| dc.contributor.author | Dincer, M | |
| dc.contributor.author | Ozdemir, N | |
| dc.contributor.author | Cukurovali, A | |
| dc.contributor.author | Yilmaz, I | |
| dc.date.accessioned | 2020-06-21T15:37:02Z | |
| dc.date.available | 2020-06-21T15:37:02Z | |
| dc.date.issued | 2005 | |
| dc.identifier.issn | 2056-9890 | |
| dc.identifier.uri | https://doi.org/10.1107/S160053680500646X | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/21132 | |
| dc.description | Ozdemir, Namik/0000-0003-3371-9874; | en_US |
| dc.description | WOS: 000228056700111 | en_US |
| dc.description.abstract | In the title compound, C15H15N3OS, the thiosemicarbazone moiety is planar, with a maximum deviation of 0.0369 (11) angstrom, and has an E configuration. The planar phenyl rings make dihedral angles of 26.56 (9) and 81.20 (5)degrees with the plane of the thiosemicarbazone moiety. In the molecule, there are two intramolecular interactions of types N-H center dot center dot center dot O and N-H center dot center dot center dot N. In the crystal structure, there are two intermolecular interactions of types O-H center dot center dot center dot S and N-H center dot center dot center dot S, leading to the formation of dimers. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Int Union Crystallography | en_US |
| dc.relation.isversionof | 10.1107/S160053680500646X | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | Benzoin thiosemicarbazone | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 61 | en_US |
| dc.identifier.startpage | O880 | en_US |
| dc.identifier.endpage | O883 | en_US |
| dc.relation.journal | Acta Crystallographica Section E-Crystallographic Communications | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
