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Updated: Jun 5, 2026

Preparation of Stable Bicyclic Aziridinium Ions and Their Ring-Opening for the Synthesis of Azaheterocycles
Published on: August 22, 2018
1,2-Bis(2-chloro-benzyl-idene)hydrazine
1Department of Chemistry, Lishui College, 323000 Lishui, ZheJiang, People's Republic of China.
This study details the crystal structure of a Schiff base compound, C14H10Cl2N2. The molecule exhibits approximate planarity and crystallizes with a unique half-molecule arrangement on an inversion center, lacking intermolecular hydrogen bonds.
Area of Science:
- Crystallography
- Organic Chemistry
- Materials Science
Background:
- Schiff base compounds are versatile organic molecules with diverse applications.
- Understanding the solid-state structure is crucial for predicting material properties.
- Crystal packing and intermolecular interactions influence bulk characteristics.
Purpose of the Study:
- To elucidate the crystal structure of the Schiff base compound C14H10Cl2N2.
- To analyze the molecular geometry and symmetry elements.
- To investigate intermolecular interactions within the crystal lattice.
Main Methods:
- Single-crystal X-ray diffraction was employed to determine the crystal structure.
- Crystallographic data were collected and refined.
- Molecular geometry and packing arrangements were analyzed.
Main Results:
- The Schiff base compound C14H10Cl2N2 crystallizes with one half-molecule in the asymmetric unit.
- The molecular skeleton is approximately planar, with minimal deviation.
- The N-N bond midpoint is located on an inversion center, indicating molecular symmetry.
- No classical intermolecular hydrogen bonds were observed in the crystal packing.
Conclusions:
- The determined crystal structure provides fundamental insights into the solid-state behavior of this Schiff base.
- The planar nature and inversion symmetry are key structural features.
- The absence of hydrogen bonds suggests alternative packing forces may dominate.
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