The synthesis and characterisation of calix[6]arene-based lasso-like molecular structures is described. These interwoven structures consist of an electrochemical responsive N,N’-dialkylviologen arm covalently anchored at the upper rim of a triphenylureido calix[6]arene-based wheel. Upon reduction of the viologen core, a hollow tridimensional macrocyclic structure can be generated. This process is reversible, and the original lasso-like structure can be regenerated by oxidizing the viologen arm to its original dicationic form. Electrochemical and EPR techniques investigated the ability of the system to perform threading/dethreading movements upon redox switching. The functionalisation of the arm ω-hydroxy ending with a bulky diphenylacetyl group converts the self-threaded structure in a blocked interwoven molecular compound belonging to the class of [1]rotaxanes. The ability to form dimeric structures in the shape of a [c2] daisy chain was also demonstrated, an unprecedented result for calixarene macrocycles.

Orlandini, G., Casimiro, L., Bazzoni, M., Cogliati, B., Credi, A., Lucarini, M., et al. (2020). Synthesis and properties of a redox-switchable calix[6]arene-based molecular lasso. ORGANIC CHEMISTRY FRONTIERS, 7, 648-659 [10.1039/C9QO01379B].

Synthesis and properties of a redox-switchable calix[6]arene-based molecular lasso

Casimiro, Lorenzo;Credi, Alberto;Lucarini, Marco;Silvi, Serena
;
2020

Abstract

The synthesis and characterisation of calix[6]arene-based lasso-like molecular structures is described. These interwoven structures consist of an electrochemical responsive N,N’-dialkylviologen arm covalently anchored at the upper rim of a triphenylureido calix[6]arene-based wheel. Upon reduction of the viologen core, a hollow tridimensional macrocyclic structure can be generated. This process is reversible, and the original lasso-like structure can be regenerated by oxidizing the viologen arm to its original dicationic form. Electrochemical and EPR techniques investigated the ability of the system to perform threading/dethreading movements upon redox switching. The functionalisation of the arm ω-hydroxy ending with a bulky diphenylacetyl group converts the self-threaded structure in a blocked interwoven molecular compound belonging to the class of [1]rotaxanes. The ability to form dimeric structures in the shape of a [c2] daisy chain was also demonstrated, an unprecedented result for calixarene macrocycles.
2020
Orlandini, G., Casimiro, L., Bazzoni, M., Cogliati, B., Credi, A., Lucarini, M., et al. (2020). Synthesis and properties of a redox-switchable calix[6]arene-based molecular lasso. ORGANIC CHEMISTRY FRONTIERS, 7, 648-659 [10.1039/C9QO01379B].
Orlandini, Guido; Casimiro, Lorenzo; Bazzoni, Margherita; Cogliati, Beatrice; Credi, Alberto; Lucarini, Marco; Silvi, Serena; Arduini, Arturo; Secchi,...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/718368
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