Search results for "One-Pot synthesis"

showing 10 items of 44 documents

One-pot synthesis of ZnO nanoparticles supported on halloysite nanotubes for catalytic applications

2020

Abstract A versatile catalyst based on halloysite and zinc oxide (HNT@ZnO) was prepared, for the first time, starting from ZnO commercial bulk form as Zn precursor source, in a one-pot procedure. This strategy gives the possibility to obtain small ZnO nanoparticles loaded on the HNT surface without the use of inorganic salts which envisage the removal of undesired anions and therefore a calcination process at high temperature. It was found that the presence of halloysite improved the UV–vis spectral absorption ability of ZnO. The hybrid was successful used as photocatalyst for the methylorange and rhodamine B degradation. In addition, after eight consecutive cycles for the methylorange phot…

Materials scienceOne-pot synthesisNanoparticle020101 civil engineering02 engineering and technologyengineering.material7. Clean energyHalloysite0201 civil engineeringCatalysislaw.inventionchemistry.chemical_compoundGeochemistry and PetrologylawRhodamine BCalcinationPhotodegradationHalloysite nanotubes Zinc oxide Heterogeneous catalyst Photodegradation reaction Biodiesel productionGeologySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnologyChemical engineeringchemistryengineeringPhotocatalysis0210 nano-technologyApplied Clay Science
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Rapid one-pot synthesis of tapered star copolymers via ultra-fast coupling of polystyryllithium chain ends

2019

Highly efficient stoichiometric coupling of sterically hindered polystyryllithium (PS-Li) chain ends was achieved using tetra[3-(chloro-dimethylsilyl)propyl]silane (TCDMSPS) as the linking agent. Based on the disparate reactivities of isoprene (I, rI = 11.0) and styrene (S, rS = 0.049) in the anionic copolymerization in nonpolar media, poly(isoprene0.5-grad-styrene0.5) (P(I0.5-grad-S0.5)) tapered 4-arm star copolymers were synthesized in only two steps. The tapered 4-arm star copolymers (Mtargetedw = 40 to 160 kg mol−1) were synthesized with high star functionalities f (Mw,star/Mw,arm = 3.68–3.98), low dispersity (Đ = 1.06–1.15) and minimal residual precursor content (2–8 wt%), avoiding fra…

Materials sciencePolymers and PlasticsOrganic ChemistryDispersitySize-exclusion chromatographyOne-pot synthesisBioengineering02 engineering and technologyNuclear magnetic resonance spectroscopy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistrySilane0104 chemical sciencesStyrenechemistry.chemical_compoundchemistryPolymer chemistryCopolymerPolystyrene0210 nano-technologyPolymer Chemistry
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Generalized “one-pot” preparative strategy to obtain highly functionalized silica-based mesoporous spherical particles

2022

In this work we present a synthesis strategy for the preparation of Stöber-type mesoporous particles functionalized with inorganic species. The procedure is based on a combination of the Atrane and the Stöber methods. Both as a source of silicon and of the incorporated heteroelements (Fe, Zn, Al, Ti) the corresponding atrane complexes are used as hydrolytic reagents. These complexes are easily formed by reaction with triethanolamine. Mesoporosity is achieved using surfactant micelles as templates. Obtaining uniform spherical particles is achieved by optimizing the amount of water-ethanol in the reaction medium. The particle sizes have been modulated by controlling simple parameters such as …

Mechanics of Materialsone-pot synthesisfunctionalizationGeneral Materials ScienceGeneral Chemistrymesoporous silicaUNESCO::CIENCIAS TECNOLÓGICASCondensed Matter Physicssize modulationspherical particles
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Selective "one-pot" synthesis of functionalized cyclopentenones.

2012

Double addition (1,2-1,4) of vinyl magnesium bromide to squaric acid derivatives allows the preparation of polyoxygenated cyclopentenones (8) in a "one-pot" procedure. The reaction occurs through the intermediate formation of octatetraenes (6). Protonation of this latter intermediate at -78 °C with TFE occurs selectively at the vinyl CH(2) closer to the metallic centers. DFT studies of the cyclization step justify the observed diastereoselectivity.

