Abstract:
Five conjugated -ketoesters (HL1
to HL5
) with the keto group connected to carbon-carbon double bond have been prepared
through the condensation of methyl acetoacetate with aromatic aldehydes (4-nitrobenzaldehyde; 4-methoxybenzaldehyde;
3,4-dihydroxybenzaldehyde; 3,4-dimethoxybenzaldehyde and indole-3-carbaldehyde). Structural characterization by
physicochemical techniques indicated the occurrence of HL1
in the keto form and HL2
to HL5 in the intra-molecularly
hydrogen bonded enol form. Details on the formation and nature of bonding in the [Cu(HL)(OAc)2] complex of HL1 and
[CuL2] complexes of HL2
to HL5 are confirmed by analytical and spectral techniques.