Abstract
Conjugated polycarbosilanes with diacetylene and aromatic groups of thiophene or phenylene simultaneously present in the polymer backbone such as poly[[1,4-bis(thiophenyl)buta-1,3-diyne]-alt-(dimethylsilane)], poly [[1,4- bis(thiophenyl)buta-1,3-diyne]-alt-(diphenylsilane)], poly[[1,4- bis(phenyl)buta-1,3-diyne]-alt-(dimethylsilane)], and poly[[1,4- bis(phenyl)buta-1,3-diyne]-alt-(diphenylsilane)] have been prepared. The characteristic C≡C stretching frequencies appear at 2177-2179 cm-1 in the IR spectra of the polymers. The molecular weights of these polymers were determined by GPC. All of these materials are soluble in organic solvents such as THF and chloroform, and thermally stable up to 200 °C in general without any weight loss under nitrogen. The prepared materials in THF solvent show a maximum absorption peak in the range of 334-356 nm with a molar absorptivity of 103-105 L/(cm·mol) in the UV-visible absorption spectra. A maximum emission peak in the range of 403-550 nm is also observed in the fluorescence emission spectra. Both absorption and emission spectra strongly indicate that the obtained polycarbosilanes contain the new conjugated systems along the polymer main chain.
| Original language | English |
|---|---|
| Pages (from-to) | 677-682 |
| Number of pages | 6 |
| Journal | Bulletin of the Korean Chemical Society |
| Volume | 20 |
| Issue number | 6 |
| Publication status | Published - 1999 Jun 20 |
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All Science Journal Classification (ASJC) codes
- Chemistry(all)
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Synthesis and properties of conjugated polycarbosilanes with 1,4- bis(thiophene or phenylene)-buta-1,3-diyne. / Seo, Il Kwon; Park, Young Tae; Kim, Yong Rok.
In: Bulletin of the Korean Chemical Society, Vol. 20, No. 6, 20.06.1999, p. 677-682.Research output: Contribution to journal › Article
TY - JOUR
T1 - Synthesis and properties of conjugated polycarbosilanes with 1,4- bis(thiophene or phenylene)-buta-1,3-diyne
AU - Seo, Il Kwon
AU - Park, Young Tae
AU - Kim, Yong Rok
PY - 1999/6/20
Y1 - 1999/6/20
N2 - Conjugated polycarbosilanes with diacetylene and aromatic groups of thiophene or phenylene simultaneously present in the polymer backbone such as poly[[1,4-bis(thiophenyl)buta-1,3-diyne]-alt-(dimethylsilane)], poly [[1,4- bis(thiophenyl)buta-1,3-diyne]-alt-(diphenylsilane)], poly[[1,4- bis(phenyl)buta-1,3-diyne]-alt-(dimethylsilane)], and poly[[1,4- bis(phenyl)buta-1,3-diyne]-alt-(diphenylsilane)] have been prepared. The characteristic C≡C stretching frequencies appear at 2177-2179 cm-1 in the IR spectra of the polymers. The molecular weights of these polymers were determined by GPC. All of these materials are soluble in organic solvents such as THF and chloroform, and thermally stable up to 200 °C in general without any weight loss under nitrogen. The prepared materials in THF solvent show a maximum absorption peak in the range of 334-356 nm with a molar absorptivity of 103-105 L/(cm·mol) in the UV-visible absorption spectra. A maximum emission peak in the range of 403-550 nm is also observed in the fluorescence emission spectra. Both absorption and emission spectra strongly indicate that the obtained polycarbosilanes contain the new conjugated systems along the polymer main chain.
AB - Conjugated polycarbosilanes with diacetylene and aromatic groups of thiophene or phenylene simultaneously present in the polymer backbone such as poly[[1,4-bis(thiophenyl)buta-1,3-diyne]-alt-(dimethylsilane)], poly [[1,4- bis(thiophenyl)buta-1,3-diyne]-alt-(diphenylsilane)], poly[[1,4- bis(phenyl)buta-1,3-diyne]-alt-(dimethylsilane)], and poly[[1,4- bis(phenyl)buta-1,3-diyne]-alt-(diphenylsilane)] have been prepared. The characteristic C≡C stretching frequencies appear at 2177-2179 cm-1 in the IR spectra of the polymers. The molecular weights of these polymers were determined by GPC. All of these materials are soluble in organic solvents such as THF and chloroform, and thermally stable up to 200 °C in general without any weight loss under nitrogen. The prepared materials in THF solvent show a maximum absorption peak in the range of 334-356 nm with a molar absorptivity of 103-105 L/(cm·mol) in the UV-visible absorption spectra. A maximum emission peak in the range of 403-550 nm is also observed in the fluorescence emission spectra. Both absorption and emission spectra strongly indicate that the obtained polycarbosilanes contain the new conjugated systems along the polymer main chain.
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M3 - Article
VL - 20
SP - 677
EP - 682
JO - Bulletin of the Korean Chemical Society
JF - Bulletin of the Korean Chemical Society
SN - 0253-2964
IS - 6
ER -