Syntéza, absorpce, fluorescence a fotoisomerisace 2-aryl-4-arylmethyliden-pyrrolin-5-onů.

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F08%3A00007956" target="_blank" >RIV/00216275:25310/08:00007956 - isvavai.cz</a>

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

The synthesis, absorption, fluorescence and photoisomerisation of 2-aryl-4-arylmethylidene-pyrroline-5-ones.

Popis výsledku v původním jazyce

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.

Název v anglickém jazyce

The synthesis, absorption, fluorescence and photoisomerisation of 2-aryl-4-arylmethylidene-pyrroline-5-ones.

Popis výsledku anglicky

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.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CC - Organická chemie

OECD FORD obor

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Projekt

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Návaznosti

Z - Vyzkumny zamer (s odkazem do CEZ)

Rok uplatnění

2008

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Dyes and Pigments

ISSN

0143-7208

e-ISSN

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Svazek periodika

77

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

11

Strana od-do

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Kód UT WoS článku

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EID výsledku v databázi Scopus

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