133708-14-2Relevant academic research and scientific papers
Substituent Effect of 1,4-Benzenedicarbonitriles as Sensitizers on the Photoinduced Electron Transfer Reactions in Alcohol
Suzuki, Masanori,Ikeno, Taketo,Osoda, Kazuhiko,Narasaka, Koichi,Suenobu, Tomoyoshi,Fukuzumi, Shunichi,Ishida, Akito
, p. 2269 - 2277 (1997)
In the photosensitized electron transfer reaction of 6,6-diphenyl-1,4-dioxaspiro[4.5]decane in methanol (MeOH), the quantum yield is increased by the use of 2-methylbenzene-1,4-dicarbonitrile (2-methyl-BDC) or 2,5-dirnethylbenzene-1,4-dicarbonitrile (2,5-
1,n-Radical ions. Photosensitized (electron transfer) carbon-carbon bond cleavage. Formation of 1,6-radical cations
Arnold, Donald R.,Lamont, Laurie J.,Perrott, Allyson L.
, p. 225 - 233 (2007/10/02)
The reactivity of the radical cations of methyl 2,2-diphenylcyclohexyl ether (7), 6,6-diphenyl-1,4-dioxaspirodecane (8), methyl cis- and trans-2-phenylcyclohexyl ether (9cis and trans), and 6-phenyl-1,4-dioxaspirodecane (10), generated by photos
