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SYNTHESIS, SYNERGISTIC EFFECT AND SCAVENGING ACTIVITY OF SCHIFF BASE LIGANDS

机译:Schiff基配体的合成,协同效应和清除活性

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The ligands HL1/HL4 were synthesized by Schiff base condensation of o-hydroxyacetophenone/thiophene-2-carboxylic acid with phenyl hydrazine in 1:1 mole ratio and the ligands HL2, HL3 were synthesized using o-hydroxyacetophenone and corresponding diamine (N, N-bis(3-aminopropyl)methylamine/N, N-bis(3-aminopropyl)-1,2-ethylenedi ammine) in 2 : 1 mole ratio.All the ligands were characterized by electronic, IR and 1H NMR spectral studies.IR and 1H NMR spectral studies confirmed the formation of azomethine (HC=N-) group.The scavenging activity for the ligands were carried out by DPPH method.The ligands HL1 and HL4 had higher than other ligands.
机译:通过在1:1摩尔比和配体HL2中与苯基肼的苯肼基 - 2-羧酸合成配体HL1 / HL4,使用O-羟基乙酮和相应的二胺合成HL 3(N,N -BIS(3-氨基丙基)甲胺/ N,N-双(3-氨基丙基)-1,2-乙二胺氨)在2:1摩尔比中以电子,IR和1H NMR光谱研究表征了配体的表征.IR和1H NMR光谱研究证实了氮杂甲磺酸酐(HC = N-)组的形成。通过DPPH方法进行配体的清除活性。配体HL1和HL4具有高于其他配体。

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