Search results for "Mono"

showing 10 items of 6843 documents

Cyclodextrins in Polymer Synthesis: Enantiodiscrimination in Free-Radical Polymerization of Cyclodextrin-Complexed Racemic N -Methacryloyl-D,L -pheny…

2003

The enantiodiscriminating polymerization of racemic cyclodextrin-complexed N-methacryloylphenylalanine methyl ester is investigated 1 H NMR spectra of the complexes with methylated β-cyclodextrin in D 2 O manifest splittings due to chiral recognition. The different stabilities of the diastereomeric complexes influence the kinetics of the homopolymerization, particularly at 0°C. An enrichment of the residual N-methacryloyl-L-phenylalanine methyl ester of 14% was achieved after 21 h of polymerization.

chemistry.chemical_classificationReaction mechanismPolymers and PlasticsCyclodextrinOrganic ChemistryRadical polymerizationtechnology industry and agricultureDiastereomerPolymerchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistrypolycyclic compoundsMaterials ChemistryProton NMRMacromolecular Rapid Communications
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NMR and Quantum-Chemical Study on the Structure of Ester Enolate−Aluminum Alkyl Complexes as Models of the Active Center in the Anionic Polymerizatio…

1999

6Li and 13C NMR on ethyl α-lithioisobutyrate (EiBLi) and quantum-chemical (DFT) calculations on methyl α-lithioisobutyrate (MiBLi) were used to elucidate the structure of the active center in the anionic polymerization of methacrylates in the presence of triethylaluminum (AlEt3) in toluene. This study reveals ester enolate/aluminum alkyl complexes with different degrees of association, (MiBLi·AlEt3)n (n = 1, 2, 4), and different stoichiometries, MiBLi·xAlEt3 (x = 1, 2). In the presence of methyl pivalate (MPiv), which is taken as a model compound for the monomer and polymer, complexes such as (MiBLi·MPiv·AlEt3)n (n = 1, 2) are formed. These complexes can dissociate into MiBLi·2AlEt3 and MPi…

chemistry.chemical_classificationReaction mechanismPolymers and PlasticsOrganic ChemistrySolution polymerizationPolymerCarbon-13 NMRTolueneInorganic ChemistryActive centerchemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymer chemistryMaterials ChemistryMacromolecules
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Polymerization of ε-caprolactone using heterobimetallic lanthanocene complexes

1997

The chiral heterobimetallic complexes Li[Ln(η 5 :η 1 -C 5 R 4 1 SiMe 2 NCH 2 CH 2 R 2 ) 2 ] (ln= Y, Lu; C 5 R 4 1 = C 5 Me 4 , C 5 H 4 , 3-C 5 H 3 tBu; R 2 = OMe, NMe 2 ) have been found to polymerize e-caprolactone to give a polymer of high molecular weight (M n > 20000) and moderate polydispersity (M w /M n < 2). Failure to observe a correlation between monomer/initiator ratio and molecular weight suggest a polymerization mechanism different from a pseudo-anionic mechanism

chemistry.chemical_classificationReaction mechanismPolymers and PlasticsStereochemistryOrganic ChemistryDispersitySolution polymerizationPolymerMedicinal chemistryRing-opening polymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationMaterials ChemistryCaprolactoneMacromolecular Rapid Communications
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Glutathione-dependent defence system and monooxygenase enzyme activities in Arctic charr Salvelinus alpinus (L.) exposed to ozone

2000

Abstract One of the major obstacles of the increasing usage of ozone in aquaculture is the lack of relevant risk assessment in culture conditions. Before the apparent advantages of ozonation can be utilised efficiently, the safety margins and biological basis of ozone toxicity should be assessed. In this research, 1-year-old Arctic charr ( Salvelinus alpinus (L.)) were exposed to an ozone concentration high enough to inactivate Aeromonas sp. bacteria in freshwater, but too low to be directly lethal to the fish themselves. The effects of ozone exposure on the activity of glutathione-dependent antioxidant enzymes and monooxygenase reactions were studied in blood and in liver. The fish were ac…

chemistry.chemical_classificationReactive oxygen speciesOzoneAntioxidantbiologymedicine.medical_treatmentGlutathioneAquatic ScienceMonooxygenasemedicine.disease_causeEnzyme assaychemistry.chemical_compoundchemistryBiochemistryToxicitybiology.proteinmedicineFood scienceOxidative stressAquaculture
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Formation of covalent di-tyrosine dimers in recombinant α-synuclein

2015

Parkinson's disease is associated with fibril deposition in the diseased brain. Misfolding events of the intrinsically disordered synaptic protein α-synuclein are suggested to lead to the formation of transient oligomeric and cytotoxic species. The etiology of Parkinson's disease is further associated with mitochondrial dysfunction and formation of reactive oxygen species. Oxidative stress causes chemical modification of native α-synuclein, plausibly further influencing misfolding events. Here, we present evidence for the spontaneous formation of covalent di-tyrosine α-synuclein dimers in standard recombinant protein preparations, induced without extrinsic oxidative or nitrative agents. The…

chemistry.chemical_classificationReactive oxygen speciesParkinson's diseasealphasynucleinamyloids di-tyrosine dimers EOM Parkinson’s disease SAXSSAXSOxidative phosphorylationFibrilmedicine.disease_causeIndustrial and Manufacturing Engineeringchemistry.chemical_compoundα-synucleinMonomerchemistryBiochemistryCovalent bondmedicinedi-tyrosine dimersamyloidsTyrosineProtein secondary structureEOMOxidative stressResearch PaperIntrinsically Disordered Proteins
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Validation strategies for antibodies targeting modified ribonucleotides

