Abstract
For cost-efficient organic electronic devices, the consecutive deposition of active layers by solution-based processes is a key benefit. We report a synthetic approach enabling solubility reduction of bis(cyclopentadienyl)-substituted polyfluorenes as emissive layers in organic light-emitting diodes (OLEDs). Thermally induced retro-Diels–Alder reaction liberates free cyclopentadiene as “protecting group” and pending cyclopentadienyl units, which cross-link the polymer strands upon cooling via [4+2] cycloadditions. The activation temperature is tuned in the range of 180–250 °C through alkyl, alkoxy, or ester linkages. Ultimately, macrocyclic self-protected bis(cyclopentadienylene) moieties avoid extrusion of volatile cyclopentadiene during activation. The solvent resistance of the emissive layers after cross-linking is examined by absorption spectroscopy and white light scanning interferometry. The influence of the desolubilization procedure on the performance of solution-processed OLEDs is investigated.
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