Design and Synthesis of a Selective Chemosensor for Zn2+
β Scribed by Nan Xie; Yi Chen
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 78 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0256-7660
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
A hydroxyl substituted phenolic Schiff base 1, used as sensor for detection of Zn^2+^, was synthesized and investigated. It was found that a strong fluorescence emission was observed when 1 bound to Zn^2+^ in acetonitrile, whereas no fluorescence emission was detected when 1 bound to other metal ions (Fe^2+^, Co^2+^, Ni^2+^, Cu^2+^, Cd^2+^, Hg^2+^, Mg^2+^, Pb^2+^, Ca^2+^, Ba^2+^, Sr^2+^) except for Mg^2+^, for which a weak fluorescence emission was detected in the same condition. Competition experiment showed that no obvious interference was observed in its fluorescence while 1 performed the titration with Zn^2+^ in the different mixtures of metal ions. To understand the site where Zn^2+^coordinated to the ligand and the mechanism of binding, three other hydroxyl substituted phenolic Schiff bases 2β4 were synthesized and their binding reactions with Zn^2+^were also investigated.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
A potassium selective fluorescent chemosensor, 2, was designed and synthesized. The molecular sensor is weakly luminescent in acetonitrile solution, but exhibits a significant increase in intensity upon addition of K + . The luminescence
## Abstract The receptor (I) binds in a cooperative fashion to both a potassium cation and a carboxylate anion.