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Updated: Jun 1, 2026

05:59
Green Synthesis of Quinoline-Based Ionic Liquid
Published on: September 27, 2024
2-Cyano-quinolin-1-ium hydrogen sulfate
Wan-Sin Loh1, Madhukar Hemamalini, Hoong-Kun Fun
1X-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, 11800 USM, Penang, Malaysia.
Summary
The protonation of 2-cyano-quinoline by sulfuric acid forms a title salt. This study details the crystal structure and hydrogen bonding network of this new salt.
Area of Science:
- Crystallography
- Supramolecular Chemistry
- Organic Chemistry
Background:
- 2-cyano-quinoline is a heterocyclic aromatic organic compound.
- Sulfuric acid is a strong mineral acid.
- Proton transfer reactions are fundamental in acid-base chemistry.
Purpose of the Study:
- To synthesize and characterize the title salt formed from 2-cyano-quinoline and sulfuric acid.
- To investigate the crystal structure and intermolecular interactions of the title salt.
Main Methods:
- Crystallization of 2-cyano-quinoline with sulfuric acid.
- X-ray diffraction analysis to determine the crystal structure.
- Analysis of hydrogen bonding networks.
Main Results:
- The title salt, C(10)H(7)N(2) (+)·HSO(4) (-), was successfully formed via proton transfer.
- The quinoline ring system exhibits near planarity.
- A layered network structure was observed, stabilized by N-H⋯O, O-H⋯O, and C-H⋯O hydrogen bonds between cations and anions.
Conclusions:
- The crystallization process leads to the formation of a well-defined salt structure.
- Hydrogen bonding plays a crucial role in organizing the crystal lattice.
- The study provides insights into the solid-state behavior of 2-cyano-quinoline in the presence of a strong acid.
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