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Updated: Jun 1, 2026

Preparation of Contiguous Bisaziridines for Regioselective Ring-Opening Reactions
Published on: July 28, 2022
N'-[1-(2-Hydroxy-phen-yl)ethyl-idene]-2-nitro-benzohydrazide methanol solvate
1School of Chemistry and Biological Engineering, Changsha University of Science and Technology, Changsha, Hunan 410004, People's Republic of China.
This study details the crystal structure of a Schiff base methanol solvate. It highlights intramolecular hydrogen bonding within the molecule and intermolecular hydrogen bonds forming chains in the crystal lattice.
Area of Science:
- Crystallography
- Supramolecular Chemistry
- Organic Chemistry
Background:
- Schiff bases are versatile organic compounds with diverse applications.
- Understanding molecular interactions is crucial for designing new materials.
- Crystal engineering aims to control solid-state structures and properties.
Purpose of the Study:
- To elucidate the crystal structure of a novel Schiff base compound.
- To investigate the intra- and intermolecular hydrogen bonding patterns.
- To characterize the solid-state assembly of the Schiff base solvate.
Main Methods:
- Single-crystal X-ray diffraction analysis was performed.
- The crystal structure was solved and refined.
- Hydrogen bonding networks were analyzed.
Main Results:
- The compound crystallizes as a methanol solvate (C(15)H(13)N(3)O(4)·CH(3)OH).
- A significant dihedral angle of 66.7° exists between the two benzene rings.
- An intramolecular O-H⋯N hydrogen bond was identified within the Schiff base molecule.
- Intermolecular O-H⋯O and N-H⋯O hydrogen bonds link molecules into chains along the a-axis.
Conclusions:
- The crystal structure reveals specific conformational preferences and bonding interactions.
- The observed hydrogen bonding dictates the supramolecular architecture.
- This structural information is valuable for understanding Schiff base chemistry and crystal engineering.
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