A Transient Absorption Spectrum Attributable to the Triplet-Triplet Transition of HCN

1984 ◽  
Vol 17 (8) ◽  
pp. 401-407 ◽  
Author(s):  
S. L. N. G. Krishnamachari ◽  
R. Venkatasubramanian
2003 ◽  
Vol 0 (7) ◽  
pp. 2606-2609
Author(s):  
M.-S. Nomura ◽  
M. Arita ◽  
S. Ashihara ◽  
S. Kako ◽  
M. Nishioka ◽  
...  

2018 ◽  
Vol 97 (3) ◽  
Author(s):  
Andrew Chew ◽  
Nicolas Douguet ◽  
Coleman Cariker ◽  
Jie Li ◽  
Eva Lindroth ◽  
...  

1992 ◽  
Vol 47 (12) ◽  
pp. 1243-1247 ◽  
Author(s):  
I. Timtcheva ◽  
N. Getoff ◽  
P. Nikolov ◽  
R. M. Quint

Steady state as well as flash photolysis experiments of 2-aryl-3-imino-1-indones (2-AIID) have been carried out with the aim to learn more about their photochemical properties. It was established that in ethanol these substances exist solely in the keto-enamine-form and are rather photostable under the influence of uv-light. Illumination in dichloroethane, acetonitrile and dioxane is leading to stable photoproducts. A typical transient absorption spectrum of 2-AIID is presented. Probable reaction mechanisms are given.


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