About: Structure, absorption and fluorescence of (bi)thiophene substituted methylidene-pyrrolinones     Goto   Sponge   NotDistinct   Permalink

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  • Four thiophene and bithiophene substituted methylidene-pyrrolinones were synthesized and thein absorption and fluorescence properties were compared with previously reported behavior of their fenyl and biphenyl substituted analogues. Their structures were estimated theoretically by density functional theory (DFT) and proved by X-ray diffraction in two cases. Thiophene derivatives show a considerable bathochromic shifts in absorption with respect to phenyl analogues, in accordance with theoretical predictions based on time dependent DFT. Conjugation extension caused a bathochromic shift in absorption, too. All compounds show fluorescence in low temperature solvent glass, while only one bithiophene substituted derivative fluoresce weakly in room temperature solution. Three of four N-methylated derivatives show strong yellow, orange and red solid-state fluorescence. An ability of solid-state fluorescence was correlated with nearest neighbor out-of-plane interactions in crystal.
  • Four thiophene and bithiophene substituted methylidene-pyrrolinones were synthesized and thein absorption and fluorescence properties were compared with previously reported behavior of their fenyl and biphenyl substituted analogues. Their structures were estimated theoretically by density functional theory (DFT) and proved by X-ray diffraction in two cases. Thiophene derivatives show a considerable bathochromic shifts in absorption with respect to phenyl analogues, in accordance with theoretical predictions based on time dependent DFT. Conjugation extension caused a bathochromic shift in absorption, too. All compounds show fluorescence in low temperature solvent glass, while only one bithiophene substituted derivative fluoresce weakly in room temperature solution. Three of four N-methylated derivatives show strong yellow, orange and red solid-state fluorescence. An ability of solid-state fluorescence was correlated with nearest neighbor out-of-plane interactions in crystal. (en)
Title
  • Structure, absorption and fluorescence of (bi)thiophene substituted methylidene-pyrrolinones
  • Structure, absorption and fluorescence of (bi)thiophene substituted methylidene-pyrrolinones (en)
skos:prefLabel
  • Structure, absorption and fluorescence of (bi)thiophene substituted methylidene-pyrrolinones
  • Structure, absorption and fluorescence of (bi)thiophene substituted methylidene-pyrrolinones (en)
skos:notation
  • RIV/62690094:18470/13:50001295!RIV14-MSM-18470___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • I, N, S
http://linked.open...iv/cisloPeriodika
  • 5.7.2013
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 108375
http://linked.open...ai/riv/idVysledku
  • RIV/62690094:18470/13:50001295
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Density functional theory; X-ray diffraction; Fluorescence; Absorption (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • NL - Nizozemsko
http://linked.open...ontrolniKodProRIV
  • [44FE5380CE6A]
http://linked.open...i/riv/nazevZdroje
  • Journal of molecular structure
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 1043
http://linked.open...iv/tvurceVysledku
  • Hrdina, Radim
  • Luňák, Stanislav
  • Padělková, Zdeňka
  • Vyňuchal, Jan
  • Lyčka, Antonín
  • Eliáš, Zdeněk
http://linked.open...ain/vavai/riv/wos
  • 000320221900006
issn
  • 0022-2860
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.molstruc.2013.03.055
http://localhost/t...ganizacniJednotka
  • 18470
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