Search results for " POLYMER"

showing 10 items of 3533 documents

Synthesis and solution properties of star-shaped poly(tert-butyl acrylate)

2000

A series of star polymers consisting of poly(tert-butyl acrylate) arms and an ethyleneglycol dimethacrylate (EGDMA) microgel core were synthesized using anionic polymerization. The effect of various parameters (precursor length, ratio [[EGDMA]/[Initiator], reaction time, and overall concentrations) on the average number of arms was investigated. Molecular weights were determined using GPC coupled with an online viscometer and MALLS. The exponents for the relation between intrinsic viscosity or radius of gyration and molecular weight, respectively, are extremely low, indicating that the dimensions of the star polymers only slightly increase with the number of arms. After a certain number of …

AcrylateTert-butyl acrylateMaterials sciencePolymers and PlasticsMolecular massIntrinsic viscosityOrganic ChemistryViscometerStar (graph theory)Condensed Matter PhysicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundAnionic addition polymerizationchemistryPolymer chemistryMaterials ChemistryRadius of gyrationPhysical chemistryAstrophysics::Galaxy AstrophysicsMacromolecular Symposia
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1993

The influence of lithium tert-butoxide (tBuOLi) and of lithium chloride on the oligomerization of tert-butyl acrylate (tBuA) initiated by tert-butyl α-lithioisobutyrate (tBiB-Li) was investigated. These additives affect both the kinetics and the product distribution. Whereas the addition of LiCl leads to a narrower molecular-weight distribution (MWD) the presence of tBuOLi induces broader MWD's, characterized by a very high fraction of the dimer. Both additives decrease the rates of propagation to different degrees. These effects are discussed on the basis of the formation of aggregates and adducts, the lithiated dimer having a higher tendency to form aggregates than the other oligomers. Th…

Acrylatechemistry.chemical_compoundAnionic addition polymerizationchemistryDimerPolymer chemistryKineticsAlkoxideLithium chloridechemistry.chemical_elementSolution polymerizationLithiumDie Makromolekulare Chemie
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Different pathways for the nuclear import of yeast RNA polymerase II

2015

Recent studies suggest that RNA polymerase II (Pol II) has to be fully assembled before being imported into the nucleus, while other reports indicate a distinct mechanism to import large and small subunits. In yeast, Iwr1 binds to the holoenzyme assembled in the cytoplasm and directs its nuclear entry. However, as IWR1 is not an essential gene, Iwr1-independent pathway(s) for the nuclear import of Pol II must exist. In this paper, we investigate the transport into the nucleus of several large and small Pol II subunits in the mutants of genes involved in Pol II biogenesis. We also analyse subcellular localization in the presence of drugs that can potentially affect Pol II nuclear import. Our…

Active Transport Cell NucleusBiophysicsRNA polymerase IISaccharomyces cerevisiaeBiochemistrychemistry.chemical_compoundStructural BiologyRNA polymeraseGeneticsmedicineMolecular BiologyCell NucleusbiologyProcessivitySubcellular localizationMolecular biologyCell biologyCell nucleusmedicine.anatomical_structurechemistrybiology.proteinRNA Polymerase IITranscription factor II DNuclear transportCarrier ProteinsBiogenesisBiochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms
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Prediction of Maxwell – Stefan diffusion coefficients in polymer – multicomponent fluid systems

2014

Abstract Calculations of mass fluxes in multicomponent fluids based on the system of generalized Maxwell–Stefan equations (GMSE) is preferably used because Maxwell–Stefan (M–S) diffusion coefficients are symmetrical and have a clear physical meaning, as they reflect the binary friction forces between compounds in the system. For the calculation of the mass transport of a multicomponent fluid in the polymer basing on GMSE, it is necessary to have M–S diffusion coefficients. This paper proposes a method that allows their calculation using widely available self-diffusion coefficients and binary diffusion coefficients for infinitely diluted mixtures. The proposed method was compared with the me…

Activity coefficientMolar concentrationChemistryDiffusionThermodynamicsFiltration and SeparationMole fractionBiochemistrychemistry.chemical_compoundMaxwell–Stefan diffusionVinyl acetateGeneral Materials ScienceDiffusion; Multicomponent; Polymer; Free volume; Maxwell–StefanPhysical and Theoretical ChemistryTernary operationMass fractionJournal of Membrane Science
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Die kationische ɛ-caprolactam-polymerisation. IV. Isolierung und strukturermittlung der oligomeren als beitrag zur aufklärung des polymerisationsmech…

1966

Molekulareinheitliche Oligomere von Polykondensations- und Polyadditionsreaktionen konnen zur Aufklarung von Struktur und Bildungsmechanismus der Polymeren dienen. Auf diesem Wege wird der fruher vorgeschlagene Mechanismus der kationischen Lactampolymerisation mit wasserfreien Sauren erhartet, der in einer Acylierung des Lactams durch Lactamsalz unter Bildung von Aminoacyllactamsalz und nachfolgendem Kettenwachstum durch Addition weiterer Lactammolekule an die entstandene und immer wieder neu gebildete Ammonium-Endgruppe besteht. Dazu werden aus Caprolactam und Chlorwasserstoff als Initiator unter geeigneten Bedingungen Oligomerengemische gewonnen und elektrophoretisch aufgetrennt. Mikropra…

