摘要
A novel alternating D-A copolymer, PPor-BT, with dioctylporphyrin (Por) as a donor unit and 5,6-bis(octyloxy)benzo-2,1,3-thiadiazole (BT) as an acceptor unit, was designed and synthesized by Pd-catalyzed Sonogashira-coupling reaction. The copolymer showed good solubility and film-forming ability. PPor-BT exhibited a broad absorption band from 350 to 950聽nm with two peaks centered at 456 and 818聽nm corresponding to the Soret band and Q-bands absorption of porphyrin segments, respectively. The employment of electron deficient BT unit to construct donor-acceptor structure observably broadened the absorption spectrum and enhanced the Q-band absorption of the porphyrin-based polymer. The HOMO and LUMO energy levels of the polymer are聽鈭?.06聽eV and聽鈭?.63聽eV, respectively. The solution-processed organic field-effect transistors (OFETs) were fabricated with bottom gate/top-contact geometry. The mobility of PPor-BT based OFEFs reached 4.3聽脳聽10鈭?聽cm2聽V鈭?聽s鈭? with an on/off current ratio of 104. This mobility is among the highest values for porphyrin-based polymers.