Cyclic side-chain phenylazo naphthalene polymers: enhanced fluorescence emission and surface relief grating formation

Macromol Rapid Commun. 2012 Nov 14;33(21):1845-51. doi: 10.1002/marc.201200415. Epub 2012 Sep 11.

Abstract

Well-defined cyclic-polymers (cyclic-PAzoMMAs), bearing side-chain phenylazo naphthalene chromophore, were successfully synthesized by the combination of atom transfer radical polymerization (ATRP) and copper(I)-catalyzed azide/alkyne cycloaddition "click" reaction, as verified by GPC, (1) H NMR, FTIR, and MALDI-TOF mass spectrometry. The cyclic-PAzoMMA showed higher glass transition temperatures than the linear-PAzoMMA with the same molecular weight. Interestingly, the cyclic-PAzoMMA exhibited deeper modulation depth (M.D.) induced by SRG, larger value of the photoinduced birefringence, increased fluorescence emission, and longer fluorescence lifetime in comparison with its linear counterpart.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry
  • Azides / chemistry*
  • Fluorescence
  • Molecular Structure
  • Naphthalenes / chemistry*
  • Polymerization
  • Polymers / chemical synthesis
  • Polymers / chemistry*
  • Surface Properties

Substances

  • Alkynes
  • Azides
  • Naphthalenes
  • Polymers
  • naphthalene