Host-guest chemistry of a bis-calix[4]pyrrole derivative containing a trans/cis-switchable azobenzene unit with several aliphatic bis-carboxylates

Chemistry. 2015 Mar 27;21(14):5323-7. doi: 10.1002/chem.201406183. Epub 2015 Feb 24.

Abstract

The azobenzene unit used as a photochemically and thermally switchable linker in the assembly of a bis-calix[4]pyrrole receptor provides a means to modulate the binding of bis-carboxylates of significant biological importance in cancer research. Conversely, the complexation of different bis-anionic guests has significant kinetic effects on both the photochemical and thermal trans/cis isomerization of the azobenzene unit.

Keywords: anion binding; azocompounds; calixpyrroles; carboxylates; host-guest systems.