0000000000123793

AUTHOR

Mihail Mondeshki

0000-0002-0772-8585

showing 35 related works from this author

Trapping Amorphous Intermediates of Carbonates – A Combined Total Scattering and NMR Study

2018

Crystallization via metastable phases plays an important role in chemical manufacturing, biomineralization, and protein crystallization, but the kinetic pathways leading from metastable phases to the stable crystalline modifications are not well understood. In particular, the fast crystallization of amorphous intermediates makes a detailed characterization challenging. To circumvent this problem, we devised a system that allows trapping and stabilizing the amorphous intermediates of representative carbonates (calcium, strontium, barium, manganese, and cadmium). The long-term stabilization of these transient species enabled a detailed investigation of their composition, structure, and morpho…

StrontiumCoordination numberchemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCatalysisAmorphous calcium carbonate0104 chemical scienceslaw.inventionAmorphous solidCondensed Matter::Materials Sciencechemistry.chemical_compoundColloid and Surface ChemistrychemistryChemical engineeringlawMetastabilityCrystallization0210 nano-technologyProtein crystallizationBiomineralizationJournal of the American Chemical Society
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Anhydrous Amorphous Calcium Oxalate Nanoparticles from Ionic Liquids: Stable Crystallization Intermediates in the Formation of Whewellite

2015

The mechanisms by which amorphous intermediates transform into crystalline materials are not well understood. To test the viability and the limits of the classical crystallization, new model systems for crystallization are needed. With a view to elucidating the formation of an amorphous precursor and its subsequent crystallization, the crystallization of calcium oxalate, a biomineral widely occurring in plants, is investigated. Amorphous calcium oxalate (ACO) precipitated from an aqueous solution is described as a hydrated metastable phase, as often observed during low-temperature inorganic synthesis and biomineralization. In the presence of water, ACO rapidly transforms into hydrated whewe…

Aqueous solutionChemistryWhewelliteOrganic ChemistryCalcium oxalateGeneral Chemistryengineering.materialCatalysislaw.inventionAmorphous solidchemistry.chemical_compoundChemical engineeringlawengineeringAnhydrousWater of crystallizationOrganic chemistryCrystallizationDissolutionChemistry - A European Journal
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Synthesis of Au, Ag, and Au–Ag Bimetallic Nanoparticles Using Pulicaria undulata Extract and Their Catalytic Activity for the Reduction of 4-Nitrophe…

2020

Plant extract of Pulicaria undulata (L.) was used as both reducing agent and stabilizing ligand for the rapid and green synthesis of gold (Au), silver (Ag), and gold&ndash

Reducing agentGeneral Chemical EngineeringAlloycatalytic activityNanoparticleengineering.materialCatalysisMetallcsh:Chemistrychemistry.chemical_compound<i>Pulicaria undulata</i>General Materials SciencesilverBimetallic stripAqueous solutiontechnology industry and agriculture4-Nitrophenolgoldchemistrylcsh:QD1-999bimetallicvisual_artvisual_art.visual_art_mediumengineeringplant extractnanoparticlesNuclear chemistryNanomaterials
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27Al NMR Study of the pH Dependent Hydrolysis Products of Al2(SO4)3 in Different Physiological Media

2018

Soluble inorganic aluminium compounds like aluminium sulfate or aluminium chloride have been challenged by the European Chemical Agency to induce germ cell mutagenicity. Before conducting mutagenicity tests, the hydrolysis products in water and in physiological solutions should be determined as a function of the concentration and pH. We used different 27Al NMR spectroscopic techniques (heteronuclear Overhauser effect spectroscopy (HOESY), exchange spectroscopy (EXSY), diffusion ordered (DOSY)) in this work to gain the information to study the aluminium species in solutions with Al2(SO4)3 concentrations of 50.0, 5.0, and 0.5 g/L and their pH and time dependent transformation. At low pH, thre…

0301 basic medicineAluminium chlorideInorganic chemistryPharmaceutical Sciencechemistry.chemical_elementNuclear Overhauser effectAluminium sulfate010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-44103 medical and health scienceschemistry.chemical_compoundHydrolysislcsh:Organic chemistryAluminiumDrug DiscoverymedicinePhysical and Theoretical Chemistrychemistry.chemical_classificationOrganic ChemistryNMR0104 chemical sciences030104 developmental biologyhydrolysischemistryHeteronuclear moleculeChemistry (miscellaneous)REACHMolecular MedicineCounterionaluminium sulfate; hydrolysis; NMR; REACHaluminium sulfateTwo-dimensional nuclear magnetic resonance spectroscopymedicine.drugMolecules; Volume 23; Issue 4; Pages: 808
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Die Reaktion von Neopentyllithium mit Kalium-tert -butoxid: Bildung einer alkanlöslichen Lochmann-Schlosser-Superbase