Acylationchemistry.chemical_compoundHydroxylamineMonomerCondensation polymerchemistryHydrochloridePolymer chemistryCationic polymerizationCaprolactamLactamDie Makromolekulare Chemie
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2014

Carbon-centered radicals represent highly useful reactive intermediates in organic synthesis. Their nucleophilic character is reflected by fast additions to electron deficient C=X double bonds as present in iminium ions or cationic heterocycles. This review covers diverse reactions of preformed or in situ-generated cationic substrates with various types of C-radicals, including alkyl, alkoxyalkyl, trifluoromethyl, aryl, acyl, carbamoyl, and alkoxycarbonyl species. Despite its high reactivity, the strong interaction of the radical’s SOMO with the LUMO of the cation frequently results in a high regioselectivity. Intra- and intermolecular processes such as the Minisci reaction, the Porta react…

Addition reactionChemistryOrganic ChemistryReactive intermediateCationic polymerizationPharmaceutical ScienceIminiumRegioselectivityPhotoredox catalysisPhotochemistryMedicinal chemistryAnalytical ChemistryNucleophileChemistry (miscellaneous)Drug DiscoveryMolecular MedicinePhysical and Theoretical ChemistryMinisci reactionMolecules
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ChemInform Abstract: Radical Addition to Iminium Ions and Cationic Heterocycles

2015

Carbon-centered radicals represent highly useful reactive intermediates in organic synthesis. Their nucleophilic character is reflected by fast additions to electron deficient C=X double bonds as present in iminium ions or cationic heterocycles. This review covers diverse reactions of preformed or in situ-generated cationic substrates with various types of C-radicals, including alkyl, alkoxyalkyl, trifluoromethyl, aryl, acyl, carbamoyl, and alkoxycarbonyl species. Despite its high reactivity, the strong interaction of the radical’s SOMO with the LUMO of the cation frequently results in a high regioselectivity. Intra- and intermolecular processes such as the Minisci reaction, the Porta react…

Addition reactionNucleophileChemistryReactive intermediateCationic polymerizationPhotoredox catalysisIminiumRegioselectivityGeneral MedicineMedicinal chemistryMinisci reactionChemInform
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Machine learning of reverse transcription signatures of variegated polymerases allows mapping and discrimination of methylated purines in limited tra…

2020

AbstractReverse transcription (RT) of RNA templates containing RNA modifications leads to synthesis of cDNA containing information on the modification in the form of misincorporation, arrest, or nucleotide skipping events. A compilation of such events from multiple cDNAs represents an RT-signature that is typical for a given modification, but, as we show here, depends also on the reverse transcriptase enzyme. A comparison of 13 different enzymes revealed a range of RT-signatures, with individual enzymes exhibiting average arrest rates between 20 and 75%, as well as average misincorporation rates between 30 and 75% in the read-through cDNA. Using RT-signatures from individual enzymes to trai…

AdenosineAcademicSubjects/SCI00010Machine learningcomputer.software_genre[SDV.BBM.BM] Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologyMethylationMachine Learning03 medical and health sciences0302 clinical medicineComplementary DNA[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]GeneticsMolecular BiologyPolymerase030304 developmental biologychemistry.chemical_classification0303 health sciencesOligoribonucleotidesGuanosinebiologybusiness.industryRNA-Directed DNA PolymeraseRNARNA-Directed DNA Polymerase[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologyReverse TranscriptionMethylationReverse transcriptaseEnzymechemistryTransfer RNAbiology.protein[SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]Artificial intelligenceTranscriptomebusinesscomputer030217 neurology & neurosurgery
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Green composites: A brief review

2011

The rising concern towards environmental issues and, on the other hand, the need for more versatile polymer-based materials has led to increasing interest about polymer composites filled with natural-organic fillers, i.e. fillers coming from renewable sources and biodegradable. The composites, usually referred to as "green", can find several industrial applications. On the other hand, some problems exist, such as worse processability and reduction of the ductility. The use of adhesion promoters, additives or chemical modification of the filler can help in overcoming many of these limitations. These composites can be further environment-friendly when the polymer matrix is biodegradable and c…

Adhesion promotersA. Polymer-matrix composites (PMCs)Materials scienceB. Mechanical propertieMechanics of MaterialsFiller (materials)A. WoodCeramics and CompositesengineeringPolymer compositesCeramics and Compositeengineering.materialComposite material
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Use of the polymerase chain reaction to demonstrate hepatitis B virus DNA in serum of children with chronic hepatitis B.

1992

The polymerase chain reaction was used to investigate the presence of hepatitis B virus DNA in sera of 61 children with chronic hepatitis B and negative results on dot biot hybridization tests. Our results demonstrate that most chronic carriers of hepatitis B surface antigen in childhood have hepatitis B virus DNA detectable by polymerase chain reaction in their serum and must be considered infectious.

AdolescentHepatitis B virus DNA polymeraseHepatitis B virus DNAmedicine.disease_causePolymerase Chain ReactionVirusHepatitis B virus PRE betalaw.inventionChronic hepatitislawMedicineHumansHepatitis B e AntigensHepatitis B AntibodiesChildPolymerase chain reactionHepatitis B virusbiologybusiness.industryInfantbiology.organism_classificationHepatitis BVirologyHepadnaviridaeChild PreschoolPediatrics Perinatology and Child HealthChronic DiseaseDNA ViralbusinessThe Journal of pediatrics
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