Crystal and Molecular Structure of N-Trityl-m-aminophenol Chloroform Solvate
| dc.contributor.author | Çelik, İsmail | |
| dc.contributor.author | Ersanlı, Cem Cüneyt | |
| dc.contributor.author | Akkurt, Mehmet | |
| dc.contributor.author | Demirtaş, İ. | |
| dc.date.accessioned | 2014-08-26T07:01:34Z | |
| dc.date.available | 2014-08-26T07:01:34Z | |
| dc.date.issued | 2007 | |
| 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)°. | |
| dc.identifier.citation | Çelik, İ., Ersanlı, Cem C., Akkurt, M., Demirtaş, İ. "Crystal and Molecular Structure of N-Trityl-m-aminophenol Chloroform Solvate". Analytical Sciences, Vol. 23 (2007) P x231-x232. | |
| dc.identifier.doi | 10.2116/analscix.23.x231 | |
| dc.identifier.issn | 0910-6340 (Print) | |
| dc.identifier.issn | 1348-2246 (Online) | |
| dc.identifier.uri | https://www.jstage.jst.go.jp/article/analscix/23/0/23_0_x231/_pdf | |
| dc.identifier.uri | https://hdl.handle.net/11486/456 | |
| dc.identifier.uri | https://doi.org/10.2116/analscix.23.x231 | |
| dc.language.iso | en | |
| dc.publisher | Analytical Sciences | |
| dc.relation.publicationcategory | Makale - Kategorisiz | |
| dc.title | Crystal and Molecular Structure of N-Trityl-m-aminophenol Chloroform Solvate | |
| dc.type | Article |
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