Related Experiment Video
Updated: Feb 25, 2026

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Erecting buckybowls onto their edge: 2D self-assembly of terphenylcorannulene on the Cu(111) surface
Quirin S Stöckl1, Tsun-Cheng Wu, Anaïs Mairena
1Empa - Swiss Federal Laboratories for Materials Science and Technology, Überlandstrasse 129, 8600 Dübendorf, Switzerland. karl-heinz.ernst@empa.ch.
Abstract:
A 2D self-assembly of a C32H12 buckybowl on the Cu(111) surface has been studied by means of scanning tunnelling microscopy. Additional aromatic rings at the rim of the corannulene core cause the bowl-shaped molecule to stand on its edge. This adsorption mode allows distinct π-π and C-Hπ interactions between the convex bowl surfaces as well as between the hydrogen-terminated rim and the convex bowl faces.
More Related Videos
Related Concept Videos
Conformations of Cyclohexane
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal...
Chair Conformation of Cyclohexane
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this...
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Newman Projections
The organic molecules rotate across the single bonds leading to numerous temporary three-dimensional structures of varying energy known as...

