Affiliation:
1. Institute for Chemical Technology and Polymer Chemistry (ITCP) Karlsruhe Institute of Technology (KIT) 76131 Karlsruhe Germany
2. Research Fellow of Japan Society for the Promotion of Science Tokyo 102‐0083 Japan
3. Faculty of Textile Science and Technology Shinshu University Nagano 386‐8567 Japan
4. Soft Matter Synthesis Laboratory – Institute for Biological Interfaces III (IBG‐3) Karlsruhe Institute of Technology (KIT) 76344 Eggenstein‐Leopoldshafen Germany
Abstract
AbstractSynthesis of polyurethane‐type poly[3]rotaxanes is achieved by polyaddition between a cyclodextrin (CD)‐based [3]rotaxane diol and various diisocyanate species, which provide a more defined structure compared to conventional polyrotaxane syntheses. In this study, hydroxyl groups on CDs of [3]rotaxane diol are initially acetylated, and deprotected after the polyaddition to introduce polyurethane backbone structure into polyrotaxane framework. Despite a relatively complicated chemical structure, [3]rotaxane diol monomer is successfully synthesized in a high yield (overall 67%) without any taxing purification process, which is beneficial for practical applications. The polymerization itself proceeds well under a standard polyaddition reaction condition to afford corresponding polyurethanes around 80% yield with Mn > 30 kDa. The poly[3]rotaxanes show different aggregation behavior or optical properties, whether or not acetyl groups are present, and are analyzed by XRD, SEM, and fluorescence measurements.
Funder
Japan Society for the Promotion of Science
Cited by
1 articles.
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