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Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
2-Chloro-4-{(E)-[(4-chloro-phen-yl)imino]-meth-yl}phenol
Zarife Sibel Sahin1, Samil Işık
1Department of Physics, Faculty of Arts and Sciences, Ondokuz Mayıs University, Kurupelit, TR-55139 Samsun, Turkey.
This study details the crystal structure of a novel Schiff base compound, C(13)H(9)Cl(2)NO. Its structure is stabilized by hydrogen bonds and π-π stacking interactions.
Area of Science:
- Crystallography
- Supramolecular Chemistry
- Organic Chemistry
Background:
- Schiff base compounds are versatile organic molecules with diverse applications.
- Understanding the crystal packing and intermolecular interactions is crucial for predicting material properties.
Purpose of the Study:
- To elucidate the crystal structure of the Schiff base compound C(13)H(9)Cl(2)NO.
- To investigate the intermolecular interactions, including hydrogen bonding and π-π stacking, that stabilize the crystal lattice.
Main Methods:
- Single-crystal X-ray diffraction was employed to determine the molecular and crystal structure.
- Analysis of the crystal structure involved identifying hydrogen bond donors and acceptors, and measuring π-π stacking distances.
Main Results:
- The crystal structure of C(13)H(9)Cl(2)NO was successfully determined.
- A notable dihedral angle of 10.20(10)° was observed between the benzene rings.
- The crystal lattice is stabilized by O-H⋯N hydrogen bonds and weak π-π stacking interactions with a centroid-centroid distance of 3.757(1) Å.
Conclusions:
- The study provides detailed structural information for the Schiff base compound C(13)H(9)Cl(2)NO.
- The identified hydrogen bonding and π-π stacking interactions are key factors in the compound's solid-state organization.
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