| dc.contributor.author | Çelik I. | |
| dc.contributor.author | Ersanli C.C. | |
| dc.contributor.author | Akkurt M. | |
| dc.contributor.author | Demirtaí I. | |
| dc.date.accessioned | 2020-06-21T09:27:22Z | |
| dc.date.available | 2020-06-21T09:27:22Z | |
| dc.date.issued | 2007 | |
| dc.identifier.issn | 1348-2238 | |
| dc.identifier.uri | https://doi.org/10.2116/analscix.23.x231 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/4028 | |
| dc.description.abstract | The 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.iso | eng | en_US |
| dc.publisher | Japan Society for Analytical Chemistry | en_US |
| dc.relation.isversionof | 10.2116/analscix.23.x231 | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.title | Crystal and molecular structure of N-Trityl-m-aminophenol chloroform solvate | en_US |
| dc.type | note | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 23 | en_US |
| dc.identifier.issue | 11 | en_US |
| dc.identifier.startpage | x231 | en_US |
| dc.identifier.endpage | x232 | en_US |
| dc.relation.journal | Analytical Sciences: X-ray Structure Analysis Online | en_US |
| dc.relation.publicationcategory | Diğer | en_US |
