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

被引:25
作者
Dupuy, N
Barbry, D
Bria, M
Marquis, S
Vrielynck, L
Kister, J
机构
[1] Univ Aix Marseille 3, GOAE, UMR 6171, F-13397 Marseille, France
[2] Univ Sci & Tech Lille Flandres Artois, Chim Organ Lab, F-59655 Villeneuve Dascq, France
[3] Univ Sci & Tech Lille Flandres Artois, Serv Commun RMN, F-59655 Villeneuve Dascq, France
[4] Univ Sci & Tech Lille Flandres Artois, Ctr Etudes & Rech Lasers & Applicat, Lab Spectrochim Infrarouge & Raman, UMR 8516, F-59655 Villeneuve Dascq, France
关键词
NMR; isoproturon; monuron; diuron; fenuron; inclusion;
D O I
10.1016/j.saa.2004.04.031
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Proton nuclear magnetic resonance spectroscopy (H-1 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 3-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. (c) 2004 Published by Elsevier B.V.
引用
收藏
页码:1051 / 1057
页数:7
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