Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2005-04-01

1H NMR study of inclusion compounds of phenylurea derivatives in beta-cyclodextrin.

N Dupuy, D Barbry, M Bria, S Marquis, L Vrielynck, J Kister

Index: Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 61(6) , 1051-7, (2005)

Full Text: HTML

Abstract

Proton nuclear magnetic resonance spectroscopy ((1)H NMR), which has become an important tool for the study "in situ" of beta-cyclodextrin (beta-CD) complexes, was used to study and structurally characterize the inclusion complexes formed between beta-CD and isoproturon, fenuron, monuron and diuron. The high variation of the chemical shifts from the proton located inside the cavity (H-3, H-5 and H-6) coupled with the non variation of the one located outer sphere of the beta-CD (H-1, H-2 and H-4) provided clear evidence of the inclusion phenomena. Two-dimensional rotating frame Overhauser effect spectroscopy (ROESY) experiments were carried out to further support the proposed inclusion mode.