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现代光谱技术在席夫碱大环配体及其与过渡金属配合物表征中的应用

Modern spectroscopic techniques in the characterization of Schiff base macrocyclic ligand and its complexes with transition metals.

作者信息

Chandra Sulekh, Gupta Lokesh Kumar

机构信息

Department of Chemistry, Zakir Husain College, University of Delhi, JLN Marg, New Delhi 110002, India.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2005 Nov;62(1-3):307-12. doi: 10.1016/j.saa.2004.12.044.

Abstract

Mn(II), Co(II), Ni(II), and Cu(II) complexes with a new azamacrocyclic tetradentate [N(4)] ligand i.e. 2,3,9,10-tetraphenyl;l,4,8,11-tetraazacyclotetradeca;1,3,8,10-tetraene (L) have been synthesized and characterized by elemental analysis, molar conductance measurements, magnetic susceptibility measurements, mass, (1)HNMR, IR, electronic and EPR spectral studies. On the basis of their non-electrolytic nature, the probable formula of the complexes is proposed to be [M(L)X(2)], where M=Mn(II), Co(II), Ni(II), and Cu(II), X=Cl(-) and NO(3)(-), in dimethylformamide (DMF). All the complexes are of high-spin type and found to have six coordinated, octahedral geometry for Mn(II), Co(II), and Ni(II) complexes, and tetragonal for Cu(II) complexes. Macrocyclic ligand and its complexes have also been screened against pathogenic bacteria and fungi in vitro as growth inhibiting agent.

摘要

已合成了锰(II)、钴(II)、镍(II)和铜(II)与一种新型氮杂大环四齿[N(4)]配体即2,3,9,10-四苯基;1,4,8,11-四氮杂环十四烷;1,3,8,10-四烯(L)形成的配合物,并通过元素分析、摩尔电导率测量、磁化率测量、质谱、(1)HNMR、红外光谱、电子光谱和电子顺磁共振光谱研究对其进行了表征。基于它们的非电解质性质,提出配合物的可能化学式为[M(L)X₂],其中M = 锰(II)、钴(II)、镍(II)和铜(II),X = Cl⁻和NO₃⁻,在二甲基甲酰胺(DMF)中。所有配合物均为高自旋型,发现锰(II)、钴(II)和镍(II)配合物具有六配位八面体几何构型,铜(II)配合物具有四方几何构型。大环配体及其配合物也已作为生长抑制剂在体外针对病原菌和真菌进行了筛选。

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