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Phototautomeric fluorescence

A system undergoing excited-state intramolecular proton transfer was suggested as a solar energy collector. Moreover, since such systems reveal a very large Stokes shift due to the excited-state intramolecular proton transfer (ESIPT) reactions, resulting in the phototautomeric fluorescence with a relatively high quantum yield (about 30%), they are recommended as potential solar energy concentrators. [Pg.1290]

Other Processes - The phototautomerism of A-salicylideneanilines has been studied at 77 A study of the fluorescent behaviour of the... [Pg.256]

Figure 3.14 Double proton transfer in pyrroloquinolines in alcohol solutions, (a) Structure of 1 H-pyrrolo[3,2-h]quinoline (7) and a scheme of the photoinduced tau-tomerization leading from a normal form to a phototautomeric form [52, 61, 62]. (b) Structure of 7,8,9,10-tetrahydropyrido[2,3-o] carbazole (30) [52] and pyrido[2,3-o] car-bazole (31) [52]. (c) Fluorescence of 7, 30, and 31 (solid lines) and of the corresponding tautomeric model structures (dotted lines), shown as 7m, 30m, and 31 m. The... Figure 3.14 Double proton transfer in pyrroloquinolines in alcohol solutions, (a) Structure of 1 H-pyrrolo[3,2-h]quinoline (7) and a scheme of the photoinduced tau-tomerization leading from a normal form to a phototautomeric form [52, 61, 62]. (b) Structure of 7,8,9,10-tetrahydropyrido[2,3-o] carbazole (30) [52] and pyrido[2,3-o] car-bazole (31) [52]. (c) Fluorescence of 7, 30, and 31 (solid lines) and of the corresponding tautomeric model structures (dotted lines), shown as 7m, 30m, and 31 m. The...

See other pages where Phototautomeric fluorescence is mentioned: [Pg.284]    [Pg.301]    [Pg.284]    [Pg.301]    [Pg.586]    [Pg.131]    [Pg.95]    [Pg.501]    [Pg.586]    [Pg.195]    [Pg.16]    [Pg.372]    [Pg.586]    [Pg.195]    [Pg.13]    [Pg.173]    [Pg.586]    [Pg.501]    [Pg.305]    [Pg.323]    [Pg.333]    [Pg.334]    [Pg.263]    [Pg.49]    [Pg.52]    [Pg.53]    [Pg.65]    [Pg.95]   
See also in sourсe #XX -- [ Pg.1290 ]




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