Search results for " polymerization"

showing 10 items of 1054 documents

Effect of cationic polyamidoamine dendrimers on ionic transport through nanochannels

2021

Abstract The effect of polyamidoamine (PAMAM) dendrimers (generations G0–G3) on the ion transport properties of nanochannels (conical and cylindrical) is studied either by surface functionalization or by addition to the electrolyte solution. Surface functionalization with cationic dendrimers lead to inversion of the ion current rectification, indicating the anion selectivity of the modified nanochannels. This anion selectivity increases by immobilizing higher-generation dendrimers, as expected for an increase in the surface density of amino groups. However, compared to PAMAM G2, functionalization with PAMAM G3 results in higher cation and lower anion fluxes. Diffusion experiments of charged…

ChemistryGeneral Chemical EngineeringCationic polymerizationIonic bondingCharge density02 engineering and technologyElectrolyte010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesIonMembraneChemical engineeringDendrimerElectrochemistrySurface modification0210 nano-technologyElectrochimica Acta
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Crystal structures, spectral and magnetic properties of cobalt(II) pyridinecarboxylates: A novel polymeric chain in {[{2,6-(MeO)2nic}2(H2O)2Co(μ-H2O)…

2006

Abstract Synthesis and characterization of two new cobalt(II) complexes, namely monomeric [Co(2-MeSnic)2(H2O)4] · 4H2O (2-MeSnic is 2-methylthionicotinate) and polymeric {[{2,6-(MeO)2nic}2(H2O)2Co(μ-H2O)Co(H2O)4(μ-H2O)]{2,6-(MeO)2nic}2 · 6H2O}n (2,6-(MeO)2nic is 2,6-dimethoxynicotinate), are reported. The characterizations were based on elemental analysis, infrared and electronic spectra as well as magnetic measurements. Crystal structures of both complexes have been determined. In both of them – ([Co(2-MeSnic)2(H2O)4] · 4H2O and {[{2,6-(MeO)2nic}2(H2O)2Co(μ-H2O)Co(H2O)4(μ-H2O)]{2,6-(MeO)2nic}2 · 6H2O}n) – the CoII atom is six-coordinated. In the 2nd complex, there are two nonequivalent CoI…

ChemistryHydrogen bondStereochemistryCationic polymerizationchemistry.chemical_elementCrystal structureSpectral lineInorganic ChemistryCrystallographychemistry.chemical_compoundMonomerAtomMaterials ChemistryMoleculePhysical and Theoretical ChemistryCobaltInorganica Chimica Acta
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Synthesis and X-ray structure of cationic β-diimine palladium complexes containing π-methallyl ligand

2005

High yield of cationic palladium β-diimine complexes [(CH 2 (MeCNAr) 2 )Pd(η 3 -C 4 H 7 )][Y] (Ar = C 6 H 5 , Y = PF 6 (8); 2-Me-C 6 H 4 , Y = PF 6 (9); 2,6-Me 2 -C 6 H 3 , Y = PF 6 (10); 2,6-iPr 2 -C 6 H 3 , Y = PF 6 (11), Y = B(3,5-(CF 3 ) 2 -C 6 H 3 ) 4 (12)) have been obtained by an oxidative addition of the methallyloxyphosphonium salts (5, 6) to a preformed complex Pd(dba) 2 (7) in the presence of the β-iminoamine ligands (1-4). These complexes are thermally stable and have been characterized by 'H and 1 3 C{ 1 H} NMR as well as IR spectroscopy. The structure of the cationic allyl palladium complex (12) has been solved by X-ray crystallography.

ChemistryLigandOrganic ChemistryX-rayCationic polymerizationInfrared spectroscopychemistry.chemical_elementPhotochemistryBiochemistryMedicinal chemistryOxidative additionInorganic ChemistryYield (chemistry)Materials ChemistryPhysical and Theoretical ChemistryDiiminePalladiumJournal of Organometallic Chemistry
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The first member of a second generation family of ligands derived from metal-ion assisted reactivity of di-2,6-(2-pyridylcarbonyl)pyridine: Synthesis…

2012

Abstract Nucleophilic attack by the carbanion −CH2COCH3 at the carbonyl carbon atoms of 2,6-di-(2-pyridylcarbonyl)pyridine, pyCOpyCOpy, in the presence of Mnn+ ions under basic conditions has yielded the cationic cluster [Mn4(OH)2(L)2(H2O)2](ClO4)4 (1), where L2− is the (py)C(CH2COCH3)(O−)(py)C(CH2COCH3)(O−)(py) dianion. The cluster cation possesses a planar {MnII2MnIII2(μ3-OH)2(μ-OR)4}4+ rhombus core, resulting from two μ3-OH− ions and two η1:η2:η1:η1:η1:η2:η1:μ3 bridging L2− groups from the in situ formed ligand. Complex 1 is antiferromagnetically coupled with an unusual S = 2 ground state resulting from spin frustration effects within the triangular Mn3 subunits of the cluster.

