About: The synthesis, absorption, fluorescence and photoisomerisation of 2-aryl-4-arylmethylidene-pyrroline-5-ones.     Goto   Sponge   NotDistinct   Permalink

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Description
  • Syntéza, absorpce, fluorescence a fotoisomerisace 2-aryl-4-arylmethyliden-pyrrolin-5-onů. (cs)
  • Base catalyzed ClaiseneSchmidt type condensation of ethyl-4,5-dihydro-5-oxo-2-phenyl(1H)pyrrole-3-carboxylate and its 2-biphenylyl analogue with various aldehydes was studied. The absorption and fluorescence spectra of ethyl-4,5-dihydro-5-oxo-2-aryl-4-(arylmethylidene)-(1H)pyrrole-3-carboxylate at both room (300 K) and low (77 K) temperatures were analyzed. EeZ photoisomerisation was observed for all derivatives; the Z-isomer was confirmed as being thermodynamically stable by NMR spectroscopy. PM3 quantum chemical Metod was used for ground state geometry calculations of the Z-isomers, while INDO/S calculations enabled interpretation of the absorption spectral shifts. Photoisomerisation forms the main deactivation channel after excitation in fluid solution, in contrast to rigid frozen glass, where fluorescence is preferred.
  • Base catalyzed ClaiseneSchmidt type condensation of ethyl-4,5-dihydro-5-oxo-2-phenyl(1H)pyrrole-3-carboxylate and its 2-biphenylyl analogue with various aldehydes was studied. The absorption and fluorescence spectra of ethyl-4,5-dihydro-5-oxo-2-aryl-4-(arylmethylidene)-(1H)pyrrole-3-carboxylate at both room (300 K) and low (77 K) temperatures were analyzed. EeZ photoisomerisation was observed for all derivatives; the Z-isomer was confirmed as being thermodynamically stable by NMR spectroscopy. PM3 quantum chemical Metod was used for ground state geometry calculations of the Z-isomers, while INDO/S calculations enabled interpretation of the absorption spectral shifts. Photoisomerisation forms the main deactivation channel after excitation in fluid solution, in contrast to rigid frozen glass, where fluorescence is preferred. (en)
Title
  • The synthesis, absorption, fluorescence and photoisomerisation of 2-aryl-4-arylmethylidene-pyrroline-5-ones.
  • The synthesis, absorption, fluorescence and photoisomerisation of 2-aryl-4-arylmethylidene-pyrroline-5-ones. (en)
  • Syntéza, absorpce, fluorescence a fotoisomerisace 2-aryl-4-arylmethyliden-pyrrolin-5-onů. (cs)
skos:prefLabel
  • The synthesis, absorption, fluorescence and photoisomerisation of 2-aryl-4-arylmethylidene-pyrroline-5-ones.
  • The synthesis, absorption, fluorescence and photoisomerisation of 2-aryl-4-arylmethylidene-pyrroline-5-ones. (en)
  • Syntéza, absorpce, fluorescence a fotoisomerisace 2-aryl-4-arylmethyliden-pyrrolin-5-onů. (cs)
skos:notation
  • RIV/00216275:25310/08:00007956!RIV09-MSM-25310___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM0021627501), Z(MSM0021627502)
http://linked.open...iv/cisloPeriodika
  • 2
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  • 398711
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  • RIV/00216275:25310/08:00007956
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http://linked.open.../riv/klicovaSlova
  • 2-Aryl-4-arylmethylidene-pyrroline-5-ones; Photoisomerisation; Fluorescence; Pyrrolinone ester (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [AE333D50B6EE]
http://linked.open...i/riv/nazevZdroje
  • Dyes and Pigments
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http://linked.open...ichTvurcuVysledku
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http://linked.open...v/svazekPeriodika
  • 77
http://linked.open...iv/tvurceVysledku
  • Hrdina, Radim
  • Luňák, Stanislav
  • Vyňuchal, Jan
  • Jirásko, Robert
  • Lyčka, Antonín
  • Vyňuchalová, Kateřina
  • Havel, Lukáš
  • Hatlapatková, Aneta
http://linked.open...n/vavai/riv/zamer
issn
  • 0143-7208
number of pages
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  • 25310
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