Chem. J. Chinese Universities ›› 1988, Vol. 9 ›› Issue (2): 140.

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Study on the Kinetics of β-Cyclodextrin-Catalyzed Hydrolysis of Phenolic Esters Containing a Ferrocenyl Group——A Probe to the Substituent Effects

Zhang Daodao, Liang Guibai   

  1. Department of Chemistry, Fudan University, Shanghai
  • Received:1986-09-10 Online:1988-02-24 Published:1988-02-24

Abstract: In this work, we have determined the pKα valuc of 4-nitro-2, 3, 5, 6-tetrafl-uorophenol and studied the relationship between pKα and the acceleration rales of β-cyclodextrin-catalyzed hydrolysis of subslituled phcnyl esters of trans-fcrrocenc-acrylic acid and ferrocenylcyclopropanccarboxylic acid.It has been found that the acceleration rates are dependent on the electronic nature of the substituents. It obeys Hammett linear free-energy relationship since the phcnyl. groups of subslratcs do not enter but the fcrroccnyl groups enter the cavities of the β-cyclodextrin.

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