ChemistryLigandStereochemistryCationic polymerizationIonInorganic ChemistryMetalCrystallographychemistry.chemical_compoundNucleophilevisual_artPyridineMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryGround stateCarbanionInorganic Chemistry Communications
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Average versus local structure in K2NiF4-type LaSrAlO4: direct experimental evidence of local cationic ordering

2012

The long-range ordering of a crystalline material can be accurately determined by analyzing the Bragg intensities and positions. In contrast, direct observation of short-range ordering in crystalline materials, which is increasingly considered of fundamental importance to unravel the structure-property relationships that underpin their technological applications, is a challenging task. In this study we have investigated the structure of LaSrAlO4, a representative example of compounds with the K2NiF4-type structure. By the combined use of synchrotron and neutron diffraction, pair distribution function analysis, Al-27 MQMAS NMR and atomistic simulations we have highlighted differences between…

ChemistryNeutron diffractionCationic polymerizationStructure (category theory)Pair distribution function02 engineering and technologyGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryType (model theory)010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesLocal structureSynchrotron0104 chemical scienceslaw.inventionCrystallographylawChemical physicsK2NiF4 neutron diffraction 27Al MAS NMR quadrupolar interaction local structureMaterials ChemistryRange (statistics)Local structure NMR0210 nano-technologyComputingMilieux_MISCELLANEOUS
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Radical cations and dications of bis[1]benzothieno[1,4]thiazine isomers

2021

Bis[1]benzothieno[1,4]thiazines (BBTT) are particularly electron-rich S,N-heteropentacenes and their radical cations and dications can be relevant intermediates in charge transport materials. All three regioisomers of N-p-fluorophenyl-BBTT (syn–syn, syn–anti, and anti–anti) were studied. A reliable preparation of radical cations and dications using antimony pentachloride as an oxidant gives deeply colored salts. The electronic structure of the radical cations was assessed by EPR spectroscopy, whereas dicationic structures were characterized by NMR spectroscopy. In addition, a deeper insight into the electronic structure was experimentally and computationally obtained by UV/Vis spectroscopy …

ChemistryOrganic ChemistryAntimony pentachlorideCationic polymerizationNuclear magnetic resonance spectroscopyTime-dependent density functional theoryPhotochemistrylaw.inventionchemistry.chemical_compoundlawThiazineStructural isomerElectron paramagnetic resonanceSpectroscopyOrganic Chemistry Frontiers
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Poly(glycolide) multi-arm star polymers: Improved solubility via limited arm length.

2010

Due to the low solubility of poly(glycolic acid) (PGA), its use is generally limited to the synthesis of random copolyesters with other hydroxy acids, such as lactic acid, or to applications that permit direct processing from the polymer melt. Insolubility is generally observed for PGA when the degree of polymerization exceeds 20. Here we present a strategy that allows the preparation of PGA-based multi-arm structures which significantly exceed the molecular weight of processable oligomeric linear PGA (<1000 g/mol). This was achieved by the use of a multifunctional hyperbranched polyglycerol (PG) macroinitiator and the tin(II)-2-ethylhexanoate catalyzed ring-opening polymerization of gly…

ChemistryPGAOrganic Chemistryblock copolymerhyperbranchedDegree of polymerizationstar polymerGraftingFull Research PaperLactic acidlcsh:QD241-441Polyesterchemistry.chemical_compoundChemistrypolyglycerollcsh:Organic chemistryPolymerizationPolymer chemistryCopolymerlcsh:QpolyesterSolubilitylcsh:Sciencepoly(glycolide)Glycolic acidBeilstein journal of organic chemistry
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Üuber eine abgekürzte Fraktioniermethode zur Bestimmung von Molekulargewichtsverteilungen

1950

Es wird ein Verfahren beschrieben, welches die Breite und ungefahre Gestalt der Verteilungskurve cines polymolekularen Stoffs auf Grund folgender experimenteller Daten zu bestimmen erlaubt: 1 Mittlerer Polymerisationsgrad (z. B. durch eine osmotische Bestimmung). 2 Gewichtsanteil und mittlerer Polymerisationsgrad einer obersten Fraktion. 3 Gewichtsanteil und mittlerer Polymerisationsgrad einer untersten Fraktion. Anwendungsbereich und Grenzen des neuen Verfahrens werden experimentell ermittelt. A method is described permitting to determine latitude and approximate shape of the distribution curve of a polymolecular substance by means of the following experimental data: 1 Average degree of po…

ChemistryPolymer chemistryAnalytical chemistryDegree of polymerizationDie Makromolekulare Chemie
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Isolation of Free Phenylide-like Carbanions with N-Heterocyclic Carbene Frameworks

2009

A series of 1,3-bis(2,6-diisopropylphenyl)-5-methyl-1,3-diaza-4,6-diborabenzenes with methyl, phenyl, and dimethylamino substituents on the ring boron atoms were prepared using the cyclocondensation reaction between N,N'-bis(2,6-diisopropylphenyl)trimethylsilylformamidine and the appropriately substituted 1,1-bis(organochloroboryl)ethane, followed by deprotonation of the cationic ring intermediate. The planar, heterocyclic benzene analogues could be further deprotonated at the other ring carbon using an additional equivalent of potassium hexamethyldisilazide to yield organometallic derivatives akin to the potassium phenylide. The potassium cations could be efficiently sequestered in both so…

ChemistryPotassiumCationic polymerizationchemistry.chemical_elementGeneral ChemistryRing (chemistry)PhotochemistryBiochemistryMedicinal chemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryDeprotonationYield (chemistry)BenzeneCarbeneCarbanionJournal of the American Chemical Society
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Surface composition analysis during the oxidation of ferrites: A necessity

1998

The cationic composition of a titanium ferrite (Fe 2.5 Ti 0.5 O 4 ) has been followed by XPS during its oxidation in cation deficient phases (without crystallographic transformation) in order to reveal a dynamic segregation phenomenon. Indeed, during this oxidation, an important modification of the chemical composition of the first layers of the material has been revealed: below 350 °C, the titanium ferrites surface becomes richer in iron and poorer in titanium. But, if the reaction is extended above 400 °C, some titanium can move to the surface. This phenomenon has been interpreted on the basis of the differences of mobility of the different ions which are present in the material. Finally,…

ChemistrySpinelInorganic chemistryCationic polymerizationchemistry.chemical_elementComposition analysisengineering.materialCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsIonX-ray photoelectron spectroscopyengineeringFerrite (magnet)InstrumentationChemical compositionTitaniumThe European Physical Journal Applied Physics
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