The role of the molecular environment for the primary photoprocesses of phenol in solution

1980 ◽  
Vol 58 (19) ◽  
pp. 2006-2010 ◽  
Author(s):  
J. Zechner ◽  
G. Köhler ◽  
G. Grabner ◽  
N. Getoff

Quantum yields of fluorescence as well as of solvated electron and H atom formation have been measured for phenol in several pure solvents and mixtures of varying polarity. The influence of excitation energy has been studied by excitation of phenol in the first and second excited singlet states. The solvent dependences of fluorescence and photoejection parameters are strongly correlated. The results are interpreted in terms of specific solute–solvent interactions, in particular H-bonded structures.


1985 ◽  
Vol 107 (10) ◽  
pp. 2831-2837 ◽  
Author(s):  
A. Maciejewski ◽  
D. R. Demmer ◽  
D. R. James ◽  
A. Safarzadeh-Amiri ◽  
R. E. Verrall ◽  
...  


1985 ◽  
Vol 16 (42) ◽  
Author(s):  
A. MACIEJEWSKI ◽  
D. R. DEMMER ◽  
D. R. JAMES ◽  
A. SAFARZADEH-AMIRI ◽  
R. E. VERRALL ◽  
...  


2000 ◽  
Vol 112 (15) ◽  
pp. 6603-6607 ◽  
Author(s):  
Yasushi Nomura ◽  
Takashi Miyamoto ◽  
Toshiki Hara ◽  
Susumu Narita ◽  
Tai-ichi Shibuya


1989 ◽  
Vol 44 (12) ◽  
pp. 1585-1588 ◽  
Author(s):  
Wojciech Boszczyk ◽  
Tadeusz Latowski

Interactions were studied of aniline, 4-methoxyaniline and 4-ethoxyaniline with tetrachloromethane, chloroform and dichloromethane in their ground and first excited singlet states. Stability constants of the complexes of these amines with the chloromethanes in cyclohexane were determined as well as their quantum yields of fluorescence in this solvent. The quenching of fluorescence of aniline and its derivatives by the chloromethanes was ascertained and characterized. Quantum yields of the formation of hydrogen chloride, ψΗCl, were measured during photochemically induced reaction of the amines in tetrachloromethane, chloroform and dichloromethane.



1960 ◽  
Vol 38 (2) ◽  
pp. 233-239 ◽  
Author(s):  
Robin M. Hochstrasser

The relative fluorescence and/or phosphorescence yields of a number of methyl- and halogeno-quinolines, isoquinolines, and acridines have been measured as a function of the wavelength of the exciting light. In all cases the solvent was absolute ethanol. The results show that the efficiency of internal conversion processes between excited singlet states is extremely high in comparison to other intramolecular steps. The effect of substituted heavy atoms is discussed, as well as the fluorescence of the conjugate acids of the bases.





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