• Title/Summary/Keyword: Dibromopyridine

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Synthesis and Characterization of Oligomers Composed of Alternating 2,5-Bis(ethynylenedimethylsilylene)thienylene and Arylene Units

  • Kwak, Young-Woo;Lee, Kyung-Koo;Cha, Seung-Hun;Lee, Sang-Koo;Lee, In-Sook;Park, Yong-Tae;Lee, Jae-Keun;Yoh, Soo-Dong;Kim, Woo-Sik
    • Bulletin of the Korean Chemical Society
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    • v.24 no.4
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    • pp.479-483
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    • 2003
  • The reactions of 2,5-bis(ethynyldimethylsilyl)thiophene (1) with aromatic dihalides(1,4-dibromobenzene, 4,4'- dibromobiphenyl, 9,10-dibromoanthracene, 2,5-dibromopyridine, 2,5-dibromothiophene, and 2,6-diiodo-4- nitroaniline) were carried out in the presence of a $[(PPh_3)_2PdCl_2]$-CuI catalyst in refluxing triethylamine to give poly{[2,5-bis(ethynylenedimethylsilylene)thienylene](arylene)} (2-7) with molecular weights of 2200-7400. The oligomers reveal characteristic absorption in the UV/visible region. The thermal behavior of 2-7 was examined by thermogravimetric analysis in an argon atmosphere.

Synthesis and Characterization of Poly(arylene-ethynylene)s with Ferrocene Unit by Reaction of 1,1'-Bis(ethynyldimethylsilyl)ferrocene and Aromatic Dihalides

  • Lee, In-Sook;Lee, Chong-Gu;Kwak, Young-Woo;Gal, Yeong-Soon
    • Bulletin of the Korean Chemical Society
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    • v.30 no.2
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    • pp.309-314
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    • 2009
  • New poly(arylene-ethynylene)s with silicon-containing ferrocene moiety in the polymer main chain were synthesized via the C-C bond forming reactions of 1,1´-bis(ethynyldimethylsilyl)ferrocene and various aromatic dihalides in high yields. The aromatic dihalides include 1,4-dibromobenzene, 4,4´-dibromobiphenyl, 9,10-dibromoanthracene, 2,5-dibromopyridine, 2,5-dibromothiophene, and 2,6-diiodo-4-nitroaniline. The polymer structures and properties were characterized by such instrumental methods as NMR $(^1H-,\;^{13}C-,\;and\;^{29}Si-)$, IR, UV-visible spectroscopies and TGA/DSC. The spectral data indicated that the present polymers have the regular alternating structure of 1,1´-bis(ethynyldimethylsilyl)ferrocenylene and arylene units. The resulting polymers were completely soluble in such organic solvents as methylene chloride, chloroform, benzene, chlorobenzene, and THF. The thermal behaviors of the resulting polymers were examined.