Search results for "modification"

showing 10 items of 853 documents

New insights into the water-solubilization of thiol-sensitive fluorogenic probes based on long-wavelength 7-hydroxycoumarin scaffolds

2014

Abstract The synthesis and photophysical properties of novel water-soluble phenol-based fluorophores derived from 3-benzothiazolyl-7-hydroxycoumarin and emitting in the range 485–631 nm are described. Further conversion into thiol-sensitive fluorogenic probes through the chemical modification of their hydroxyl group was next investigated. Depending on the type of thiol-reactive quenching moiety used (2,4-dinitrobenzenesulfonyl ester, 2,4-dinitrophenyl ether or benzoquinone-type Michael acceptors) and the water-solubilizing group(s) pre-introduced into the coumarin core, dramatic differences in the thiol-induced fluorescence activation of these pro-fluorophores under physiological conditions…

chemistry.chemical_classificationQuenching (fluorescence)[CHIM.ORGA]Chemical Sciences/Organic chemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringChemical modificationEther[CHIM.CATA]Chemical Sciences/Catalysis[CHIM.THER]Chemical Sciences/Medicinal ChemistryPhotochemistryCoumarinFluorescence[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundchemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistryThiolPhenolMoietyComputingMilieux_MISCELLANEOUS[CHIM.CHEM]Chemical Sciences/CheminformaticsDyes and Pigments
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Inorganic Polymers: Morphogenic Inorganic Biopolymers for Rapid Prototyping Chain

2013

In recent years, considerable progress has been achieved towards the development of customized scaffold materials, in particular for bone tissue engineering and repair, by the introduction of rapid prototyping or solid freeform fabrication techniques. These new fabrication techniques allow to overcome many problems associated with conventional bone implants, such as inadequate external morphology and internal architecture, porosity and interconnectivity, and low reproducibility. However, the applicability of these new techniques is still hampered by the fact that high processing temperature or a postsintering is often required to increase the mechanical stability of the generated scaffold, …

chemistry.chemical_classificationRapid prototypingScaffoldBiocompatibilityNanotechnologyPolymerBiologyInterconnectivityBone tissue engineeringlaw.inventionchemistrylawBioactive glassSurface modification
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Isoreticular two-dimensional magnetic coordination polymers prepared through pre-synthetic ligand functionalization

2018

Chemical functionalization is a powerful approach to tailor the physical and chemical properties of two-dimensional (2D) materials, increase their processability and stability, tune their functionalities and, even, create new 2D materials. This is typically achieved through post-synthetic functionalization by anchoring molecules on the surface of an exfoliated 2D crystal, but it inevitably alters the long-range structural order of the material. Here we present a pre-synthetic approach that allows the isolation of crystalline, robust and magnetic functionalized monolayers of coordination polymers. A series of five isostructural layered magnetic coordination polymers based on Fe(ii) centres a…

chemistry.chemical_classificationSolucions polimèriquesChemistryLigandMagnetismGeneral Chemical EngineeringNanotechnology02 engineering and technologyGeneral ChemistryPolymerCiència dels materials010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesExfoliation joint0104 chemical sciencesMonolayerSurface modificationMoleculeIsostructural0210 nano-technologyNature Chemistry
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Solvent-free ruthenium-catalysed triflate coupling as a convenient method for selective azole-o-C-H monoarylation.

2019

Metal-catalysed ortho-directed C–H functionalization usually faces selectivity issues in the competition between mono- and disubstitution processes. We report herein the ruthenium-catalysed N-directed C–H monoarylation of arylpyrazoles with a selectivity of up to 96% or that generally reaches values above 80%. This selectivity is an effect of solvent-free conditions associated with sulfonate reagents, in the absence of frequently used acidic additives.

chemistry.chemical_classificationSolvent free010405 organic chemistryChemistryOrganic Chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesRutheniumchemistry.chemical_compoundSulfonateReagentSurface modificationAzolePhysical and Theoretical ChemistrySelectivityTrifluoromethanesulfonateOrganicbiomolecular chemistry
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Silica-Immobilized NHC-Gold(I) Complexes: Versatile Catalysts for the Functionalization of Alkynes under Batch and Continuous Flow Conditions

2017

Immobilized sterically demanding NHC-Au(I) complexes silica-[(IPrR)Au]Cl and silica-[(IAdPrR)Au]Cl are synthesized and characterized. These complexes are suitable catalysts in typical homogeneous Au(I)-catalyzed alkyne reactions such as hydration, hydroamination, hydroarylation, or cycloisomerization. The results obtained with the immobilized catalysts in reactions in batch are comparable to those obtained with their homogeneous counterparts with the advantage of easily recovered and recycled in successive reactions. Their catalytic activity decreases when reused in batch reactions, probably because of crushing that is associated with magnetic stirring. In contrast, these immobilized cataly…

chemistry.chemical_classificationSteric effects010405 organic chemistryContinuous flowInorganic chemistryAlkyneGeneral ChemistryFlow chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisCycloisomerizationchemistrySurface modificationHydroaminationACS Catalysis
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Synthetic approaches towards new polymer systems by the combination of living carbocationic and anionic polymerizations

