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聚乙烯吡咯烷酮与苯磺酸铕相互作用研究
引用本文:刘俊,刘少轩,高云龙,范晓坤,关妍,翁诗甫,杨展澜,徐怡庄,吴瑾光. 聚乙烯吡咯烷酮与苯磺酸铕相互作用研究[J]. 光谱学与光谱分析, 2013, 33(6): 1487-1490. DOI: 10.3964/j.issn.1000-0593(2013)06-1487-04
作者姓名:刘俊  刘少轩  高云龙  范晓坤  关妍  翁诗甫  杨展澜  徐怡庄  吴瑾光
作者单位:1. 文山学院生化系,云南 文山 663000
2. 北京大学化学与分子工程学院,北京 100871
3. 辽宁中医药大学药学院,辽宁 大连 116600
4. 河北师范大学化学与材料科学学院,河北 石家庄 050016
基金项目:国家自然科学基金项目,国家科技部(863)重大项目
摘    要:用变温红外光谱法和荧光光谱法研究了聚乙烯吡咯烷酮与苯磺酸铕的相互作用。聚乙烯吡咯烷酮的酰胺基团可与苯磺酸铕中的铕离子发生络合配位作用,导致聚乙烯吡咯烷酮的酰胺Ⅰ带发生红移。这种络合配位作用,使原本不溶于氯仿的苯磺酸铕可溶于含聚乙烯吡咯烷酮的氯仿溶液。在苯磺酸铕固体的发射光谱中,只能观察到铕离子的f—f跃迁特征发射峰,而在苯磺酸铕浓水溶液的荧光光谱中,亦可观测到苯磺酸根的π*→π跃迁峰,说明苯磺酸铕在水溶液中存在解络合现象。苯磺酸铕在溶液中的解络合行为使铕离子周围的可配位空间增大,这为PVP的酰胺基团与铕离子发生络合配位作用创造了条件。

关 键 词:聚乙烯吡咯烷酮  苯磺酸铕  红外光谱   
收稿时间:2012-10-22

On the Interaction between PVP and Europium Benzenesulfonate
LIU Jun,LIU Shao-xuan,GAO Yun-long,FAN Xiao-kun,GUAN Yan,WENG Shi-fu,YANG Zhan-lan,XU Yi-zhuang,WU Jin-guang. On the Interaction between PVP and Europium Benzenesulfonate[J]. Spectroscopy and Spectral Analysis, 2013, 33(6): 1487-1490. DOI: 10.3964/j.issn.1000-0593(2013)06-1487-04
Authors:LIU Jun  LIU Shao-xuan  GAO Yun-long  FAN Xiao-kun  GUAN Yan  WENG Shi-fu  YANG Zhan-lan  XU Yi-zhuang  WU Jin-guang
Affiliation:1. Department of Biochemistry, Wenshan University, Wenshan 663000, China2. College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China3. College of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian 116600, China4. College of Chemistry and Materials Science, Hebei Normal University, Shijiazhuang 050016, China
Abstract:The interaction between polyvinylpyrrolidone (abbreviated as PVP) and europium benzenesulfonate was investigated by using temperature-dependent FTIR and fluorescence spectra. Europium compounds show strong coordination ability with amide groups of PVP. In order to remove the undesired H—O—H scissoring bands from the adsorbed water in FTIR spectra, temperature-dependent FTIR was utilized to reveal the spectral behavior of amide Ⅰ band after being coordinated with europium ions from europium compounds. As a result, the bond order of the carbonyl groups decreased, leading to a red-shift of amide Ⅰ band in the FTIR spectra. Furthermore, fluorescence spectra demonstrate that the interaction between PVP and europium benzenesulfonate enhanced the solubility of europium benzenesulfonate in chloroform. As a matter of fact, europium benzenesulfonate, which is insoluble in chloroform, becomes soluble in chloroform containing 10 Wt% PVP. In the fluorescence spectrum of europium benzenesulfonate crystals, only the f—f transition peaks of europium ions can be found. However, the emission peak of the π*—π transition of benzenesulfonate group appears in concentrated aqueous solution of europium benzenesulfonate. The phenomenon shows that part of benzenesulfonate undergoes decomplexation from europium benzenesulfonate complex and isolated benzenesulfonate occurs in the aqueous solution. Energy transfer pathway from excited triplet state of benzenesulfonate to europium ions is blocked in isolated benzenesulfonate. As a result, π*—π transition band of benzenesulfonate can be observed in the florescence spectrum. The decomplexation provides larger coordination space around europium ions, which favors the coordination between europium benzenesulfonate and PVP.
Keywords:Polyvinylpyrrolidone  Europium benzenesulfonate  FTIR
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