The Photoinduced Hydrogen Atom Transfer andtrans–cisIsomerization of the C=C Double Bond in 1-(1-Hydroxy-2-naphthyl)-3-(1-naphthyl)-2-propen-1-one and Related Compounds Studied Using Nanosecond Time-Resolved Infrared Spectroscopy

2004 ◽  
Vol 77 (8) ◽  
pp. 1529-1535 ◽  
Author(s):  
Kaoru Kaneda ◽  
Shin Sato ◽  
Hiro-o Hamaguchi ◽  
Tatsuo Arai
2005 ◽  
Vol 127 (45) ◽  
pp. 15684-15685 ◽  
Author(s):  
Jie Zhang ◽  
David C. Grills ◽  
Kuo-Wei Huang ◽  
Etsuko Fujita ◽  
R. Morris Bullock

2003 ◽  
Vol 107 (40) ◽  
pp. 8239-8250 ◽  
Author(s):  
H. Lippert ◽  
V. Stert ◽  
L. Hesse ◽  
C. P. Schulz ◽  
I. V. Hertel ◽  
...  

2007 ◽  
Vol 20 (11) ◽  
pp. 864-871 ◽  
Author(s):  
Yousuke Azechi ◽  
Keiko Takemura ◽  
Yoshihiro Shinohara ◽  
Yoshinobu Nishimura ◽  
Tatsuo Arai

2015 ◽  
Vol 17 (7) ◽  
pp. 4888-4898 ◽  
Author(s):  
Igor Reva ◽  
Maciej J. Nowak ◽  
Leszek Lapinski ◽  
Rui Fausto

The photochemistry of thiophenol monomers confined in cryogenic argon matrices is dominated by hydrogen atom transfer reactions and leads to the formation of two new thione isomers, which were characterized in this work by infrared spectroscopy and theoretical calculations.


1985 ◽  
Vol 63 (4) ◽  
pp. 944-950 ◽  
Author(s):  
Guy J. Collin ◽  
Hélène Deslauriers

The photolysis of cis-3-hexene and 4-methyl-cis-2-pentene has been studied at 147.0 and 184.9 nm. The fragmentation pattern of the photoexcited molecule is normal: it requires, mainly, the split of a C—C bond located in the β position relative to the double bond [Formula: see text]. Some α(C—C), β(C—H), and α(C—H) primary splits complete this mechanism. The formation of α-ethallyl and α,γ-dimethallyl radicals is important in 3-hexene and 4-methyl-2-pentene, respectively. An isomerization process, involving these two radicals, is necessary to explain the formation of part of the 1,3-pentadiene in the 3-hexene system and of all the 1,3-butadiene in the 4-methyl-2-pentene system. This process involves a 1,4-hydrogen atom transfer.


1988 ◽  
Vol 24 (3) ◽  
pp. 314-319
Author(s):  
Yu. P. Tsentalovich ◽  
A. A. Obynochnyi ◽  
M. V. Burlov ◽  
R. Z. Sagdeev ◽  
P. Burkhard

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