期刊文献+

含芘环的缩氨基硫脲类化合物的合成及其对汞离子的识别 被引量:6

Synthesis of Some Thiosemicarbazones Containing Pyrene Group and Their Mercury Ion Recognition Properties
原文传递
导出
摘要 合成了芘甲醛-4-甲基缩氨基硫脲(1)、芘甲醛-4-(4-乙苯基)缩氨基硫脲(2)、芘甲醛-4,4-二甲基缩氨基硫脲(3)三个化合物,并通过质谱、元素分析、傅立叶红外光谱和核磁共振氢谱进行了结构表征.利用荧光激发和发射光谱,对其荧光活性进行研究,并考察了对溶液中汞离子的识别作用.在分别向三种化合物的溶液中逐步滴加汞离子时,其特征的荧光发射波长处对应的强度值都呈现规律性变化.因此可利用比率荧光法实现对汞离子配合过程的观测.结果表明,三种化合物都能与汞离子形成1:1的配合物,配合常数分别为4.57×104,5.54×104和2.12×104L/mol,其检测下限分别为4.56×10-6,2.61×10-6和5.49×10-6mol/L. Novel pyrenecarboxaldehyde-4-methyl-3-thiosemicarbazone(1),pyrenecarboxaldehyde-4-(4-ethylphenyl)-3-thiosemicarbazone(2) and pyrenecarboxaldehyde-4,4-dimethyl-3-thiosemicarbazone(3) have been synthesized and characterized by elemental analysis,FT-IR,1H NMR MS techniques.Their fluorescence and recognition properties to the mercury ion were studied by the fluorescence excitation and emission spectra.With adding mercury ion into their solutions respectively,their fluorescence emission intensities at different characteristic wavelength changed continually.Hence the ratiometric fluorescence measurement was used for detecting the complex process.It was found that a 1:1 stoichiometry complex is formed between the mercury ion and the three compounds with the association constants were 4.57×104,5.54×104 and 2.12×104 L/mol,respectively.And the detection limits of the mercury ion were 4.56×10-6,2.61× 10-6 and 5.49×10-6 mol/L.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2010年第10期1563-1566,共4页 Chinese Journal of Organic Chemistry
基金 后勤工程学院研究生创新基金资助项目
关键词 缩氨基硫脲 芘类衍生物 阳离子识别 合成 荧光光谱 thiosmicarbazone pyrene derivative cation recognition synthesis fluorescence spectrum
  • 相关文献

参考文献2

二级参考文献36

  • 1Joby,T.; Geetha,P.Asian J.Chem.2002,14(3~4),1370.
  • 2Klayman,D.L.; Bartosevich,J.F.; Mason,C.J.; Griffin,T.S.; Scovill,J.P.J.Med.Chem.1979,22(7),855.
  • 3Scovill,J.P.; Klayman,D.L.; Franchino,C.F.J.Med.Chem.1982,25,1261.
  • 4Jeno,K.DE 1934089,1970[Chem.Abstr.1970,72,100334s].
  • 5Omaima M,A.; Hamida,A.S.; Omar,A.; Mohsen,M.E.Alexandria J.Pharm.Sci.1990,4(2),1687.
  • 6Manish,S.; Pankaj,P.; Hansa,P.Orient.J.Chem.2002,18(1),159.
  • 7Rajasekaran,A.; Murugesan,S.J.Indian Chem.Soc.2002,79(6),544.
  • 8Narashima,M.; Dharmarajan,T.S.Asian J.Chem.2002,14(3~4),1325.
  • 9Klayman,D.L.; Scovill,J.P.; Bartosevich,J.; Mason,C.J.J.Med.Chem.1979,22(11),1367.
  • 10Andrei,G.M.; Pieroni,O.I.; Gatica,H.S.; Coto,C.E.Drugs Exp.Clin.Res.1985,11(12),869.

共引文献23

同被引文献64

引证文献6

二级引证文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部