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 |
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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