The assignment of the absorption spectra of 2-hydroxytropone (2-HT) is reported by measuring the circular dichroism spectra of the &cycIodextrin complexes \vith 2-HT and 2-H-f anion It is concluded that the fEst (270-400 nm) and second (210-270 MI) bands of 2-HT are respectively composed of two elec
Improvement of the desorption of the pesticide 2,4-D via complexation with HP-β-cyclodextrin
✍ Scribed by José I Pérez-Martínez; Juan M Ginés; Esmeralda Morillo; María L González-Rodríguez; José R Moyano Méndez
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 184 KB
- Volume
- 56
- Category
- Article
- ISSN
- 1526-498X
No coin nor oath required. For personal study only.
✦ Synopsis
Inclusion complex formation of 2,4-dichlorophenoxyacetic acid (2,4-D) with hydroxypropylb-cyclodextrin (HP-b-CD) has been proposed as a way of modifying the behaviour of the pesticide in the soil environment. The present study assesses the effect of complex formation on 2,4-D physicochemical properties (aqueous solubility, crystallinity and dissolution rate) and its behaviour on soils.
The solid complexes were prepared using different methods (spray drying, kneading and heating in a sealed container). To con®rm the complex formation in the solid state differential scanning calorimetry, hot stage microscopy and x-ray diffraction techniques were employed. Complex formation in solution was studied by phase solubility. The presence of HP-b-CD increased the 2,4-D solubility nine times approximately. The apparent stability constant was determined as 98.6 M À1 . The dissolution rates of the 2,4-D/HP-b-CD complexes were examined and compared with that of the pure pesticide. The results indicated that the complex may have great utility as a rapid way of dissolving the pesticide. Batch experiments were performed to study the adsorption±desorption of 2,4-D on soils and the in¯uence of the HP-b-CD over these processes. The results showed that HP-b-CD could increase the desorption of 2,4-D previously adsorbed on soils.
📜 SIMILAR VOLUMES
The crystal of the 1: 1 complex of cyclomaltoheptaose (p-cyclodextrin, PCD) with 4-tert-butylbenzoic acid is triclinic Pl with a = 18.244(3), b = 15.476(3), c = 15.417(2) A; (Y = 102.94(l), p = 113.08(l), y = 99.69(2)"; V = 3740(l) As; and Z = 2. The final R was determined to be 0.0932 for 8111 obse
Molecular mechanics calculations were employed to study the inclusion of 2-methyl naphthoate in alpha- and beta-cyclodextrin in vacuo and in the presence of water as a solvent. The driving forces for complexation are dominated by nonbonded van der Waals host:guest interactions in both environments.
Phase-solubility techniques were used to assess the effect of pH on itraconazole complexation with 2-hydroxypropyl-beta-cyclodextrin (HPbetaCD). In addition, molecular modeling using beta-cyclodextrin as a surrogate for HPbetaCD was completed. Data suggested A(p)-type solubility relationships, indic
A diastereomeric mixture of iloprost (16R: 16s = 55 :45) was co-crystallized with cyclomaltoheptaose (P-cyclodextrin, PCD) from aqueous solution as the complex (P-cyclodextrin),\*iloprost 020.5 H,O. The crystals are triclinic Pl; a = 15.474(10), b = 15.446(10), c = 18.081(10) A, (Y = 99.40(3); p = 1