6533b821fe1ef96bd127b646

RESEARCH PRODUCT

Switchable Supramolecular Crosslinking of Cyclodextrin-Modified Hyperbranched Polyethylenimine via Anthraquinone Dyes

Ute KolbS. Katharina KrethRobert BranscheidHelmut RitterIndra Böhm

subject

chemistry.chemical_classificationPolyethyleniminePolymers and PlasticsCyclodextrinOrganic ChemistrySupramolecular chemistryCondensed Matter PhysicsAnthraquinonechemistry.chemical_compoundchemistryCovalent bondOrganic dyePolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryWater soluble polymers

description

Two anthraquinone dyes, 5,8-di-N-adamantylamino-1,4-dihydroxyanthraquinone (AQ-OH) and 1,4-di-N-adamantylaminoanthraquinone (AQ-H), are synthesized. The combination of AQ-OH and AQ-H with hyperbranched polyethylenimine (PEI) bearing covalently attached β-cyclodextrin spontaneously formed host–guest complexes with hydrodynamic diameters of about 260 nm. Even enlarged structures of the trifunctional AQ-H were observed via DLS. Repeated measurements show that their assembly and disassembly is reversible with a critical point at 26 °C and therefore switchable via temperature. Also superstructures up to 100 μm were detected via TEM, cryo-TEM-, and SEM. Hence, a smart colored network of switchable size consisting of a supramolecular approach involving an organic dye is described.

https://doi.org/10.1002/macp.201100259