Synthesis and optoelectronic characterization of some star-shaped oligomers with benzene and triphenylamine cores.

ISRN Organic Chemistry Pub Date : 2012-08-22 eCollection Date: 2012-01-01 DOI:10.5402/2012/976178
Teofilia Ivan, Loredana Vacareanu, Mircea Grigoras
{"title":"Synthesis and optoelectronic characterization of some star-shaped oligomers with benzene and triphenylamine cores.","authors":"Teofilia Ivan, Loredana Vacareanu, Mircea Grigoras","doi":"10.5402/2012/976178","DOIUrl":null,"url":null,"abstract":"<p><p>Six star-shaped oligomers containing triphenylamine (D1-D3) and benzene unit (D4-D6) as cores have been synthesized by Wittig condensation or Heck coupling reaction using aromatic aldehydes and triphenylphosphonium salts or aromatic halogenated compounds with vinyl triphenylamine. All oligomers have well-defined molecular structure and high purity. Characterization of the oligomers was made by FT-IR, (1)H-NMR spectroscopy, UV-Vis, and fluorescence spectroscopy. The electrochemical behavior was studied by cyclic voltammetry (CV). The cyclic voltammograms have revealed that oligomers undergo quasireversible or irreversible redox processes. The irreversible process is associated with electrochemical polymerization of oligomers by dimerization of unsubstituted triphenylamine groups. Thermal characterization was accomplished by TGA and DSC methods and evidenced that all oligomers were stable materials until 250°C and have formed stable molecular glasses after first heating scan. </p>","PeriodicalId":14730,"journal":{"name":"ISRN Organic Chemistry","volume":"2012 ","pages":"976178"},"PeriodicalIF":0.0000,"publicationDate":"2012-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767318/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ISRN Organic Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5402/2012/976178","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2012/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Six star-shaped oligomers containing triphenylamine (D1-D3) and benzene unit (D4-D6) as cores have been synthesized by Wittig condensation or Heck coupling reaction using aromatic aldehydes and triphenylphosphonium salts or aromatic halogenated compounds with vinyl triphenylamine. All oligomers have well-defined molecular structure and high purity. Characterization of the oligomers was made by FT-IR, (1)H-NMR spectroscopy, UV-Vis, and fluorescence spectroscopy. The electrochemical behavior was studied by cyclic voltammetry (CV). The cyclic voltammograms have revealed that oligomers undergo quasireversible or irreversible redox processes. The irreversible process is associated with electrochemical polymerization of oligomers by dimerization of unsubstituted triphenylamine groups. Thermal characterization was accomplished by TGA and DSC methods and evidenced that all oligomers were stable materials until 250°C and have formed stable molecular glasses after first heating scan.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
一些以苯和三苯胺为核心的星形低聚物的合成与光电特性。
利用芳香醛和三苯基膦盐或芳香卤代化合物与乙烯基三苯胺通过威蒂希缩合或赫克偶联反应合成了六种以三苯胺(D1-D3)和苯单元(D4-D6)为核心的星形低聚物。所有低聚物都具有明确的分子结构和高纯度。利用傅立叶变换红外光谱、(1)H-核磁共振光谱、紫外-可见光谱和荧光光谱对这些低聚物进行了表征。电化学行为通过循环伏安法(CV)进行了研究。循环伏安图显示,低聚物会发生类逆转或不可逆的氧化还原过程。不可逆过程与低聚物通过未取代的三苯胺基团的二聚化进行电化学聚合有关。通过 TGA 和 DSC 方法完成了热表征,结果表明所有低聚物在 250°C 之前都是稳定的材料,并且在第一次加热扫描后形成了稳定的分子玻璃。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Synthesis, Spectral Analysis, In Vitro Microbiological Evaluation, and Molecular Docking Studies of Some Novel 1-(1-Aryl-1H-tetrazol-5-yl)-2-(piperidin-1-yl)ethanone Derivatives. A facile stereoselective total synthesis of (R)-rugulactone. Asymmetric organocatalysis at the service of medicinal chemistry. Efficient electrochemical N-alkylation of N-boc-protected 4-aminopyridines: towards new biologically active compounds. Synthesis and biological activities of 4-aminoantipyrine derivatives derived from betti-type reaction.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1