Search results for "polymerization"

showing 10 items of 1689 documents

Influence of theZ/EIsomerism on the Pathway Complexity of a Squaramide‐Based Macrocycle

2020

The rising interest on pathway complexity in supramolecular polymerization has prompted the finding of novel monomer designs able to stabilize kinetically trapped species and generate supramolecular polymorphs. In the present work, the exploitation of the Z/E (geometrical) isomerism of squaramide (SQ) units to produce various self-assembled isoforms and complex supramolecular polymerization pathways in methylcyclohexane/CHCl3 mixtures is reported for the first time. This is achieved by using a new bissquaramidic macrocycle (MSq) that self-assembles into two markedly different thermodynamic aggregates, AggA (discrete cyclic structures) and AggB (fibrillar structures), depending on the solven…

Supramolecular chemistry02 engineering and technology010402 general chemistry01 natural sciencesPolymerizationBiomaterialschemistry.chemical_compoundIsomerismSpectroscopy Fourier Transform InfraredGeneral Materials ScienceConformational isomerismchemistry.chemical_classificationQuinineHydrogen bondSquaramideHydrogen BondingGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSupramolecular polymersCrystallographyMonomerPolymerizationchemistryMethylcyclohexane0210 nano-technologyBiotechnologySmall
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A Stereochemically Driven Supramolecular Polymerisation

2018

Anthracyclines self-assemble in water into dimers. In the presence of sufficiently high salt (NaCl) concentrations, solutions of the antibiotic doxorubicin, but not those of the closely related molecules daunomycin and epirubicin, turn into gels barely compatible with the presence of small oligomers. The use of spectroscopic, scattering, imaging and computational techniques, allowed light to be shed on the self-assembly process that triggered doxorubicin gelification. A complex picture emerged, with doxorubicin molecules assembled into long, highly chiral, supramolecular aggregates made of hundreds of units, showing redshifted fluorescence spectra, very short fluorescence lifetimes and smal…

Supramolecular chemistry02 engineering and technology010402 general chemistryPhotochemistrydoxorubicin01 natural sciencesCatalysisTurn (biochemistry)chemistry.chemical_compoundMolecular dynamicsanthracyclines; doxorubicin; fluorescence; circular dichroism; SAXS; molecular dynamicsMoleculeanthracyclinesScatteringOrganic ChemistrySAXSGeneral Chemistry021001 nanoscience & nanotechnologyFluorescencemolecular dynamicscircular dichroism0104 chemical sciencesMonomerchemistryPolymerizationfluorescence0210 nano-technologyChemistry - A European Journal
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Synthesis, structural studies and reactivity of vanadium complexes with tridentate (OSO) ligand

2007

The direct reaction between [VCl3(thf)3] or [VO(OEt)3] and 2,2′-thiobis{4-(1,1,3,3-tetramethyl-butyl)phenol (tbopH2) leads to the formation of [V2(µ-tbop-κ3O,S,O)2Cl2(CH3CN)2] (1)·4CH3CN or [V2(µ-OEt)2(O)2(tbop-κ3O,S,O)2] (2), respectively, in high yield. Compounds 1 and 2 were characterized by chemical and physical techniques including X-ray crystallography and variable temperature magnetic susceptibility studies (J = −29.1 cm−1) for 1. Complexes 1 and 2 were supported on MgCl2 and when activated with aluminium alkyls, were found to effectively polymerize ethene to produce polyethylene with a narrow molecular weight distribution Mw/Mn ∼ 3.

Synthesis (chemical)ComplexationX ray crystallographyPolyethylenesPolymerizationThermal effectsDalton Transactions
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Oxadiazolyl-Pyridinium as Cationic Scaffold for Fluorinated Ionic Liquid Crystals

2021

The synthesis and characterization of a new class of 1,2,4-oxadiazolylpyridinium as a cationic scaffold for fluorinated ionic liquid crystals is herein described. A series of 12 fluorinated heterocyclic salts based on a 1,2,4-oxadiazole moiety, connected through its C(5) or C(3) to an N-alkylpyridinium unit and a perfluoroheptyl chain, differing in the length of the alkyl chain and counterions, has been synthesized. As counterions iodide, bromide and bis(trifluoromethane)sulfonimide have been considered. The synthesis, structure, and liquid crystalline properties of these compounds are discussed on the basis of the tuned structural variables. The thermotropic properties of this series of sa…

