About: Synthesis and thermal behavior of telechelic poly(butadiene)diols with azobenzene-based liquid-crystalline units in side chains     Goto   Sponge   NotDistinct   Permalink

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  • Mesogenic thiols with azobenzene as a rigid part and with various substituent (H-, methoxy-, butoxy- or octyloxy-) in para-position of azobenzene ring were synthesized by multi-step syntheses. The thiols were grafted onto double bonds of telechelic poly(butadiene)diol (M (n) similar to 2,400, functionality f (n) = 2, 60 mol.% of 1,2-butadiene units) via radical addition in the presence of 2,2'-azobis(2-methylpropionitrile) (AIBN). Initial mole ratio of thiol/double bonds varied in the range of 0.2-1.0. Influence of the azobenzene substituent on the extent of modification reaction was estimated using elemental analysis, size-exclusion chromatography and H-1 NMR spectroscopy. The substituent on mesogen plays also an important role in thermal behavior of both the thiols and the obtained comb-like polymers, as determined by differential scanning calorimetry and polarizing optical microscopy.
  • Mesogenic thiols with azobenzene as a rigid part and with various substituent (H-, methoxy-, butoxy- or octyloxy-) in para-position of azobenzene ring were synthesized by multi-step syntheses. The thiols were grafted onto double bonds of telechelic poly(butadiene)diol (M (n) similar to 2,400, functionality f (n) = 2, 60 mol.% of 1,2-butadiene units) via radical addition in the presence of 2,2'-azobis(2-methylpropionitrile) (AIBN). Initial mole ratio of thiol/double bonds varied in the range of 0.2-1.0. Influence of the azobenzene substituent on the extent of modification reaction was estimated using elemental analysis, size-exclusion chromatography and H-1 NMR spectroscopy. The substituent on mesogen plays also an important role in thermal behavior of both the thiols and the obtained comb-like polymers, as determined by differential scanning calorimetry and polarizing optical microscopy. (en)
Title
  • Synthesis and thermal behavior of telechelic poly(butadiene)diols with azobenzene-based liquid-crystalline units in side chains
  • Synthesis and thermal behavior of telechelic poly(butadiene)diols with azobenzene-based liquid-crystalline units in side chains (en)
skos:prefLabel
  • Synthesis and thermal behavior of telechelic poly(butadiene)diols with azobenzene-based liquid-crystalline units in side chains
  • Synthesis and thermal behavior of telechelic poly(butadiene)diols with azobenzene-based liquid-crystalline units in side chains (en)
skos:notation
  • RIV/61389013:_____/10:00339561!RIV10-AV0-61389013
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GA202/09/2078), Z(AV0Z40500505)
http://linked.open...iv/cisloPeriodika
  • 4
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
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http://linked.open...dnocenehoVysledku
  • 291497
http://linked.open...ai/riv/idVysledku
  • RIV/61389013:_____/10:00339561
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • azobenzene mesogens; radical addition; poly(butadiene)diols (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • DE - Spolková republika Německo
http://linked.open...ontrolniKodProRIV
  • [470435CDE06E]
http://linked.open...i/riv/nazevZdroje
  • Polymer Bulletin
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 64
http://linked.open...iv/tvurceVysledku
  • Látalová, Petra
  • Poláková, Lenka
  • Sedláková, Zdeňka
http://linked.open...ain/vavai/riv/wos
  • 000274099400001
http://linked.open...n/vavai/riv/zamer
issn
  • 0170-0839
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