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首页> 外文期刊>Dyes and Pigments >New water soluble phenoxy phenyl diazenyl benzoic acid substituted phthalocyanine derivatives: Synthesis, antioxidant activities, atypical aggregation behavior and electronic properties
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New water soluble phenoxy phenyl diazenyl benzoic acid substituted phthalocyanine derivatives: Synthesis, antioxidant activities, atypical aggregation behavior and electronic properties

机译:新型水溶性苯氧基苯基二氮烯基苯甲酸取代的酞菁衍生物:合成,抗氧化活性,非典型聚集行为和电子性质

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摘要

Novel substituted phthalonitrile derivatives were obtained by the reaction of 2-(4-hydroxyphenylazo) benzoic acid and 4,5-dichloro-1,2-dicyanobenzene, or 4-nitrophthalonitrile. Peripherally phenoxy phenyl diazenyl benzoic acid substituted zinc (II) phthalocyanine complexes, and their sodium salts were synthesized and characterized for the first time. The newly synthesized phthalocyanine complexes show excellent solubility in water. The aggregation investigations carried out in different concentrations indicate that phenoxy phenyl diazenyl benzoic acid-substituted phthalocyanine compounds do not have any aggregation behavior for the concentration range of 7.00 × 10~(-5)-4.38 × 10~(-6) M in DMF. The antioxidant activities of DMF solution of compounds were analyzed through radical scavenging, and chelating ability to Fe~(2+) cation. Additionally, new compounds did not show any antibacterial activity against some selected bacteria cultures. Moreover, the ground-state geometries of the complexes were optimized using density functional theory (DFT) methods at B3LYP/6-31G(d,p) level in order to obtain information about the 3D geometries and electronic structure.
机译:通过2-(4-羟基苯基偶氮)苯甲酸与4,5-二氯-1,2-二氰基苯或4-硝基苯甲腈的反应获得新型取代的邻苯二甲腈衍生物。首次合成并表征了苯氧基苯基二氮烯基苯甲酸取代的酞菁锌(II)配合物及其钠盐。新合成的酞菁配合物在水中显示出极好的溶解性。在不同浓度下进行的聚集研究表明,对于DMF中7.00×10〜(-5)-4.38×10〜(-6)M的浓度范围,苯氧基苯基二氮烯基苯甲酸取代的酞菁化合物没有任何聚集行为。 。通过自由基清除和对Fe〜(2+)阳离子的螯合能力分析了化合物DMF溶液的抗氧化活性。此外,新化合物对某些选定的细菌培养物未显示任何抗菌活性。此外,使用B3LYP / 6-31G(d,p)级的密度泛函理论(DFT)方法优化了配合物的基态几何,以获得有关3D几何和电子结构的信息。

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