Ontology highlight
ABSTRACT:
SUBMITTER: Bohm I
PROVIDER: S-EPMC3167151 | biostudies-literature | 2011
REPOSITORIES: biostudies-literature
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]