期刊文献+

新型芳并吡喃类多环化合物的合成与光谱性质研究 被引量:1

Synthesis and Optical Properties of Novel Aryl-fused Pyran-containing Polycyclic Compounds
下载PDF
导出
摘要 本文设计并经由分子内碳-碳偶联反应合成了一系列基于芳并吡喃供电子功能片段的有机功能小分子,包括萘并[2,1-b:6,5-b’]二苯并吡喃4a,萘并[2,1-b:6,5-b’]二萘并吡喃4b,萘并[2,1-b:6,5-b’]二[2-(5-己基噻吩基)]苯并吡喃4c。通过紫外光谱和荧光光谱研究表明,这类化合物在370~400 nm波长范围内具有最大紫外吸收,在417~462 nm波长范围内具有最大荧光发射。说明随着共轭平面的增大或共轭链长度的增加,化合物的吸收和荧光光谱均发生显著的红移,是一类具有丰富光电活性的有机功能分子。 A series of functional small organic molecules based on electron-donating aryl-fused pyran functional motifs have been designed and synthesized by intramolecular carbon- carbon coupling reaction,including naphtho[2,1-b:6,5-b']bisbenzopyran 4a,naphtho[2,1-b:6,5-b']bisnaphthopyran 4b,naphtho[2,1-b:6,5-b']bis[2-(5-hexyl thienyl)]benzopyran 4c.Their UV-Vis spectra showed the maxima absorption at 370-400 nm,and their fluorescence spectra exhibited the maxima emission in the range of 417-462 nm.The increasing of conjugated plane or conjugated chain length in these compounds caused remarkable red shifts in both of their absorption and emission spectra,indicative of their rich optical properties.
出处 《影像科学与光化学》 CAS CSCD 北大核心 2014年第3期282-288,共7页 Imaging Science and Photochemistry
基金 国家自然科学基金项目(21174083)资助
关键词 有机小分子 芳并吡喃 光谱性质 small organic molecules aryl-fused pyran optical properties
  • 相关文献

参考文献16

  • 1Mishra A,Ma C Q.Bauerle P.Functional oligothiophenes:molecular design for multidimensional nanoarchitectures and their application[J].Chemical Reviews,2009,109(3):1141-1276.
  • 2Murphy A R,and Frechet J M J.Organic semiconducting oligomers for use in thin film transistors[J].Chemical Reviews,2007,107(4):1066-1096.
  • 3Zaumseil J,Sirringhaus H.Electron and ambiolar transport inorganic field-effect transistor[J].Chemical Reviews,2007,107(4):1296-1323.
  • 4Toby L N,Tomasz M Y,Jun Y L,Mishra S P,Belot J A,Balliet C L,Javier A E,Kowalewski T,McCullough R D.Transistor paint:high mobilities in small bandgap polymer semiconductor based on the strong acceptor,diketopyrrolopyrrole and strong donor,dithienopyrrole[J].Advanced Materials,2010,22(41):4617-4621.
  • 5Mitsui C,Soeda J,Miwa K.Tsuji H,Takeya J,Nakamura E.Naphtho[2,l-b:6,5-b']difuran:a versatile motif available for solution-processed single-crystal organic field-effect transistors with high hole mobility[J].Journal of the American Chemical Society,2012,134(12):5448-5451.
  • 6Gidron O,Diskin-Posner Y,and Bendikov M.crOligofurans[J].Journal of the American Chemical Society,2010,132(7):2148-2150.
  • 7Dou L T.Chen C C,Yoshimura K.Ohya K.Chang W H.Gao J.Liu Y S,Richard E,and Yang Y.Synthesis of 5Hdithieno[3,2-b:2,3'-d]pyran as an electron-rich building block for donor-acceptor type low-bandgap po-lymers[J].Macromolecules,2013,46(9):3384-3390.
  • 8You J B,Dou L T,Yoshimura K,Ohya K,Moriarty T,Emery K,Chen C C,Gao J,Li G,Yang Y.A poly-mer tandem solar cell with 10.6%power conversion efficiency[J].Nature Communications,2013.4:1-10.
  • 9You J B,Chen C C,Hong Z,Yoshimura K,Ohya K,Gao J,Li G.and Yang Y.10.2%power conversion efficiency polymer tandem solar cells consisting of two identical subcells[J].Advanced Materials,2013,25(29):3973-3978.
  • 10Mocydlahz J W,Canonne P,Lfitch L C.Synthesis of 2,5,8-trimethylphellalene[J].Communications Synthesis,1974,23:566-568.

同被引文献4

引证文献1

二级引证文献1

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