"Clickable" pillar[5]arenes

Chem Commun (Camb). 2011 Jun 28;47(24):6927-9. doi: 10.1039/c1cc11864a. Epub 2011 May 23.

Abstract

Introduction of bulky substituents such as benzyl and pyrenyl groups using click reactions inhibited or slowed the rotation of the units on the NMR chemical shift timescale. The perpyrenylated pillar[5]arene showed a thermally-responsive excimer emission, but a unit model of the perpyrenylated pillar[5]arene did not exhibit such a response.