| Abstract: | We theoretically predicted that acetylene‐bridged benzo1,2‐c ;4,5‐c ′]bis1,2,5]thiadiazole (BBT) oligomers would show a quick increase of diradical character with the extension of chain length. To validate the hypothesis, six stable BBT‐based diradicaloids were synthesized and fully characterized by X‐ray crystallographic analysis and various spectroscopic measurements. Three of them showed prominent paramagnetic activity at elevated temperatures due to thermal population from the open‐shell singlet ground state to triplet excited state. It was also found that substitution by electron‐donating triphenylamine groups at the termini promoted the diradical character and reduced the singlet–triplet energy gap, and at the same time, resulted in intense near‐infrared absorption. |
