Azo dyes containing the quinoxaline nucleus. II. Their preparation and spectroscopic studies

1972 ◽  
Vol 314 (1) ◽  
pp. 15-23 ◽  
Author(s):  
Sayed Sherif ◽  
R. M. Issa ◽  
S. S. Aggour
ChemInform ◽  
2015 ◽  
Vol 46 (17) ◽  
pp. no-no
Author(s):  
M. A. Rauf ◽  
S. Hisaindee ◽  
N. Saleh

RSC Advances ◽  
2015 ◽  
Vol 5 (23) ◽  
pp. 18097-18110 ◽  
Author(s):  
M. A. Rauf ◽  
S. Hisaindee ◽  
N. Saleh

Keto–enol tautomeric equilibrium of an azo dye is shifted to the keto form as the solvent polarity is increased.


ChemInform ◽  
2010 ◽  
Vol 29 (38) ◽  
pp. no-no ◽  
Author(s):  
Y. M. ISSA ◽  
W. F. EL-HAWARY ◽  
M. E. MOUSTAFA ◽  
M. REFAAT

2013 ◽  
Vol 187 ◽  
pp. 43-48 ◽  
Author(s):  
Nosrat O. Mahmoodi ◽  
Meysam Pasandideh Nadamani ◽  
Tahereh Behzadi

RSC Advances ◽  
2015 ◽  
Vol 5 (82) ◽  
pp. 67165-67167 ◽  
Author(s):  
Liudmil Antonov ◽  
Poul Erik Hansen ◽  
Gert van der Zwan

The paper mentioned in the title contains inaccuracies and misleading interpretations that misrepresent basic knowledge about tautomerism in azo dyes. This Letter gives a better understanding of the basic principles of the tautomerisation process.


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