Photochromism of a Furylfulgide, 2-[1-(2,5-Dimethyl-3-furyl)ethylidene]-3-isopropylidenesuccinic Anhydride in Solvents and Polymer Films
- 1 June 1990
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 63 (6) , 1607-1610
- https://doi.org/10.1246/bcsj.63.1607
Abstract
The quantum yields of the photochromic reaction between (E)- and (Z)-2-[1-(2,5-dimethyl-3-furyl)ethylidene]-3-isopropylidenesuccinic anhydride and the cyclized valence isomer were determined in various solvents and polymers. In both media the ring-opening quantum yield (ΦCE) depended on the dielectric constant of the media. In some polymer films, ΦCE were larger, and the cyclization quantum yield (ΦEC) and olefinic isomerization quantum yields (ΦEZ) and (ΦZE) were smaller than those in the corresponding solvents.Keywords
This publication has 7 references indexed in Scilit:
- Photochromic thiophenefulgide absorption spectra and kinetics of photochemical isomerizationsChemical Physics Letters, 1989
- Photochemical Fatigue Resistances and Thermal Stabilities of Heterocyclic Fulgides in PMMA FilmBulletin of the Chemical Society of Japan, 1988
- Rapid chromatographic technique for preparative separations with moderate resolutionThe Journal of Organic Chemistry, 1978
- Temperature dependence of photoisomerization. VI. Viscosity effectJournal of the American Chemical Society, 1968
- Second‐order transitions in solutions of cellulose triacetateJournal of Polymer Science, 1961
- Die Farbe der „Fulgensäuren”︁ und „Fulgide”︁. (7. Abhandlung über Butadiënverbindungen.)European Journal of Inorganic Chemistry, 1905
- ButadiëndicarbonsäurenEuropean Journal of Inorganic Chemistry, 1904