3 research outputs found

    New Chelating Ion-Exchange Resin Synthesized via the Cyclopolymerization Protocol and Its Uptake Performance for Metal Ion Removal

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    Azoisobutyronitrile-initiated cycloterpolymerization of [(diallylamino)­propyl]­phosphonic acid hydrochloride (90 mol %), cross-linker 1,1,4,4-tetraallylpiperazinium dichloride (10 mol %), and SO<sub>2</sub> (100 mol %) afforded a new pH-responsive cross-linked polyzwitterionic acid which, upon alkaline treatment, was transformed to a cross-linked dianionic polyelectrolyte (CDAPE). Chelating ion-exchange resin CDAPE was tested for the uptake of Pb<sup>2+</sup> and Cu<sup>2+</sup> ions; the adsorption process followed pseudo-second-order kinetics with respective <i>E</i><sub>a</sub> values of 13.4 and 13.8 kJ mol<sup>–1</sup>. The adsorption data fitted well to the Langmuir, Freundlich, and Temkin as well as Dubinin–Radushkevich isotherm models. The maximum uptakes of Pb<sup>2+</sup> and Cu<sup>2+</sup> were determined to be 3.83 and 10.1 mmol g<sup>–1</sup>, respectively. The scanning electron microscopy images and energy-dispersive X-ray spectroscopy analysis confirmed that the CDAPE adsorbed the metal ions on the surface as well as throughout the polymer. The negative Δ<i>G</i>° and positive Δ<i>H</i>° ensured the adsorption process as favorable and endothermic in nature. The excellent adsorption and desorption efficiencies demonstrated by the resin would enable its use for the removal of toxic metal ions from wastewater. A comparison of CDAPE with several other adsorbents in recent works ascertains the excellent efficiency of the current resin for the removal of toxic metal ions

    Enantioselective [4 + 2]-Annulation of Oxadienes and Allenones Catalyzed by an Amino Acid Derived Phosphine: Synthesis of Functionalized Dihydropyrans

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    An enantioselective [4 + 2]-annulation process between cyano-activated oxadienes and allenones is developed. An l-valine-derived phosphine was efficient in catalyzing the reaction, and a wide range of highly functionalized dihydropyrans were prepared in high yields and with excellent enantioselectivities
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