Search results for "polymer chemistry"

showing 10 items of 3410 documents

1988

Negatively charged lipid molecules were converted into polymerizable lipids by introduction of polymerizable mono- or bifunctional counterions. As an attempt to mimic the cytoskeleton of biomembranes, unsymmetrical polymeric vesicles were prepared, where the polyelectrolyte is attached either only to the inner or to the outer bilayer surfaces. Polymerizable cations were introduced to the outer surface of preformed small unilamellar vesicles via ion-exchange. The outer counterions of vesicles bearing polymerizable counterions at both sides of the membrane were replaced by Na+. Polymerization of these systems leads to unsymmetrical vesicles. The introduction, separation and polymerization of …

inorganic chemicalschemistry.chemical_classificationVesicleBilayertechnology industry and agricultureCationic polymerizationPolymerPolyelectrolytechemistry.chemical_compoundMembranePolymerizationchemistryPolymer chemistryBifunctionalDie Makromolekulare Chemie
researchProduct

Titanium (IV) chloride complexes with salen ligands supported on magnesium carrier: Synthesis and use in ethylene polymerization

2009

The magnesium support with the formula MgCl 2 (THF) 0.32 (Et 2 AlCl) 0.36 was used for immobilization of salen complexes of titanium [Ti(salen)Cl 2 , Ti(salen(O-Me) 2 )Cl 2 ]. The effects of the catalyst composition (i.e. type of titanium complex and type of activator), polymerization temperature, polymerization time, and the effect of comonomer (1-octene) on the activity of the obtained supported catalysts, on the polymer characteristics (molecular weight, molecular weight distribution, melting point), and on the polymer morphology were studied. The findings were compared to those obtained for corresponding unsupported systems. Catalysts immobilization results in considerable changes in ca…

inorganic chemicalschemistry.chemical_classificationpolyethyleneZiegler‐Natta polymerizationPolymers and PlasticssupportsComonomerOrganic Chemistrychemistry.chemical_elementPolymerPolyethylenecatalystsCatalysischemistry.chemical_compoundchemistryPolymerizationMetal salen complexesPolymer chemistryMaterials ChemistryMolar mass distributiontitanium (IV) salen complexesTitaniumJournal of Polymer Science. Part A : Polymer Chemistry
researchProduct

ortho-(Dimesitylboryl)phenylphosphines: Positive Boryl Effect in the Palladium-Catalyzed Suzuki-Miyaura Coupling of 2-Chloropyridines

2013

The presence of ortho-dimesitylboryl moiety in the catalyst is crucial to enhance the catalytic performance.

inorganic chemicalsintegumentary systemorganic chemicalschemistry.chemical_elementGeneral ChemistryPhotochemistryCatalysisCoupling (electronics)chemistryPolymer chemistrybacteriaMoietyheterocyclic compoundsPalladiumAdvanced Synthesis & Catalysis
researchProduct

Synthese mehrerer polymerhomologer reihen von diol-oligo-urethanen. Synthese von makromolekeln einheitlicher größe. V. Mitt.

1961

Mit Hilfe des Duplikationsverfahrens und durch schrittweise Synthese werden mehrere polymerhomologe Reihen von Diol-oligo-urethanen synthetisiert. Die Anwendbarkeit dieser Methode wird eingehend diskutiert. Die Diol-oligo-urethane werden durch Endgruppenanalyse charakterisiert. Several homologous polymeric series of diol-oligo-urethanes are prepared by the method of duplication and by synthesis step by step. The application of these methods is discussed thoroughly. The diol-oligo-urethanes are characterized by end-group analysis.

integumentary systemChemistryStereochemistryorganic chemicalsPolymer chemistrypolycyclic compoundsheterocyclic compoundshormones hormone substitutes and hormone antagonistsDie Makromolekulare Chemie
researchProduct

Preparation of Polymeric Nanoparticles by Photo-Crosslinking of an Acryloylated Polyaspartamide in w/o Microemulsion

2004

Biodegradable polymeric nanoparticles have been prepared by UV irradiation of an acryloylated water soluble polymer by an inverse microemulsion. The starting polymer was a α,β‐poly(N‐2‐hydroxyethyl)‐D,L‐aspartamide (PHEA) partially functionalized with glycidyl methacrylate (GMA) in order to introduce reactive vinyl groups in the side chain. The PHEA‐GMA copolymer obtained (PHG) was crosslinked by UV irradiation of the inverse microemulsion prepared by mixing an aqueous solution of PHG with propylene carbonate (PC)/ethyl acetate (EtOAc) in the presence of sorbitan trioleate (SPAN 85) as surfactant. Nanoparticles obtained were characterized by FTIR spectrophotometry, transmission electron mic…

inverse microemulsionGlycidyl methacrylatePHGAqueous solutionPolymers and PlasticsChemistryOrganic ChemistryNanoparticleCondensed Matter Physicsacryloylated polyaspartamide inverse microemulsion irradiation nanoparticles PHG photo‐crosslinkingphoto-crosslinkingchemistry.chemical_compoundSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPolymer chemistryMaterials ChemistryZeta potentialSide chainCopolymernanoparticlesMicroemulsionPhysical and Theoretical ChemistryDrug carrieracryloylated polyaspartamideMacromolecular Chemistry and Physics
researchProduct

From isolated 1H-pyrazole cryptand anion receptors to hybrid inorganic-organic 1D helical polymeric anion receptors

