Disorder within dicarboxylates and supramolecular structural control in hydrogen-bonded networks
Related documents:This repository does not currently have the full-text of this item.
You may be able to access a copy if URLs are provided below.
The crystal structures of two hydrogen-bonded adducts containing omicron-bromoterephthalate have been determined and shown to be virtually identical to those of their terephthalate analogues. Consequently, the strategy of manipulating the relative orientation of the carboxylate groups by adding a bromine atom to terephthalate, which has previously been used to give metal-organic frameworks with predictable structure, can be frustrated with the observation of disorder in the bromine position.
|Creators||Burke, N. J., Burrows, A. D., Mahon, M. F. and Pritchard, L. S.|
|Departments||Faculty of Science > Chemistry|
|Additional Information||ID number: ISI:000185630700001|
Actions (login required)