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Updated: Jun 15, 2025

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
A corannulene-based metallobox for the encapsulation of fullerenes
Susana Ibáñez1, Carmen Mejuto1, Katherin Cerón1
1Institute of Advanced Materials (INAM), Centro de Innovación en Química Avanzada (ORFEO-CINQA), Universitat Jaume I Av. Vicente Sos Baynat s/n Castellón E-12071 Spain maella@uji.es eperis@uji.es.
Abstract:
A corannulene-bis-N-imidazolium salt was used for the synthesis of two corannulene-bis-N-heterocyclic carbenes of dirhodium(i) complexes of formula (corannulene-di-NHC)[RhCl(COD)]2 and (corannulene-di-NHC)[RhCl(CO)2]2. Both complexes were characterized by spectroscopic techniques, and the electron-donating properties of the corannulene-di-NHC ligand were studied by means of infrared spectroscopy and cyclic voltammetry. The complex (corannulene-di-NHC)[RhCl(COD)]2 was used for the encapsulation of fullerenes C60 and C70, generating host-guest complexes with 2 : 1 stoichiometry, as evidenced by 1H NMR and ITC titrations. Then, a tetra-rhodium(i) metallo-rectangle supported by two corannulene-bis-imidazolylidene ligands and two cofacial 4,4'-bipyridine ligands was prepared and characterized. This metallobox is capable of quantitatively encapsulating fullerenes C60 and C70, forming complexes that are highly stable even at high temperatures. The molecular structure of the metallobox with encapsulated C60 reveals a perfect size and shape complementarity that benefits from the concave-convex π-π interaction between the polyaromatic surfaces of the host and the guest.