TechnologyQH301-705.5QC1-999heterocyclicThermotropic crystalSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni Culturaliionic liquidsfluorinated saltsmesogenschemistry.chemical_compoundliquid crystalsLiquid crystalBromidePolymer chemistryMoietyGeneral Materials ScienceBiology (General)QD1-999InstrumentationAlkylFluid Flow and Transfer Processeschemistry.chemical_classificationTPhysicsProcess Chemistry and TechnologyGeneral EngineeringCationic polymerizationSettore CHIM/06 - Chimica OrganicaEngineering (General). Civil engineering (General)Computer Science ApplicationsChemistrychemistryddc:540Ionic liquidPyridiniumTA1-2040Applied Sciences
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Correction: Mechanical properties of provisional dental materials: A systematic review and meta-analysis.

2018

Provisional restorations represent an important phase during the rehabilitation process, knowledge of the mechanical properties of the available materials allows us to predict their clinical performance. At present, there is no systematic review, which supports the clinicians’ criteria, in the selection of a specific material over another for a particular clinical situation. The purpose of this systematic review and meta-analysis was to assess and compare the mechanical properties of dimethacrylates and monomethacrylates used in fabricating direct provisional restorations, in terms of flexural strength, fracture toughness and hardness. This review followed the PRISMA guidelines. The searche…

TeethComputer sciencePolymerslcsh:MedicineChemical Composition02 engineering and technologycomputer.software_genre01 natural sciencesPolymerizationMathematical and Statistical TechniquesMedicine and Health Scienceslcsh:Science010302 applied physicsMultidisciplinaryChemical ReactionsResearch Assessment021001 nanoscience & nanotechnologyChemistryMacromoleculesMeta-analysisPhysical SciencesAnatomy0210 nano-technologyPlasticsNatural language processingStatistics (Mathematics)Research ArticleSystematic ReviewsMaterials by StructureMaterials ScienceMaterial PropertiesResearch and Analysis MethodsText mining0103 physical sciencesMechanical PropertiesStatistical MethodsMaterials by Attributebusiness.industrylcsh:RBiology and Life SciencesPolymer ChemistryJawlcsh:QArtificial intelligencebusinesscomputerDigestive SystemHeadMathematicsMeta-AnalysisPLoS ONE
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Thermo- and Light-Responsive Polymers Containing Photoswitchable Azobenzene End Groups

2009

Telechelic thermo- and light-responsive polymers based on poly(oligo(ethylene glycol) methyl ether methacrylate) P(OEGMA) with azobenzene functionalities at the end groups were synthesized. In a reversible addition−fragmentation chain transfer (RAFT) polymerization using a functionalized chain transfer agent (CTA) containing a pentafluorophenyl (PFP) activated ester, oligo(ethylene glycol) methyl ether methacrylate (OEGMA, Mn ∼ 300 g mol−1) could successfully be polymerized with good control over molecular weight, very high conversions, and narrow molecular weight distributions. Polymers derived from this CTA possessed an activated ester at the α-end of the polymer chain as well as a dithio…

Telechelic polymerAzo compoundPolymers and PlasticsOrganic ChemistryRadical polymerizationChain transferMethacrylateInorganic Chemistrychemistry.chemical_compoundAzobenzenechemistryPolymerizationPolymer chemistryMaterials ChemistryOrganic chemistryEthylene glycolMacromolecules
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Synthesis of Reactive Telechelic Polymers Based on Pentafluorophenyl Esters

2008

A diazo initiator and a chain transfer agent (CTA), both containing a pentafluorophenyl (PFP) activated ester, were synthesized. In a RAFT polymerization using the functionalized chain transfer agent (PFPCTA), methyl methacrylate (MMA), diethylene glycol monomethyl ether methacrylate (DEGMA), poly(ethylene glycol) monomethyl ether methacrylate (PEGMA), and lauryl methacrylate (LMA) could successfully be polymerized into homopolymers and diblock copolymers with good control over molecular weight, very high conversions, and narrow molecular weight distributions. Polymers derived from the PFP-CTA possessed an activated ester at the R-end of the polymer chain, which could be reacted with amines…