2015

We report a novel 1-D helical coordination polymer formed by protonated polyamine 1H-pyrazole cryptands interconnected by Cu2+ metal ions that are able to encapsulate anionic species behaving as a multianion receptor. Switching from a monomeric receptor to a polymeric receptor is activated by metal ions and pH.

kemiaChemistryStereochemistryCoordination polymerMetal ions in aqueous solutionCryptandreceptorsProtonationPyrazolechemistryInorganic Chemistrychemistry.chemical_compoundMonomerPolymer chemistryPolyamineReceptorta116Dalton Transactions 44: 7761-7764 (2015)
researchProduct

The S … Hal and Se … Hal chalcogen bonding in a series of thiourea, selenourea and their derivatives

2021

The chalcogen bonding (ChB) in a series of thiourea, selenourea and their derivatives has been investigated in the present paper. Thus, selenourea and dimethylselenourea undergo dimerization and trimerization processes in the presence of various halogen species (1–5). Selenourea and dimethylselenourea form trimers 3–4 in the presence of lighter halogens (chlorine and bromine) through Se⋯Se chalcogen bonding. When moving to heavier halogen (iodine), the dimers 1–2 are formed. Thiourea and its derivatives also tend to make very strong S⋯S bonds and form dimers in the case of lighter halogens chlorine and bromine (compounds 6–7). However, the monomers separated by the iodine species are formed…

kemiaSelenoureachemistry.chemical_element02 engineering and technologyCrystal structure010402 general chemistry01 natural sciencesInorganic Chemistryjodichemistry.chemical_compoundChalcogenkemialliset sidoksetklooriPolymer chemistryMaterials ChemistryChlorinechalcogen bondingbromiPhysical and Theoretical ChemistryselenoureathioureaBrominehalogeenitChemistry021001 nanoscience & nanotechnologyCondensed Matter Physicshalogen0104 chemical sciencesElectronic Optical and Magnetic MaterialsMonomerThioureaHalogenCeramics and Composites0210 nano-technology
researchProduct

Rapid self-healing and anion selectivity in metallosupramolecular gels assisted by fluorine-fluorine interactions.

2017

Simple ML2 [M = Fe(II), Co(II), Ni(II)] complexes obtained from a perfluoroalkylamide derivative of 4-aminophenyl-2,2′,6,2′-terpyridine spontaneously, yet anion selectively, self-assemble into gels, which manifest an unprecedented rapid gel strength recovery, viz. self-healing, and thermal rearrangement in aqueous dimethyl sulfoxide. The key factor for gelation and rheological properties emerges from the fluorine–fluorine interactions between the perfluorinated chains, as the corresponding hydrocarbon derivative did not form metallogels. The perfluoro-terpyridine ligand alone formed single crystals, while its Fe(II), Co(II) or Ni(II) complexes underwent rapid gelation leading to highly enta…

kemiachemistry.chemical_element02 engineering and technology010402 general chemistrychemistry01 natural sciencesMetalInorganic Chemistrychemistry.chemical_compoundTheoretical and Computational ChemistryfluorinePolymer chemistryOrganic chemistryThermal stabilitymoleculeshydrocarbonsta116chemistry.chemical_classificationgeelitAqueous solutionta114Ligandmolekyylit021001 nanoscience & nanotechnologygelsfluorihiilivedyt0104 chemical sciencesHydrocarbonchemistryvisual_artFluorinevisual_art.visual_art_mediumInorganic & Nuclear Chemistry0210 nano-technologySelectivityOther Chemical SciencesDerivative (chemistry)
researchProduct

Halogen Bonding between Thiocarbonyl Compounds and 1,2- and 1,4-Diiodotetrafluorobenzenes

2021

The halogen bonding (XB) between 1,2-diiodotetrafluorobenzene (1,2-DITFB) or 1,4-diiodotetrafluorobenzene (1,4-DITFB) and the selection of different thiocarbonyl acceptors was studied by the single-crystal X-ray diffraction method. Diiodotetrafluorobenzenes (DITFBs) were found to form C-I···S halogen-bonded 1:1, 2:1, and 1:2 (donor/acceptor ratio) complexes with thiocarbonyls. Lengths of contacts were found to be clearly shorter than the sum of van der Waals radii of iodine and sulfur as well as the contact angles showed values close to linear, so the XB interactions could be verified. One sulfur atom showed the ability to accept one, two, or four XB interactions, and the acceptor angle can…

kemialliset sidoksetMaterials scienceHalogen bondhalogeenit010405 organic chemistryPolymer chemistryGeneral Materials ScienceGeneral Chemistrykompleksiyhdisteet010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciences
researchProduct

Selective Synthesis of Z -Silyl Enol Ethers via Ni-Catalyzed Remote Functionalization of Ketones

2021

Journal of the American Chemical Society : JACS 143(22), 8375-8380 (2021). doi:10.1021/jacs.1c01797

ketonesSilylationDimerketonit010402 general chemistry01 natural sciencesBiochemistrytransition metalsCatalysisCatalysischemistry.chemical_compoundkatalyytitColloid and Surface ChemistryPolymer chemistryhydrocarbonsoligomerseetteritkemiallinen synteesiOlefin fiberGeneral ChemistrySilyl enol ether540Enolhiilivedyt3. Good health0104 chemical sciencesoligomeerietherschemistryChain walkingddc:540nikkeliSelectivityJournal of the American Chemical Society
researchProduct