Novel chiral Schiff base macrocycles containing azobenzene chromophore: gelation and guest inclusion |
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Authors: | Koichi Tanaka Shingo Fukuoka Hiroki Takahashi |
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Affiliation: | a Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering & High-Tech Research Centre, Kansai University, Suita, Osaka 564-8680, Japan b Graduate School of Human and Environmental Studies, Kyoto University, Kyoto 606-8501, Japan |
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Abstract: | A novel chiral Schiff base macrocycle 1 was synthesized by [3+3] condensation of enantiomerically pure trans-1,2-diaminocyclohexane with azobenzene-4,4′-dicarbaldehyde. Subsequent reduction of 1 afforded macrocyclic hexamine 2 having three azobenzene units. The former could be converted into a benzene gel, while the latter could include several aromatic guest molecules. |
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