“…The synthesis of BT , BT2 , DTBT , DTBT2 , PSN , and PSeN are reported elsewhere. − DPP , isoindigo , NDI , and BBT were newly synthesized by the following general procedure (Scheme ): A solution of 3,6-di- tert -butyl-1,8-diethynyl-9-hexadecyl-9 H -carbazole (0.1134 g 0.2000 mmol) and dibromo-comonomer (0.2000 mmol), namely, 3,6-bis(5-bromothiophen-2-yl)-2,5-dioctyl-2,5-dihydropyrrolo[3,4- c ]pyrrole-1,4-dione, ( E )-6,6′-dibromo-1,1′-dioctyl-[3,3′-biindolinylidene]-2,2′-dione, 4,9-dibromo-2,7-dioctylbenzo[ lmn ][3,8]phenanthroline-1,3,6,8(2 H ,7 H )-tetraone, and 4,7-bis[5-bromo-4-(2-butyloctyl)thiophen-2-yl]benzo[1,2- c :4,5- c ’]bis[1,2,5]thiadiazole, respectively, in 3 mL of toluene and 1 mL of i Pr 2 NH was degassed with nitrogen for 15 min. PdCl 2 (PPh 3 ) 2 (5.7 mg, 0.008 mmol) and CuI (1.5 mg, 0.008 mmol) were added.…”