Related Experiment Video
Updated: Nov 9, 2025

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
A three-shell supramolecular complex enables the symmetry-mismatched chemo- and regioselective bis-functionalization
Ernest Ubasart1, Oleg Borodin2, Carles Fuertes-Espinosa1
1Institut de Química Computacional i Catàlisi and Departament de Química, Universitat de Girona, Girona, Spain.
Abstract:
Molecular Russian dolls (matryoshkas) have proven useful for testing the limits of preparative supramolecular chemistry but applications of these architectures to problems in other fields are elusive. Here we report a three-shell, matryoshka-like complex-in which C60 sits inside a cycloparaphenylene nanohoop, which in turn is encapsulated inside a self-assembled nanocapsule-that can be used to address a long-standing challenge in fullerene chemistry, namely the selective formation of a particular fullerene bis-adduct. Spectroscopic evidence indicates that the ternary complex is sufficiently stable in solution for the two outer shells to affect the addition chemistry of the fullerene guest. When the complex is subjected to Bingel cyclopropanation conditions, the exclusive formation of a single trans-3 fullerene bis-adduct was observed in a reaction that typically yields more than a dozen products. The selectivity facilitated by this matryoshka-like approach appears to be a general phenomenon and could be useful for applications where regioisomerically pure C60 bis-adducts have been shown to have superior properties compared with isomer mixtures.
More Related Videos
Related Concept Videos
Stereoisomerism of Cyclic Compounds
Prochirality
Woodward–Hoffmann Selection Rules and Microscopic Reversibility
Molecules with Multiple Chiral Centers
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.
[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement

