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
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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.File | Dimensione | Formato | |
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