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dc.contributor.authorHökelek, Tuncer
dc.contributor.authorDal, Hakan
dc.contributor.authorTercan,B.
dc.contributor.authorGülle , S.
dc.contributor.authorErgün ,Yavuz
dc.date.accessioned2019-12-13T06:29:33Z
dc.date.available2019-12-13T06:29:33Z
dc.date.issued2009
dc.identifier.issn1600-5368
dc.identifier.urihttps://doi.org/10.1107/S1600536809021035
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969395/
dc.identifier.urihttp://hdl.handle.net/11655/18335
dc.description.abstractIn the title compound, C22H19NO5S, the carbazole skeleton is nearly planar [maximum deviation = 0.043 (1) Å] with the pyrrole ring oriented at dihedral angles of 2.32 (6) and 1.77 (6)° with respect to the adjacent benzene rings. The dihedral angle between the benzene ring of the tosyl group and the carbazole skeleton is 82.25 (5)°. Intra­molecular O—H⋯O hydrogen bonding results in the formation of a planar six-membered ring, which is oriented at a dihedral angle of 3.06 (4)° with respect to the adjacent carbazole skeleton. In the crystal structure, weak inter­molecular C—H⋯O inter­actions link the mol­ecules into infinite chains and π–π contacts between the benzene rings and between the pyrrole and benzene rings [centroid–centroid distances = 3.374 (1) and 3.730 (1) Å, respectively] may further stabilize the structure. A weak C—H⋯π inter­action is also present.
dc.relation.isversionof10.1107/S1600536809021035
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleEthyl 4-Hydr­Oxy-9-Tosyl-9H-Carbazole-3-Carboxyl­Ate
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalActa Crystallographica Section E: Structure Reports Online
dc.contributor.departmentFizik Mühendisliği
dc.identifier.volume65
dc.identifier.issuePt 7
dc.identifier.startpageo1515
dc.identifier.endpageo1516
dc.description.indexPubMed
dc.description.indexWoS
dc.description.indexScopus


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