首页> 外文期刊>Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry >COPPER(II), NICKEL(II), OXOVANADIUM(IV) AND DIOXOURANIUM(VI) COMPLEXES OF NOVEL ASYMMETRIC TETRADENTATE SCHIFF BASE LIGANDS DERIVED FROM 6-METHYL-3-FORMYL-4-HYDROXY-2-(1H)-QUINOLONE .4.
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COPPER(II), NICKEL(II), OXOVANADIUM(IV) AND DIOXOURANIUM(VI) COMPLEXES OF NOVEL ASYMMETRIC TETRADENTATE SCHIFF BASE LIGANDS DERIVED FROM 6-METHYL-3-FORMYL-4-HYDROXY-2-(1H)-QUINOLONE .4.

机译:从6-甲基-3-甲酰基-4-羟基-2-(1H)-喹诺酮.4衍生而来的新型不对称四齿丁香席夫夫基配体的铜(II),镍(II),氧钒(IV)和二氧铀(VI)络合物。

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摘要

The novel, half-unit ligand obtained by the single condensation of 6-methyl-3-formyl-4-hydroxy-2-(1H)-quinolone and p-phenylenediamine, was condensed with either acetylacetone or salicylaldehyde to yield novel, asymmetric tetradentate Schiff base ligands, H(2)L(a) and H(2)L(b), respectively. The reactions of the ligands with Cu2+, Ni2+, VO2+ and UO22+ salts yielded complexes of the general formula [L(2)M(2)]nH(2)O, except that of the uranyl complex of the ligand H(2)L(a) which has the formula [L(a)(UO2)(2)(OAc)(2)(OH2)(2)] The ligands and metal complexes were characterized by elemental analyses IR, UV-visible, mass and ESR spectra and magnetic measurements. The Cu2+ complexes are distored tetrahedral, the Ni2+ complexes are octahedral. [References: 19]
机译:通过6-甲基-3-甲酰基-4-羟基-2-(1H)-喹诺酮和对苯二胺的单缩合获得的新型半单元配体与乙酰丙酮或水杨醛缩合,生成新型不对称四齿希夫碱配体H(2)L(a)和H(2)L(b)。配体与Cu2 +,Ni2 +,VO2 +和UO22 +盐的反应生成通式[L(2)M(2)] nH(2)O的配合物,但配体H(2)L的铀酰配合物除外具有式[L(a)(UO2)(2)(OAc)(2)(OH2)(2)的(a)的配位体和金属配合物通过红外,紫外可见,质量和ESR元素分析进行​​表征光谱和磁测量。 Cu2 +络合物是扭曲的四面体,Ni2 +络合物是八面体的。 [参考:19]

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