Synthesis of annulated thiophene perylene bisimide analogues: their applications to bulk heterojunction organic solar cells was written by Choi, Hyunbong;Paek, Sanghyun;Song, Juman;Kim, Chulwoo;Cho, Nara;Ko, Jaejung. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2011.Quality Control of 2,9-Di(tridecan-7-yl)anthra[2,1,9-def:6,5,10-d’e’f’]diisoquinoline-1,3,8,10(2H,9H)-tetraone This article mentions the following:
Annulated thiophene perylene bisimides and their triphenyl-amine based oligomers were synthesized. One of the oligomers FPTTPA was demonstrated to be an efficient electron donor in bulk heterojunction organic solar cells, giving a power conversion efficiency of 1.42%. In the experiment, the researchers used many compounds, for example, 2,9-Di(tridecan-7-yl)anthra[2,1,9-def:6,5,10-d’e’f’]diisoquinoline-1,3,8,10(2H,9H)-tetraone (cas: 110590-84-6Quality Control of 2,9-Di(tridecan-7-yl)anthra[2,1,9-def:6,5,10-d’e’f’]diisoquinoline-1,3,8,10(2H,9H)-tetraone).
2,9-Di(tridecan-7-yl)anthra[2,1,9-def:6,5,10-d’e’f’]diisoquinoline-1,3,8,10(2H,9H)-tetraone (cas: 110590-84-6) belongs to isoquinoline derivatives. Isoquinoline is a structural isomer of quinoline, which have antiseptic, antipyretic and anti-cyclic properties, and can be used as antimalarial drugs and for the preparation of other antimalarial medicine. Lewis acid activation and nucleophilic attack can produce multiple regioisomers in quinolines and pyridines; isoquinolines generally only undergo attack at the 1-position.Quality Control of 2,9-Di(tridecan-7-yl)anthra[2,1,9-def:6,5,10-d’e’f’]diisoquinoline-1,3,8,10(2H,9H)-tetraone
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem