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Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
4-Chloro-2-[(E)-(2-chloro-phen-yl)imino-meth-yl]phenol
1Department of Chemistry, Baoji University of Arts and Science, Baoji, Shaanxi 721007, People's Republic of China.
This study details the crystal structure of a novel compound derived from 5-chloro-salicylaldehyde and o-chloro-aniline. The molecule exhibits a trans configuration and features an intramolecular hydrogen bond, contributing to its structural stability.
Area of Science:
- Crystallography
- Organic Chemistry
- Molecular Structure
Background:
- Understanding the structural properties of organic compounds is crucial in chemistry.
- Schiff bases, formed from aldehydes and amines, are versatile intermediates.
Purpose of the Study:
- To characterize the crystal structure of a compound synthesized from 5-chloro-salicylaldehyde and o-chloro-aniline.
- To investigate the molecular geometry, including bond configurations and intermolecular interactions.
Main Methods:
- Single crystal X-ray diffraction was employed to determine the molecular and crystal structure.
- Analysis of bond lengths, bond angles, and non-bonded contacts.
Main Results:
- The synthesized compound, C(13)H(9)Cl(2)NO, was successfully crystallized.
- The molecule adopts a trans configuration around the imine (C=N) double bond.
- An intramolecular O-H⋯N hydrogen bond was identified, stabilizing the structure.
- The two aromatic rings are nearly coplanar (dihedral angle 7.1°).
- A C-H⋯π interaction was observed within the crystal lattice.
Conclusions:
- The crystal structure reveals key features of the title compound, including its trans imine configuration and stabilizing intramolecular hydrogen bonding.
- The near-planar aromatic rings and C-H⋯π interaction provide insights into crystal packing forces.
- This structural data contributes to the understanding of Schiff base derivatives.
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