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- W2093962621 abstract "Abstract Substitution of the phenyl group in 2‐hydroxychalcones by a 4‐pyridine unit dramatically changes the network of chemical reactions of this compound: trans ‐chalcone‐type ( Ct ), cis ‐chalcone‐type ( Cc ), and a hemiketal (hydroxy‐4‐pyridinechromene) ( B ) and their protonated forms are formed, but the presence of a flavylium‐type cation could not be detected even at very acidic pH values. Moreover, whereas in 2‐phenyl‐2‐benzopyrylium compounds B and Cc are generally elusive species whose kinetic processes in aqueous solutions occur on the sub‐second timescale, in the present compound these species equilibrate on a timescale four orders of magnitude lower. Complete characterization of the equilibrium and kinetics of the reaction network could thus be achieved by 1 H NMR spectroscopy and UV/Vis spectrophotometry. The network of chemical reactions exhibits cis – trans photoisomerization, as well as photochromism between the hemiketal and the chalcone‐type species. The irradiation of Ct in MeOH/H 2 O (1:1) at 365 nm produces B almost quantitatively through two consecutive photochemical reactions: Ct → Cc photoisomerization followed by Cc → B photo ring closure with a global quantum yield of 0.02. On the other hand, irradiation of B at 254 nm leads to a photostationary state composed by 80 % Ct and 20 % B , with a quantum yield of 0.21." @default.
- W2093962621 created "2016-06-24" @default.
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- W2093962621 date "2009-12-28" @default.
- W2093962621 modified "2023-10-18" @default.
- W2093962621 title "Hydroxypyridinechromene and Pyridinechalcone: Two Coupled Photochromic Systems" @default.
- W2093962621 cites W1965554479 @default.
- W2093962621 cites W1966638831 @default.
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- W2093962621 cites W1972155932 @default.
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- W2093962621 doi "https://doi.org/10.1002/chem.200901884" @default.
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