Cu (II)、Ni (II)、Co (II)和La (III)离子与2-[(吡啶-2-基甲基)氨基]苯酚和杂环氮碱的三元配合物

O. Ali, S. M. El‐Medani, Doaa A. Nassar
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引用次数: 0

摘要

席夫碱是配位化学领域中最普遍和重要的混合给体体系之一。2-氨基吡啶也作为有用的螯合配体应用于各种无机和金属器官[1,2]。氨基吡啶及其衍生物在大多数情况下作为单齿配体,通过环的氮来配位金属离子[3,4]。此外,氨基吡啶已被提出作为治疗许多疾病的药物,如心肌梗死的抗血栓剂和腹泻的抗菌药物[5,6]。此外,氨基吡啶通常存在于合成和天然产物中[7]。它们在许多大分子中形成重复的片段,具有有趣的光物理、电化学和催化应用[8]。具有不同类型杂环的配合物,如胺类、亚胺类、恶唑类、咪唑类和含吡啶配体等,在生物和医学领域发挥着重要作用。这些配体因其抗菌活性等药理特性而常用于医学中[9,10]。另一方面,由2吡啶羧醛衍生物与cu (II)、Co(II)、Cd(II)和Zn(II)等过渡金属衍生的席夫碱配体配合物显示出显著的生物活性[11,12]。此外,发光化合物由于其广泛的应用,包括用于有机发光二极管的发光材料、用于光催化的光收集材料以及用于有机或无机分析物的荧光传感器等,而引起了当前的研究兴趣[13-17]。过氧化氢的分解已被用作模型反应来研究各种金属配合物的催化活性[18]。例如,研究了壳聚糖与4,6 -二乙酰间苯二酚合成的壳聚糖衍生物铜(II)配合物对过氧化氢分解的催化活性[19]。混合配体络合物[Fe(2-AP)(Ala)Cl3]4H2O (2-AP = 2-乙酰吡啶,Ala =丙氨酸)催化H2O2分解,生成O2[20]。本文报道了由2-吡啶甲酸醛与2-氨基酚缩合而成的席夫碱过渡金属配合物。与2-氨基吡啶反应得到三元配合物。通过分析和光谱技术对这些配合物的结构特征进行了研究。摘要:一种新的三元席夫碱过渡金属配合物[M(HL)(2-AP)Cl2]通式。H2O,其中M= Cu(II), Ni(II)和Co(II)离子以及配合物[La(HL)(2- ap)(NO3)2]。采用模板合成法制备了no3。用光谱技术对合成的金属配合物进行了表征。DMF中配合物的摩尔电导率除La(III)配合物外均表现出非电解行为。红外光谱表明,希夫碱(HL)通过吡啶- n、偶氮- n和苯酚- o的NNO给体位与金属离子呈三联位配位,而2-氨基吡啶则通过其吡啶- n与金属离子配位。配体(HL)及其混合配体配合物表现出配体内(-*)荧光,可作为光活性材料。考察了配合物对过氧化氢分解反应的催化活性。对其配体(HL)和混合配体配合物进行了抗菌活性筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ternary Complexes of Cu (II), Ni (II), Co (II) and La (III) Ions with 2-[(Pyridin-2-Ylmethylidene) Amino] Phenol and Heterocyclic Nitrogen Base
Schiff bases are one of the most prevalent and important of the mixed donor systems in the field of coordination chemistry.2-Aminopyridines also serve as useful chelating ligands in a variety of inorganic and organ metallic applications [1,2].Amino pyridines and their derivatives in most cases act as monodentate ligands which coordinate the metal ions through the nitrogen of the ring [3,4]. Also, amino pyridines have been proposed as drugs for the treatment of many diseases such as myocardial infarction as antithrombus agents and diarrhea as antimicrobial agents [5,6]. Moreover, amino pyridines are commonly present in synthetic and natural products [7]. They form repeated moiety in many large molecules with interesting photophysical, electrochemical and catalytic applications [8].The complexes with different types of heterocyclic such asamines, imines, oxazole, imidazole and ligands containing pyridine play an important role in biology and medicine areas. These ligands are often used in medicine, because of their pharmacological properties such as antibacterial activity [9,10].On the other hand, complexes of Schiff base ligands derived from 2pyridinecarboxaldehyde derivatives with some transition metals such asCu(II), Co(II), Cd(II) and Zn(II) show significant biological activity [11,12]. Moreover, luminescent compounds are attracting much current research interest because of their many applications including emitting materials for organic light emitting diodes, light harvesting materials for photo catalysis and fluorescent sensors for organic or inorganic analytes [13-17].The decomposition of hydrogen peroxide has been used as a model reaction for the investigation of the catalytic activity of various metal complexes [18]. For example, the catalytic activity of copper (II) complex of chitosan derivative which derived from chitosan and 4, 6-diacetylresorcinol was investigated on hydrogen peroxide decomposition [19]. Also, the mixed ligand complex [Fe(2-AP)(Ala)Cl3]4H2O (2-AP = 2-acetylpyridine, Ala = alanine) catalyzed the decomposition of H2O2 and O2 was evolved [20]. Herein, we report the transition metal complexes of Schiff base derived from the condensation of 2-pyridinecarboxaldehyde with 2aminophenol.The ternary complexes were obtained by reaction with 2-aminopyridine. The structural features of these complexes were examined by analytical and spectral techniques. Abstract: A new ternary Schiff base transition metal complexes of general formula [M(HL)(2-AP)Cl2].H2O where M= Cu(II), Ni(II) and Co(II) ions in addition to the complex [La(HL)(2-AP)(NO3)2].NO3have been prepared by template synthesis. The synthesized metal complexes were characterized using spectroscopic techniques. The molar conductivities of the complexes in DMF indicated non electrolytic behavior except La(III) complex.IR spectra show that the Schiff base (HL) is coordinated to the metal ions in a tridentate manner with NNO donor sites of the pyridine-N, azomethine-N and phenolic-O,while 2-aminopyridine coordinated to the metal ions via its pyridine-N. The ligand (HL) and its mixed ligand complexes exhibited intraligand (-*) fluorescence and can potentially serve as photoactive materials. The catalytic activity of the complexes towards hydrogen peroxide decomposition reaction was investigated. Both the ligand (HL) and mixed ligand complexes have been screened for antibacterial activities.
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