首页 | 本学科首页   官方微博 | 高级检索  
     检索      

苯基羧甲基亚砜体系中高氯酸铥对高氯酸铽的荧光增强效应研究
引用本文:李文先,武国军,刘中仕,韩凤梅.苯基羧甲基亚砜体系中高氯酸铥对高氯酸铽的荧光增强效应研究[J].光谱学与光谱分析,2002,22(6):905-907.
作者姓名:李文先  武国军  刘中仕  韩凤梅
作者单位:内蒙古大学化学化工学院,内蒙古,呼和浩特,010021
基金项目:本项目由内蒙古自然科学基金资助,项目批准号 :2 0 0 0 1 30 1
摘    要:合成了不同摩尔比的苯基羧甲基亚砜高氯酸铽、铥异核配合物 ,对配合物进行了组成分析 ,确定了配合物组成为 (Tb1 -xTmx) L2 (ClO4 ) ·2H2 O(x=0 0 0 0~ 0 2 0 0 ,L=C6 H5SOCH2 COO- )。通过IR光谱及摩尔电导的测定推测了配位情况 ,溶解性实验表明配合物在乙醇、丙酮等极性溶剂中具有很高的溶解性。荧光光谱实验表明 :当 x =0 0 0 1~ 0 10 0时铥对铽的荧光均产生敏化增强效应 ,当x =0 0 0 1时敏化强度最大 ,可使Tb3+ 荧光强度增加 32 6 %。

关 键 词:高氯酸铥  高氯酸铽  苯基羧甲基亚砜  异核高氯酸  荧光增强效应  稀土配合物  稀土离子  发光
文章编号:1000-0593(2002)06-0905-03
修稿时间:2001年12月10

Fluorescence Enhancement Character of Terbium Perchlorate and Thulium Perchlorate with Phenylcarboxymethyl Sulfoxide Coordination Compounds
Wen-xian Li,Guo-jiun Wu,Zhong-shi Liu,Feng-mei Han.Fluorescence Enhancement Character of Terbium Perchlorate and Thulium Perchlorate with Phenylcarboxymethyl Sulfoxide Coordination Compounds[J].Spectroscopy and Spectral Analysis,2002,22(6):905-907.
Authors:Wen-xian Li  Guo-jiun Wu  Zhong-shi Liu  Feng-mei Han
Institution:College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China.
Abstract:(Tb1-x Tmx).L2.(ClO4).2H2O(x = 0.000 to 0.200, L = C6H5SOCH2COO-) have been synthesized. The coordination compounds have been studied by means of composition analysis, molar conductivity, IR, and the condition of coordination have been inferred. In the fluorescent spectra it was found that Tm3+ has a strongly sensitization effect to the fluorescence of Tb3+. The fluorescent emission intensity of Terbium perchlorate with phenylcarboxymethyl sulfoxide coordination compounds would be enhanced by Tm3+ in mixing. Tm3+ has a sensitization to the fluorescence of Tb3+ in the ratio of Tb3+:Tm3+ = 0.999:0.001-0.900:0.100. In the solubility experiment it was found that the complexes have high solubility in ethanol.
Keywords:Terbium perchlorate  Thulium perchlorate  Phenylcarboxymethyl sulfoxide  Fluorescence enhancement character
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号