Related Experiment Video
Updated: Nov 26, 2025

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
The shape selectivity of corannulene dimers based on concave-convex and convex-convex shape complementarity as hosts
Li Wang1, Yan-Li Liu, Sheng-Hui Chen
1School of Physics and Optoelectronics Engineering, Ludong University, Yantai, 264025, Shandong, China. wangl@ldu.edu.cn mswang1971@163.com.
Abstract:
In the formation of noncovalent complexes, the stacking arrangements of corannulene and fullerene are diverse, most of which are combinations of multiple corannulenes and fullerene. Here, a composition ratio of 2 : 1 was selected for the complex between corannulene and fullerene (C60 and C70) to investigate the effects of different superposition modes, including concave-convex and convex-convex interactions, on the stability and third-order nonlinear optical (NLO) properties of the composite materials. It was found that the concave-convex interaction was stronger and it was reported to stabilize the charge-transfer (CT) complex more effectively than the convex-convex interaction. The dispersion range of the concave-convex interaction was larger than that of the convex-convex interaction, which is consistent with the interaction energy results. The packing design with the double convex-convex interactions exhibited the largest linear optical response and third-order NLO response, which showed that the convex-convex interaction was more likely to be excited and cause intermolecular CT as compared to the concave-convex interaction. This work confirmed that the packing arrangement significantly affected the NLO response and will advance the development of NLO crystals.
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...
Molecular Shape and Polarity
Stability of Conjugated Dienes
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
Stability of Substituted Cyclohexanes
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
Conformations of Cycloalkanes

