Search results for "GELATORS"

showing 6 items of 6 documents

Synthesis of fluorinated oxadiazoles with gelation and oxygen storage ability

2012

A new family of fluorinated low molecular weight (LMW) gelators has been synthesized through SNAr substitution of 5-polyfluoroaryl-3-perfluoroheptyl-1,2,4-oxadiazoles with glycine ester. The obtained compounds give thermal and pH-sensitive hydrogels or thermo-reversible organogels in DMSO. Oxygen solubility studies showed the ability to maintain high oxygen levels in solution and in gel blend with plate counter agar (PCA).

HalogenationOxygen storageGlycinechemistry.chemical_elementBiochemistryPhase TransitionNucleophilic aromatic substitutionOrganic chemistryDimethyl SulfoxidePhysical and Theoretical ChemistrySolubilityOxadiazolesHydrogen bondChemistryOrganic ChemistryHalogenationEstersHydrogen BondingFluorineSettore CHIM/06 - Chimica OrganicaHydrogen-Ion ConcentrationMolecular WeightOxygenSolubilityGlycineSelf-healing hydrogelsFluorineMicroscopy Electron Scanninglow molecular weight gelators(LMWG) oxadiazoles fluorinated compounds oxgyen carriersThermodynamicsGels
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Synthesis of new fluorinated low molecular weight (LMW) gelators

2011

Oxadiazoles fluorinated compounds LMW gelators organogels hydrogelsSettore CHIM/06 - Chimica Organica
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A coumarin based gold(i)-alkynyl complex: a new class of supramolecular hydrogelators.

2014

A phosphine-gold(I)-alkynyl-coumarin complex, [Au{7-(prop-2-ine-1-yloxy)-1-benzopyran-2-one}(DAPTA)] (1), was synthesized and the formation of long luminescent fibers in solution was characterized via fluorescence microscopy and dynamic light scattering. The fibers presented strong blue and green luminescence, suggesting that the gold(I) in the complex increased intersystem crossing due to the heavy atom effect, resulting in a significant increase in triplet emission. The X-ray structure of the fibers indicates that both aurophilic, π–π interactions and hydrogen bonding contribute to their formation in aqueous solvents.

PhotoluminescenceAqueous solutionChemistryHydrogen bondOrganic ChemistrySupramolecular chemistryPhotochemistryBiochemistrycoumarin basedMetalIntersystem crossingDynamic light scatteringvisual_artgold(I)-alkynyl complexvisual_art.visual_art_mediumPhysical and Theoretical ChemistryhydrogelatorsLuminescenceta116supramolecularOrganicbiomolecular chemistry
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Subcomponent Self-Assembly A Quick Way to New Metallogels

2013

Subcomponent self-assembly, introduced by the Nitschke group,[1] is a process which allow complex structures to be generated from simple building blocks (generally aldehydes and amines). In this bottom-up approach, the building blocks spontaneously self-assemble around templates (usually metal ions) leading to a simultaneous covalent (C=N) and dative (N– metal) bonds formation. The method has been successfully used to construct well-defined metal-organic macrocycles, helicates, catenanes, rotaxanes, grids,[2] and cages.[3] Our field of interest lies not in building-up of defined structures but in designing gelator molecules for a formation of supramolecular gels as functional nanomaterials.…

SUPRAMOLECULAR GELSMetal ions in aqueous solutionta221GELATORSSupramolecular chemistryNanoparticleNanotechnologymetallogeelimultistimuli responsive010402 general chemistrySmart material01 natural sciencesCatalysisMOLECULESMoleculeta116ta218ta214ta114010405 organic chemistryChemistryIN-SITUOrganic ChemistryGeneral Chemistryself-assemblygelsGELATION0104 chemical sciencesin situ gelationMETALnanoparticlesSelf-assemblymetallogelCHEMISTRY: A EUROPEAN JOURNAL
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A coumarin based gold(I)-alkynyl complex: a new class of supramolecular hydrogelators

2015

A phosphine-gold(I)-alkynyl-coumarin complex, [Au{7-(prop-2-ine-1-yloxy)-1-benzopyran-2-one}- (DAPTA)] (1), was synthesized and the formation of long luminescent fibers in solution was characterized via fluorescence microscopy and dynamic light scattering. The fibers presented strong blue and green luminescence, suggesting that the gold(I) in the complex increased intersystem crossing due to the heavy atom effect, resulting in a significant increase in triplet emission. The X-ray structure of the fibers indicates that both aurophilic, π–π interactions and hydrogen bonding contribute to their formation in aqueous solvents. peerReviewed

gold(I)-alkynyl complexhydrogelatorscoumarin basedsupramolecular
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Solid state NMR studies of gels derived from low molecular mass gelators

2016

solid state NMRmass gelatorsgelsta116Soft Matter
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