Synthesis and properties of conjugated polycarbosilanes with 1,4- bis(thiophene or phenylene)-buta-1,3-diyne

Il Kwon Seo, Young Tae Park, Yong Rok Kim

Research output: Contribution to journalArticle

12 Citations (Scopus)

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 languageEnglish
Pages (from-to)677-682
Number of pages6
JournalBulletin of the Korean Chemical Society
Volume20
Issue number6
Publication statusPublished - 1999 Jun 20

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Thiophenes
Polymers
Chloroform
Organic solvents
Stretching
Absorption spectra
Nitrogen
Fluorescence
Molecular weight

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

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title = "Synthesis and properties of conjugated polycarbosilanes with 1,4- bis(thiophene or phenylene)-buta-1,3-diyne",
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.",
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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 journalArticle

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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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