Helical Poly(5-alkyl-2,3-thiophene)s: Controlled Synthesis and Structure Characterization

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• 作者：Hong-Hai Zhang ; Chuanxu Ma ; Peter V. Bonnesen ; Jiahua Zhu ; Bobby G. Sumpter ; Jan-Michael Y. Carrillo ; Panchao Yin ; Yangyang Wang ; An-Ping Li ; Kunlun Hong
• 刊名：Macromolecules
• 出版年：2016
• 出版时间：July 12, 2016
• 年：2016
• 卷：49
• 期：13
• 页码：4691-4698
• 全文大小：496K
• 年卷期：0
• ISSN：1520-5835

文摘

Whereas poly(3-alkyl-2,5-thiophene)s (P3AT), with many potential applications, have been extensively investigated, their ortho-connected isomers, poly(5-alkyl-2,3-thiophene)s (P5AT), have never been reported because of the difficulty in their syntheses. We herein present the first synthesis of regioregular P5AT via controlled Suzuki cross-coupling polymerization with PEPPSI-IPr as catalyst, affording the polymers with tunable molecular weight, narrow polydispersity (PDI), and well-defined functional end groups at the gram scale. The helical geometry of P5AT was studied by a combination of NMR, small-angle X-ray scattering (SAXS), and scanning tunneling microscopy (STM). Particularly, the single polymer chain of poly(5-butyl-2,3-thiophene) (P5BT) on highly oriented pyrolytic graphite (HOPG) substrates with either M or P helical conformation was directly observed by STM. The comparison of UV–vis absorption between poly(5-hexyl-2,3-thiophene) (P5HT) (λ = 345 nm) and poly(3-hexyl-2,5-thiophene) (P3HT) (λ = 450 nm) indicated that the degree of conjugation of the backbone in P5HT is less than in P3HT, which may be a consequence of the helical geometry of the former compared to the more planar geometry of the latter. Moreover, we found that P5HT can emit green fluorescence under UV (λ = 360 nm) irradiation.