Rigid, Y-shaped imidazole compounds containing the bis(thienyl)ethene moiety were designed and synthesized. The 4,5-bis(benzothienyl)-2-phenylimidazolium cations were then used as axles for [2]pseudorotaxane formation with 24-membered crown ether wheels. It was demonstrated using 1H NMR spectroscopy, UV-Vis absorption and emission spectroscopies that this host-guest interaction results in significant changes in the photochromic properties of the imidazolium axles. This is a rare example of gated photochromism, which exploits the recognition event of an interpenetrated molecular system to tune the photochromic properties in one of the components.

Baggi, G., Casimiro, L., Baroncini, M., Silvi, S., Credi, A., Loeb, S.J. (2019). Threading-gated photochromism in [2]pseudorotaxanes. CHEMICAL SCIENCE, 10, 1-7 [10.1039/C9SC00913B].

Threading-gated photochromism in [2]pseudorotaxanes

Casimiro, Lorenzo;Baroncini, Massimo;Silvi, Serena
;
Credi, Alberto;
2019

Abstract

Rigid, Y-shaped imidazole compounds containing the bis(thienyl)ethene moiety were designed and synthesized. The 4,5-bis(benzothienyl)-2-phenylimidazolium cations were then used as axles for [2]pseudorotaxane formation with 24-membered crown ether wheels. It was demonstrated using 1H NMR spectroscopy, UV-Vis absorption and emission spectroscopies that this host-guest interaction results in significant changes in the photochromic properties of the imidazolium axles. This is a rare example of gated photochromism, which exploits the recognition event of an interpenetrated molecular system to tune the photochromic properties in one of the components.
2019
Baggi, G., Casimiro, L., Baroncini, M., Silvi, S., Credi, A., Loeb, S.J. (2019). Threading-gated photochromism in [2]pseudorotaxanes. CHEMICAL SCIENCE, 10, 1-7 [10.1039/C9SC00913B].
Baggi, Giorgio; Casimiro, Lorenzo; Baroncini, Massimo; Silvi, Serena; Credi, Alberto; Loeb, Stephen J.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/685368
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