Chem. J. Chinese Universities ›› 1990, Vol. 11 ›› Issue (4): 376.

• Articles • Previous Articles     Next Articles

Study on Intramolecular Hydrogen-Bonding and Keto-Enol Tautomerism of Some Asymmetrical β-Diketones by1H NMR

Zhang Benli, Zhuo Jincong, Gui Mingde, Gao Zhenheng   

  1. Department of Chemistry, Nankai University, Tianjin
  • Received:1988-12-02 Online:1990-04-24 Published:1990-04-24

Abstract: The intramolecular hydrogen-bonding and keto-enol tautomerism of a series of 1-aryl-3-tolyl-1,3-propanediones were studied by 1H NMR. Both δOHand lgK(K=[enol]/[keto]) can be correlated with substituent constants satisfactorily. +1 and +Rsubstituents enhance the hydrogenbond-ing and decrease the content of enol form.

Key words: β-Dlketone, Hydrogen-bonding, Keto-enol tautomerism

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