2016

Gemische aus Alkyllithium und Alkoxiden der schweren Alkalimetalle eignen sich zur Herstellung der entsprechenden Alkylverbindungen. Sie zeichnen sich ebenfalls durch ihre Reaktivitat bei Metallierungsreaktionen aus. Diese metallorganischen Mischungen werden oft als LiC-KOR-Superbasen bezeichnet, doch trotz vieler Bemuhungen ist nur wenig uber ihren Aufbau bekannt. Hier werden dimetallische Alkalimetall-Alkyl/Alkoxy-Verbindungen vorgestellt, die durch die Reaktion von Neopentyllithium und Kalium-tert-butoxid gebildet werden. Dank guter Loslichkeit in Alkanen und Temperaturbestandigkeit der Neopentylverbindungen konnten die Losungen in n-Hexan bei Umgebungstemperatur gehandhabt werden und er…

010405 organic chemistryGeneral Medicine010402 general chemistry01 natural sciences0104 chemical sciencesAngewandte Chemie
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Combining Neopentyllithium with Potassium tert-Butoxide: Formation of an Alkane-Soluble Lochmann-Schlosser Superbase.

2016

Mixtures of alkyllithium and heavier alkali-metal alkoxides are often used to form alkyl compounds of heavier alkali metals, but these mixtures are also known for their high reactivity in deprotonative metalation reactions. These organometallic mixtures are often called LiC-KOR superbases, but despite many efforts their constitution remains unknown. Herein we present mixed alkali-metal alkyl/alkoxy compounds produced by reaction of neopentyllithium with potassium tert-butoxide. The key to success was the good solubility and temperature-stability of neopentyl alkali-metal compounds, leading to hexane-soluble mixtures, which allowed handling at ambient temperatures and isolation by crystalliz…

chemistry.chemical_classification010405 organic chemistryMetalationPotassiumSuperbasechemistry.chemical_elementGeneral Chemistry010402 general chemistryAlkali metal01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryPotassium tert-butoxideAlkoxy groupOrganic chemistryReactivity (chemistry)AlkylAngewandte Chemie (International ed. in English)
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Multistep Crystallization Pathways in the Ambient‐Temperature Synthesis of a New Alkali‐Activated Binder

2021

Materials scienceSodium silicateCondensed Matter PhysicsElectronic Optical and Magnetic Materialslaw.inventionBiomaterialschemistry.chemical_compoundCalcium carbonatechemistryChemical engineeringlawElectrochemistryAlkali activatedCalcium silicate hydrateCrystallizationAdvanced Functional Materials
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Mechanochemical Access to Defect-Stabilized Amorphous Calcium Carbonate

2018

Amorphous calcium carbonate (ACC) is an important precursor in the biomineralization of crystalline CaCO3. The lifetime of transient ACC in nature is regulated by an organic matrix, to use it as an intermediate storage buffer or as a permanent structural element. The relevance of ACC in material science is related to our understanding of CaCO3 crystallization pathways. ACC can be obtained by liquid–liquid phase separation, and it is typically stabilized with the help of macromolecules. We have prepared ACC by milling calcite in a planetary ball mill. The ball-milled amorphous calcium carbonate (BM-ACC) was stabilized with small amounts of Na2CO3. The addition of foreign ions in form of Na2C…

CalciteMaterials scienceGeneral Chemical EngineeringRecrystallization (metallurgy)02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAmorphous calcium carbonate0104 chemical scienceslaw.inventionchemistry.chemical_compoundchemistryChemical engineeringlawMaterials ChemistryAnhydrousCrystallization0210 nano-technologyBall millMacromoleculeBiomineralizationChemistry of Materials
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Hydrothermal growth mechanism of SnO2 nanorods in aqueous HCl

2018

Abstract Rutile-type nanorods of SnO2 were obtained in a one-pot hydrothermal synthesis starting from SnCl4·5H2O and HCl in a temperature range between 200 and 240°C. Although the nanorods are polydisperse, the average length of the nanorods could be adjusted from 13 to 65 nm by varying of the reaction temperature. The resulting anisotropic nanocrystals were characterized using powder X-ray diffraction (PXRD), (high resolution-) transmission electron microscopy (HR-TEM), and selected area electron diffraction (SAED). The particle growth proceeds via a dissolution-recrystallization process with soluble [SnCl5(H2O)]− intermediates, as confirmed by PXRD, Raman spectroscopy, and magic angle spi…

Aqueous solutionChemistryTin dioxideCrystal growth02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesHydrothermal circulation0104 chemical scienceschemistry.chemical_compoundChemical engineeringNanorod0210 nano-technologyMechanism (sociology)Zeitschrift für Naturforschung B
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Polycationic Monomeric and Homodimeric Asymmetric Monomethine Cyanine Dyes with Hydroxypropyl Functionality—Strong Affinity Nucleic Acids Binders