Telechelic polymerCondensation polymerPolymers and PlasticsOrganic ChemistryChain transferPentafluorophenyl estersMethacrylateInorganic ChemistryEnd-groupchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryOrganic chemistryReversible addition−fragmentation chain-transfer polymerizationMethyl methacrylateMacromolecules
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Long-Distance Magnetic Interaction of Exchange-Coupled Copper Dimers with Nitronyl Nitroxide and tert-Butyl Nitroxide Radicals

2009

To study long-distance magnetic interactions between exchange-coupled metal centers and coordinated radical moieties, two new homodimetallic Cu(II) complexes held together by the chelating ligand L(nPr) = N,N,N',N'-tetrakis(N-propyl-2-benzimidazolyl)-2-hydroxy-1,3-diaminopropane and additionally bridged by either a nitronyl nitroxide (NIT) or a tert-butyl nitroxide (NOA) radical-substituted benzoate have been prepared. The complexes have been investigated by X-ray crystallography, magnetic susceptibility measurements, electron paramagnetic resonance (EPR) spectroscopy, and density functional theory (DFT) calculations. For comparison additionally the related copper dimer with the bridging di…

Tert butylNitroxide mediated radical polymerizationChemistryRadicalchemistry.chemical_elementCopperInorganic ChemistryMetalvisual_artPolymer chemistryvisual_art.visual_art_mediumOrganic chemistryChelationPhysical and Theoretical ChemistryMagnetic interactionInorganic Chemistry
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Dimeric Capsules Formed by Tetra-CMPO Derivatives of (Thia)Calix[4]arenes

2010

Thiacalix[4]arene 2, calix[4]arene 3 a and its tetraether fixed in the cone conformation 3 b form homo- and heterodimeric capsules in apolar solvents, which are held together by a seam of NH⋅⋅⋅O=P hydrogen bonds between carbamoylmethyl phospine oxide functions attached to their wide rim. Their internal volume of ∼370 A3 requires the inclusion of a suitable guest. Although neutral molecules such as adamantane (derivatives) or tetraethylammonium cations form kinetically stable complexes (1H- and 31P-time scale), the included solvent is rapidly exchanged. The internal mobility of the included tetraethylammonium cation is distinctly higher (ΔG=42.5 and 49.7 kJ mol−1 for 3 a and 3 b) than that f…

TetraethylammoniumbiologyHydrogen bondAdamantaneOrganic ChemistryCationic polymerizationGeneral Chemistrybiology.organism_classificationBiochemistrySolventchemistry.chemical_compoundchemistryCalixarenePolymer chemistryMoleculeTetraChemistry - An Asian Journal
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The role of the dual nature of ionic liquids in the reversed-phase liquid chromatographic separation of basic drugs.

2010

The cationic nature of basic drugs gives rise to broad asymmetrical chromatographic peaks with conventional C18 columns and hydro-organic mixtures, due to the ionic interaction of the positively charged solutes with the free silanol groups on the alkyl-bonded reversed-phase packing. Ionic liquids (ILs) have recently attracted some attention to reduce this undesirable silanol activity. ILs are dual modifiers (with a cationic and anionic character), which means that both cation and anion can be adsorbed on the stationary phase, giving rise to interesting interactions with the anionic free silanols and the cationic basic drugs. A comparative study of the performance of four imidazolium-based I…

TetrafluoroborateIonic bondingIonic LiquidsBiochemistryAnalytical Chemistrychemistry.chemical_compoundPhase (matter)BoratesEthylaminesTriethylamineChromatography Reverse-PhaseChromatographyOrganic ChemistryCationic polymerizationImidazolesSodium Dodecyl SulfateGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationSilanesSilanolchemistryModels ChemicalPharmaceutical PreparationsIonic liquidLinear ModelsJournal of chromatography. A
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