Resonance Raman intensity analysis of the excited-state proton transfer in 2-hydroxyacetophenone

1992 ◽  
Vol 96 (17) ◽  
pp. 6910-6916 ◽  
Author(s):  
Linda A. Peteanu ◽  
Richard A. Mathies
1983 ◽  
Vol 61 (5) ◽  
pp. 809-816 ◽  
Author(s):  
J. W. Lewis ◽  
C. Sandorfy

The infrared and resonance Raman spectra of the two long-lived forms of triphenylformazan and several of its derivatives have been examined. The spectra of unsymmetrically 15N-labelled derivatives suggest that two tautomers exist for each of the two forms. This observation is confirmed by the spectra of 1-(p-halophenyl)-3,5-diphenylformazans. The spectra of the non-chelate forms of these latter compounds demonstrate that the position of the tautomeric equilibrium is influenced by the electron-attracting ability of the para-halo-substituent. A comparison of the resonance Raman spectra of the two forms leads to the conclusion that excited state proton transfer is the initial photoevent in the photochromism of the triphenylformazans.


2016 ◽  
Vol 18 (20) ◽  
pp. 13874-13887 ◽  
Author(s):  
Sayan Mondal ◽  
Mrinalini Puranik

Instantaneous structural distortions of 6-chloroguanine in Bb electronic state from resonance Raman intensity analysis.


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