Summary
The keto-enol tautomerism of the 2- and 3-isomers of thianaphthenoyltrifluoroacetone has been studied and the results explained by considering the relative negativities of the 2- and 3-position of thianaphthene. The results of the comparison of the keto-enol tautomerism of 3-thianaphthenoyltrifluoroacetone to that of 2-thenoyltrifluoroacetone in 80% benzene-20% ethanol may explain in part the greater sensitivity of the former in trace metal analysis.
Zusammenfassung
Die Keto-Enol-Tautomerie der 2- und 3-Isomeren des Thianaphthenoyltrifluoracetons wurde untersucht und mit der relativen Negativität der 2- und 3-Stellung des Thianaphtens zu erklären versucht. Der Vergleich der Keto-Enol-Tautomerie von II mit der des 2-Thenoyltrifluoracetons in BenzolÄthanol (80+20) könnte eine Erklärung für die größere Sensitivität von II bei der Spurenmetallanalyse bieten.
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Johnston, J.R., Holland, W.J. Thianaphthenoyltrifluoroacetone as an analytical reagent: The keto-enol tautomerism of the 2- and 3-isomers of thianaphthenoyltrifluoroacetone. Mikrochim Acta 60, 763–767 (1972). https://doi.org/10.1007/BF01239143
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DOI: https://doi.org/10.1007/BF01239143