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American Chemical Society, Crystal Growth and Design, 3(5), p. 1041-1047, 2005

DOI: 10.1021/cg049650v

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Crystal Engineering Based on Polymeric Hydrogen-Bonded Supramolecules by Self-Assembling of 4,4‘-(9-Fluorenylidene)diphenol and 4,4‘-Cyclohexylidenebisphenol with Bipyridines

This paper is available in a repository.
This paper is available in a repository.

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Abstract

4,4‘-(9-Fluorenylidene)diphenol (FDP) and/or 4,4‘-cyclohexylidenebisphenol (CBP) is crystallized with bipyridine bases 4,4‘-bipyridyl (bipy), 1,2-bis(4-pyridyl)ethane (bipy-eta), 1,2-di(4-pyridyl)ethylene (dipy-ete), and 4,4‘-dipyridyl N,N‘-dioxide (dipy-dox) to afford molecular complexes (FDP)·(bipy) 1, (FDP)·(bipy-eta)0.5 2, (FDP)2·(dipy-ete) 3, (FDP)·(dipy-dox) 4, and (CBP)·(bipy) 5. The crystal structures of 1−5 have been determined by single-crystal X-ray diffraction. All these molecular complexes exhibit polymeric supramolecular structures via O−H···N or O−H···O hydrogen-bonding. 1 forms double helices. 2 forms an infinite honeycomblike supramolecular structure. 3 forms a brick supramolecular structure. 4 forms an X-shaped supramolecular structure. 5 forms a single strand infinite helix. Thus, by changing the guest molecule, we can obtain different supramolecular hydrogen-bonded polymers through interactions of host−guest systems.