| Autor: |
Solanko KA; Department of Physics and Chemistry, University of Southern Denmark, Campusvej 55, Odense, DK-5230, Denmark., Bond AD |
| Jazyk: |
angličtina |
| Zdroj: |
Acta crystallographica. Section B, Structural science [Acta Crystallogr B] 2011 Oct; Vol. 67 (Pt 5), pp. 437-45. Date of Electronic Publication: 2011 Sep 16. |
| DOI: |
10.1107/S0108768111035786 |
| Abstrakt: |
The crystal structures of the six dichlorobenzaldehyde isomers, four of them newly determined, are analyzed in terms of the geometry and energies of their intermolecular interactions, quantified using the semi-classical density sums (SCDS-PIXEL) method. A consistent feature in all six structures is molecular stacks propagating along a short crystallographic axis of ca 3.8 Å. The stacks have a closely comparable geometry in each isomer, but the interaction energies between stacked molecules are variable on account of the differing relative positions of the Cl substituents. In the majority of the isomers the stacking interactions are the most stabilizing in the structure. Exceptions are the 2,4- and 3,5-isomers, where more stabilizing interactions are made between stacks. In general, the most stabilizing non-stacking intermolecular interactions in the structures are those involving C-H...O contacts. Observed motifs based on Cl...Cl interactions appear to be largely imposed by the constraints of other more stabilizing intermolecular interactions. The isomeric series displays the following noteworthy features: (i) the 2,3- and 2,6-isomers are isostructural despite having different orientations of the Cl and aldehyde functionalities; (ii) the 2,5-isomer exhibits whole-molecule disorder; (iii) the 2,5- and 3,5-isomers have more than one molecule in the crystallographic asymmetric unit (Z' > 1). These features in particular are considered on the basis of the intermolecular interaction energies. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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