Search results for "fragmentation"

showing 10 items of 798 documents

Functionalization and patterning of reactive polymer brushes based on surface reversible addition and fragmentation chain transfer polymerization

2012

We present the synthesis of reactive polymer brushes prepared by surface reversible addition–fragmentation chain transfer polymerization of pentafluorophenyl acrylate. The reactive ester moieties can be used to functionalize the polymer brush film with virtually any functionality by simple post-polymerization modification with amines. Dithiobenzoic acid benzyl-(4-ethyltrimethoxylsilyl) ester was used as the surface chain transfer agent (S-CTA) and the anchoring group onto the silicon substrates. Reactive polymer brushes with adjustable molecular weight, high grafting density, and conformal coverage through the grafting-from approach were obtained. Subsequently, the reactive polymer brushes …

chemistry.chemical_classificationAcrylateMaterials sciencePolymers and PlasticsOrganic ChemistryChain transferPolymerPolymer brushchemistry.chemical_compoundchemistryChemical engineeringPolymerizationPolymer chemistryMaterials ChemistrySurface modificationReversible addition−fragmentation chain-transfer polymerizationWettingJournal of Polymer Science Part A: Polymer Chemistry
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Substrate-Independent Stable and Adherent Reactive Surface Coatings and their Conversion with Amines

2007

To create stable, adherent and reactive surface coatings, a hybrid polymer composed of poly(methylsilsesquioxane) (PMSSQ) and poly(pentafluorophenyl acrylate) PFPA with a M n of 32000 g/mol was prepared by a RAFT polymerization procedure. These hybrid polymer has been used for coating experiments. The PFPA part enabled a variable functionalization of the coating afterwards. The stability on various substrates (e.g. glass, PMMA, steel) was tested in an ISO tape test. These reactive surface coatings were modified using different amines, such as amino-terminated PEG, dodecyl amine and N-isopropyl amine. The conversion was analyzed by FT-IR and contact angle measurements.

chemistry.chemical_classificationAcrylateMaterials sciencePolymers and PlasticsOrganic ChemistryChain transferPolymerengineering.materialCondensed Matter PhysicsContact anglechemistry.chemical_compoundCoatingchemistryPolymer chemistryMaterials ChemistryengineeringSurface modificationThermal stabilityReversible addition−fragmentation chain-transfer polymerizationMacromolecular Symposia
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Self-assembly and intra-cluster reactions of erbium and ytterbium bis(2-ethylhexyl)sulfosuccinates in the gas phase

2014

RATIONALE The study of surfactant organization in vacuum allows surfactant–surfactant interaction to be unveiled in the absence of surrounding solvent molecules. Knowledge on their chemical-physical properties may also lead to the definition of more efficient gas-phase carriers, air-cleaning agents and nanoreactors. In addition, the presence of lanthanide-group ions adds unique photochemical properties to surfactants. METHODS The structural features, stability and fragmentation patterns of charged aggregates formed by lanthanide-functionalized surfactants, ytterbium and erbium bis(2-ethylhexyl)sulfosuccinate ((AOT)3Yb and (AOT)3Er), have been investigated by electrospray ionization mass spe…

chemistry.chemical_classificationAggregation numberChemistryElectrospray ionizationOrganic ChemistryAnalytical chemistryMass spectrometryPhotochemistryAnalytical ChemistrySupramolecular assemblyMassFragmentation (mass spectrometry)MoleculeSpectroscopyAlkylRapid Communications in Mass Spectrometry
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Langmuir-Blodgett films of biocompatible poly(HPMA)-block-poly(lauryl methacrylate) and poly(HPMA)-random-poly(lauryl methacrylate): influence of pol…

2010

Membranes based on functional biocompatible polymers can be regarded as a useful model system to study biological interactions, e.g. antibody-antigen interactions or protein polymer interactions. These model systems may give a better insight into these processes and may help to find suitable polymeric structures offering biocompatibility as well as reduced polymer protein interaction. In this respect, Langmuir-Blodgett (LB) layer formation at the air/water (A/W) interface is studied in respect to polymer architecture in this article. For this purpose, narrowly distributed N-(2-hydroxypropyl)-methacrylamide (HPMA) random and block copolymers have been prepared by the RAFT polymerization meth…

chemistry.chemical_classificationAqueous solutionMaterials scienceMagnetic Resonance SpectroscopyBiocompatibilityPolymersPolymer architectureBiocompatible MaterialsMembranes ArtificialSurfaces and InterfacesPolymerCondensed Matter PhysicsMicroscopy Atomic ForceLangmuir–Blodgett filmMembranechemistryPolymer chemistryElectrochemistryCopolymerMethacrylatesGeneral Materials ScienceReversible addition−fragmentation chain-transfer polymerizationSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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A detailed MSn study for the molecular identification of a dimer formed from oxidation of pinene

2016

Abstract Dimeric products formed in the oxidation of α- and β-pinene have been frequently observed in laboratory and field studies of biogenic SOA formation. While their existence is undoubted, their exact chemical structures remain unclear. This study uses a combined two step approach aiming on the molecular identification of the most important of the various dimers that have been observed in biogenic secondary organic aerosol formation, a dimer with the molecular weight 358 g mol−1. The first step is the application of a functional group derivatization technique (esterification) to quantify the number of carboxylic acid groups in the target molecule. Based on the detailed interpretation o…

chemistry.chemical_classificationAtmospheric Science010504 meteorology & atmospheric sciencesDimerCarboxylic acid010501 environmental sciencesMass spectrometry01 natural scienceschemistry.chemical_compoundchemistryFragmentation (mass spectrometry)Computational chemistryReagentFunctional groupOrganic chemistryMoleculeDerivatization0105 earth and related environmental sciencesGeneral Environmental ScienceAtmospheric Environment
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Radioactive labeling of defined HPMA-based polymeric structures using [18F]FETos for in vivo imaging by positron emission tomography.

