Synthesis and properties of tricarbazole-functionalized poly(norbornene-dicarboximide)

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

A series of poly(norbornene-dicarboximide)s with donor-acceptor pendants were synthesized by ring-opening metathesis polymerization, and their photophysical and thermal properties have been investigated. By linking different electron-withdrawing groups to electron-donating tricarbazole on the side chain of poly(norbornene) backbone, the polymers displayed various fluorescence emission color as purplish blue (418 nm), greenish blue (489 nm), green (515 nm), and orange yellow (594 nm). The fluorescence quantum yield of polymer bearing tricarbazole-aldehyde group in CHCl3 was reached to 0.42. The highest occupied molecular orbital level of polymers was close to -5.3 eV, and the lowest unoccupied molecular orbital varied between -2.34 and -3.02 eV. All polymers exhibited high thermal stability with decomposition temperature exceeding 400 °C.

Original languageEnglish
Pages (from-to)110-121
Number of pages12
JournalEuropean Polymer Journal
Volume76
DOIs
StatePublished - Mar 2016

Keywords

  • Polynorbornene
  • Properties
  • Ring-opening metathesis polymerization
  • Tricarbazole

Fingerprint

Dive into the research topics of 'Synthesis and properties of tricarbazole-functionalized poly(norbornene-dicarboximide)'. Together they form a unique fingerprint.

Cite this