N'-(2-Chloro-5-nitro-benzyl-idene)isonicotinohydrazide.
1Modern Medical Research Center, Third Affiliated Hospital of Soochow University, Changzhou 213003, People's Republic of China.
Researchers synthesized a new chemical compound, C(13)H(9)ClN(4)O(3), using a condensation reaction. The study details its molecular structure and crystal packing, revealing intermolecular hydrogen bonds that form dimers.
Area of Science:
- Organic Chemistry
- Crystallography
- Molecular Structure
Background:
- Synthesis of novel organic compounds is crucial for developing new materials and pharmaceuticals.
- Understanding molecular configurations and crystal packing provides insights into chemical properties and potential applications.
Purpose of the Study:
- To synthesize and characterize a novel chemical compound with the formula C(13)H(9)ClN(4)O(3).
- To elucidate the molecular geometry, including bond configurations and dihedral angles between aromatic rings.
- To investigate the intermolecular interactions and crystal structure through hydrogen bonding.
Main Methods:
- Condensation reaction between 2-chloro-5-nitro-benzaldehyde and isonicotinohydrazide in methanol.
- X-ray crystallography to determine the crystal structure and molecular conformation.
- Analysis of bond angles, dihedral angles, and intermolecular hydrogen bonding (N-H⋯O).
Main Results:
- Successful synthesis of the target compound C(13)H(9)ClN(4)O(3).
- The molecule exhibits a trans configuration around the C=N and C-N bonds.
- A dihedral angle of 12.1(2)° was measured between the benzene and pyridine rings.
- Crystal structure analysis revealed the formation of dimers through intermolecular N-H⋯O hydrogen bonds.
Conclusions:
- The study successfully synthesized and characterized a new organic compound.
- The determined molecular and crystal structure provides fundamental data for this class of compounds.
- The identified hydrogen bonding pattern is key to the compound's self-assembly in the solid state.
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