2009

During the last decades polymer-based nanomedicine has turned out to be a promising tool in modern pharmaceutics. The following article describes the synthesis of well-defined random and block copolymers by RAFT polymerization with potential medical application. The polymers have been labeled with the positron-emitting nuclide fluorine-18. The polymeric structures are based on the biocompatible N-(2-hydroxypropyl)-methacrylamide (HPMA). To achieve these structures, functional reactive ester polymers with a molecular weight within the range of 25,000-110,000 g/mol were aminolyzed by 2-hydroxypropylamine and tyramine (3%) to form (18)F-labelable HPMA-polymer precursors. The labeling procedure…

chemistry.chemical_classificationBiodistributionAcrylamidesFluorine RadioisotopesPolymers and PlasticsPolymersRadical polymerizationSize-exclusion chromatographyRadiochemistryBioengineeringChain transferPolymerPolymerizationRatsBiomaterialsPolymerizationchemistryIsotope LabelingPositron-Emission TomographyPolymer chemistryMaterials ChemistryAnimalsReversible addition−fragmentation chain-transfer polymerizationPreclinical imagingBiotransformationBiomacromolecules
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Deglycosylated bleomycin triggers apoptosis in laryngeal carcinoma cells in a caspase and reactive oxygen species independent manner

2008

Background:  Bleomycin-A2, a member of a family of glycopeptide antibiotics, has potent antitumor activity against a range of lymphomas, head and neck cancer and germ cell tumors. However, little is known about the biologic activity of the carbohydrate moiety in Bleomycin-A2-induced cytotoxicity. Methods:  We compared the capacity of Bleomycin-A2 and its deglycosylated form (deglycoBleomycin-A2) to induce cell death. Apoptosis was analyzed by cell nuclear staining with Hoechst 33342 dye and DNA fragmentation. The signal transduction pathway was measured through Western blotting and production of reactive oxygen species (ROS). Results:  When tested on HEp-2 laryngeal carcinoma cells, Bleomyc…

chemistry.chemical_classificationCancer ResearchReactive oxygen speciesProgrammed cell deathbiologyMolecular biologyPathology and Forensic MedicineOtorhinolaryngologyBleomycin A2chemistryApoptosisImmunologybiology.proteinPeriodonticsDNA fragmentationViability assayOral SurgeryCytotoxicityCaspaseJournal of Oral Pathology & Medicine
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Functionalization of TiO2Nanoparticles with Semiconducting Polymers Containing a Photocleavable Anchor Group and Separation via Irradiation Afterward

2014

The controlled radical polymerization (RAFT polymerization) of semiconducting polymers based on poly(4,4′-dimethyl-triphenylamine) is described. These polymers are afterward end-functionalized with a photocleavable group and an anchor unit (catechol) for oxidic nanoparticles (NPs). Serving as a reference, polystyrene oligomers with the same end groups are also synthesized. Using these polymers allows functionalization of the TiO2-NPs, leading to an improved solubility and miscibility in organic solvents or polymer matrices. Irradiation in the UV region is used to split the photocleavable group and remove the polymer chains from the NPs, which leads to their aggregation.

chemistry.chemical_classificationCatecholPolymers and PlasticsOrganic ChemistryRadical polymerizationtechnology industry and agricultureNanoparticlePolymerCondensed Matter PhysicsMiscibilitychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistrySurface modificationReversible addition−fragmentation chain-transfer polymerizationPolystyrenePhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Collision-Induced Dissociation of Imidazolium-Based Zwitterionic Liquids

2009

Fragmentation pathways of some imidazolium based zwitterionic liquids—3-(3-alkyl-1-imidazolio)-propane sulfonates and 3-(2-methyl-3-alkyl-1-imidazolio)-propane sulfonates—have been studied by tandem electrospray mass spectrometry and collision-induced dissociation. The relative abundances of the lowest energy fragment ions depend on the length of the alkyl chain at the IIN of the imidazolium ring and the cone voltage. The first fragment ions originate from the scission of Cnon aromatic–N bond of compounds investigated, but with increasing collision energy, scission of C–C bonds occurs. Aggregates of the general formula [(M + H) x + (M) y]+ ( x;y = 1–2) formed. Methyl substituted zwitterion…

chemistry.chemical_classificationCollision-induced dissociationChemistryElectrospray ionizationGeneral MedicineMass spectrometryMedicinal chemistryAtomic and Molecular Physics and OpticsDissociation (chemistry)IonFragmentation (mass spectrometry)Organic chemistrySpectroscopyAlkylBond cleavageEuropean Journal of Mass Spectrometry
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2017

Abstract. Further development and optimisation of a previously described ion trap aerosol mass spectrometer (IT-AMS) are presented, which resulted in more reproducible and robust operation and allowed for the instrument's first field deployment. Results from this 11-day-long measurement indicate that the instrument is capable of providing quantitative information on organics, nitrate, and sulfate mass concentrations with reasonable detection limits (0.5–1.4 µg m−3 for 1 h averages) and that results obtained with the IT-AMS can directly be related to those from Aerodyne aerosol mass spectrometers. The capability of the IT-AMS to elucidate the structure of fragment ions is demonstrated via an…

chemistry.chemical_classificationDetection limitAtmospheric Science010504 meteorology & atmospheric sciences010401 analytical chemistryAnalytical chemistryMass spectrometry01 natural sciencesOrganic compound0104 chemical sciencesAerosolIonchemistryFragmentation (mass spectrometry)MoleculeIon trap0105 earth and related environmental sciencesAtmospheric Measurement Techniques
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