Acidity Dependence of the Tautomeric Equilibrium Between the First Conjugated Acids of 4-Aminoazobenzenes
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Acidity functions based upon primary anilines which have no ortho substituents have been established in 20% ethanol-80% aqueous sulfuric acid solutions, and compared with those based upon o-substituted anilines and azobenzenes. It was found that the tautomeric equilibrium between azonium and anilinium forms in 4-aminoazobenzene derivatives invariably shifts to the azonium form with increase in acidity. This observation has been interpreted in terms of acidity functions.
2005 ◽
Vol 152
(7)
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pp. E212
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1977 ◽
Vol 26
(3)
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pp. 621-623
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2005 ◽
Vol 5
(6)
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pp. 1577-1587
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1959 ◽
Vol 62
(12)
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pp. 1914-1918
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1963 ◽
Vol 85
(11)
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pp. 1555-1561
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