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showing 10 items of 70 documents

Chemoenzymatic Synthesis of Functional Sialyl LewisX Mimetics with a Heteroaromatic Core

2014

Functional mimetics of the sialyl Lewis(X) tetrasaccharide were prepared by the enzymatic sialylation of a 1,3-diglycosylated indole and a glycosyl azide, which was subsequently transformed into a 1,4-diglycosylated 1,2,3-triazole, by using the trans-sialidase of Trypanosoma cruzi. These compounds inhibited the binding of E-, L-, and P-selectin-coated nanoparticles to polyacrylamide-bound sialyl-Lewis(X) -containing neighboring sulfated tyrosine residues (sTyr/sLe(X) -PAA) at low or sub-millimolar concentrations. Except for E-selectin, the mimetics showed higher activities than the natural tetrasaccharide.

Spectrometry Mass Electrospray IonizationStereochemistryProton Magnetic Resonance SpectroscopyTrypanosoma cruziMolecular Sequence DataNeuraminidaseOligosaccharidessaccharide mimeticsBiochemistryenzyme catalysisEnzyme catalysischemistry.chemical_compoundSulfationTetrasaccharideAnimalsGlycosylTyrosineCarbon-13 Magnetic Resonance SpectroscopySialyl Lewis X AntigenGlycoproteinsIndole testheterocyclesOrganic ChemistryMolecular Mimicrycell adhesionGeneral ChemistryFull Paperscarbohydrates (lipids)Sialyl-Lewis XchemistryCarbohydrate SequenceSelectinsAzideChemistry, an Asian Journal
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Binding Sites, Vibrations and Spin-Lattice Relaxation Times in Europium(II)-Based Metallofullerene Spin Qubits.

2021

Abstract To design molecular spin qubits with enhanced quantum coherence, a control of the coupling between the local vibrations and the spin states is crucial, which could be realized in principle by engineering molecular structures via coordination chemistry. To this end, understanding the underlying structural factors that govern the spin relaxation is a central topic. Here, we report the investigation of the spin dynamics in a series of chemically designed europium(II)‐based endohedral metallofullerenes (EMFs). By introducing a unique structural difference, i. e. metal‐cage binding site, while keeping other molecular parameters constant between different complexes, these manifest the ke…

Spin statesFOS: Physical scienceschemistry.chemical_element010402 general chemistry01 natural sciencesMolecular physicsCatalysischemistry.chemical_compoundVery Important PaperPhysics - Chemical PhysicsPhysics::Atomic and Molecular ClustersPhysics - Atomic and Molecular Clustersspin-vibration couplingQuantumeuropiumSpin-½Chemical Physics (physics.chem-ph)Full Paper010405 organic chemistryChemistryNanotecnologiaOrganic ChemistryRelaxation (NMR)Spin–lattice relaxationfullerenesGeneral ChemistryQuímicaFull Papers0104 chemical sciences3. Good healthQubitMetallofullerenemagnetic propertiesAtomic and Molecular Clusters (physics.atm-clus)Europiumspin qubitsChemistry (Weinheim an der Bergstrasse, Germany)
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Asymmetric Disulfanylbenzamides as Irreversible and Selective Inhibitors of Staphylococcus aureus Sortase A

2020

Abstract Staphylococcus aureus is one of the most frequent causes of nosocomial and community‐acquired infections, with drug‐resistant strains being responsible for tens of thousands of deaths per year. S. aureus sortase A inhibitors are designed to interfere with virulence determinants. We have identified disulfanylbenzamides as a new class of potent inhibitors against sortase A that act by covalent modification of the active‐site cysteine. A broad series of derivatives were synthesized to derive structure‐activity relationships (SAR). In vitro and in silico methods allowed the experimentally observed binding affinities and selectivities to be rationalized. The most active compounds were f…

Staphylococcus aureusmedicine.drug_classdrug designAntibioticsVirulenceMicrobial Sensitivity Testsmedicine.disease_cause01 natural sciencesBiochemistrybiofilmMicrobiology570 Life sciencesStructure-Activity RelationshipBacterial ProteinsAntibioticssortase ADrug DiscoverymedicineGeneral Pharmacology Toxicology and PharmaceuticsEnzyme InhibitorsCytotoxicityPharmacologyFull PaperDose-Response Relationship DrugMolecular Structure010405 organic chemistryChemistryOrganic ChemistryBiofilmFull PapersAminoacyltransferasesIn vitro0104 chemical sciencesAnti-Bacterial Agents010404 medicinal & biomolecular chemistryCysteine EndopeptidasesStaphylococcus aureusSortase Addc:540BenzamidesMolecular MedicineCysteine570 BiowissenschaftenChemmedchem
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Shedding Light on the Interactions of Hydrocarbon Ester Substituents upon Formation of Dimeric Titanium(IV) Triscatecholates in DMSO Solution

