Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.polymer.2005.02.090
Title: PH-Controllable cyclic threading/dethreading of polypseudorotaxane obtained from cyclodextrins and poly(amino ester)
Authors: Sun, G.
Wu, D.
Liu, Y.
He, C.
Chung, T.S. 
Goh, S.H. 
Keywords: Cyclodextrins
Polyrotaxanes
Self-assembly
Issue Date: 25-Apr-2005
Citation: Sun, G., Wu, D., Liu, Y., He, C., Chung, T.S., Goh, S.H. (2005-04-25). PH-Controllable cyclic threading/dethreading of polypseudorotaxane obtained from cyclodextrins and poly(amino ester). Polymer 46 (10) : 3355-3362. ScholarBank@NUS Repository. https://doi.org/10.1016/j.polymer.2005.02.090
Abstract: Cyclic threading/dethreading of novel polypseudorotaxane obtained from β-cyclodextrins and poly(amino ester), poly(BDA-DEEDA), obtained from the Michael addition polymerization of 1,4-butanediol diacrylate (BDA) and N, N′-diethyl ethylenediamine (DEEDA), was realized by adjusting pH of the aqueous solutions between ca. 9.0 and 3.2 alternatively. 1H NMR, XRD profiles, and 13C CP/MAS NMR verified the formation of polypseudorotaxane, and acid titration induced dethreaded structures were characterized using 2D ROESY NMR, 1H NMR and XRD. The appearance/disappearance of precipitates, the kinetics, and the cyclic performance of pH controllable threading/dethreading processes were monitored by the changes in absorbance or transmittance of the solutions as reflected by UV experiments. Further pH-induced protonated and deprotonated states of poly(BDA-DEEDA) were demonstrated by 1H NMR, which indicated the mechanism of the threading/dethreading processes. © 2005 Elsevier Ltd. All rights reserved.
Source Title: Polymer
URI: http://scholarbank.nus.edu.sg/handle/10635/89770
ISSN: 00323861
DOI: 10.1016/j.polymer.2005.02.090
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