| dc.contributor.author | Icbudak, H | |
| dc.contributor.author | Bulut, A | |
| dc.contributor.author | Cetin, N | |
| dc.contributor.author | Kazak, C | |
| dc.date.accessioned | 2020-06-21T15:37:26Z | |
| dc.date.available | 2020-06-21T15:37:26Z | |
| dc.date.issued | 2005 | |
| dc.identifier.issn | 2053-2296 | |
| dc.identifier.uri | https://doi.org/10.1107/S0108270104028574 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/21227 | |
| dc.description | Kazak, Canan/0000-0003-2475-8775 | en_US |
| dc.description | WOS: 000227376400005 | en_US |
| dc.description | PubMed: 15640564 | en_US |
| dc.description.abstract | The crystal structure of the first acesulfame - metal complex, namely tetraaquabis[6-methyl-1,2,3-oxathiazin-4(3H)-onato 2,2-dioxide-kappaN] cobalt(II), [Co(C4H4NO4S)(2)(H2O)(4)], is reported. The Co-II ion resides on a twofold axis and is coordinated by four aqua ligands defining the basal plane and by two monodentate acesulfamate ligands, via their ring N atoms, in the axial positions. Two intra- and three intermolecular hydrogen-bonding interactions stabilize the crystal structure and form an infinite three-dimensional lattice. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Int Union Crystallography | en_US |
| dc.relation.isversionof | 10.1107/S0108270104028574 | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | Bis(acesulfamato)tetraaquacobalt(II) | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 61 | en_US |
| dc.identifier.startpage | M1 | en_US |
| dc.identifier.endpage | M3 | en_US |
| dc.relation.journal | Acta Crystallographica Section C-Structural Chemistry | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
