Abstract

In the title compound, C27H20ClNO, the quinoline ring forms a dihedral angle of 62.53 (5)° with the substituent benzene ring. In the crystal, inter­molecular C—H⋯Cl inter­actions link the mol­ecules into chains along the b axis. Inter­molecular C—H⋯N and C—H⋯O hydrogen bonds further consolidate the structure into a three-dimensional network. The unit cell contains four solvent-accessible voids, each with a volume of 35 Å3, but no significant electron density was found in them.

Highlights

  • In the title compound, C27H20ClNO, the quinoline ring forms a dihedral angle of 62.53 (5) with the substituent benzene ring

  • H atoms treated by a mixture of independent and constrained refinement max = 0.38 e Å3

  • In continuation our interest in synthesis of chalcones we report a new chalcone (Loh et al, 2010a,b; Shahani et al, 2010)

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Summary

Bruker APEXII DUO CCD areadetector diffractometer

H atoms treated by a mixture of independent and constrained refinement max = 0.38 e Å3. R factor = 0.040; wR factor = 0.116; data-to-parameter ratio = 17.6. C27H20ClNO, the quinoline ring forms a dihedral angle of 62.53 (5) with the substituent benzene ring. Intermolecular C—H Cl interactions link the molecules into chains along the b axis. H N and C—H O hydrogen bonds further consolidate the structure into a three-dimensional network. The unit cell contains four solvent-accessible voids, each with a volume of. 35 Å3, but no significant electron density was found in them

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