Abstract

Techniques for the assembly of hierarchical nanostructures from soft matter have opened the door to many new applications of nanotechnology. Despite these achievements, nanoscale syntheses that rely on self-assembly can be highly dependent on conditions such as solvent and temperature if the integrity of the nanomaterial is to be maintained. Bottlebrush copolymers provide a compelling bottom-up approach to the synthesis of hierarchical nanostructures from soft material, allowing for the preparation of multicompartment structures that remain nanosegregated by virtue of their covalent chemistry. Here we describe methods for the preparation of fiber-like nanomaterials that mimic the multilayer structure of organic electronic devices on individual polymer chains. Narrowly dispersed fibers are prepared from materials commonly used as the hole transport, electron transport, and host materials in organic electronics, with molecular weights on the order of 106 Da. Energy transfer interactions can be regulated by the reversible expansion and collapse of polymer chains, creating dramatic fluorescence changes or activating thermaly activated delayed fluorescence (TADF).

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