Abstract
Development of new efficient organic luminophores for optoelectronic applications (OLEDs, sensors) remains a pressing challenge in modern materials science. The 1,3,5-triazine unit, owing to its pronounced electron-accepting character, serves as a versatile building block for the design of luminescent materials with tunable optical properties1. In this work, we present the synthesis of a series of novel 2,1,3-benzothiadiazole derivatives incorporating various peripheral 1,3,5-triazine fragments. The fluorescence quantum yield reaches 78% in cyclohexane while dropping to 6% in THF, a behavior rationalized by conformational effects.