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Updated: Jun 5, 2026

Facile Preparation of (2Z,4E)-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
Bis[4-(2-hydr-oxy-3-methoxy-benzyl-ideneamino)phen-yl] ether
Hong-Wu Xu1, Jin-Xia Li, Yin-Hua Li
1Department of Materials and Chemical Engineering, ZhongYuan University of Technology, Zhengzhou, Henan 450007, People's Republic of China.
A flexible Schiff base ligand was synthesized using a condensation reaction. Structural analysis revealed its unique molecular geometry and hydrogen bonding, highlighting its potential applications.
Area of Science:
- Organic Chemistry
- Crystallography
Background:
- Schiff bases are versatile ligands with diverse applications in coordination chemistry and materials science.
- Understanding the structure-property relationships of flexible ligands is crucial for designing novel functional molecules.
Purpose of the Study:
- To synthesize and characterize a novel flexible Schiff base ligand.
- To elucidate the molecular structure and conformation of the synthesized ligand.
Main Methods:
- Schiff base condensation reaction between 3-methoxy-salicylaldehyde and bis-(4-amino-phenyl) ether.
- Single-crystal X-ray diffraction analysis to determine molecular structure and conformation.
Main Results:
- The title compound, C(28)H(24)N(2)O(5), was prepared in high yield.
- The molecule crystallizes with the formula C(28)H(24)N(2)O(5) and lies on a twofold rotation axis.
- Detailed crystallographic analysis revealed specific dihedral angles (69.22° and 24.29°) between benzene rings, indicating significant molecular flexibility and twisting.
Conclusions:
- A novel flexible Schiff base ligand was successfully synthesized and characterized.
- The crystal structure provides insights into the conformational flexibility and hydrogen bonding of the ligand.
- The study contributes to the understanding of structure-property relationships in flexible organic molecules.
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