Abstract
Examination of the solid state structures of bromo- and fluoro:substituted ethynylbenzenes, determined by single crystal X-ray diffraction, has demonstrated that the halogen and ethynyl substituents on these 1,4- and 1,3,5-substituted benzene rings can be interchanged without significant changes in their average solid state structures. Consideration of these structures, together with those of 1,4- and 1,3,5-substituted halogenobenzenes, suggests that, in most cases, shape complementarity may be of equal importance to interactional complementarity when attempting to rationalise the packing of these molecules in the solid state.
| Original language | English |
|---|---|
| Pages (from-to) | 2459-2469 |
| Journal | Journal of Chemical Society, Perkin Transactions 2 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - Nov 1998 |
Keywords
- DOT-PI-INTERACTIONS
- POLYNUCLEAR AROMATIC-HYDROCARBONS
- SUPRAMOLECULAR SYNTHONS
- CRYSTAL-STRUCTURE
- INTERMOLECULAR INTERACTIONS
- STRUCTURE SIMPLIFICATION
- MOLECULAR RECOGNITION
- TERMINAL ALKYNES
- FORCES
- BOND
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