An investigation of the photophysics of Ir(III) complexes with controlled ligand structures and our quantum chemical calculations attest that the most probable explanation for the reported 'aggregation-induced phosphorescent emission', which was originally claimed to be related to an intermolecular excimer, is restricted intramolecular motion.
Selective removal of t-Boc protecting groups in a polymer film imbedded, pyrene-containing calixarene derivative results in the generation of a patterned fluorescence image without employing wet developing processes.
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