Protonation activates anion binding and alters binding selectivity in new inherently fluorescent 2,6-bis(2-anilinoethynyl)pyridine bisureas

Chem Commun (Camb). 2009 May 14:(18):2520-2. doi: 10.1039/b901643k. Epub 2009 Mar 27.

Abstract

A new class of 2,6-bis(2-anilinoethynyl)pyridine-based bisureas forms 1 : 1 complexes with halides; protonation enhances binding by over one order of magnitude, alters the binding selectivity, and provides a colorimetric indication of anion binding.