Related Experiment Video
Updated: Apr 16, 2026

Microscopic Visualization of Porous Nanographenes Synthesized through a Combination of Solution and On-Surface Chemistry
Published on: March 4, 2021
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Ruth Dorel1, Carlos Manzano, Maricarmen Grisolia
1Institute of Chemical Research of Catalonia (ICIQ), Av. Països Catalans 16, 43007 Tarragona, Spain. aechavarren@iciq.es.
Researchers synthesized a novel disc-shaped nanographene called tetrabenzocircumpyrene. Scanning tunnelling microscopy proved effective for characterizing this highly insoluble molecule.
Area of Science:
- Materials Science
- Nanotechnology
- Organic Chemistry
Background:
- Graphenic molecules are crucial in advanced materials.
- Synthesizing and characterizing large, insoluble graphenes presents significant challenges.
Purpose of the Study:
- To synthesize a novel, highly symmetric C54H20 nanographene fragment.
- To characterize the synthesized molecule using advanced microscopy techniques.
- To evaluate the utility of scanning tunnelling microscopy for insoluble graphenic compounds.
Main Methods:
- Chemical synthesis of tetrabenzocircumpyrene (C54H20).
- Characterization using scanning tunnelling microscopy (STM).
Main Results:
- Successful synthesis of the disc-shaped, highly symmetric tetrabenzocircumpyrene nanographene.
- STM imaging confirmed the molecular structure and high symmetry.
- Demonstrated STM's capability in analyzing highly insoluble graphenic molecules.
Conclusions:
- Tetrabenzocircumpyrene represents a new class of nanographene fragments.
- Scanning tunnelling microscopy is a powerful tool for characterizing insoluble graphenes.
- This work opens avenues for exploring complex graphenic structures.
More Related Videos
Related Concept Videos
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Structure of Benzene: Molecular Orbital Model
Thermal and Photochemical Electrocyclic Reactions: Overview
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous...
π Molecular Orbitals of 1,3-Butadiene
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the...
Five-Membered Heterocyclic Aromatic Compounds: Overview

