Related Experiment Video
Updated: Jul 7, 2026

Paradigms for Pharmacological Characterization of C. elegans Synaptic Transmission Mutants
Published on: August 18, 2008
Adsorption-induced asymmetric assembly from an achiral adsorbate
Yuguang Cai1, Steven L Bernasek
1Department of Chemistry, Princeton University, Princeton, New Jersey 08540, USA.
Abstract:
Symmetry breaking in the self-assembled monolayer (SAM) structure of 1-octadecanol on highly ordered pyrolytic graphite (HOPG) is observed. Due to the slight mismatch of the octadecanol molecule with the graphite lattice, the alkane chain undergoes distortion upon adsorption on the surface. The asymmetric distortion of the octadecanol SAM unit cell pair is observed by scanning tunneling microscopy at the liquid/solid interface. Asymmetric distortion is due to the requirement for planarity of the hydrogen bond connecting the two octadecanol molecules in the chevron-shaped unit cell. This very simple structure provides the first example of an adsorption-induced distortion to form a supramolecular asymmetric structure, which is formed by achiral molecules adsorbed on an achiral surface. What makes this system interesting and different from other examples of adsorption-induced chirality is that the adsorbate itself undergoes asymmetric distortion due to the existence of the substrate and the adsorbate conformation is different from the molecule in solution.
Related Concept Videos
Drug-Receptor Interactions
Several parameters, such as the drug's affinity for its receptor and its efficacy, which is its ability to activate the receptor, determine the drug's effect on the tissue.
Drug-Receptor Interaction: Agonist
Agonists can bind to receptors in different ways. Some agonists bind directly to the receptor's active site, mimicking the endogenous ligand's action.
Drug-Receptor Interaction: Antagonist
Antagonists can be classified as competitive or noncompetitive based on their...
Combined Effects of Drugs: Antagonism
The most common type is receptor antagonism, where one drug acts as an antagonist to block the effects of another drug by...
Adrenergic Agonists: Indirect-Acting Agents
One mechanism involves depleting stored catecholamines by displacing them from synaptic vesicles. These agents, known as "displacers," are transported into vesicles at the expense of noradrenaline. Examples include amphetamine and tyramine, which lack a catechol moiety, resulting in prolonged action, improved oral bioavailability, and...
Adrenergic Agonists: Chemistry and Structure-Activity Relationship
Aromatic ring substitutions: Substituting the aromatic ring with –OH groups at positions 3 and 4 yields catecholamines (e.g., epinephrine), which have a high affinity for adrenoceptors. Hydrogen bonding between –OH groups and receptors enhances adrenergic activity.
Separation of the aromatic...

