Abstract
[Cu2(carboxylate)4] paddlewheel molecular building blocks, MBBs, are capable of generating square grid or Kagomé lattice supramolecular isomers when dicarboxylates such as 1,3-benzenedicarboxylate (1,3-bdc) and 1,4-benzenedicarboxylate (1,4-bdc) are exploited to link the paddlewheel MBBs. In this contribution we demonstrate that it is possible to use a solvent-free reaction (cocrystal controlled solid-state synthesis) to prepare a tetracarboxylic acid, H4BIPA-TC, formed by rigidly linking two 1,3-bdc moieties at the 5-position. BIPA-TC can pillar both square grid and Kagomé lattice supramolecular isomers, thereby generating nets that exhibit lvt or nbo topologies, respectively. © 2011 The Royal Society of Chemistry.
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CITATION STYLE
Perman, J. A., Cairns, A. J., Wojtas, Ł., Eddaoudi, M., & Zaworotko, M. J. (2011). Cocrystal controlled solid-state synthesis of a rigid tetracarboxylate ligand that pillars both square grid and Kagomé lattice layers. CrystEngComm, 13(9), 3130–3133. https://doi.org/10.1039/c0ce00542h
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