Related Experiment Video
Updated: Jun 1, 2026

Synthesis and Structure Determination of µ-Conotoxin PIIIA Isomers with Different Disulfide Connectivities
Published on: October 2, 2018
4-Acetyl-pyridinium hydrogen sulfate
1Ordered Matter Science Research Center, Southeast University, Nanjing 210096, People's Republic of China.
The crystal structure reveals hydrogen sulfate anions forming chains via O-H⋯O bonds. These anions also link to 4-acetyl-pyridinium cations through N-H⋯O hydrogen bonds.
Area of Science:
- Crystallography
- Materials Science
- Chemical Physics
Background:
- Understanding the intermolecular interactions in crystalline solids is crucial for predicting material properties.
- Pyridinium salts and their derivatives are important in various chemical applications.
- Hydrogen sulfate anions play a significant role in hydrogen-bonding networks.
Purpose of the Study:
- To elucidate the crystal structure of the 4-acetyl-pyridinium hydrogen sulfate salt.
- To investigate the hydrogen bonding patterns within the crystal lattice.
- To characterize the interactions between the organic cation and inorganic anion.
Main Methods:
- Single-crystal X-ray diffraction was employed to determine the crystal structure.
- Analysis of bond lengths, bond angles, and intermolecular distances.
- Identification of hydrogen bonding interactions (O-H⋯O and N-H⋯O).
Main Results:
- The crystal structure is characterized by extended chains of hydrogen sulfate anions linked by O-H⋯O hydrogen bonds.
- Each hydrogen sulfate anion acts as a bridge, connecting to a 4-acetyl-pyridinium cation.
- A significant N-H⋯O hydrogen bond was observed between the pyridinium nitrogen and a sulfate oxygen.
Conclusions:
- The crystal structure is dominated by a network of hydrogen bonds involving both anions and cations.
- The observed hydrogen bonding pattern dictates the packing and stability of the crystal.
- This study provides fundamental insights into the solid-state chemistry of pyridinium salts with hydrogen sulfate counterions.
More Related Videos
08:21Optimized Procedure for Determining the Adsorption of Phosphonates onto Granular Ferric Hydroxide using a Miniaturized Phosphorus Determination Method
Published on: May 18, 2018
10:48Electrochemical Preparation of Poly(3,4-Ethylenedioxythiophene) Layers on Gold Microelectrodes for Uric Acid-Sensing Applications
Published on: July 28, 2021
Related Concept Videos
Phosphate Buffer
Sodium dihydrogen phosphate does not fully dissociate in neutral or acidic solutions. When a strong base, such as sodium hydroxide (NaOH), is introduced into the solution, sodium dihydrogen phosphate...
Acidity of 1-Alkynes
The acidic strength of hydrocarbons follows the order: Alkynes > Alkenes > Alkanes. The strength of an acid is commonly expressed in units of pKa — the lower the pKa, the stronger the acid. Among the hydrocarbons, terminal alkynes have lower pKa values and are, therefore, more acidic. For example, the pKa values for ethane, ethene, and acetylene are 51, 44, and 25, respectively, as shown here.
Polyprotic Acids
Composition of Polyprotic Acid Solutions as a Function of pH
A graph with the alpha values is plotted against the volume of base added during titration. Here, a...
Relative Strengths of Conjugate Acid-Base Pairs
Titration of Polyprotic Acids with a Strong Base