Matches in SemOpenAlex for { <https://semopenalex.org/work/W2067996489> ?p ?o ?g. }
- W2067996489 abstract "Abstract The fluorescence properties and photoisomerization behavior for trans and cis isomers of 1-(9-anthryl)-2-(2-pyrazinyl)ethene (APzE). a diaza analogue of 1-(9-anthryl)-2-phenylethene (9-APE), were studied. The fluorescence maximum (λ 1 ). quantum yield ( Φ t ) and lifetime ( τ t ) of t -APZE were solvent-dependent reflecting the intramolecular charge transfer character in the lowest excited singlet state. However, in polar protic solvent, some discrepancy was observed probably due to protonation on the nitrogen atoms. The photoisomerization of t -APzE was observed even in very nonpolar solvent, in contrast that the parent t -9-APE did not photoisomerize in any solvent and photoisomerization of monoaza analogues t 1-(9-anthryl)-2-( n -pyridyl)ethenes ( n -APyE) was very inefficient in nonpolar solvent. The quantum yield of the trans → cis photoisomerization ( Φ t → c ) of t -APzE was also solvent-dependent. Not only the inverse dependence for Φ f -and Φ t → c , of t -APzE on the temperature and the solvent polarity but also hiacetyl-sensitized photoisomerization experiment indicate that the photoisomerization of t -APzE occurs, at least in part, via the excited singlet state. In air-saturated solution, another side photoproduct was observed in all solvent examined and identified as anthraquinone, a photo-oxidation product. For c -APzE, the τ t , is too short to measure and Φ t , is relatively low. Quantum yields of fluorescence and cis→trans photoisomerization of c -APzE in various solvent and temperature indicate singlet mechanism for the cis → trans photoisomerization of c -APzE in polar solvent but mixed singlet/triplet mechanism in nonpolar solvent. On irradiation of c -APzE, the photo-oxidation product was not generated at all in any solvent. In n -hexane, photocyclization competing with photoisomerization was observed both for t - and c -APzE." @default.
- W2067996489 created "2016-06-24" @default.
- W2067996489 creator A5007262375 @default.
- W2067996489 creator A5091537747 @default.
- W2067996489 date "1998-03-01" @default.
- W2067996489 modified "2023-09-29" @default.
- W2067996489 title "Photoisomerization behavior of 1-(9-anthryl)-2-(2-pyrazinyl)ethene, a diaza analogue of 1-(9-anthryl)-2-phenylethene" @default.
- W2067996489 cites W1964204207 @default.
- W2067996489 cites W1967147771 @default.
- W2067996489 cites W1967890626 @default.
- W2067996489 cites W1974474781 @default.
- W2067996489 cites W1981228594 @default.
- W2067996489 cites W1986312673 @default.
- W2067996489 cites W1989649581 @default.
- W2067996489 cites W1996731160 @default.
- W2067996489 cites W1997669020 @default.
- W2067996489 cites W1997951235 @default.
- W2067996489 cites W1999448471 @default.
- W2067996489 cites W2007741875 @default.
- W2067996489 cites W2019692325 @default.
- W2067996489 cites W2020587360 @default.
- W2067996489 cites W2023456153 @default.
- W2067996489 cites W2025704729 @default.
- W2067996489 cites W2030897550 @default.
- W2067996489 cites W2059875103 @default.
- W2067996489 cites W2069907581 @default.
- W2067996489 cites W2071412186 @default.
- W2067996489 cites W2076586233 @default.
- W2067996489 cites W2088016822 @default.
- W2067996489 cites W2089208674 @default.
- W2067996489 cites W2157299937 @default.
- W2067996489 cites W2316309054 @default.
- W2067996489 cites W2950468689 @default.
- W2067996489 doi "https://doi.org/10.1016/s1010-6030(98)00197-x" @default.
- W2067996489 hasPublicationYear "1998" @default.
- W2067996489 type Work @default.
- W2067996489 sameAs 2067996489 @default.
