Quantum yields for the sensitized photoisomerization of cis- and trans-stilbene

1969 ◽  
Vol 91 (18) ◽  
pp. 5180-5181 ◽  
Author(s):  
Howell A. Hammond ◽  
D. E. DeMeyer ◽  
Jack L. R. Williams
1970 ◽  
Vol 3 (6) ◽  
pp. 711-715 ◽  
Author(s):  
H. A. Hammond ◽  
J. C. Doty ◽  
T. M. Laakso ◽  
J. L. R. Williams
Keyword(s):  

1979 ◽  
Vol 71 (7) ◽  
pp. 2892 ◽  
Author(s):  
Keitaro Yoshihara ◽  
Akira Namiki ◽  
Minoru Sumitani ◽  
Nobuaki Nakashima

1991 ◽  
Vol 69 (1) ◽  
pp. 146-150 ◽  
Author(s):  
M. Hamity ◽  
R. H. Lema

The photolyses of electron donor–acceptor (EDA) complexes formed between both cis-stilbene (cS) and trans-stilbene (tS) as donors and mefhylviologen (MV+2) as acceptor have been carried out in homogeneous ethanolic and in micellar sodium dodecyl sulfate (SDS) solutions, in the presence of oxygen. The stilbene loss quantum yields (Φ−S) have been determined in both media. Quantum yields were observed to be dependent upon methylviologen concentration and the acidity of media. A reaction scheme is proposed, which accounts for experimental results and can be related to the photochemistry of MV+2 and its cation radical MV•+. Key words: EDA complexes, micelles, methyl viologen, stilbene.


1976 ◽  
Vol 7 (30) ◽  
pp. no-no
Author(s):  
SHIGENOBU NAKAYAMA ◽  
MASAAKI YOSHIFUJI ◽  
RENJI OKAZAKI ◽  
NAOKI INAMOTO
Keyword(s):  

1984 ◽  
Vol 106 (21) ◽  
pp. 6459-6459
Author(s):  
Jack Saltiel ◽  
Gary Marchand ◽  
Ewa Kirkor-Kaminska ◽  
William Smothers ◽  
Warren Mueller ◽  
...  

1967 ◽  
Vol 32 (11) ◽  
pp. 3726-3726
Author(s):  
Robert Buckles ◽  
James Miller ◽  
Roland Thurmaier

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