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2000
Volume 7, Issue 6
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A new type of perylenebisimide-based imidazolium chemosensor was synthesized for selective recognition of anions. Imidazolium-anchored receptor PBI-1 showed high binding affinity to F- due to the role of the phenolic hydroxyl group as an additional binding site. The hydroxyl-protected receptor PBI-2 could serve as highly selective and sensitive colorimetric and fluorometric sensor for H2PO4-. The study indicated that the C2-H of the imidazolium ring played an essential role in the anion recognition via synergistic effects of multiple hydrogen-bonding and electrostatic interactions. In addition, it was noteworthy that the phenolic hydroxy of the receptor was not indispensable for binding H2PO4 -, but very pivotal for binding F-.

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/content/journals/loc/10.2174/157017810791824928
2010-09-01
2025-10-03
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/content/journals/loc/10.2174/157017810791824928
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