Chinese Journal of Magnetic Resonance ›› 1999, Vol. 16 ›› Issue (6): 559-562.

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1H NMR STUDIES OF 2, 3, 6-TRI-O-METHYLATED β-CYCLODEXTRIN INCLUSION-COMPLEXES WITH SUBSTITUTED PHENOLS

YIN Kailiang1, XU Duanjun2, XU Yuanzhi2   

  1. 1. Department of Chemical Engineering, Jiangsu institute of Petrochemical Technology, Changzhou 213016;
    2. Department of Chemistry, Zhejiang University, Hangzhou 310027
  • Received:1999-07-12 Revised:1999-09-06 Published:1999-12-05 Online:2018-01-13

Abstract: In this paper we report on the result of study on aqueous solution of inclusion-complexesof host 2, 3, 6-tri-O-methylated β-Cyclodextrin with guest hydroquinone and cresols by 1HNMR spectroscopy. The study shows that every four different substituted phenol can bebond by the host through inserting into the host hydrophobic cavity, and the correspondingbinding constant in aqueous solution can be calculated according to the relation betweenchemical shift changes of the host methoxyl protons and the concentration changing of thehost and different guests.

Key words: 2,3,6-tri-O-methylated β-Cyclodextrin, Hydroquinone, Cresols, 1H NMR, Inclusion-complexion, Binding constant