| dc.creator |
SEVINDIR, HC |
|
| dc.date |
1995-01-01T01:00:00Z |
|
| dc.date.accessioned |
2021-12-03T11:14:51Z |
|
| dc.date.available |
2021-12-03T11:14:51Z |
|
| dc.identifier |
09f75730-41fc-468c-96fa-5fd08028aefe |
|
| dc.identifier |
10.1080/15533179508014680 |
|
| dc.identifier |
https://avesis.sdu.edu.tr/publication/details/09f75730-41fc-468c-96fa-5fd08028aefe/oai |
|
| dc.identifier.uri |
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/89834 |
|
| dc.description |
anti-Chloroglyoxime, CGH(2), has been synthesized by chlorination of anti-glyoxime. The reaction of CGH(2) with thiophenol, 4-methyIthiophenol and 4-methoxythiophenol in ethanol between -5 degrees C and -10 degrees C gives unsymmetrical vic-dioximes, designated as thiophenologlyoxime [L(a)H(2)], 4-methylthiophenologlyoxime [L(b)H(2)] and 4-methoxythiophenologlyoxime [L(c)H(2)]. The Cu(II) and Ni(II) complexes of these ligands were prepared and are proposed to be square-planar, while the corresponding Co(II) complexes are proposed to be octahedral with water molecules as axial ligands. Structural assiguments are supported by H-1 NMR, IR and elemental analyses. |
|
| dc.language |
eng |
|
| dc.rights |
info:eu-repo/semantics/closedAccess |
|
| dc.title |
SYNTHESIS AND COMPLEX-FORMATION OF SUBSTITUTED THIO-GLYOXIMES OF UNSYMMETRICAL VIC-DIOXIMES |
|
| dc.type |
info:eu-repo/semantics/article |
|