Naphthalonitriles featuring efficient emission in solution and in the solid state

In this work, a series of gamma-substituted diphenylnaphthalonitriles were synthesized and characterized. They show efficient emission in solution and in the aggregated state and their environment responsiveness is based on having variable substituents at the para-position of the two phenyl moieties. The excited state properties were fully investigated in tetrahydrofuran (THF) solutions and in THF/H2O mixtures. The size of the aggregates in aqueous media were measured by dynamic light scattering (DLS). The steadystate and time-resolved photoluminescence spectroscopy studies revealed that all the molecules show intense fluorescence both in solution and in the aggregated state. In THF solutions, a blue emission was observed for the unsubstituted (H), methyl(Me) and tert-butyl(t-Bu) substituted gamma-diphenylnaphthalonitriles, which can be attributed to a weak pi-donor capability of these groups. On the other hand, the methoxy(OMe), methylsulfanyl(SMe) and dimethylamino(NMe2) substituted compounds exhibit a progressive red-shift in emission compared to H, Me and t-Bu due to a growing pi-electron donating capability. Interestingly, upon aggregation in water-containing media, H, Me and t-Bu show a slight red-shift of the emission and a blue-shift is observed for OMe, SMe and NMe2. The crystal structure of Me allowed a detailed discussion of the structure-property relationship. Clearly, N-containing substituents such as NMe2 possess more electron-donating ability than the S-based moieties such as SMe. Moreover, it was found that NMe2 showed higher luminescence quantum yields (Phi(F)) in comparison to SMe, indicating that N-substituted groups could enhance the fluorescence intensity. Therefore, the pi-donor nature of the substituents on the phenyl ring constitutes the main parameter that influences the photophysical properties, such as excited state lifetimes and photoluminescence quantum yields. Hence, a series of highly luminescent materials from deep blue to red emission depending on substitution and environment is reported with potential applications in sensing, bioimaging and optoelectronics.