Related Experiment Video
Updated: May 13, 2026

Synthesis and Characterization of Supramolecular Colloids
Published on: April 22, 2016
Generating long supramolecular pathways with a continuous density of states by physically linking conjugated
Roozbeh Shokri1, Marie-Agnés Lacour, Thibaut Jarrosson
1Institut de Sciences des Matériaux de Mulhouse IS2M, LRC 7228-CNRS-UHA, 4 rue des frères Lumière, 68093 Mulhouse, France.
Abstract:
Self-assembly of conjugated 2,5-dialkoxy-phenylene-thienylene-based oligomers on epitaxial monolayer graphene was studied in ultrahigh vacuum by low-temperature scanning tunneling microscopy (STM). The formation of long one-dimensional (1D) supramolecular chain-like structures has been observed, associated to a physical linking of their ends which involved the rotation of the end thiophene rings in order to allow π-π stacking of these end-groups. dI/dV maps taken at an energy corresponding to the excited states showed a continuous electronic density of states, which tentatively suggests that within such molecular chains conjugation of electrons is preserved even across physically linked molecules. Thus, in a self-organization process conjugation may be extended by appropriately adapting conformations of neighboring molecules. Our STM results on such self-organized end-linked molecules potentially represent a direct visualization of J-aggregates.
Related Concept Videos
Step-Growth Polymerization: Overview
Many natural and synthetic polymers are produced by...
Cationic Chain-Growth Polymerization: Mechanism
Ziegler–Natta Chain-Growth Polymerization: Overview
Cycloaddition Reactions: Overview
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 number...
¹H NMR: Long-Range Coupling
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene π orbitals.

