Rational design strategies for nonconventional luminogens with efficient and tunable emission in dilute solution

The design and synthesis of organic nonconventional luminescent (NL) materials with efficient emission have attracted significant attention. However, these materials usually suffer from the fact of low photoluminescent quantum efficiency (Φ), poor tunability of emission wavelength, and non-luminescence in dilute solution, limiting their further application. Herein, rational molecular design strategies for NL compounds with efficient and tunable emission in dilute solution were presented via theoretical calculation and practical verification. Firstly, increasing the ratio of π → π* transition in the excited state to suppress the n → π* transition, inhibit intersystem crossing, and avoid the generation of triplet excitons which can be easily quenched by water or oxygen. Secondly, introducing strong intramolecular hydrogen bonds to suppress intramolecular rotation and inhibit non-radiative transitions. Besides, D-π-A structure can effectively adjust the luminescence color. Based on the proposed design strategies, two novel compounds named LJ-1 and LJ-2 were synthesized, both compounds can emit bright green fluorescence in dilute solution with Φ of up to 59.8 %, and their photophysical properties are pH-dependent. The results showed that pH had a great impact on the strength of intramolecular hydrogen bonds and the degree of conjugation. For example, the emission wavelength of LJ-1 exhibited red-shift as the increase of pH value. Furthermore, LJ-1 can be used for visual detection of Ag+ in water solution in naked eye and the precise localization of lysosomes. We believe that our work will greatly broaden the application range of nonconventional luminogenic compounds in future.