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Synthesis and complex formation of unsymmetrically substituted arylthio-p-chlorophenyl vic-dioximes

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dc.creator Sevindir, HC
dc.date 2002-07-01T00:00:00Z
dc.date.accessioned 2021-12-03T11:30:04Z
dc.date.available 2021-12-03T11:30:04Z
dc.identifier 6aa1fde8-a2eb-4757-8d27-920933bdb237
dc.identifier 10.1081/sim-120005619
dc.identifier https://avesis.sdu.edu.tr/publication/details/6aa1fde8-a2eb-4757-8d27-920933bdb237/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/92378
dc.description anti-Chlorophenylchloroglyoxime, 4-ClC6H4C=NOH)CCl(=NOH), has been synthesized by chlorination of anti-p-cholorophenylglyoxime. The reaction. of 4-ClC6H4C(=NOH)CCl(=NOH) with thiophenol, 4-methylthiophenol and 4-methoxythiophenol in ethanol between -5 and -10degreesC gives the unsymmetrical vic-dioximes, designated as thiophenolo-p-chlorophenylglyoxime, 4-ClC6H4C(=NOH)C(SC6H5)(=NOH), 4-methylthiophenolo-p-chlorophenylglyoxime, 4-ClC6H4C(=NOH)C(SC6H4-CH3-p)(=NOH), and 4-methoxylthiophenolo-p-chlorophenylglyoxime, 4-ClC6H4C(=NOH)C(SC6H4-OCH3-p)(=NOH). 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. The 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 unsymmetrically substituted arylthio-p-chlorophenyl vic-dioximes
dc.type info:eu-repo/semantics/article


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