfeu.ru/handle/123456789/8887-
dc.description.abstractThe crystal structure of 1-phenyl-3-isopropyl-5-(benzothiazol-2-yl)formazan is investigated using X-ray diffraction. The compound crystallizes in the form of two crystallographically independent molecules (A and B) in identical conformations that are stabilized by intermolecular hydrogen bonds. The intermolecular hydrogen bonds N-H ⋯ N (N⋯N, 2.892 and 2.939 Å) link molecules into AB dimers. Both molecules have a flattened structure, except for the isopropyl fragment. The bonds in the formazan chains are delocalized. Molecules A and B have close geometric characteristics. © 2008 Pleiades Publishing, Inc.en
dc.description.sponsorshipThis study was supported by the Russian Foundation for Basic Research, project nos. 05-03-32023a and 06-03-08040-ofi.en
dc.language.isoenen
dc.publisherPleiades Publishingen
dc.rightsinfo:eu-repo/semantics/restrictedAccessen
dc.sourceCrystallography Reportsen
dc.subjectCRYSTAL STRUCTUREen
dc.subjectHYDROGEN BONDSen
dc.subjectMOLECULAR STRUCTUREen
dc.subjectX RAY DIFFRACTIONen
dc.subjectCOMPOUND CRYSTALLIZESen
dc.subjectFORMAZAN CHAINSen
dc.subjectIDENTICAL CONFORMATIONSen
dc.subjectBENZENEen
dc.titleX-ray diffraction investigation of 1-phenyl-3-isopropyl-5-(benzothiazol-2- yl)formazanen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
local.description.firstpage88-
local.description.lastpage91-
local.issue1-
local.volume53-
local.identifier.wosWOS:000252797600011-
local.identifier.doi10.1134/S1063774508010112-
local.affiliationPostovskiǐ Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, ul. Akademicheskaya 20/22, Yekaterinburg 620041, Russian Federationen
local.affiliationUral State Forestry Engineering University, Sibirskiǐ trakt 37, Yekaterinburg 620100, Russian Federationen
local.affiliationUral State Technical University (UPI), ul. Mira 19, Yekaterinburg 620078, Russian Federationen
local.contributor.employeeSlepukhin, P.A., Postovskiǐ Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, ul. Akademicheskaya 20/22, Yekaterinburg 620041, Russian Federation-
local.contributor.employeePervova, I.G., Ural State Forestry Engineering University, Sibirskiǐ trakt 37, Yekaterinburg 620100, Russian Federation-
local.contributor.employeeRezinskikh, Z.G., Ural State Forestry Engineering University, Sibirskiǐ trakt 37, Yekaterinburg 620100, Russian Federation-
local.contributor.employeeLipunova, G.N., Ural State Technical University (UPI), ul. Mira 19, Yekaterinburg 620078, Russian Federation-
local.contributor.employeeGorbatenko, Yu.A., Ural State Forestry Engineering University, Sibirskiǐ trakt 37, Yekaterinburg 620100, Russian Federation-
local.contributor.employeeLipunov, I.N., Ural State Forestry Engineering University, Sibirskiǐ trakt 37, Yekaterinburg 620100, Russian Federation-
local.identifier.rsi13590581-
local.identifier.eid2-s2.0-38749110402-
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