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.

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

CAFEO, GRAZIA
Primo
;
KOHNKE, Franz Heinrich
Secondo
;
MEZZATESTA, GIOVANNI;VILLARI, Antonino Gaet.
Penultimo
;
2015-01-01

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.
2015
Inglese
STAMPA
21
14
5323
5327
5
http://onlinelibrary.wiley.com/doi/10.1002/chem.201406183/pdf
Internazionale
Esperti anonimi
anion binding, azocompounds, calixpyrroles, carboxylates, host-guest systems
info:eu-repo/semantics/article
Cafeo, Grazia; Kohnke, Franz Heinrich; Mezzatesta, Giovanni; Profumo, Aldo; Rosano, Camillo; Villari, Antonino Gaet.; White, Andrew J. P.
14.a Contributo in Rivista::14.a.1 Articolo su rivista
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Descrizione: Host-guest chemistry of a bis-calix[4]pyrrole derivative containing a trans/cis-switchable azobenzene unit with several aliphatic bis-carboxylates
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/3081741
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