- W2067996489 citedByCount "6" @default.
- W2067996489 crossrefType "journal-article" @default.
- W2067996489 hasAuthorship W2067996489A5007262375 @default.
- W2067996489 hasAuthorship W2067996489A5091537747 @default.
- W2067996489 hasConcept C120665830 @default.
- W2067996489 hasConcept C121332964 @default.
- W2067996489 hasConcept C126661725 @default.
- W2067996489 hasConcept C132439834 @default.
- W2067996489 hasConcept C145148216 @default.
- W2067996489 hasConcept C161790260 @default.
- W2067996489 hasConcept C171001562 @default.
- W2067996489 hasConcept C178790620 @default.
- W2067996489 hasConcept C181500209 @default.
- W2067996489 hasConcept C185544564 @default.
- W2067996489 hasConcept C185592680 @default.
- W2067996489 hasConcept C2780471494 @default.
- W2067996489 hasConcept C30095370 @default.
- W2067996489 hasConcept C33062035 @default.
- W2067996489 hasConcept C71240020 @default.
- W2067996489 hasConcept C75079739 @default.
- W2067996489 hasConcept C75473681 @default.
- W2067996489 hasConcept C85311670 @default.
- W2067996489 hasConcept C91881484 @default.
- W2067996489 hasConceptScore W2067996489C120665830 @default.
- W2067996489 hasConceptScore W2067996489C121332964 @default.
- W2067996489 hasConceptScore W2067996489C126661725 @default.
- W2067996489 hasConceptScore W2067996489C132439834 @default.
- W2067996489 hasConceptScore W2067996489C145148216 @default.
- W2067996489 hasConceptScore W2067996489C161790260 @default.
- W2067996489 hasConceptScore W2067996489C171001562 @default.
- W2067996489 hasConceptScore W2067996489C178790620 @default.
- W2067996489 hasConceptScore W2067996489C181500209 @default.
- W2067996489 hasConceptScore W2067996489C185544564 @default.
- W2067996489 hasConceptScore W2067996489C185592680 @default.
- W2067996489 hasConceptScore W2067996489C2780471494 @default.
- W2067996489 hasConceptScore W2067996489C30095370 @default.
- W2067996489 hasConceptScore W2067996489C33062035 @default.
- W2067996489 hasConceptScore W2067996489C71240020 @default.
- W2067996489 hasConceptScore W2067996489C75079739 @default.
- W2067996489 hasConceptScore W2067996489C75473681 @default.
- W2067996489 hasConceptScore W2067996489C85311670 @default.
- W2067996489 hasConceptScore W2067996489C91881484 @default.
- W2067996489 hasLocation W20679964891 @default.
- W2067996489 hasOpenAccess W2067996489 @default.
- W2067996489 hasPrimaryLocation W20679964891 @default.
- W2067996489 hasRelatedWork W1970083849 @default.
- W2067996489 hasRelatedWork W1977184582 @default.
- W2067996489 hasRelatedWork W1997951235 @default.
- W2067996489 hasRelatedWork W2005948909 @default.
- W2067996489 hasRelatedWork W2011314355 @default.
- W2067996489 hasRelatedWork W2014405144 @default.
- W2067996489 hasRelatedWork W2016056182 @default.
- W2067996489 hasRelatedWork W2021501887 @default.
- W2067996489 hasRelatedWork W2046315608 @default.
- W2067996489 hasRelatedWork W2049176995 @default.
- W2067996489 hasRelatedWork W2055976940 @default.
- W2067996489 hasRelatedWork W2062795560 @default.
- W2067996489 hasRelatedWork W2068420814 @default.
- W2067996489 hasRelatedWork W2070696701 @default.
- W2067996489 hasRelatedWork W2073079183 @default.
- W2067996489 hasRelatedWork W2074994232 @default.
- W2067996489 hasRelatedWork W2075972687 @default.
- W2067996489 hasRelatedWork W2131382247 @default.