Search results for "Ionic polymerization"

showing 10 items of 481 documents

2017

Two cationic Ir(III) complexes bearing 2-phenylpyridinato cyclometalating ligands and bithiazole-type ancillary ligands have been synthesized and optoelectronically characterised. These emitters exhibit unusually deep red-to-near-infrared emission at room temperature, thereby rendering them as attractive emitters in solution-processed light emitting electrochemical cell (LEEC) electroluminescent devices.

Materials sciencebusiness.industryGeneral Chemical EngineeringNear-infrared spectroscopyCationic polymerization02 engineering and technologyGeneral ChemistryElectroluminescence010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesElectrochemical cellOptoelectronicsLight-emitting electrochemical cell0210 nano-technologybusinessRSC Advances
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O-Doped Nanographenes: A Pyrano/Pyrylium Route Towards Semiconducting Cationic Mixed-Valence Complexes

2020

Herein we report an efficient synthesis to prepare O‐doped nanographenes, which derive from the longitudinally and latitudinally p‐extension of pyrene. The derivatives are highly fluorescent and feature low‐oxidation potentials. Exploiting electrooxidation, crystals of cationic mixed valence (MV) complexes were grown in which the organic salts organize into face‐to‐face p‐ p stacks, a favorable solid‐state arrangement for organic electronics. Variable‐temperature EPR measurements and relaxation studies suggest a strong electron delocalization along the longitudinal axis of the columnar p‐stacking architectures. Electric measurements of single crystals of the MV salts exhibited a semiconduct…

Materials sciencemolecular graphenespolycyclic aromatic hydrocarbonsHeteroatom010402 general chemistry01 natural sciencesCatalysislaw.inventionchemistry.chemical_compoundCompostos orgànicslaw[CHIM]Chemical ScienceselectrocrystallizationElectron paramagnetic resonanceOrganic electronicsValence (chemistry)[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryDopingCationic polymerizationGeneral MedicineGeneral Chemistryelectrocrystallization; electron paramagnetic resonance; heteroatom doping; molecular graphenes; polycyclic aromatic hydrocarbonsFluorescence0104 chemical sciencesElectroquímicaCrystallographyelectron paramagnetic resonancechemistryPyreneheteroatom doping
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EMPLOYMENT OF CATIONIC SOLID-LIPID NANOPARTICLES AS RNA CARRIERS

2007

Gene transfer represents an important advance in the treatment of both genetic and acquired diseases. In this article, the suitability of cationically modified solid-lipid nanoparticles (SLN) as a nonviral vector for gene delivery was investigated, in order to obtain stable materials able to condense RNA. Cationic SLN were produced by microemulsion using Compritol ATO 888 as matrix lipid, Pluronic F68 as tenside, and dimethyldioctadecylammonium bromide (DDAB) as cationic lipid. The resulting particles were approximately 100 nm in size and showed a highly positive surface charge (+41 mV) in water. Size and shape were further characterized by scanning electron microscopy (SEM) measurements. M…

MicroinjectionsCell SurvivalBiomedical EngineeringPharmaceutical ScienceNanoparticleBioengineeringNanotechnologyElectrophoretic Mobility Shift AssayPoloxamerGene deliveryTransfectionParacentrotus lividusCationsSolid lipid nanoparticleAnimalsNanotechnologyeducationcationic solid lipid nanoparticles gene deliveryOvumPharmacologyeducation.field_of_studyDrug CarriersbiologyChemistryOrganic ChemistryFatty AcidsCationic polymerizationRNAMembrane ProteinsTransfectionbiology.organism_classificationLipidsQuaternary Ammonium CompoundsSea UrchinsBiophysicsMicroscopy Electron ScanningNanoparticlesRNAEmulsionsDimethyldioctadecylammonium bromideBiotechnology
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QSAR of Natural Sesquiterpene Lactones as Inhibitors of Myb-dependent Gene Expression

2017

Background Protein c-Myb is a therapeutic target. Some sesquiterpene lactones suppress Myb-dependent gene expression, which results in their potential anti-cancer activity. Material & methods Database ChEMBL is a representative of lactones for physicochemical and physiochemical properties. Data presented for 31 natural lactones are discussed in terms of quantitative structureactivity relationships with the objective to predict inhibitors of Myb-induced gene expression. Several constitutional descriptors are related to structure-activity. α-Methylene-γ-lactone groups enhance while OH functions worsen potency. The latter feature is in agreement with the fact that the more lipophilic the lacto…

