Synthesis, characterization and thermal analysis of the copper(II) complexes with 2,2-bipyridyl and 1,10-phenanthroline

S. Chandraleka, G. Chandramohan
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引用次数: 16

Abstract

The Cu(II) complexes were synthesized by the addition of Cu(II) acetate monohydrate to ligand in aqueous solution with 1,10-phenanthroline and 2,2'-bipyridyl which led to the precipitation of complexes. The synthesized Cu(II) complexes [Cu(SAla)phen(H2O)].H2O, [Cu(SAla)bpy(H2O)].H2O were found to be soluble in water, ethanol, methanol and DMSO. The electronic spectra and the magnetic moment support the stereochemistry of the complexes. The electronic spectra of all the complexes display a broad band with maximum at 14765 to 15503 cm -1 , which suggested an octahedral geometry of the metal ion. The magnetic moment at the room temperature lying in the range of 1.78 to 2.09 BM corresponds to one unpaired electron which are slightly greater than the spin only value of 1.73 BM, which was expected for one unpaired electron which offer possibility of the paramagnetic nature. The electronic spectra of free ligand shows band at 35651 cm -1 which are intra ligand charge transfer band (INCT). The electronic absorption spectra of the schiff base complexes were recorded using DMSO solvent. The spectrum of Cu(II) complexes display a broad band at 14765 cm -1 , which attributed to 2 Eg 2 T2g transition, which strongly favours the octahedral geometry around the central metal ion. The thermal gravimetric analysis (TGA), derivative thermogravimetric analysis (DTG), differential thermal analysis (DTA) experiments were carried out to explore the thermal stability of the complexes. The thermal behaviours of all the metal complexes were studied in the temperature range of 0 to 1400°C. The TGA, DTG and DTA studies of complexes reveal that the decomposition proceeds in three steps.
2,2-联吡啶和1,10-菲罗啉铜配合物的合成、表征和热分析
采用1,10-菲罗啉和2,2′-联吡啶在配体上加成一水乙酸铜(II),使配合物沉淀,合成了Cu(II)配合物。合成的Cu(II)配合物[Cu(SAla)phen(H2O)]。水,铜(大厅)bpy (H2O)]。H2O可溶于水、乙醇、甲醇和二甲基亚砜。电子谱和磁矩支持配合物的立体化学性质。所有配合物的电子光谱都显示出较宽的频带,最大频带在14765 ~ 15503 cm -1处,表明金属离子具有八面体几何结构。室温下的磁矩为1.78 ~ 2.09 BM,对应1个未配对电子,比仅自旋的磁矩1.73 BM略大,这是对1个未配对电子的预期,为顺磁性提供了可能。自由配体的电子能谱在35651 cm -1处显示为配体内部电荷转移带。用DMSO溶剂记录了希夫碱配合物的电子吸收光谱。Cu(II)配合物的光谱在14765 cm -1处显示出较宽的波段,这归因于2 Eg - 2 t2跃迁,这强烈地有利于中心金属离子周围的八面体几何结构。通过热重分析(TGA)、导数热重分析(DTG)、差热分析(DTA)等实验考察了配合物的热稳定性。研究了所有金属配合物在0 ~ 1400℃范围内的热行为。配合物的热重分析(TGA)、差热分析(DTG)和差热分析(DTA)表明,分解分三步进行。
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