引用本文:
Er Fu Huo, Yong Zou, Hui Qin Sun, Yan Huang, Zhi Yun Lu, Qing Jiang. Synthesis and characterization of novel conjugated polymers based on 3-cyclobutene-l,2-dione moiety[J]. Chinese Chemical Letters,
2011, 22(11): 1326-1330.
doi:
10.1016/j.cclet.2011.05.025
Citation: Er Fu Huo, Yong Zou, Hui Qin Sun, Yan Huang, Zhi Yun Lu, Qing Jiang. Synthesis and characterization of novel conjugated polymers based on 3-cyclobutene-l,2-dione moiety[J]. Chinese Chemical Letters, 2011, 22(11): 1326-1330. doi: 10.1016/j.cclet.2011.05.025

Citation: Er Fu Huo, Yong Zou, Hui Qin Sun, Yan Huang, Zhi Yun Lu, Qing Jiang. Synthesis and characterization of novel conjugated polymers based on 3-cyclobutene-l,2-dione moiety[J]. Chinese Chemical Letters, 2011, 22(11): 1326-1330. doi: 10.1016/j.cclet.2011.05.025

Synthesis and characterization of novel conjugated polymers based on 3-cyclobutene-l,2-dione moiety
摘要:
Three novel conjugated polymers bearing 3, 4-bis (4-hexylthiophen-2-yl)-3-cyclobutene-l, 2-dione unit in their main chain have been synthesized successfully in good yields through Suzuki or Stille coupling reaction. Their molecular structures have been confirmed by FT-IR, 1H NMR and 13C NMR. All these copolymers exhibit broad and strong absorption bands in UV-vis region, and their optical band gaps are calculated to be 1.6-2.0 eV, suggesting that they have good coverage with the solar spectrum. These polymers have good thermostability and solubility in common organic solvents. Moreover, all these objective macromolecules possess high electron affinity of~3.8 eV determined from cyclic voltammetry measurement, implying that they are potential n-type polymeric photovoltaic materials.
English
Synthesis and characterization of novel conjugated polymers based on 3-cyclobutene-l,2-dione moiety
Abstract:
Three novel conjugated polymers bearing 3, 4-bis(4-hexylthiophen-2-yl)-3-cyclobutene-l, 2-dione unit in their main chain have been synthesized successfully in good yields through Suzuki or Stille coupling reaction. Their molecular structures have been confirmed by FT-IR, 1H NMR and 13C NMR. All these copolymers exhibit broad and strong absorption bands in UV-vis region, and their optical band gaps are calculated to be 1.6-2.0 eV, suggesting that they have good coverage with the solar spectrum. These polymers have good thermostability and solubility in common organic solvents. Moreover, all these objective macromolecules possess high electron affinity of~3.8 eV determined from cyclic voltammetry measurement, implying that they are potential n-type polymeric photovoltaic materials.

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