Characterization of the triplet charge-transfer state of 4-amino-N-methylphthalimide in aprotic and protic media by laser flash photolysis

1997 ◽  
Vol 93 (17) ◽  
pp. 2991-2996 ◽  
Author(s):  
Sanjukta Aich ◽  
Chitra Raha ◽  
Samita Basu
2006 ◽  
Vol 16 (2) ◽  
pp. 216-220 ◽  
Author(s):  
Hermenegildo García ◽  
Jose Manuel López-Nieto ◽  
Emilio Palomares ◽  
Heinz D. Roth ◽  
Benjamín Solsona

2018 ◽  
Vol 20 (30) ◽  
pp. 19819-19828
Author(s):  
Götz Bucher ◽  
Mukul Lal ◽  
Anup Rana ◽  
Michael Schmittel

Photolysis of a dioxolanyl Barton ester results in formation of the vinyloxy radical, via nonstatistical reaction dynamics. The nonstatistical reaction involves ester cleavage, CO2 loss and fragmentation of the intermediate dioxolanyl radical.


2015 ◽  
Vol 68 (11) ◽  
pp. 1707 ◽  
Author(s):  
H. Dushanee M. Sriyarathne ◽  
Kosala R. S. Thenna-Hewa ◽  
Tianeka Scott ◽  
Anna D. Gudmundsdottir

Laser flash photolysis of 2-methyl-1-phenylbut-3-en-1-one (1) conducted at irradiation wavelengths of 266 and 308 nm results in the formation of triplet 1,2-biradical 2 that has λmax at 370 and 480 nm. Biradical 2 is formed with a rate constant of 1.1 × 107 s–1 and decays with a rate constant of 2.3 × 105 s–1. Isoprene-quenching studies support the notion that biradical 2 is formed by energy transfer from the triplet-excited state of the ketone chromophore of 1. Density functional theory calculations were used to verify the characterization of triplet biradical 2 and validate the mechanism for its formation. Thus, it has been demonstrated that intramolecular sensitization of simple alkenes can be used to form triplet 1,2-biradicals with the two radical centres localized on the adjacent carbon atoms.


1989 ◽  
Vol 67 (5) ◽  
pp. 927-932 ◽  
Author(s):  
D. R. Boate ◽  
L. J. Johnston ◽  
J. C. Scaiano

Decafluorobenzophenone triplets, which have a triplet energy very close to that of benzophenone, are much more reactive than benzophenone in quenching reactions that involve hydrogen transfer and/or charge transfer. An excellent correlation has been observed between the rate constants for charge transfer quenching and the oxidation potential of the substrate. In the case of 2-propanol, where the reactivity can be fully accounted for by hydrogen transfer, decafluorobenzophenone is 35 times more reactive than benzophenone. Pentafluorobenzophenone shows intermediate behaviour. Keywords: laser photolysis, benzophenones, triplet states, charge transfer, photoreduction.


2016 ◽  
Vol 15 (3) ◽  
pp. 431-439 ◽  
Author(s):  
Ivan P. Pozdnyakov ◽  
Wei Ding ◽  
Jing Xu ◽  
Long Chen ◽  
Feng Wu ◽  
...  

An Fe(iii)–As(iii) complex was characterized by UV/Vis spectra and its laser flash photolysis via ligand-to-metal charge transfer resulted in the intermediate of Fe(ii)–As(iv).


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