Models Molecular0301 basic medicine030103 biophysicsQuantitative structure–activity relationshipStereochemistryQuantitative Structure-Activity RelationshipSesquiterpene lactoneSesquiterpeneLactonesProto-Oncogene Proteins c-myb03 medical and health scienceschemistry.chemical_compoundDrug DiscoveryGene expressionHumansStructure–activity relationshipMYBCytotoxicitychemistry.chemical_classificationBiological ProductsDose-Response Relationship DrugMolecular StructureCationic polymerizationGeneral MedicinechEMBLGene Expression RegulationchemistrySesquiterpenesLactoneCurrent Topics in Medicinal Chemistry
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Antisymmetric exchange in triangular tricopper(II) complexes: correlation among structural, magnetic, and electron paramagnetic resonance parameters.

2011

Two new trinuclear copper(II) complexes, [Cu(3)(μ(3)-OH)(daat)(Hdat)(2)(ClO(4))(2)(H(2)O)(3)](ClO(4))(2)·2H(2)O (1) and [Cu(3)(μ(3)-OH)(aaat)(3)(H(2)O)(3)](ClO(4))(2)·3H(2)O (2) (daat = 3,5-diacetylamino-1,2,4-triazolate, Hdat = 3,5-diamino-1,2,4-triazole, and aaat = 3-acetylamino-5-amino-1,2,4-triazolate), have been prepared from 1,2,4-triazole derivatives and structurally characterized by X-ray crystallography. The structures of 1 and 2 consist of cationic trinuclear copper(II) complexes with a Cu(3)OH core held by three N,N-triazole bridges between each pair of copper(II) atoms. The copper atoms are five-coordinate with distorted square-pyramidal geometries. The magnetic properties of 1 …

Models MolecularAntisymmetric exchangeMolecular StructureX-rayCationic polymerizationElectron Spin Resonance SpectroscopyTemperaturechemistry.chemical_elementCrystal structureAtmospheric temperature rangeTriazolesCrystallography X-RayLigandsCopperlaw.inventionInorganic ChemistryCrystallographyMagneticschemistrylawOrganometallic CompoundsMoleculePhysical and Theoretical ChemistryElectron paramagnetic resonanceCopperInorganic chemistry
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Morphology of hybrid polystyrene-block-poly(ethylene oxide) micelles: Analytical ultracentrifugation and SANS studies

2006

Abstract Morphology and structure of aqueous block copolymer solutions based on polystyrene- block -poly(ethylene oxide) (PS- b -PEO) of two different compositions, a cationic surfactant, cetyl pyridinium chloride (CPC), and either platinic acid (H 2 PtCl 6 ⋅6H 2 O) or Pt nanoparticles were studied using a combination of analytical ultracentrifugation (AUC), transmission electron microscopy (TEM), and small angle neutron scattering (SANS). These studies combining methods contributing supplemental and analogous structural information allowed us to comprehensively characterize the complex hybrid systems and to discover an isotope effect when H 2 O was replaced with D 2 O. In particular, TEM s…

Models MolecularBlock copolymerHybrid micellesMicellePolyethylene GlycolsBiomaterialsSurface-Active Agentschemistry.chemical_compoundColloid and Surface ChemistrySurfactantPolymer chemistryCopolymerMicellesAqueous solutionCalorimetry Differential ScanningEthylene oxideIsotope effectCationic polymerizationSmall-angle neutron scatteringSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMicroscopy ElectronchemistryPolystyrenesPhysical chemistryPolystyrenePyridiniumUltracentrifugationJournal of Colloid and Interface Science
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Pores Formed by Baxα5 Relax to a Smaller Size and Keep at Equilibrium

2010

AbstractPores made by amphipathic cationic peptides (e.g., antimicrobials and fragments of pore-forming proteins) are typically studied by examining the kinetics of vesicle leakage after peptide addition or obtaining structural measurements in reconstituted peptide-lipid systems. In the first case, the pores have been considered transient phenomena that allow the relaxation of the peptide-membrane system. In the second, they correspond to equilibrium structures at minimum free energy. Here we reconcile both approaches by investigating the pore activity of the α5 fragment from the proapoptotic protein Bax (Baxα5) before and after equilibrium of peptide/vesicle complexes. Quenching assays on …

