4.3 Article

Synthesis and Characterization of Novel Conjugated Polymer with Thiophene and Benzimidazole

Journal

BULLETIN OF THE KOREAN CHEMICAL SOCIETY
Volume 32, Issue 8, Pages 3045-3050

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.5012/bkcs.2011.32.8.3045

Keywords

Polymer; PLED; Thiophene; Benzimidazole

Funding

  1. National Research Foundation of Korea (NRF)
  2. Ministry of Education, Science and Technology [2009-0071669]
  3. National Research Foundation of Korea [2009-0071669] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The synthesis of copolymers containing thiophene and benzimidazole unit by Stille polymerization is reported. The polymers with many unsubstituted thiophene units in the backbone have been reported to show low solubility, which has been a problem for spin-coating for the device fabrication. In dihexyl-2H-benzimidazole, the sulfur at 2-position of BT unit was replaced with dialkyl substituted carbon, while keeping the 1,2-quinoid form, to improve the solubility of the polymers. The PL emission spectra of the PHBIT1, PHBIT2 and PHBIT3 in chloroform solutions show maximum peaks at 500 similar to 561 nm. In thin films, maximum peaks of the PHBITs appeared at 529, 562 and 569 nm, respectively. The EL emission maxima of the PHBIT1 and PHBIT2 appear at around 588 and 576 nm, respectively. The current density and maximum luminescence of the LED with the configuration of ITO/PEDOT/PHBIT2/Ca/Al are 552 mA/cm(2) and 46 cd/m(2), respectively.

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