Insights into the Aggregation Behaviour of a Benzoselenadiazole‐Based Compound and Generation of White Light Emission

We have designed and synthesized the benzoselenadiazole (BDS) based donor‐acceptor‐donor (D‐A‐D) π‐conjugated compound 4,7‐di((E)styryl)benzo[2,1,3]selenadiazole (1). A single‐crystal study of 1 shows J‐type molecular aggregation in the solid state. The crystal packing of 1 shows head‐to‐head dimeric intermolecular assembly via Se⋅⋅⋅N interactions while staircase‐type interlock molecular packing has occurred via Se⋅⋅⋅π interaction. The staircase‐type interlock packing of dimeric molecular arrangement induces sheet‐type, herringbone type architecture along crystallographic a axis and ab plane via CH⋅⋅⋅π interactions. Interestingly, the J‐type aggregation of 1 in solid state changes to H‐type aggregation upon UV‐irradiation. Moreover, our spectroscopic findings in solution state reveal H‐type of aggregation of 1 in 90 % aqueous THF. We have further demonstrated white light emission in the binary mixture of 1 and 1‐pyrenemethanol (2) in 90 % aqueous THF. Our study reveals solvent specific co‐assembly of H‐aggregated 1 and 2 in 90 % aqueous THF solution, which shows white light emissive properties with the Commission Internationale de l'Eclairage (CIE) chromaticity coordinates (0.32, 0.31). The observed white light emission arises mainly due to the combination of red light from H‐aggregated 1, blue light from monomeric 2 and green light from excimers of 2. A binary mixture containing the donor‐acceptor‐donor compound 4,7‐di((E)styryl)benzo[2,1,3]selenadiazole (1) and 1‐pyrenemethanol (2) in 90 % aqueous THF shows white‐light emission, which arises mainly from the combination of red light from H‐aggregated 1, blue light from monomeric 2, and green light from excimers of 2.