2021

New analogs of the commercial asymmetric monomethine cyanine dyes thiazole orange (TO) and thiazole orange homodimer (TOTO) with hydroxypropyl functionality were synthesized and their properties in the presence of different nucleic acids were studied. The novel compounds showed strong, micromolar and submicromolar affinities to all examined DNA ds-polynucleotides and poly rA–poly rU. The compounds studied showed selectivity towards GC-DNA base pairs over AT-DNA, which included both binding affinity and a strong fluorescence response. CD titrations showed aggregation along the polynucleotide with well-defined supramolecular chirality. The single dipyridinium-bridged dimer showed intercalatio…

antiproliferative activityCircular dichroismSupramolecular chiralityDimerIntercalation (chemistry)cyanine dye010402 general chemistry01 natural sciencesBiochemistryMicrobiologyArticlechemistry.chemical_compoundCell Line TumorHumansCyanineDNA bindingColoring AgentsBiologyMolecular BiologyBinding Sites010405 organic chemistrycyanine dye ; DNA binding ; RNA binding ; fluorescence ; circular dichroism ; antiproliferative activityDNARNA bindingCombinatorial chemistryQR1-502Intercalating Agents3. Good health0104 chemical sciencescircular dichroismchemistryPolynucleotideNucleic acidcyanine dye; DNA binding; RNA binding; fluorescence; circular dichroism; antiproliferative activityfluorescenceDNA
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Cell adhesion on UV-crosslinked polyurethane gels with adjustable mechanical strength and thermoresponsiveness

2021

Temperature-responsive polyurethane (PU) hydrogels represent a versatile material platform for modern tissue engineering and biomedical applications. However, besides intrinsic advantages such as high mechanical strength and a hydrolysable backbone composition, plain PU materials are generally lacking bio-adhesive properties. To overcome this shortcoming, the authors focus on the synthesis of thermoresponsive PU hydrogels with variable mechanical and cell adhesive properties obtained from linear precursor PUs based on poly(ethylene glycol)s (pEG) with different molar masses, isophorone diisocyanate, and a dimerizable dimethylmaleimide (DMMI)-diol. The cloud point temperatures of the dilute,…

chemistry.chemical_classification540 Chemistry and allied sciencesMaterials scienceMolar massTissue EngineeringPolymers and PlasticsPolyurethanesOrganic ChemistryHydrogelsPolymerLight intensitychemistry.chemical_compoundchemistryChemical engineeringAdhesives540 ChemieSelf-healing hydrogelsCell AdhesionMaterials ChemistryAdhesiveIsophorone diisocyanateEthylene glycolPolyurethane
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Gram-scale selective synthesis of WO3−x nanorods and (NH4)xWO3 ammonium tungsten bronzes with tunable plasmonic properties

2021

Localized surface plasmon resonance properties in unconventional materials like metal oxides or chalcogenide semiconductors have been studied for use in signal detection and analysis in biomedicine and photocatalysis. We devised a selective synthesis of the tungsten oxides WO3-x and (NH4)xWO3 with tunable plasmonic properties. We selectively synthesized WO3-x nanorods with different aspect ratios and hexagonal tungsten bronzes (NH4)xWO3 as truncated nanocubes starting from ammonium metatungstate (NH4)6H2W12O40·xH2O. Both particles form from the same nuclei at temperatures >200 °C; monomer concentration and surfactant ratio are essential variables for phase selection. (NH4)xWO3 was the prefe…

Materials scienceOxidechemistry.chemical_elementNanoparticleTungstenchemistry.chemical_compoundchemistryNanocrystalChemical engineeringOleylamineMagic angle spinningGeneral Materials ScienceNanorodSurface plasmon resonanceNanoscale
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Polymer-Functionalised Nanograins of Mg-Doped Amorphous Calcium Carbonate via a Flow-Chemistry Approach

2019

Calcareous biominerals typically feature a hybrid nanogranular structure consisting of calcium carbonate nanograins coated with organic matrices. This nanogranular organisation has a beneficial effect on the functionality of these bioceramics. In this feasibility study, we successfully employed a flow-chemistry approach to precipitate Mg-doped amorphous calcium carbonate particles functionalized by negatively charged polyelectrolytes&mdash

SorbentMaterials sciencemicrofluidicschemistry.chemical_element02 engineering and technologyCalcium010402 general chemistrylcsh:Technology01 natural sciencesArticlePolystyrene sulfonatechemistry.chemical_compoundGeneral Materials Sciencelcsh:Microscopynanoceramicslcsh:QC120-168.85chemistry.chemical_classificationlcsh:QH201-278.5Dopantlcsh:TPolymer021001 nanoscience & nanotechnologyAmorphous calcium carbonate0104 chemical sciencesCalcium carbonatechemistryChemical engineeringlcsh:TA1-2040flow-chemistryamorphous calcium carbonatelcsh:Descriptive and experimental mechanicslcsh:Electrical engineering. Electronics. Nuclear engineeringddc:620lcsh:Engineering (General). Civil engineering (General)0210 nano-technologylcsh:TK1-9971CalcareousDepartment WerkstoffwissenschaftenbiomaterialsMaterials
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Single nanogranules preserve intracrystalline amorphicity in biominerals.

