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dc.contributor.authorKansiz, S.
dc.contributor.authorTinmaz, F.
dc.contributor.authorIlhan, I. O.
dc.contributor.authorSaripinar, E.
dc.contributor.authorDege, N.
dc.date.accessioned2020-06-21T13:06:11Z
dc.date.available2020-06-21T13:06:11Z
dc.date.issued2018
dc.identifier.issn1063-7745
dc.identifier.issn1562-689X
dc.identifier.urihttps://doi.org/10.1134/S1063774518060160
dc.identifier.urihttps://hdl.handle.net/20.500.12712/11327
dc.descriptionDege, Necmi/0000-0003-0660-4721; Kansiz, Sevgi/0000-0002-8433-7975en_US
dc.descriptionWOS: 000452155100012en_US
dc.description.abstractThe molecule of the title pyrazole derivative, 3,5-diphenyl-1-(phenylacetyl)-4,5-dihydro-1H-pyrazol, C23H20N2O, is twisted. The compound crystallizes in the monoclinic sp. gr. I2/a with a = 15.3502(13) angstrom, b = 12.7576(8) angstrom, c = 19.625(2) angstrom, = 106.639(7)degrees, and Z = 8. In the compound, the phenyl rings form dihedral angles of 12.01(13)degrees, 80.36(8)degrees, and 86.95(9)degrees with the mean plane of the pyrazole ring (r.m.s. deviation = 0.030 angstrom). The central pyrazole ring, which approximates an envelope conformation, is almost coplanar with one of the phenyl rings. The crystal packing is stabilized by weak intermolecular C-HO hydrogen bonds.en_US
dc.language.isoengen_US
dc.publisherPleiades Publishing Incen_US
dc.relation.isversionof10.1134/S1063774518060160en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleSynthesis and Single Crystal X-Ray Structure of 3,5-Diphenyl-1-(phenylacetyl)-4,5-dihydro-1H-pyrazolen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume63en_US
dc.identifier.issue6en_US
dc.identifier.startpage937en_US
dc.identifier.endpage941en_US
dc.relation.journalCrystallography Reportsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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