| dc.creator |
SEVINDIR, HC |
|
| dc.date |
1995-01-01T01:00:00Z |
|
| dc.date.accessioned |
2021-12-03T11:19:57Z |
|
| dc.date.available |
2021-12-03T11:19:57Z |
|
| dc.identifier |
34c384cd-aebf-4324-bf3a-1dcb1e1c9a3d |
|
| dc.identifier |
10.1080/15533179508218231 |
|
| dc.identifier |
https://avesis.sdu.edu.tr/publication/details/34c384cd-aebf-4324-bf3a-1dcb1e1c9a3d/oai |
|
| dc.identifier.uri |
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/90842 |
|
| dc.description |
The reaction of anti-p-Tolylchloroglyoxime PTCGH(2) with thiophenol, 4-methylthiophenol and 4-methoxythiophenol in ethanol between -5 degrees C and 10 degrees C gives unsymmetrical vic-dioximes, designated as thiophenolo-p-tolylglyoxime [L(1)H(2)], 4-methylthiophenolo-p-tolylglyoxime [L(2)H(2)] and 4-methoxythiophenol-p-etolylglyoxime [L(3)H(2)]. The Ni(II) and Cu(II) complexes of these ligands are proposed to be square-planar, while the Co(II) complexes are proposed to be octahedral with water molecules as axial ligands. Structural assignments are supported by H-1 NMR IR and elemental analyses which are reported herein. |
|
| dc.language |
eng |
|
| dc.rights |
info:eu-repo/semantics/closedAccess |
|
| dc.title |
SYNTHESIS AND COMPLEX-FORMATION OF SUBSTITUTED THIO-P-TOLYLGLYOXIMES OF UNSYMMETRICAL VIC-DIOXIMES |
|
| dc.type |
info:eu-repo/semantics/article |
|