2020

Chemical modifications are found on almost all RNAs and affect their coding and noncoding functions. The identification of m6A on mRNA and its important role in gene regulation stimulated the field to investigate whether additional modifications are present on mRNAs. Indeed, modifications including m1A, m5C, m7G, 2′-OMe, and Ψ were detected. However, since their abundances are low and tools used for their corroboration are often not well characterized, their physiological relevance remains largely elusive. Antibodies targeting modified nucleotides are often used but have limitations such as low affinity or specificity. Moreover, they are not always well characterized and due to the low abun…

chemistry.chemical_classificationRegulation of gene expression0303 health sciencesMessenger RNAbiologyNucleotidesmedicine.drug_class030302 biochemistry & molecular biologyMethodComputational biologyRibonucleotidesMonoclonal antibodyAntibodies03 medical and health sciencesLow affinitychemistrybiology.proteinmedicineRNANucleotideRNA MessengerAntibodyMolecular Biology030304 developmental biologyRNA
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Sodium Dodecylsulphate Electrophoresis

1994

Sodium dodecylsulphate (SDS) consists of an aliphatic chain of 12 C atoms to which at one end a sulphate residue is bound. It forms complexes with both the polar and non- polar amino acid residues of proteins irrespective of their sizes and shapes, leaving the primary structure uninfluenced. In electrophoresis SDS is used: a) to separate (enzyme) proteins into their monomeric constituents, b) to estimate the molecular mass of unfolded (and reduced) polypeptides, and c) to keep membrane proteins in a solubilized state.

chemistry.chemical_classificationResidue (chemistry)chemistry.chemical_compoundElectrophoresisEnzymeMonomerChromatographychemistryMembrane proteinMolecular massSodiumProtein primary structurechemistry.chemical_element
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Cyclodextrins in Polymer Synthesis:  Free Radical Polymerization of a N-Methacryloyl-11-aminoundecanoic Acid/β-Cyclodextrin Pseudorotaxane in an Aque…

1999

The relatively hydrophobic monomer N-methacryloyl-11-aminoundecanoic acid (1) was incorporated as a guest into the cavity of β-cyclodextrin (β-CD) as a host, yielding the water-soluble monomer N-me...

chemistry.chemical_classificationRotaxanePolymers and PlasticsAqueous mediumCyclodextrinOrganic ChemistryRadical polymerizationSolution polymerizationmacromolecular substancesPolymerPolyelectrolyteInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryOrganic chemistryMacromolecules
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Investigation of Multicomponent Sorption in Polymers from Fluid Mixtures at Supercritical Conditions:  The Case of the Carbon Dioxide/Vinylidenefluor…

2008

The simultaneous sorption of carbon dioxide and vinylidene fluoride (VDF) in poly(vinylidenefluoride) from their supercritical (sc) mixtures was studied using an experimental method, already described in a previous publication, based on the gas-chromatographic determination of the equilibrium composition of the fluid phase in contact with the polymer. Argon was added to the system as a nonabsorbable molecular probe in the polymer to take into account the effect of the volume swelling on the measurement. Sorption behavior has been studied at 50 °C by changing the composition and the density of the supercritical phase. We have found that VDF dissolves in its polymer with concentrations much l…

chemistry.chemical_classificationSettore ING-IND/26 - Teoria Dello Sviluppo Dei Processi ChimiciPolymers and PlasticsOrganic ChemistryRadical polymerizationSorptionPolymerSettore ING-IND/27 - Chimica Industriale E TecnologicaSupercritical fluidInorganic Chemistrychemistry.chemical_compoundChemical reaction kineticsMonomerchemistryChemical engineeringCarbon dioxideMaterials ChemistryOrganic chemistryFluorideFluid mechanicsGas chromatographyPolymerizationPolymersSorptionMacromolecules
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Ferrocenyl-functionalized long chain branched polydienes

2009

A convenient two-step approach for the synthesis of ferrocenyl-functionalized long chain branched polydienes, based on both butadiene and isoprene, respectively, is presented. Classical living anionic polymerization was used to synthesize different AB n type poly(diene) macromonomers with moderate molecular weights between 1700 and 3200 g/mol and narrow polydispersity. Quantitative end-capping with chlorodimethylsilane resulted in the desired AB n macromonomer structures. In the ensuing Pt-catalyzed hydrosilylation polyaddition, branched, functionalized polydienes were obtained by a concurrent AB n + AR type of copolymerization with mono-and difunctional ferrocenyl silanes (fcSiMe 2 H or fc…

chemistry.chemical_classificationSilanesPolymers and PlasticsHydrosilylationOrganic ChemistryPolymerBranching (polymer chemistry)Macromonomerchemistry.chemical_compoundAnionic addition polymerizationchemistryPolymer chemistryMaterials ChemistryCopolymerLiving anionic polymerizationJournal of Polymer Science Part A: Polymer Chemistry
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