用户名: 密码: 验证码:
Fluorescent detection of Cu(II) by chitosan-based AIE bioconjugate
详细信息    查看全文
  • 作者:Ya-lan Liu ; Zheng-ke Wang 王征科 ; Wei Qin…
  • 关键词:Aggregation ; induced emission ; Chitosan ; Cu(II) ; Fluorescent detection
  • 刊名:Chinese Journal of Polymer Science
  • 出版年:2017
  • 出版时间:March 2017
  • 年:2017
  • 卷:35
  • 期:3
  • 页码:365-371
  • 全文大小:
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Polymer Sciences; Industrial Chemistry/Chemical Engineering; Characterization and Evaluation of Materials; Condensed Matter Physics;
  • 出版者:Chinese Chemical Society and Institute of Chemistry, CAS
  • ISSN:1439-6203
  • 卷排序:35
文摘
Detection of Cu(II) is very important in disease diagnose, biological system detection and environmental monitoring. Previously, we found that the product TPE-CS prepared by attaching the chromophores of tetraphenylethylene (TPE) to the chitosan (CS) chains showed excellent fluorescent properties. In this study, we tried to use TPE-CS for detecting Cu(II) because of the stable complexation of CS with heavy metals and the luminosity mechanism of the Restriction of Intramolecular Rotations (RIR) for aggregation-induced emission (AIE)-active materials. The fluorescence intensity changed when TPE-CS was contacted with different metal ions, to be specific, no change for Na+, slightly increase for Hg2+, Pb2+, Zn2+, Cd2+, Fe2+, Fe3+ due to the RIR caused by the complexation between CS and metal ions. However, for Cu2+, an obvious fluorescence decrease was observed because of the Photoinduced-Electron-Transfer (PET). Moreover, we found that the quenched FL intensity of TPE-CS was proportional to the concentration of Cu(II) in the range of 5 μmol/L to 100 μmol/L, which provided a new way to quantitatively detect Cu(II). Besides, TPE-CS has excellent water-solubility as well as absorbability (the percentage of removal, R = 84%), which is an excellent detection probe and remover for Cu(II).

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700