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dc.contributor.authorÇelik I.
dc.contributor.authorErsanli C.C.
dc.contributor.authorAkkurt M.
dc.contributor.authorDemirtaí I.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:12:30Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:12:30Z
dc.date.issued2007
dc.identifier.issn1348-2238
dc.identifier.urihttps://dx.doi.org/10.2116/analscix.23.x231
dc.identifier.urihttps://hdl.handle.net/20.500.12418/4346
dc.description.abstractThe title compound, (C26H23N)3·CHCl3, was synthesized by the reaction of trityl bromide with m-toluidine in chloroform and crystalized in the trigonal R3 space group (Z = 6) with the one molecule of chloroform, and with a = 20.765(5), b = 20.765(5), c = 24.924(5)Å, ? = ? = 90°, ? = 120°, V = 9307(4)Å3, Z = 6 and Dx = 1.250 Mg m-3. A least-squares refinement gave a residual index of R = 0.065 for 3540 observed reflections. Three phenyl rings of the title compound are at angles of 60.39(13), 74.10(14) and 70.17(13)° to the six-membered ring of the planar aminophenol group. The dihedral angles between three phenyl rings are 73.60(16), 87.80(15) and 56.52(15)°. 2007 © The Japan Society for Analytical Chemistry.en_US
dc.language.isoengen_US
dc.publisherJapan Society for Analytical Chemistryen_US
dc.relation.isversionof10.2116/analscix.23.x231en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleCrystal and molecular structure of N-Trityl-m-aminophenol chloroform solvateen_US
dc.typeotheren_US
dc.relation.journalAnalytical Sciences: X-ray Structure Analysis Onlineen_US
dc.contributor.departmentÇelik, I., Department of Physics, Faculty of Arts and Sciences, Cumhuriyet University, 06532 Sivas, Turkey -- Ersanli, C.C., Department of Physics, Sinop Faculty of Arts and Sciences, Ondokuz Mayis University, Sinop, Turkey -- Akkurt, M., Department of Physics, Faculty of Arts and Sciences, Erciyes University, 38039 Kayseri, Turkey -- Demirtaí, I., Department of Chemistry, Faculty of Arts and Sciences, Gaziosmanpasa University, 60250 Tokat, Turkeyen_US
dc.identifier.volume23en_US
dc.identifier.issue11en_US
dc.identifier.endpagex232en_US
dc.identifier.startpagex231en_US
dc.relation.publicationcategoryDiğeren_US


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