Unlocking Multicolor Emissions in the Crystalline State through Dimerization and Configurational Transformation of a Single Fluorophore

Multicolor luminescent materials with tunable properties hold great promise for a wide range of applications in materials science. Unfortunately, the conventional approach to achieving multicolor emissions by blending multiple types of fluorophores is hindered by limitations, notably, spectral instability, aggregation-caused quenching, and energy transfer. The pursuit of multicolor emissions from a single type of fluorophore in the solid state has, until now, remained a formidable challenge. In this study, we have introduced N,N′-diphenyl dihydrodibenzo[a,c]-phenazines (DPAC), augmented with two o-carboranyl units, to create a novel fluorophore CbDPAC. The CbDPAC crystal exhibits three distinct emission bands peaking at 405, 470, and 620 nm, respectively, arising from a rich intermolecular interaction network that generates novel emission centers, such as conformational isomers and excimers. This work inspires the rational molecular engineering of smart fluorophores with tailorable properties and inaugurates diverse possibilities for stimuli-responsive luminescent technologies

Unlocking Multicolor Emissions in the Crystalline State through Dimerization and Configurational Transformation of a Single Fluorophore

Multicolor luminescent materials with tunable properties hold great promise for a wide range of applications in materials science. Unfortunately, the conventional approach to achieving multicolor emissions by blending multiple types of fluorophores is hindered by limitations, notably, spectral instability, aggregation-caused quenching, and energy transfer. The pursuit of multicolor emissions from a single type of fluorophore in the solid state has, until now, remained a formidable challenge. In this study, we have introduced N,N′-diphenyl dihydrodibenzo[a,c]-phenazines (DPAC), augmented with two o-carboranyl units, to create a novel fluorophore CbDPAC. The CbDPAC crystal exhibits three distinct emission bands peaking at 405, 470, and 620 nm, respectively, arising from a rich intermolecular interaction network that generates novel emission centers, such as conformational isomers and excimers. This work inspires the rational molecular engineering of smart fluorophores with tailorable properties and inaugurates diverse possibilities for stimuli-responsive luminescent technologies