首页> 外文期刊>Journal of Coordination Chemistry >Synthesis, characterization and fluorescence spectra of mononuclear Zn(II), Cd(II) and Hg(II) complexes with l,10-phenanthroline-5,6-dione ligand
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Synthesis, characterization and fluorescence spectra of mononuclear Zn(II), Cd(II) and Hg(II) complexes with l,10-phenanthroline-5,6-dione ligand

机译:具有1,10-菲咯啉-5,6-二酮配体的单核Zn(II),Cd(II)和Hg(II)配合物的合成,表征和荧光光谱

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The mononuclear complexes of Zn(II), Cd(II) and Hg(II), [Zn(phen-dione)Cl_2], [Cd(phen-dione)Cl_2 and [Hg(phen-dione)Cl_2], where phen-dione= l,10-phenanthroline-5,6-dione, have been synthesized and characterized by elemental analysis and IR, ~1H NMR and electronic absorption spectroscopies. The v(C=O) of coordinated phen-dione ligands in these complexes shows that the phen-dione is not coordinated to metal ion from its C=O sites. Electronic spectra of the complexes show two absorption bands for intraligand transitions. These absorption bands show dependence on the dielectric constant of solvents. These complexes exhibit an intense fluorescence band around 545 nm in DMSO when the excitation wavelengths are 200 nm at room temperature.
机译:Zn(II),Cd(II)和Hg(II),[Zn(phen-dione)Cl_2],[Cd(phen-dione)Cl_2和[Hg(phen-dione)Cl_2]的单核络合物,其中-dione = 1,10-菲咯啉-5,6-dione已合成并通过元素分析,IR,〜1H NMR和电子吸收光谱进行了表征。这些配合物中配位的苯二酮配体的v(C = O)表明,苯二酮未从其C = O位置与金属离子配位。配合物的电子光谱显示了配体内跃迁的两个吸收带。这些吸收带显示出对溶剂的介电常数的依赖性。当激发波长在室温下为200 nm时,这些络合物在DMSO中显示约545 nm的强烈荧光带。

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