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Hyperbranched polyethylenimine bearing cyclodextrin moieties showing temperature and pH controlled dye release.


ABSTRACT: The release of anthraquinone dyes from ?-cyclodextrin modified, hyperbranched polyethylenimine (PEI-CD) was investigated. 5,8-Dichloro-1,4-dihydroxyanthraquinone (AQ-OH) was enclosed simply by ionic attraction between the phenolate groups of AQ-OH and the protonated amino groups of polyethylenimine (PEI). Additionally, the adamantyl moieties of 1,4-bis-N-adamantylaminoanthraquinone (AQ-Ada) were encapsulated by the cavity of CD modified PEI. Due to these different types of interaction, the dyes can be controllably released from the CD-cavity (AQ-Ada) by temperature variation or from salt encapsulation by pH variation (AQ-OH), as monitored by UV-vis spectroscopy.

SUBMITTER: Bohm I 

PROVIDER: S-EPMC3167151 | biostudies-literature | 2011

REPOSITORIES: biostudies-literature

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Hyperbranched polyethylenimine bearing cyclodextrin moieties showing temperature and pH controlled dye release.

Böhm Indra I   Kreth Susanne Katharina SK   Ritter Helmut H  

Beilstein journal of organic chemistry 20110818


The release of anthraquinone dyes from β-cyclodextrin modified, hyperbranched polyethylenimine (PEI-CD) was investigated. 5,8-Dichloro-1,4-dihydroxyanthraquinone (AQ-OH) was enclosed simply by ionic attraction between the phenolate groups of AQ-OH and the protonated amino groups of polyethylenimine (PEI). Additionally, the adamantyl moieties of 1,4-bis-N-adamantylaminoanthraquinone (AQ-Ada) were encapsulated by the cavity of CD modified PEI. Due to these different types of interaction, the dyes  ...[more]

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