Models MolecularCardiolipinsMacromolecular SubstancesKineticsMolecular Sequence DataBiophysicsPeptideIn Vitro TechniquesBiophysical PhenomenaAmphiphileAnimalsHumansAmino Acid SequencePeptide sequenceUnilamellar LiposomesFluorescent Dyesbcl-2-Associated X Proteinchemistry.chemical_classificationMicroscopy ConfocalChemistryBilayerVesicleMacromolecular SubstancesCationic polymerizationMembranePeptide FragmentsCrystallographyKineticsBiophysicsPhosphatidylcholinesThermodynamicsCattle
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Combining reactive triblock copolymers with functional cross-linkers: A versatile pathway to disulfide stabilized-polyplex libraries and their applic…

2017

Therapeutic nucleic acids such as pDNA hold great promise for the treatment of multiple diseases. These therapeutic interventions are, however, compromised by the lack of efficient and safe non-viral delivery systems, which guarantee stability during blood circulation together with high transfection efficiency. To provide these desired properties within one system, we propose the use of reactive triblock copolypept(o)ides, which include a stealth-like block for efficient shielding, a hydrophobic block based on reactive disulfides for cross-linking and a cationic block for complexation of pDNA. After the complexation step, bifunctional cross-linkers can be employed to bio-reversibly stabiliz…

Models MolecularLysisEndosomePolymersPharmaceutical ScienceNanotechnology02 engineering and technologyGene delivery010402 general chemistryCleavage (embryo)Transfection01 natural sciencesCell Linechemistry.chemical_compoundMiceVaccines DNAAnimalsHumansDisulfidesBifunctionalCationic polymerizationGene Transfer TechniquesTransfection021001 nanoscience & nanotechnology0104 chemical sciencesCross-Linking ReagentschemistryBiophysicsNucleic acid0210 nano-technologyPlasmidsJournal of controlled release : official journal of the Controlled Release Society
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Cationic Nanohydrogel Particles as Potential siRNA Carriers for Cellular Delivery

2012

Oligonucleotides such as short, double-stranded RNA (siRNA) or plasmid DNA (pDNA) promise high potential in gene therapy. For pharmaceutical application, however, adequate drug carriers are required. Among various concepts progressing in the market or final development, nanosized hydrogel particles may serve as novel transport media especially for siRNA. In this work, a new concept of synthesizing polymeric cationic nanohydrogels was developed, which offers a promising strategy to complex and transport siRNA into cells. For this purpose, amphiphilic reactive ester block copolymers were synthesized by RAFT polymerization of pentafluorophenyl methacrylate as reactive ester monomer together wi…

Models MolecularMaterials scienceMolecular ConformationGeneral Physics and AstronomyMethacrylateCell Linechemistry.chemical_compoundAmphiphilePolymer chemistryAnimalsGeneral Materials ScienceReversible addition−fragmentation chain-transfer polymerizationAminesRNA Small Interferingchemistry.chemical_classificationDrug CarriersGeneral EngineeringCationic polymerizationBiological TransportEstersHydrogelsPolymerCombinatorial chemistryNanostructuresRatsMonomerchemistrySolventsDrug carrierHydrophobic and Hydrophilic InteractionsEthylene glycolACS Nano
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Synthesis and reactivity of the novel hydride derivative RhHCl(TIMP3) (HTIMP3 = tris[1-(diphenylphosphino)-3-methyl-1H-indol-2-yl]methane)

2009

The reaction of HTIMP(3) (HTIMP(3) = tris[1-(diphenylphosphino)-3-methyl-1H-indol-2-yl]methane) with [RhCl(COD)](2) and Rh(acac)(CO)(2) produces RhHCl(TIMP(3)) (1H) and Rh(TIMP(3))(CO) (2), respectively, both exhibiting tetradentate kappaC,kappa(3)P-coordination of the TIMP(3) moiety. The reaction of RhHCl(TIMP(3)) with nucleophiles (L) in the presence of AgBF(4) or AgPF(6) produces different compounds depending on the nature of L. Indeed, cationic Lewis adducts of formula [RhH(L)(TIMP(3))](+) ((2H+)-(5H+)) are obtained when L is CO, CNCH(2)Ph, pyridine or CH(2)CHCN. On the other hand, when the incoming nucleophile is CH(3)COOH the hydride-free complex [Rh(CH(3)COO)(TIMP(3))](+) ((6+)) is o…

Models MolecularMolecular StructureHydrideChemistryCationic polymerizationStereoisomerismCrystallography X-RayMedicinal chemistryAdductInorganic Chemistrychemistry.chemical_compoundNucleophilePyridineOrganometallic CompoundsMoietyOrganic chemistryReactivity (chemistry)Derivative (chemistry)Dalton Transactions
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