Search results for "Ionic polymerization"

showing 10 items of 481 documents

Pyrophosphate-mediated magnetic interactions in Cu(II) coordination complexes.

2010

The reaction in water of Cu(NO(3))(2)·2.5H(2)O with 2,2'-bipyridine (bipy), 1,10-phenanthroline (phen), or 1,10-phenanthroline-5-amine (phenam), and sodium pyrophosphate (Na(4)P(2)O(7)), at various pHs, afforded three new copper(II)-pyrophosphate complexes, namely, {[Cu(bipy)(cis-H(2)P(2)O(7))](2)}·3H(2)O (1a), {[Cu(phen)(H(2)O)](4)(HP(2)O(7))(2)}(ClO(4))(2)·4H(2)O (2), and {[Cu(2)(phenam)(2)(P(2)O(7))](2)·25H(2)O}(n) (3). A solvent free crystalline phase of 1a was also isolated with formula {[Cu(bipy)(trans-H(2)P(2)O(7))](2)} (1b), which can be regarded as a pseudo-polymorph of 1a. Single crystal X-ray analyses revealed these compounds to have uncommon molecular architectures, with 3 being…

Models MolecularStereochemistryPolymersSodiumchemistry.chemical_elementCrystallography X-RayPyrophosphateInorganic Chemistrychemistry.chemical_compoundMagneticsStructure-Activity Relationship22'-DipyridylCoordination ComplexesMoleculePhysical and Theoretical ChemistryMathematical ComputingSolvent freeMolecular StructureCationic polymerizationHydrogen-Ion ConcentrationCopperDiphosphatesCrystallographychemistryThermodynamicsSingle crystalDimerizationCopperPhenanthrolinesInorganic chemistry
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Development of Bimetallic Titanocene−Ruthenium−Arene Complexes As Anticancer Agents: Relationships between Structural and Biological Properties

2010

A series of bimetallic titanium-ruthenium complexes of general formula [(η(5)-C(5)H(5))(μ-η(5):κ(1)-C(5)H(4)(CR(2))(n)PR'R'')TiCl(2)](η(6)-p-cymene)RuCl(2) (n = 0, 1, 2 or 4; R = H or Me; R' = H, Ph, or Cy; R'' = Ph or Cy) have been synthesized, including two novel compounds as well as two cationic derivatives of formula [(η(5)-C(5)H(5))(μ-η(5):κ(1)-C(5)H(4)(CH(2))(n)PPh(2))TiCl(2)] [(η(6)-p-cymene)RuCl](BF(4)) (n = 0 or 2). The solid state structure of two of these compounds was also established by X-ray crystallography. The complexes showed a cytotoxic effect on human ovarian cancer cells and were markedly more active than their Ti or Ru monometallic analogues titanocene dichloride and RA…

Models MolecularStereochemistrychemistry.chemical_elementAntineoplastic AgentsCrystal structureCrystallography X-RayRutheniumCathepsin BMetalStructure-Activity Relationshipchemistry.chemical_compoundCoordination ComplexesCell Line TumorDrug DiscoveryAnimalsHumansBimetallic stripAlkylTitaniumchemistry.chemical_classificationCationic polymerizationTitanocene dichlorideRutheniumEnzymechemistryDrug Resistance Neoplasmvisual_artvisual_art.visual_art_mediumMolecular MedicineCattleDrug Screening Assays AntitumorProtein BindingJournal of Medicinal Chemistry
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Influence of chain length on the molecular dynamics of an aliphatic ionene

1998

An aliphatic random copolymer ionene (a cationic polyelectrolyte with N + in the repeat unit), was fractionated with the continuous polymer fractionation and investigated for its molecular weight dependent properties. The fractions were analyzed with GPC and capillary viscometry for their molecular weight. Glass transition temperatures were determined with DSC and a strong molecular weight dependence was observed, but no influence in the ionic conductivity was observed. The temperature dependency of ionic conductivity in ionenes is described.

Molecular dynamicsPolymers and PlasticsChemistryGeneral Chemical EngineeringPolymer chemistryCationic polymerizationCopolymerPhysical chemistryViscometerIonic conductivityPolymer fractionationGlass transitionPolyelectrolyteActa Polymerica
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2015

AbstractThe synthesis, characterization and evaluation in solid-state devices of a series of 8 cationic iridium complexes bearing different numbers of methoxy groups on the cyclometallating ligands are reported. The optoelectronic characterization showed a dramatic red shift in the absorption and the emission and a reduction of the electrochemical gap of the complexes when a methoxy group was introduced para to the Ir-C bond. The addition of a second or third methoxy group did not lead to a significant further red shift in these spectra. Emission maxima over the series ranged from 595 to 730 nm. All complexes possessing a motif with a methoxy group at the 3-position of the cyclometalating l…

MultidisciplinaryPhotoluminescenceChemistryLigandCationic polymerizationchemistry.chemical_element02 engineering and technologyElectroluminescence010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistryPhotochemistry01 natural sciencesSpectral line0104 chemical sciencesPolar effectIridium0210 nano-technologyScientific Reports
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Synthesis and Characterization of Halloysite-Cyclodextrin Nanosponges for Enhanced Dyes Adsorption

