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Bulky hydrophobic counterions (weakly coordinating anions) can insulate ionic dyes against aggregation-caused quenching (ACQ) and enable preparation of highly fluorescent dye-loaded nanoparticles (NPs) for bioimaging, biosensing and light harvesting. Here, we introduce a family of hydrophobic anions based on fluorinated C-acyl barbiturates with delocalized negative charge and bulky non-polar groups. Similarly to fluorinated tetraphenylborates, these barbiturates prevent ACQ of cationic dye alkyl rhodamine B inside polymer NPs made of biodegradable poly(lactic-co-glycolic acid) (PLGA). Their efficiency to prevent ACQ increases for analogues with higher acidity and bulkiness. Their structure controls dye-dye communication, yielding bright NPs with on/off switching or stable emission. They enhance dye encapsulation inside NPs, allowing intracellular imaging without dye leakage. Compared to fluorinated tetraphenylborates known as cytotoxic transmembrane ion transporters, the barbiturates display a significantly lower cytotoxicity. These chemically available and versatile barbiturate derivatives are promising counterion scaffolds for preparation of bright non-toxic fluorescent nanomaterials., (© 2021 Wiley-VCH GmbH.)

Bulky hydrophobic counterions (weakly coordinating anions) can insulate ionic dyes against aggregation‐caused quenching (ACQ) and enable preparation of highly fluorescent dye‐loaded nanoparticles (NPs) for bioimaging, biosensing and light harvesting. Here, we introduce a family of hydrophobic anions based on fluorinated C‐acyl barbiturates with delocalized negative charge and bulky non‐polar groups. Similarly to fluorinated tetraphenylborates, these barbiturates prevent ACQ of cationic dye alkyl rhodamine B inside polymer NPs made of biodegradable poly(lactic‐co‐glycolic acid) (PLGA). Their efficiency to prevent ACQ increases for analogues with higher acidity and bulkiness. Their structure controls dye‐dye communication, yielding bright NPs with on/off switching or stable emission. They enhance dye encapsulation inside NPs, allowing intracellular imaging without dye leakage. Compared to fluorinated tetraphenylborates known as cytotoxic transmembrane ion transporters, the barbiturates display a significantly lower cytotoxicity. These chemically available and versatile barbiturate derivatives are promising counterion scaffolds for preparation of bright non‐toxic fluorescent nanomaterials. [ABSTRACT FROM AUTHOR]

Dye‐loaded polymeric nanoparticles emerge as powerful bioimaging tools, but their assembly is challenged by aggregation‐caused quenching (ACQ) of flat fluorophores. Aggregation‐induced emission (AIE) proposes an effective solution against ACQ by exploiting propeller‐shaped neutral fluorophores without polymeric blending. Fighting ACQ of ionic dyes in polymeric nanoparticles can be achieved by bulky hydrophobic counterions. Here, it is aimed to generate an AIE phenomenon in poorly emissive ionic dyes using bulky counterions. Three cationic hemicyanine dyes of styryl pyridinium family are synthesized: two planar fluorophores featuring ACQ and one propeller‐shaped AIE fluorophore. It is found that, in water, bulky fluorinated tetraphenylborates can light up all three dyes, including planar non‐AIE fluorophores. The described "ionic" AIE (iAIE) with bulky counterions enables preparation of 50‐nm dye‐loaded polymeric nanoparticles showing 40% quantum yield at 500 mm dye loading, whereas small anions favor poorly emissive large aggregates. Single‐particle microscopy reveals that these nanoparticles emit without blinking 50‐fold brighter than commercial quantum dots "Qdot 605" (at 470‐nm excitation). iAIE opens the route to assembling charged intrinsically non‐AIE fluorophores into bright fluorescent (nano)materials. [ABSTRACT FROM AUTHOR]