Models MolecularMolecular StructureOrganic ChemistryOne-pot synthesisProtonationSquaric acidCyclopentanesCrystallography X-RayMetalchemistry.chemical_compoundchemistryCyclizationvisual_artMagnesium bromidevisual_art.visual_art_mediumOrganic chemistryQuantum TheoryThe Journal of organic chemistry
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Asymmetric Allylation/Ring Closing Metathesis: One-Pot Synthesis of Benzo-fused Cyclic Homoallylic Amines. Application to the Formal Synthesis of Ser…

2013

A one-pot asymmetric allylation/ring closing metathesis (RCM) sequence for the synthesis of cyclic homoallylic amines has been developed. A library of six- and seven-membered benzo-fused products has been synthesized in good yields and complete diastereoselectivity. The new methodology has been applied to the formal syntheses of the antidepressant Sertraline and the epimeric Norsertraline. The methodology is amenable for the synthesis of analogs.

Molecular StructureChemistryOrganic ChemistryOne-pot synthesisStereoisomerismStereoisomerismBiochemistryCatalysisFormal synthesisRing-closing metathesisSertralineOrganic chemistryAminesPhysical and Theoretical Chemistry
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One-pot synthesis of PbS NP/sulfur-oleylamine copolymer nanocomposites via the copolymerization of elemental sulfur with oleylamine

2014

A novel synthetic and processing strategy for converting elemental sulfur into polymeric and nanocomposite materials is reported. We describe a facile one-pot reaction using elemental sulfur and oleylamine as comonomers to prepare high sulfur content copolymers and lead sulfide nanoparticle (PbS NP) nanocomposites. This process enables the preparation of solution processable copolymers and nanocomposites, where the loading and dispersion of PbS NP inclusions could be precisely controlled. We demonstrate the dual roles of oleylamine with sulfur for both the copolymerization of sulfur copolymers as well as the in situ synthesis of PbS NPs in a one-pot fashion.

NanocompositeMaterials sciencePolymers and PlasticsOrganic ChemistryOne-pot synthesisNanoparticlechemistry.chemical_elementBioengineeringBiochemistrySulfurchemistry.chemical_compoundChemical engineeringchemistryOleylaminePolymer chemistryCopolymerLead sulfideDispersion (chemistry)Polymer Chemistry
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One-Pot Synthesis of Pyrrole-2-carboxylates and -carboxamides via an Electrocyclization/Oxidation Sequence

2014

An electrocyclic ring closure is the key step of an efficient one-pot method for the synthesis of pyrrole-2-carboxylates and -carboxamides from chalcones and glycine esters or amides. The 3,4-dihydro-2H-pyrrole intermediates generated in situ are oxidized to the corresponding pyrroles by stoichiometric oxidants or by catalytic copper(II) and air in moderate to high yields. A wide range of functional groups are tolerated, and further combination with an in situ bromination gives access to polyfunctional pyrrole scaffolds.

ProlineOrganic ChemistryOne-pot synthesischemistry.chemical_elementHalogenationEstersStereoisomerismStereoisomerismElectrochemistryRing (chemistry)Combinatorial chemistryCopperCatalysisCatalysischemistry.chemical_compoundchemistryCyclizationElectrochemistryPyrrolesOxidation-ReductionCopperPyrroleThe Journal of Organic Chemistry
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New reaction of 1H-pyrazoles with selenium dioxide: one-pot synthesis of bis(1H-pyrazol-4-yl)selenides

2010

Abstract A novel reaction between 3- and 3,5-substituted pyrazoles with selenium dioxide proceeds with formation of bis(3R,5R′-1H-pyrazol-4-yl)selenides in high yield. On this basis, an efficient one-pot synthetic procedure has been developed. In the case of the unsubstituted pyrazole a selenonium compound has been obtained. The identity and structure of the isolated selenium derivatives have been confirmed by spectral methods and their molecular structures investigated by X-ray analysis.

Reaction mechanismOrganic ChemistryOne-pot synthesischemistry.chemical_elementCrystal structurePyrazoleBiochemistryChemical synthesisMedicinal chemistrychemistry.chemical_compoundNucleophilechemistryYield (chemistry)Drug DiscoveryOrganic chemistrySeleniumTetrahedron
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Glucose as an Eco‐Friendly Reductant in a One‐Pot Synthesis of 2,3‐Dihydroquinazolin‐4(1 H )‐ones

2020

SUSTENTABILIDADEChemistryOrganic ChemistryOne-pot synthesisBiomassOrganic chemistryPhysical and Theoretical ChemistryEnvironmentally friendlyEuropean Journal of Organic Chemistry
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One-Pot Synthesis of (.+-.)-Crispine A and Its C-Ring-Substituted Analogues.

2006

StereochemistryChemistryOne-pot synthesisGeneral MedicineChemInform
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