Related Experiment Video
Updated: Jul 29, 2026

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
The structure of acetylarsenocholine bromide
A Kostick1, A S Secco, M Billinghurst
1Department of Chemistry, University of Manitoba, Winnipeg, Canada.
This study reveals acetylarsenocholine bromide’s crystal structure, showing a trans-gauche conformation similar to acetylcholine. Bromide ions link the arsonium groups, providing insights into organoarsenic compounds.
Area of Science:
- Inorganic Chemistry
- Crystallography
- Structural Chemistry
Background:
- Acetylcholine is a crucial neurotransmitter with a well-studied structure.
- Organoarsenic compounds exhibit diverse chemical properties and biological activities.
- Understanding the structural nuances of acetylcholine analogs is vital for pharmacological research.
Purpose of the Study:
- To determine the crystal structure of acetylarsenocholine bromide.
- To elucidate the conformational properties of acetylarsenocholine in the solid state.
- To compare the structure of acetylarsenocholine bromide with acetylcholine salts.
Main Methods:
- Single-crystal X-ray diffraction analysis was performed.
- The crystal structure was solved and refined.
- Crystallographic data (space group, unit cell dimensions, R-factor) were obtained.
Main Results:
- Acetylarsenocholine bromide crystallizes in the orthorhombic system (P2(1)2(1)2(1)).
- The compound adopts a trans-gauche conformation in its crystalline state.
- Each bromide ion bridges four arsonium groups, indicating a specific intermolecular interaction.
Conclusions:
- The determined conformation is analogous to the solution conformation of acetylcholine.
- The crystal packing reveals a unique interaction pattern involving bromide ions and arsonium centers.
- This structural data contributes to the understanding of arsenic-containing analogs of biologically significant molecules.
More Related Videos
Related Concept Videos
Structures of Carboxylic Acid Derivatives
Carboxylic acid derivatives contain an acyl group attached to a heteroatom such as chlorine, oxygen, or nitrogen. The carbonyl carbon and oxygen are both sp2-hybridized with an unhybridized p orbital.
The three sp2 orbitals of the carbonyl carbon form three σ bonds, one each with the carbonyl oxygen, the α carbon, and the heteroatom, whereas the other two sp2 orbitals of the carbonyl oxygen are occupied by the lone pairs. Further, the unhybridized p...
Electrophilic Aromatic Substitution: Friedel–Crafts Acylation of Benzene
Direct-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship
The direct-acting...
Direct-Acting Cholinergic Agonists: Pharmacokinetics
Indirect-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship
Reversible inhibitors display short to medium durations of action. Short-acting agents include simple alcohols with...
Cholinergic Antagonists: Chemistry and Structure-Activity Relationship

