Chopra, Deepak and Row, Guru TN (2005) Dimorphic Forms in a Non-Centrosymmetric Environment from a Prochiral Molecule: Cooperative Interplay of Strong Hydrogen Bonds and Weak Intermolecular Interactions. In: Crystal Growth and Design, 5 (5). pp. 1679-1681.Full text not available from this repository. (Request a copy)
4-Fluoro-N-(2-fluorophenyl) benzamide, a prochiral molecule, exhibits dimorphic behavior. This feature has been analyzed in terms of morphology, X-ray single-crystal structure analysis, differential thermal analysis, and measurement of second harmonic generation (SHG) in both forms, which crystallize in noncentric space groups. The dimorphs have different morphologies, a major form as needles and a minor form as thin plates, occurring concomitantly in the same crystallization setup. The plates crystallize in the monoclinic space group $P2_1$, while the needles are in the orthorhombic space group $Pca2_1$. Strong N-H \cdot\cdot\cdot O hydrogen bonds and weak but highly directional C-H \cdot\cdot\cdot F interactions acting cooperatively are responsible for the observed symmetry steering the molecules to pack in noncentric environments.
|Item Type:||Journal Article|
|Additional Information:||The copyright for this article belongs to American Chemical Society.|
|Department/Centre:||Division of Chemical Sciences > Solid State & Structural Chemistry Unit|
|Date Deposited:||20 Oct 2005|
|Last Modified:||27 Aug 2008 11:30|
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