1996

This study summarizes recent efforts to obtain by combination of living carbocationic and anionic polymerizations block copolymers which are potential precursors for building new well-defined polymeric architectures with microphase separated morphology. Living carbocationic polymerization (LCCP) yields telechelic polyisobutylene (PIB) chains with a variety of useful endgroups, such as tert-chlorine, isopropenyl, primary hydroxyl, tolyl etc. When tolyl-ended PIB was used as precursor for macroinitiator of living anionic polymerization of 2-(tert-butyldimethylsilyloxy)ethyl methacrylate (tBuMe2SiOEMA), mixtures of homopolymers and block copolymers were formed due to incomplete lithiation of t…

chemistry.chemical_classificationSteric effectsMaterials sciencePolymers and PlasticsOrganic ChemistryPolymerCondensed Matter PhysicsMethacrylatechemistryPolymerizationAmphiphilePolymer chemistryMaterials ChemistryCopolymerSurface modificationOrganic chemistryLiving anionic polymerization
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Surface-Functionalized Latex Particles as Controlling Agents for the Mineralization of Zinc Oxide in Aqueous Medium

2005

Polystyrene latex particles modified at the surface with different hydrophilic functional groups were prepared by miniemulsion polymerization and used as controlling agents in the crystallization of zinc oxide from aqueous medium. The effects of the chemical nature of the surface functionalization and the latex concentration on the crystal growth, morphology, and crystalline structure of the resulting zinc oxide were analyzed. Micro- and submicrosized crystals with a broad variety of morphologies depending on the functionalization were obtained. Among the different latexes studied, the acrylic-acid-derived particles were shown to be a convenient system for further quantitative investigation…

chemistry.chemical_classificationSurface PropertiesChemistryOrganic ChemistryWaterGeneral ChemistryPolymerMicrospheresCatalysislaw.inventionMiniemulsionAdsorptionX-Ray DiffractionChemical engineeringPolymerizationlawPolymer chemistryWettabilityPolystyrenesSurface modificationWettingParticle sizeParticle SizeZinc OxideCrystallizationChemistry - A European Journal
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Identification of the 3-amino-3-carboxypropyl (acp) transferase enzyme responsible for acp3U formation at position 47 in Escherichia coli tRNAs

2019

AbstracttRNAs from all domains of life contain modified nucleotides. However, even for the experimentally most thoroughly characterized model organism Escherichia coli not all tRNA modification enzymes are known. In particular, no enzyme has been found yet for introducing the acp3U modification at position 47 in the variable loop of eight E. coli tRNAs. Here we identify the so far functionally uncharacterized YfiP protein as the SAM-dependent 3-amino-3-carboxypropyl transferase catalyzing this modification and thereby extend the list of known tRNA modification enzymes in E. coli. Similar to the Tsr3 enzymes that introduce acp modifications at U or m1Ψ nucleotides in rRNAs this protein conta…

chemistry.chemical_classificationTRNA modificationAlkyl and Aryl TransferasesNucleic Acid EnzymesNucleotidesRNASaccharomyces cerevisiaeBiologymedicine.disease_causePhenotypeEnzymechemistryBiochemistryBacterial ProteinsRNA TransferTransfer RNAGeneticsmedicineEscherichia coliTransferaseNucleic Acid ConformationNucleotideEscherichia coliNucleic Acids Research
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Heterotelechelic Ring-Opening Metathesis Polymers

2009

By combining sacrificial synthesis with the vinyl lactone termination technique, heterotelechelic polymers were synthesized. The nonterminating nature of sacrificial synthesis was utilized to introduce a hydroxyl group at the start of the polymer chain. Lactone termination was used to functionalize the chain ends with aldehydes or carboxylic acids. The synthesis of well-defined heterotelechelic polymers was thus accomplished employing the Grubbs’ first generation catalyst as the initiator. The living nature of this polymerization allowed for precise control over the molecular weight and guaranteed full functionalization of both polymer chain ends. The presence of the functional groups is sh…

chemistry.chemical_classificationTelechelic polymerPolymers and PlasticsChemistryOrganic ChemistryPolymerRing (chemistry)MetathesisInorganic Chemistrychemistry.chemical_compoundPolymerizationPolymer chemistryMaterials ChemistrySurface modificationImideLactoneMacromolecules
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Sacrificial Synthesis of Hydroxy-Telechelic Metathesis Polymers via Multiblock-Copolymers

2009

The synthesis of well-defined telechelic ring-opening metathesis polymers has been achieved by Sacrificial Synthesis. With the formation of cleavable triblock-copolymers, precise control over the molecular weight and the degree of functionalization was achieved. Introducing cleavable monomers that can be addressed separately, sequential deprotection was accomplished which opened the path to more sophisticated polymeric materials bearing different substituents at their respective chain ends. Sacrificial penta- and heptablock-copolymers are also presented which allow the synthesis of well-defined telechelic polymers in good yields and significantly improved initiator efficiency.

chemistry.chemical_classificationTelechelic polymerPolymers and PlasticsOrganic ChemistryMultiblock copolymerPolymerMetathesisInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistrySurface modificationAcetal copolymerImideMacromolecules
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