2-(4-Methoxy-phen-yl)phenanthro[9,10-d]imidazole methanol solvate
Fanpeng Kong1, Yunliang Gao, Jibang Ling
1Department of Chemistry, Shandong Normal University, Jinan 250014, People's Republic of China.
Acta Crystallographica. Section E, Structure Reports Online
|January 5, 2011
Summary
This study details a new imidazole compound formed from phenanthrene-quinone and 4-methoxy-benzaldehyde. Crystal analysis reveals specific molecular arrangements and hydrogen bonding crucial for its structure.
Area of Science:
- Organic Chemistry
- Crystallography
Background:
- Imidazole derivatives are important in various chemical applications.
- Phenanthrene-quinone and substituted benzaldehydes are common synthetic precursors.
Purpose of the Study:
- To synthesize and characterize a novel imidazole compound.
- To investigate the crystal structure and intermolecular interactions of the synthesized compound.
Main Methods:
- Condensation reaction between phenanthrene-quinone and 4-methoxy-benzaldehyde.
- Single-crystal X-ray diffraction analysis to determine molecular and crystal structure.
Main Results:
- The title compound, C(22)H(16)N(2)O·CH(4)O, was successfully synthesized.
- The crystal structure contains two imidazole and two methanol molecules in the asymmetric unit.
- Analysis showed near-parallel orientation of phenanthryl and imidazole rings (inter-planar angles 6.65° and 5.40°).
- Dihedral angles between imidazole and benzene rings were 5.40° and 6.65°.
- Intermolecular hydrogen bonds (O-H⋯N and N-H⋯O) were identified as key stabilizing forces in the crystal packing.
Conclusions:
- The synthesis yielded a novel imidazole derivative.
- The crystal structure is stabilized by a network of intermolecular hydrogen bonds.
- The specific arrangement of aromatic rings influences the overall molecular conformation and packing.
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