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Updated: Apr 27, 2026

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
2D conglomerate crystallization of heptahelicene
Johannes Seibel1, Laura Zoppi, Karl-Heinz Ernst
1Empa, Swiss Federal Laboratories for Materials Science and Technology, Überlandstrasse 129, CH-8600 Dübendorf, Switzerland. karl-heinz.ernst@empa.ch.
Scanning tunnelling microscopy revealed that heptahelicene forms homochiral domains on copper(100) surfaces. This contrasts with previous observations of racemic crystals on copper(111) surfaces.
Area of Science:
- Surface science
- Supramolecular chemistry
- Organic chemistry
Background:
- Heptahelicene is a helical aromatic hydrocarbon with unique chiral properties.
- Controlling molecular self-assembly on surfaces is crucial for advanced materials.
- Previous studies showed racemic crystallization of heptahelicene on Cu(111).
Purpose of the Study:
- To investigate the two-dimensional (2D) nucleation and crystallization of heptahelicene on a single crystalline copper(100) surface.
- To compare the self-assembly behavior of heptahelicene on Cu(100) with that on Cu(111).
Main Methods:
- Scanning tunnelling microscopy (STM) was employed to visualize and analyze the molecular arrangement.
- The study focused on the self-assembly of heptahelicene molecules on the Cu(100) surface.
Main Results:
- Heptahelicene forms distinct homochiral domains on the Cu(100) surface.
- This observation differs from the racemic 2D crystals previously reported on the Cu(111) surface.
- The specific surface crystallography of Cu(100) influences the chiral separation during crystallization.
Conclusions:
- The Cu(100) surface promotes enantioselective self-assembly of heptahelicene.
- Surface crystallography plays a critical role in dictating the chirality of 2D molecular crystals.
- This finding opens possibilities for creating surfaces with controlled chirality.
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