Article ID Journal Published Year Pages File Type
9559244 Polymer 2005 7 Pages PDF
Abstract
β-Cyclodextrin (β-CD) forms inclusion complexes (ICs) with adamantane-modified benzoxazines (2 benzoxazine and 3 benzoxazine). These benzoxazines can readily penetrate into the CD's hydrophobic cavity, causing turbidity of their solutions, from which fine crystalline powders are obtained. We characterized these complexes by powder X-ray diffraction, 13C and 13C CP/MAS NMR spectroscopies, DSC, and TGA. The X-ray diffraction and solid-state 13C CP/MAS NMR spectroscopy indicate that the IC domains of the polypseudorotaxanes maintain their channel-type structures after the ring-opening curing reactions have occurred. Furthermore, DSC measurements indicate that complexing the adamantane-modified benzoxazine units with β-CDs result in stiffer main chains and, thus, higher glass transition temperature. TGA also indicates that the inclusion complexes have enhanced its thermal stability.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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