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Nd/Dy掺杂-L-谷氨酸-邻菲啰啉三元配合物的合成及其电化学性质

Synthesis and Electrochemical Activity of Rare Earth Nd/Dy-L-glutamic acid-1,10-phenanthroline Doped Ternary Complex

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【作者】 陈华庆王卫东陆江林陈灵

【Author】 Chen Huaqing;Wang Weidong;Lu Jianglin;Chen Ling;College of Arts & Science,Hubei Normal University;Hubei Collaborative Innovation Center for Rare Metal Chemistry;Hubei Key Laboratory of Pollutant Analysis & Reuse Technology;

【机构】 湖北师范大学文理学院稀有金属化学湖北省协同创新中心污染物分析与资源化技术湖北省重点实验室

【摘要】 在乙醇-水溶液中,水浴60℃合成了一系列不同配比的稀土掺杂(Nd/Dy)-L-谷氨酸(L-Glu)-邻菲啰啉(Phen)三元固体配合物。利用元素分析、摩尔电导、紫外光谱、红外光谱、热重差热分析等表征,推测出配合物组成为[NdxDy1-x(L-Glu)3Phen]Cl3·nH2O。通过荧光光谱对配合物的发光特性进行了探讨,当Nd和Dy掺杂比达到1∶3时,配合物荧光强度最大。最后通过循环伏安法对配合物的电化学活性进行了研究,设定扫描电位-0.30-0.80V(vs.SCE),五种配合物在HAc-NaAc缓冲溶液(pH约6.0左右)中均表现出电化学活性,电化学活性中心是RE3+,电化学行为是准可逆的,配合物还原峰电流与扫描速度及浓度呈现出递增关系。

【Abstract】 In the ethanol-water medium,a series of doped ternary complexes of Nd / Dy-L-glutamic acid-1,10-phenanthroline was synthesized in different proportion of Nd / Dy. Through molar conductance,complexometric titration analysis,elemental analysis,infrared spectra( IR) and TG-DTG analysis test,the general formula of the complexes were conformed to [NdxDy1- x( L-Glu)3Phen]Cl3·nH2O. Then fluorescence spectra were used to discuss their glowing characteristics,and when Nd3+ and Dy3+doping ratio was set as 1 ∶ 3,the fluorescence intensity achieved maximum. Finally electrochemical behavior at a platinum working electrode was tested by cyclic voltammetry. The complexes showed the electrochemical activity at- 0. 30 - 0. 80 V( vs. SCE) in the HAc-Na Ac buffer solution( pH≈6. 0). The RE3+ was electrochemical active center in rare earth complex. The results showed that the complex was a quasi-reversible system and it showed the increasing relationship between the coordination compound’s reduction peak and concentration.

【关键词】 稀土掺杂配合物荧光电化学活性
【Key words】 rare earthsdopedcomplexesfluorescenceelectrochemical activity
【基金】 湖北师范大学文理学院重点科研资助项目(Ky201501);湖北省教育厅重点科研资助项目(D20082202)
  • 【文献出处】 中国稀土学报 ,Journal of the Chinese Society of Rare Earths , 编辑部邮箱 ,2016年02期
  • 【分类号】O641.4
  • 【被引频次】2
  • 【下载频次】153
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