2020

Abstract The dissociation of hierarchically formed dimeric triple lithium bridged triscatecholate titanium(IV) helicates with hydrocarbyl esters as side groups is systematically investigated in DMSO. Primary alkyl, alkenyl, alkynyl as well as benzyl esters are studied in order to minimize steric effects close to the helicate core. The 1H NMR dimerization constants for the monomer–dimer equilibrium show some solvent dependent influence of the side chains on the dimer stability. In the dimer, the ability of the hydrocarbyl ester groups to aggregate minimizes their contacts with the solvent molecules. Due to this, most solvophobic alkyl groups show the highest dimerization tendency followed by…

Steric effectscoordination compoundsesteritDimersolvent effects010402 general chemistry01 natural sciencesMedicinal chemistryCatalysishelicatechemistry.chemical_compoundthermodynamicshelicate thermodynamicsSide chainMoleculeAlkylchemistry.chemical_classificationCoordination Chemistry | Hot PaperFull Paper010405 organic chemistryOrganic ChemistrykompleksiyhdisteetGeneral ChemistryFull PapersTriple bond0104 chemical sciences3. Good healthchemistrytermodynamiikkaweak interactionsSolvent effectsSolvophobicChemistry (Weinheim an Der Bergstrasse, Germany)
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Correlating Solution‐ and Solid‐State Structures of Conformationally Flexible Resorcinarenes: Significance of a Sulfonyl Group in Intramolecular Self…

2020

Abstract The synthesis of tetramethoxyresorcinarene podands bearing p‐toluene arms connected by ‐SO3‐ (1) and ‐CH2O‐ (2) linkers is presented herein. In the solid state, the resorcinarene podand 1 forms an intramolecular self‐inclusion complex with the pendant p‐toluene group of a podand arm, whereas the resorcinarene podand 2 does not show self‐inclusion. The conformations of the flexible resorcinarene podands in solution were investigated by variable‐temperature experiments using 1D and 2D NMR spectroscopic techniques as well as by computational methods, including a conformational search and subsequent DFT optimisation of representative structures. The 1H NMR spectra of 1 and 2 at room te…

Supramolecular chemistryself-inclusionCrystal structure010402 general chemistry01 natural sciencessupramolecular chemistryCatalysissupramolekulaarinen kemiasolution structuresMoleculesolution structureX-ray crystallographySulfonylchemistry.chemical_classificationresorcinareneFull PaperResorcinarenes010405 organic chemistryChemistryinclusion compoundsOrganic ChemistryGeneral ChemistryFull PapersResorcinareneX-ray diffraction0104 chemical sciencesCrystallographyIntramolecular forceProton NMRTwo-dimensional nuclear magnetic resonance spectroscopyröntgenkristallografiaChemistry – A European Journal
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Synthesis and Comparative Catalytic Study of Zirconia-MnCO3or -Mn2O3for the Oxidation of Benzylic Alcohols

2016

Abstract We report on the synthesis of the zirconia–manganese carbonate ZrO x (x  %)–MnCO3 catalyst (where x=1–7) that, upon calcination at 500 °C, is converted to zirconia–manganese oxide ZrO x (x  %)–Mn2O3. We also present a comparative study of the catalytic performance of the both catalysts for the oxidation of benzylic alcohol to corresponding aldehydes by using molecular oxygen as the oxidizing agent. ZrO x (x  %)–MnCO3 was prepared through co‐precipitation by varying the amounts of Zr(NO3)4 (w/w %) in Mn(NO3)2. The morphology, composition, and crystallinity of the as‐synthesized product and the catalysts prepared upon calcination were studied by using scanning electron microscopy, tr…

Thermogravimetric analysisOxide02 engineering and technology010402 general chemistry01 natural sciencesCatalysislaw.inventionchemistry.chemical_compoundlawOxidizing agentThermal stabilityCalcinationmanganese oxideFull PaperChemistrymanganese carbonateGeneral ChemistryFull Papers021001 nanoscience & nanotechnology0104 chemical sciencesmixed metal oxidesBenzyl alcoholAlcohol oxidation0210 nano-technologybenzyl alcohol oxidationzirconiaNuclear chemistryChemistryOpen
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Interface Amorphization of Two‐Dimensional Black Phosphorus upon Treatment with Diazonium Salts

2021

Abstract Two‐dimensional (2D) black phosphorus (BP) represents one of the most appealing 2D materials due to its electronic, optical, and chemical properties. Many strategies have been pursued to face its environmental instability, covalent functionalization being one of the most promising. However, the extremely low functionalization degrees and the limitations in proving the nature of the covalent functionalization still represent challenges in many of these sheet architectures reported to date. Here we shine light on the structural evolution of 2D‐BP upon the addition of electrophilic diazonium salts. We demonstrated the absence of covalent functionalization in both the neutral and the r…

