Tunability of anion binding strength based on acyl-thiourea receptors containing isatin group

S Hu, Y Guo, J Xu, S Shao

Index: Hu, Shuzhen; Guo, Yong; Xu, Jian; Shao, Shijun Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2009 , vol. 72, # 5 p. 1043 - 1046

Full Text: HTML

Citation Number: 10

Abstract

Some acyl-thiourea derivatives containing isatin group were synthesized and their interactions with anions were investigated using UV–vis spectroscopy and 1H NMR titrations in DMSO and DMSO-d6, respectively. These compounds have a same molecular framework, functionalising with different groups lead to different anion binding strength of these receptors. Receptor 1 showed a higher binding affinity for AcO− than for F−, due to ...

Related Articles:

Synthesis and Antimicrobial Activity of N??[(2Z)??3??(4, 6??Substitutedpyrimidin??2??yl)??4??phenyl??1, 3??thiazol??2 (3H)??ylidene]??3, 5??dinitrobenzamide Analogues

[Saeed, Sohail; Hussain, Rizwan; Ali, Muhammad Journal of Heterocyclic Chemistry, 2013 , vol. 50, # 2 p. 237 - 243]

More Articles...