以4-氨基苯乙酮和水杨醛为原料制备了具有席夫碱的Fe(III)、Co(II)、Ni(II)和Cu(II)的热稳定配合物

IF 1.7 4区 化学 Q3 Chemistry Journal of Chemical Sciences Pub Date : 2022-11-25 DOI:10.1007/s12039-022-02113-6
Rasheeda M Ansari, Dileep Ramakrishna, Badekai Ramachandra Bhat
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引用次数: 0

摘要

以4-氨基苯乙酮和水杨醛为原料合成了希夫碱配体1-(4-(2-羟基苄基)氨基)苯基)乙二酮及其与Fe(III)、Co(II)、Ni(II)和Cu(II)的配合物。这些配合物通过FTIR光谱、元素分析和SCXRD分析进行了表征。配合物的FTIR光谱显示金属离子与配体的双齿配位,其中O和N是亚甲基的给电子位点。这些配合物的电子吸收光谱显示出Fe、Co和Ni配合物由于π→π*、n→π*跃迁所涉及的吸收带特征。通过计算得到的磁矩值和单晶XRD分析,推导出配合物的几何形状。由2-氨基苯乙酮与水杨醛缩合反应生成的希夫碱与镍、钴、铁、铜等四种不同的金属配合物形成。合成这些配合物的方法简单,产率高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Thermally stable complexes of Fe(III), Co(II), Ni(II) and Cu(II) with Schiff base derived from 4-aminoacetophenone and salicylaldehyde

The Schiff base ligand 1-(4-((2-hydroxybenzylidene)amino)phenyl)ethan-1-one, obtained from 4-aminoacetophenone and salicylaldehyde, and its complexes with Fe(III), Co(II), Ni(II) and Cu(II) have been synthesized. These complexes were characterized by FTIR spectroscopy, elemental, and SCXRD analysis. FTIR spectra of complexes show the bidentate coordination of metal ions with ligands where O and N are electron-donating sites of the azomethine group. The electronic absorption spectra of these complexes show the characteristics of absorption bands involved in the Fe, Co, and Ni complexes due to their π→π*, n→π* transitions. Further, the geometry of the complexes was deduced from the calculated magnetic moment values and single crystal XRD analysis.

Graphical abstract

A Schiff base derived from the condensation reaction between 2-aminoacetophenone and salicylaldehyde was involved in the formation of four different metal complexes, i.e., with Nickel, Cobalt, Iron, and Copper. The synthetic route to forming these complexes followed an easy process, and the complexes were obtained in good yields.

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来源期刊
Journal of Chemical Sciences
Journal of Chemical Sciences Chemistry-General Chemistry
CiteScore
2.90
自引率
5.90%
发文量
107
审稿时长
12 months
期刊介绍: Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.
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