Keto-enol tautomerization of 2-(2'-hydroxyphenyl)benzoxazole and 2-(2'-hydroxy-4'-methylphenyl)benzoxazole in the triplet state: hydrogen tunneling and isotope effects. Transient absorption kinetics

1991 ◽  
Vol 95 (25) ◽  
pp. 10503-10509 ◽  
Author(s):  
Wajih Al-Soufi ◽  
Karl H. Grellmann ◽  
Bernhard Nickel
1991 ◽  
Vol 95 (25) ◽  
pp. 10509-10518 ◽  
Author(s):  
Heike Eisenberger ◽  
Bernhard Nickel ◽  
A. Andreas Ruth ◽  
Wajih Al-Soufi ◽  
Karl H. Grellmann ◽  
...  

1977 ◽  
Vol 32 (3) ◽  
pp. 285-288 ◽  
Author(s):  
Klaus-Peter Zeller ◽  
Günther Gauglitz

The photochemical cyclisation of diphenylether to dibenzofuran is scavenged by trans-1,3-pentadiene indicating that the triplet state of the ether is the reactive species. The intramolecular, kinetic isotope effects kʜ/kᴅ for the cyclisation of 2-deuteriodiphenyl ether and 1-phenoxy-4-pentadeuteriophenoxy-benzene are 1.12 ± 0.05 and 1.19 ± 0.05, respectively. A reaction scheme consisting of a photochemical cyclisation to 1 a, 9 a-dihydrodi-benzofuran followed by dehydrogenation to dibenzofuran is suggested.


2015 ◽  
Vol 14 (2) ◽  
pp. 407-413 ◽  
Author(s):  
Martín F. Broglia ◽  
Carlos M. Previtali ◽  
Sonia G. Bertolotti

The interaction of the triplet state of the synthetic dye phenosafranine (3,7-diamino-5-phenylphenazinium chloride) with indolic compounds of biological relevance was investigated in water by means of laser flash photolysis.


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