Synthesis of Azole-fused Benzothiadiazoles as Key Units for Functional π-Conjugated Compounds

• Published in: Journal of Photopolymer Science and Technology 2017/06/26, Vol.30(5), pp.561-568
• Main Authors: Nakamura, Tomoya, Okazaki, Shuhei, Arakawa, Noriko, Satou, Motoi, Endo, Masaru, Murata, Yasujiro, Wakamiya, Atsushi
• Format: Article
• Language: English
• Subjects: Acceptor unit; Benzothiadiazole; Electronic structure; Imidazole; Nitrogen; Oxidation; Photovoltaic cells; Ring-fusion; Solar cells; Sulfur; Thiazole; Valence
• ISSN: 0914-9244; 1349-6336
• DOI: 10.2494/photopolymer.30.561

2,1,3-Benzothiadiazole (BT) is a widely used electron-accepting unit in organic electronics including organic solar cells (OSCs). As modifications of BT skeleton, two types of azole-fused BT units were designed and synthesized; thiazole-fused BT with an electron-withdrawing C=N bond and imidazole-fused BT with an electron-donating nitrogen atom as well as an electron-withdrawing C=N bond. Electrochemical measurements and theoretical calculations suggest that thiazole-fusion enhances the electron-accepting ability, whereas imidazole-fusion endows the BT skeleton with electron-donating ability while maintaining its electron-accepting ability. Moreover, in thiazole-fused BT units, the electronic structure could be further modulated by varying the oxidation state of the sulfur atom in methylthio group at the fused thiazole ring.