“…[36,37] The idea was based on the possibility of chain stacking (crystalline) changes according to the side (alkyl) groups attached to the main polymer backbones. [38][39][40] For this purpose, 2,5-bis-(2-octyldodecyl)-3,6-bis-(5-trimethylstannanylthiophen-2-yl)-2,5-dihydro-pyrrolo [3,4-c]pyrrole-1,4-dione (2Sn-ODTPPD) was reacted with 4,7-dibromo-2,1,3-benzothiadiazole (2Br-BT) in the presence of a Stille coupling catalyst. The resulting conjugated polymer, poly[{2,5-bis-(2-octyldodecyl)-3,6-bis-(thien-2yl)-pyrrolo [3,4-c]pyrrole-1,4-diyl}-co-{2,2′-(2,1,3-benzothiadiazole)-5,5′-diyl}] (PODTPPD-BT), exhibited strong optical absorptions in the NIR range.…”