Thermogravimetric analysisred phosphoruschemistry.chemical_element010402 general chemistryPhotochemistryMass spectrometryblack phosphorus01 natural sciencesCatalysislaw.inventionsymbols.namesakeX-ray photoelectron spectroscopylawElectron paramagnetic resonanceMaterialsFull Paper010405 organic chemistryChemistryPhosphorusOrganic ChemistryBalz–Schiemann productGeneral ChemistryQuímicaFull Paperssacrificial catalysts6. Clean waterMaterials Science | Hot Paperamorphization0104 chemical sciencesElectrophilesymbolsSurface modificationRaman spectroscopyddc:547Chemistry – A European Journal
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In Situ Polyphosphate Nanoparticle Formation in Hybrid Poly(vinyl alcohol)/Karaya Gum Hydrogels: A Porous Scaffold Inducing Infiltration of Mesenchym…

2018

Abstract The preparation and characterization of a porous hybrid cryogel based on the two organic polymers, poly(vinyl alcohol) (PVA) and karaya gum (KG), into which polyphosphate (polyP) nanoparticles have been incorporated, are described. The PVA/KG cryogel is prepared by intermolecular cross‐linking of PVA via freeze‐thawing and Ca2+‐mediated ionic gelation of KG to form stable salt bridges. The incorporation of polyP as amorphous nanoparticles with Ca2+ ions (Ca‐polyP‐NP) is achieved using an in situ approach. The polyP constituent does not significantly affect the viscoelastic properties of the PVA/KG cryogel that are comparable to natural soft tissue. The exposure of the Ca‐polyP‐NP w…

Vinyl alcoholGeneral Chemical EngineeringGeneral Physics and AstronomyMedicine (miscellaneous)Nanoparticle02 engineering and technologykaraya gum010402 general chemistry01 natural sciencesBiochemistry Genetics and Molecular Biology (miscellaneous)chemistry.chemical_compoundhuman mesenchymal stem cellsotorhinolaryngologic diseasesKaraya GumGeneral Materials Sciencechemistry.chemical_classificationcoacervateCoacervateintegumentary systemFull PaperChemistryPolyphosphateMesenchymal stem cellGeneral EngineeringPolymerFull Papers021001 nanoscience & nanotechnologydigestive system diseases0104 chemical sciencesChemical engineeringSelf-healing hydrogelsnanoparticles0210 nano-technologyinorganic polyphosphateAdvanced Science
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B-DNA Structure and Stability as Function of Nucleic Acid Composition. Dispersion-Corrected DFT Study of Dinucleoside-Monophosphate Single and Double…

2013

actions of the sugar-phosphate skeleton with water; (6) hydrophobic interactions of the DNA cylindrical core, made up by the hydrogen-bonded and stacked nitrogen bases, with the water solvent. Recently, there has been increasing effort in developing and applying quantum chemical methods able to reproduce the structure of native B-DNA and to correctly describe the energy involved in the intrastrand and interstrand noncovalent interactions between the nucleotide monomers. This topic has been approached by both wave function methods and density functional theory. [2] Water solvent and sodium counterions also play an important role in the formation and relative stabilization of the double-helic…

chemistry.chemical_classificationStereochemistryChemistryBase pairHydrogen bondStackingGeneral ChemistryCrystal structureFull Papersstacking interactionsNucleobaseHydrophobic effectCrystallographyDNA structuresSettore CHIM/03 - Chimica Generale E Inorganicadensity functional calculationshydrogen bondsNon-covalent interactionsDNA DFT calculations structure stabilityDensity functional theoryWatson–Crick base pairsTheoretical ChemistryGeneralLiterature_REFERENCE(e.g.dictionariesencyclopediasglossaries)
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Controlling Spin-Correlated Radical Pairs with Donor-Acceptor Dyads: A New Concept to Generate Reduced Metal Complexes for More Efficient Photocataly…

2021

Abstract One‐electron reduced metal complexes derived from photoactive ruthenium or iridium complexes are important intermediates for substrate activation steps in photoredox catalysis and for the photocatalytic generation of solar fuels. However, owing to the heavy atom effect, direct photochemical pathways to these key intermediates suffer from intrinsic efficiency problems resulting from rapid geminate recombination of radical pairs within the so‐called solvent cage. In this study, we prepared and investigated molecular dyads capable of producing reduced metal complexes via an indirect pathway relying on a sequence of energy and electron transfer processes between a Ru complex and a cova…

chemistry.chemical_element010402 general chemistryPhotochemistry7. Clean energy01 natural sciencestime-resolved spectroscopyCatalysischemistry.chemical_compoundElectron transferBipyridineMoietyPhotochemistry | Hot Paperdonor–acceptor systemsenergy transferAnthraceneFull Paper010405 organic chemistryOrganic ChemistryPhotoredox catalysisGeneral ChemistryFull Paperselectron transfer0104 chemical sciencesRutheniumchemistryPhotocatalysisFlash photolysisphotocatalysis
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