betadex and fenuron

betadex has been researched along with fenuron* in 1 studies

Other Studies

1 other study(ies) available for betadex and fenuron

Article	Year
1H NMR study of inclusion compounds of phenylurea derivatives in beta-cyclodextrin. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2005, Volume: 61, Issue:6 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. Topics: beta-Cyclodextrins; Diuron; Magnetic Resonance Spectroscopy; Methylurea Compounds; Molecular Structure; Phenylurea Compounds	2005

Article

Year

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

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2005, Volume: 61, Issue:6

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.

Topics: beta-Cyclodextrins; Diuron; Magnetic Resonance Spectroscopy; Methylurea Compounds; Molecular Structure; Phenylurea Compounds

2005