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Synthesis and optical properties of copolymers containing electron transporting 1,3,4-oxadiazole pendant groups
- Synthesis and optical properties of copolymers containing electron transporting 1,3,4-oxadiazole pendant groups
- Wang, H[Wang, Hui]; Ryu, JT[Ryu, Jeong-Tak]; Han, YS[Han, Yoon Soo]; Hur, Y[Hur, Youngjune]; Park, LS[Park, Lee Soon]; Song, M[Song, Minhyeon]; Kwon, Y[Kwon, Younghwan]
- DGIST Authors
- Han, YS[Han, Yoon Soo]
- Issue Date
- Molecular Crystals and Liquid Crystals, 459, 109-118
- Article Type
- 1,3,4-Oxadiazole; Copolymers; Electron Energy Levels; Energy Gap; Hole Transport; N-Alkylcarbazole; Organic Compounds; Polycondensation; Synthesis (Chemical); Triaryl Amine
- Well-defined copolymer, P(3,6-EHCZ-alt-MPAOXD), containing a triarylamine and N-alkylcarbazole groups (as hole transport moieties with blue emission) in the main chain and a 1,3,4-oxadiazole pendant group (as an electron transporting moiety) was synthesized by Pd-catalyzed polycondensation of N-(2-ethylhexyl)-3,6-dibromo carbazole with 2-methylphenyl-5-(4-aminophenyl)-1, 3,4-oxadiazole. For comparison, P(3,6-EHCZ-alt-AL) containing a triarylamine and a carbazole groups in the main chain was also prepared. P(3,6-EHCZ-alt-AL) exhibited λmax,UV at 309 nm and λmax,PL in the range of blue emission at 452 nm. However, P(3,6-EHCZ-alt-MPAOXD) exhibited λmax,UV at 283 nm with a new peak at 359 nm, and red-shifted PL emission at 506 nm, possibly attributed to the extended conjugation by 1,3,4-oxadiazole pendant group. The electrochemical results revealed that incorporation of 1,3,4-oxadiazole group in the polymer side chain provided a closely matched HOMO energy levels with hole-injecting PEDOT layer, and reduced the band gap energy level.
- Taylor and Francis Ltd.
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