Benzothiazolylazo derivatives of some β-dicarbonyl compounds and their Cu(II), Ni(II) and Zn(II) complexes
Author(s) -
K. Krishnankutty,
Basheer Ummathur,
Kamalakshy Babu
Publication year - 2010
Publication title -
journal of the serbian chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.227
H-Index - 45
eISSN - 1820-7421
pISSN - 0352-5139
DOI - 10.2298/jsc090816040k
Subject(s) - tautomer , chemistry , chelation , ligand (biochemistry) , enol , stoichiometry , moiety , proton nmr , paramagnetism , medicinal chemistry , carbon 13 nmr , metal ions in aqueous solution , metal , inorganic chemistry , polymer chemistry , stereochemistry , organic chemistry , catalysis , biochemistry , physics , receptor , quantum mechanics
The coupling of diazotized 2-aminobenzothiazole with 1,3-dicarbo- nyl compounds (benzoylacetone, methyl acetoacetate and acetoacetanilide) yielded a new series of tridentate ligand systems (HL). Analytical, IR, 1 H- -NMR, 13 C-NMR and mass spectral data indicated that the compounds exist in the intramolecularly hydrogen bonded azo-enol tautomeric form in which one of the carbonyl groups of the dicarbonyl moiety had enolised and hydrogen bonded to one of the azo nitrogen atoms. The compounds formed stable com- plexes with Ni(II), Cu(II) and Zn(II) ions. The Cu(II) complexes conform to (CuL(OAc)) stoichiometry while the Ni(II) and Zn(II) complexes are in agre- ement with (ML2) stoichiometry. Analytical, IR, 1 H-NMR, 13 C-NMR and mass spectral data of the complexes are consistent with the replacement of the che- lated enol proton of the ligand with a metal ion, thus leading to a stable six- -membered chelate ring involving a cyclic nitrogen, one of the azo nitrogens and the enolate oxygen. The Zn(II) chelates are diamagnetic while Cu(II) and Ni(II) complexes showed a normal paramagnetic moment.
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