2017

Inorganic-organic nanosponge hybrids based on halloysite clay and organic cyclodextrin derivatives (HNT-CDs) were developed by means of microwave irradiations in solvent-free conditions. The HNT-CDs nanomaterials characterized by FT-IR, TGA, BET, TEM, SEM, DLS, and zeta-potential have showed a hyper-reticulated network which possesses both HNT and cyclodextrin peculiarities. The new HNT-CDs nanosponge hybrids were employed as nanoadsorbents, first choosing Rhodamine B as the dye model, and furthermore for the removal of some cationic and anionic dyes, under different pH values (1.0, 4.54, and 7.4). The collected results showed that the pH solution as well as the electrostatic interactions a…

NanospongesGeneral Chemical Engineering02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesHalloysiteNanospongeNanomaterialschemistry.chemical_compoundBioremediation; Cyclodextrin; Halloysite; NanospongesAdsorptionRhodamine BEnvironmental ChemistryOrganic chemistryCyclodextrinFreundlich equationSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationCyclodextrinRenewable Energy Sustainability and the EnvironmentCationic polymerizationHalloysiteGeneral ChemistrySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesCharacterization (materials science)Halloysite Nanosponges Cyclodextrin BioremediationchemistryChemical engineeringengineering0210 nano-technologyBioremediation
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Poly(alkylidenamines) dendrimers as scaffolds for the preparation of low-generation ruthenium based metallodendrimers

2011

The aim of this article is to highlight the use of nitrile-functionalized poly(alkylidenamines) dendrimers as building blocks for the preparation of low-generation ruthenium based cationic metallodendrimers having in view potential biomedical applications. Air-stable poly(alkylidenamines) nitrile dendrimers, peripherally functionalized with the ruthenium moieties [Ru(η5-C5H5)(PPh3)2]+ or [RuCl(dppe)2]+, have been prepared, characterized and are being studied for their anticancer activity. The followed strategy is based on the biological advantages associated with low-generation dendrimers, the known activity of ruthenium compounds as anticancer drugs and the stability of these dendrimers at…

NitrileMetallodendrimersCationic polymerizationchemistry.chemical_elementPreparation of low-generation rutheniumPoly(alkylidenamines) dendrimersLow-generation rutheniumGeneral Chemistry.Combinatorial chemistryRutheniumCatalysisRutheniumFaculdade de Ciências Exatas e da Engenhariachemistry.chemical_compoundchemistryDendrimerMaterials ChemistryOrganic chemistryRuthenium Compoundsta116New Journal of Chemistry
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Nucleophilic attack by 2-pyridylpalladium(II) and platinum(II) complexes on the organic chlorides ClCH2R (R  COMe, CN, Ph, Cl)

1992

Abstract The 2-pyridyl complexes trans-[MCl(C5H4NC2)(PPh3)2] (M = Pd, 1a; M = Pt, 1b), [MCl(C5H4NC2)(dppe)] (M = Pd, 2a; M = Pt, 2b) and [M(dmtc)(C5H4NC2) (PPh3)] (M = Pd, 3a; M = Pt,3b) react with the chlorides ClCH2R(R  COMe, CN, Ph) to give cationic products containing the 2-pyridylium ligands (1-CH2R)C5H4NC2. The rate of nucleophilic displacement of the chloride ion from ClCH2R depends on the central metal (Pt > Pd), on the coordination geometry (1 ~ 3) and on the substituent R (COMe > CN > Ph for the reactions with 3b). Like 1b and 2b, complex 3b also reacts with dichloromethane to give [Pt(dmtc){(1-CH2Cl)C5H4NC2}(PPh3)]+. The reaction of the binuclear compound [{PdCl(μ-C5H4NC2,…

NitrileStereochemistryOrganic ChemistryCationic polymerizationchemistry.chemical_elementBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundPerchlorateChloroacetonechemistryNucleophileMaterials ChemistryNucleophilic substitutionPhysical and Theoretical ChemistryPlatinumCoordination geometryJournal of Organometallic Chemistry
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Growth of polyoxymethylene crystals during cationic polymerization of trioxane in nitrobenzene

1973

Nitrobenzenechemistry.chemical_compoundTrioxanePolyoxymethyleneChemistryPolymer chemistryGeneral EngineeringCationic polymerizationGeneral Materials SciencePhotochemistryJournal of Polymer Science: Polymer Letters Edition
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1993

Nitroxide mediated radical polymerizationAnionic addition polymerizationPolymerizationChemistryPolymer chemistryRadical polymerizationChain transferReversible addition−fragmentation chain-transfer polymerizationPhotochemistryIonic polymerizationLiving anionic polymerizationDie Makromolekulare Chemie, Rapid Communications
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Polyoxometalate salts of cationic nitronyl nitroxide free radicals

2008

The cationic nitronyl nitroxide free radical of the N-methylpyridinium type p-MepyNN + has been combined with [Mo 8 0 26 ] 4- and Keggin [SiW 12 0 40 ] 4- polyanions to afford salts ( p-MepyNN) 4 [Mo 8 0 26 ] DMSO (DMSO = dimethylsulfoxide) (1) and (p-MepyNN)4[SiW 12 0 40 ] 6DMF (DMF = dimethylformamide) (2). Herein, their structural and magnetic properties are described.

Nitroxide mediated radical polymerizationChemistryMagnetismRadicalCationic polymerizationGeneral ChemistryCondensed Matter PhysicsPhotochemistrychemistry.chemical_compoundMetallatePolyoxometalatePolymer chemistryDimethylformamideGeneral Materials ScienceGroup 2 organometallic chemistrySolid State Sciences
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