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To investigate new concepts for such materials and to broaden their applicability, the previously reported non\u2010fluorescent zinc(II) complex <jats:bold>[Zn(L)]<\/jats:bold> that shows coordination\u2010induced turn\u2010on emission was encapsulated into a family of non\u2010fluorescent polystyrene\u2010block\u2010poly(4\u2010vinylpyridine) (PS\u2010b\u2010P4VP) diblock copolymer micelles leading to brightly emissive materials. Coordination\u2010induced turn\u2010on emission upon incorporation and ligation of the <jats:bold>[Zn(L)]<\/jats:bold> in the P4VP core outperform parent <jats:bold>[Zn(L)]<\/jats:bold> in pyridine solution with respect to lifetimes, quantum yields, and temperature resistance. The quantum yield can be easily tuned by tailoring the selectivity of the employed solvent or solvent mixture and, thus, the tendency of the PS\u2010b\u2010P4VP diblock copolymers to self\u2010assemble into micelles. 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