[1] Rasmussen, S. C. Conjugated and Conducting Organic Polymers: The First 150 years. ChemPlusChem2020, 85, 1412-1429. [2] Rasmussen S. C.; Pomerantz M.Low Bandgap Conducting Polymers. In Conjugated Polymers: Theory, Synthesis, Properties, and Characterization, Eds.: Skotheim, T. A.; Reynolds, J. R., Handbook of Conducting Polymers, 3rd Ed., CRC Press, Boca Raton, FL, 2007, pp. 421-462. [3] Rasmussen S. C.Low-Bandgap Polymers. In Encyclopedia of Polymeric Nanomaterials, Eds.: Muellen, K.; Kobayashi, S., Springer, Heidelberg, 2015, pp. 1155-1166. [4] Dou L.; Liu Y.; Hong Z.; Li G.; Yang, Y. Low-Bandgap Near-IR Conjugated Polymers/Molecules for Organic Electronics. Chem. Rev.2015, 115, 12633-12665. [5] Holliday S.; Li Y.; Luscombe, C. K. Recent advances in high performance donor-acceptor polymers for organic photovoltaics. Prog. Polym. Sci.2017, 70, 34-51. [6] Scharber M. C.; Sariciftci N. S.Low Band Gap Conjugated Semiconducting Polymers.Adv. Mater. Technol. 2021, 2000857. [7] Mikie T.; Osaka, I. Small-bandgap quinoid-based π-conjugated polymers. J. Mater. Chem. C2020, 8, 14262-14288. [8] Ji X.; Fang, L. Quinoidal conjugated polymers with open-shell character. Polym. Chem.2021, 12, 1347-1361. [9] Evenson S. J.; Mulholland M. E.; Anderson T. E.; Rasmussen, S. C. Minimizing Polymer Band gap via Donor-Acceptor Frameworks: Poly(dithieno[3,2-b:2',3'-d]pyrrole-alt-thieno[3 4- b]pyrazine)s as Illustrative Examples of Challenges and Misconceptions. Asian J. Org. Chem.2020, 9, 1333-1339. [10] Anderson T. E.; Culver E. W.; Badía-Domínguez I.; Wilcox W. D.; Buysse C. E.; Delgado M. C. R.; Rasmussen, S. C. Probing the Nature of Donor-Acceptor Effects in Conjugated Materials: A Joint Experimental and Computational Study of Model Conjugated Oligomers. Phys. Chem. Chem. Phys.2021, 23, 26534-26546. [11] Liu X.; He B.; Garzón-Ruiz A.; Navarro A.; Chen T. L.; Kolaczkowski M. A.; Feng S. F.; Zhang L.; Anderson C. A.; Chen J.; Liu Y. Unraveling the Main Chain and Side Chain Effects on Thin Film Morphology and Charge Transport in Quinoidal Conjugated Polymers. Adv. Funct. Mater.2018, 28, 1801874. [12] Liu C.; Xuncheng Liu X.; Zheng G.; Gong X.; Yang C.; Liu H.; Zhang L.; Anderson C. L.; He B.; Xie L.; Zheng R.; Liang H.; Zhou Q.; Zhang Z.; Chen J.; Liu, Y. An unprecedented quinoid-donor-acceptor strategy to boost the carrier mobilities of semiconducting polymers for organic field-effect transistors. J. Mater. Chem. A2021, 9, 23497-23505. [13] Wen L.; Heth C. L.; Rasmussen, S. C. Thieno[3,4-b]pyrazine- based Oligothiophenes: Simple Models of Donor-Acceptor Polymeric Materials. Phys. Chem. Chem. Phys.2014, 16, 7231-7240. [14] Culver E. W.; Anderson T. E.; Navarrete J. T.L.; Delgado, M. C. R.; Rasmussen, S. C. Poly(thieno[3,4-b]pyrazine-alt-2,1,3- benzothiadiazole)s: A new design paradigm in low band gap polymers. ACS Macro Lett. 2018, 7, 1215-1219. [15] Anderson T. E.; Culver E. W.; Almyahi F.; Dastoor P. C.; Rasmussen S. C. Poly(2,3-dihexylthieno[3,4-b]pyrazine-alt-2 3- dihexylquinoxaline): Processible, Low Bandgap, Ambipolar- Acceptor Frameworks via Direct Arylation Polymerization. Synlett2018, 29, 2542-2546. |