期刊文献+

Electronic Structures and Spectroscopic Characters of Modified Oligo(alkylenedioxypyrrole)

Electronic Structures and Spectroscopic Characters of Modified Oligo(alkylenedioxypyrrole)
原文传递
导出
摘要 Polyalkylenedioxypyrrole (PADOP) exhibited an excellent conductivity experimentally. A series of oligomers for the electron-rich monomer alkylenedioxypyrrole (ADOP) were designed in order to study properties of PADOP. The structures of these oligomers were optimized using density function theory (DFT) at B3LYP/6-31G(d) level. The energy gaps and thermal stabilities of the oligomers were decreased when the chain lengths were increased. These properties were also decreased with the enlargement of the neighboring substituted rings. The 13C nuclear magnetic resonance (NMR) spectra and nucleus independent chemical shifts (NICS) of the oligomers were calcu- lated at B3LYP/6-31G(d) level. The chemical shifts at J 96.! of the linking carbon atoms in the dimer of 3,4-methylenedioxypyrrole (MDOP) were moved downfield relative to those at d 89.5 of the same carbon atoms in the monomer of MDOP. The aromaticity of the central pyrrole ring in the oligomers is improved with the enlargement of the neighboring substituted rings. Polyalkylenedioxypyrrole (PADOP) exhibited an excellent conductivity experimentally. A series of oligomers for the electron-rich monomer alkylenedioxypyrrole (ADOP) were designed in order to study properties of PADOP. The structures of these oligomers were optimized using density function theory (DFT) at B3LYP/6-31G(d) level. The energy gaps and thermal stabilities of the oligomers were decreased when the chain lengths were increased. These properties were also decreased with the enlargement of the neighboring substituted rings. The 13C nuclear magnetic resonance (NMR) spectra and nucleus independent chemical shifts (NICS) of the oligomers were calcu- lated at B3LYP/6-31G(d) level. The chemical shifts at J 96.! of the linking carbon atoms in the dimer of 3,4-methylenedioxypyrrole (MDOP) were moved downfield relative to those at d 89.5 of the same carbon atoms in the monomer of MDOP. The aromaticity of the central pyrrole ring in the oligomers is improved with the enlargement of the neighboring substituted rings.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2011年第5期888-892,共5页 中国化学(英文版)
关键词 alkylenedioxypyrrole oligomers conductive polymer AROMATICITY NICS scanning alkylenedioxypyrrole oligomers, conductive polymer, aromaticity, NICS scanning
  • 相关文献

参考文献1

共引文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部