Predicted geometries of porphyrin excited states and radical cations and anions

1991 ◽  
Vol 95 (24) ◽  
pp. 9728-9736 ◽  
Author(s):  
Kristine Prendergast ◽  
Thomas G. Spiro
1994 ◽  
Vol 23 (8) ◽  
pp. 1371-1374 ◽  
Author(s):  
Yasunao Kuriyama ◽  
Fumiko Hashimoto ◽  
Masahiro Tsuchiya ◽  
Hirochika Sakuragi ◽  
Katsumi Tokumaru

1995 ◽  
Vol 236 (1-2) ◽  
pp. 167-176 ◽  
Author(s):  
M.P. Fülscher ◽  
S. Matzinger ◽  
T. Bally

2020 ◽  
Author(s):  
Shangze Wu ◽  
Jonas Zurauskas ◽  
Michal Domanski ◽  
Patrick Hitzfeld ◽  
Valeria Butera ◽  
...  

<p>Electrochemically-mediated Photoredox Catalysis emerged as a powerful synthetic technique in recent years, overcoming fundamental limitations of electrochemistry and photoredox catalysis in the single electron transfer activation of small organic molecules. However, the mechanism of how photoexcited radical ion species with ultrashort (picosecond-order) lifetimes could ever undergo productive photochemistry has eluded synthetic chemists. We report tri(<i>para</i>-substituted)biarylamines as a tunable class of electroactivated photocatalysts that become superoxidants in their photoexcited states, even able to oxidize molecules (such as dichlorobenzene and trifluorotoluene) beyond the solvent window limits of cyclic voltammetry. Furthermore, we demonstrate that precomplexation not only permits the excited state photochemistry of tris(<i>para</i>-substituted)biarylaminium cations, but enables and rationalizes the surprising photochemistry of their <i>higher-order</i> doublet (D<i><sub>n</sub></i>) excited states.</p>


2009 ◽  
Vol 131 (14) ◽  
pp. 144311 ◽  
Author(s):  
Jan Hendrik Starcke ◽  
Michael Wormit ◽  
Andreas Dreuw

1984 ◽  
Vol 106 (14) ◽  
pp. 3927-3933 ◽  
Author(s):  
Thomas Bally ◽  
Stephan Nitsche ◽  
Kuno Roth ◽  
Edwin Haselbach

1986 ◽  
pp. 248-265 ◽  
Author(s):  
Dongho Kim ◽  
Lisa Miller ◽  
Oliver Su ◽  
James Terner ◽  
Thomas G. Spiro

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