2015

We revisit the ultrastructural features of different calcareous biominerals and identify remarkable similarities: taxonomically very distant species show a common nanogranular structure, even if different extracellular secretion patterns are employed or calcium carbonate polymorphs formed. By these analyses, we elucidate the locus of the small fraction of intracrystalline organic matrix revealing its intergranular character and localize the intracrystalline amorphous calcium carbonate moiety commonly found in mesocrystalline biominerals and provide a first explanation for the pathway by which it is preserved.

0301 basic medicineMaterials scienceMechanical EngineeringMineralogy02 engineering and technology[ SDV.IB.BIO ] Life Sciences [q-bio]/Bioengineering/Biomaterials021001 nanoscience & nanotechnologyAmorphous calcium carbonate[SDV.IB.BIO] Life Sciences [q-bio]/Bioengineering/Biomaterials03 medical and health scienceschemistry.chemical_compound030104 developmental biologyCalcium carbonatechemistryMechanics of MaterialsBiophysicsGeneral Materials ScienceOrganic matrix0210 nano-technologyMesocrystalCalcareousComputingMilieux_MISCELLANEOUSBiomineralization
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Nonclassical crystallization in vivo et in vitro (I): Process-structure-property relationships of nanogranular biominerals.

2016

A distinct nanogranular fine structure is shared by a wealth of biominerals from several species, classes and taxa. This nanoscopic organization affects the properties and behavior of the biogenic ceramic material and confers on them attributes that are essential to their function. We present a set of structure-relationship properties that are rooted in the nanogranular organization and we propose that they rest on a common pathway of formation, a colloid-driven and hence nonclassical mode of crystallization. With this common modus operandi, we reveal the most fundamental and wide spread process-structure-property relationship in biominerals. With the recent increase in our understanding of…

MineralsMaterials scienceStructure propertyNanotechnology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionCalcification PhysiologicStructural BiologylawScientific methodAnimalsNanoparticlesColloidsCrystallization0210 nano-technologyCrystallizationNanoscopic scaleBiomineralizationJournal of structural biology
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Monitoring Thiol–Ligand Exchange on Au Nanoparticle Surfaces

2018

Surface functionalization of nanoparticles (NPs) plays a crucial role in particle solubility and reactivity. It is vital for particle nucleation and growth as well as for catalysis. This raises the quest for functionalization efficiency and new approaches to probe the degree of surface coverage. We present an (in situ) proton nuclear magnetic resonance (1H NMR) study on the ligand exchange of oleylamine by 1-octadecanethiol as a function of the particle size and repeated functionalization on Au NPs. Ligand exchange is an equilibrium reaction associated with Nernst distribution, which often leads to incomplete surface functionalization following “standard” literature protocols. Here, we show…

LigandNanoparticle02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsPhotochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundsymbols.namesakechemistryOleylamineElectrochemistryProton NMRsymbolsSurface modificationGeneral Materials ScienceReactivity (chemistry)Nernst equationParticle size0210 nano-technologySpectroscopyLangmuir
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Pseudomorphic transformation of amorphous calcium carbonate films follows spherulitic growth mechanisms and can give rise to crystal lattice tilting

2015

Amorphous calcium carbonate films synthesized by the polymer-induced liquid-precursor (PILP) process convert into crystallographically complex calcite spherulites. Tuning the experimental parameters allows for the generation of crystal lattice tilting similar to that found in calcareous biominerals. This contribution evidences the role of spherulitic growth mechanisms in pseudomorphic transformations of calcium carbonate.

CalciteMaterials scienceTechnische FakultätMineralogy02 engineering and technologyGeneral ChemistryCrystal structure-010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesTransformation (music)Amorphous calcium carbonate0104 chemical scienceschemistry.chemical_compoundCalcium carbonatechemistryChemical engineeringGeneral Materials Science0210 nano-technologyCalcareousddc:600
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Supramolecular Linear-g-Hyperbranched Graft Polymers: Topology and Binding Strength of Hyperbranched Side Chains

2013

Complex, reversible hyperbranched graft polymer topologies have been obtained by spontaneous self-assembly. Well-defined adamantyl- and β-cyclodextrin-functionalized polymers were employed to generate linear-g-(linear–hyperbranched) supramolecular graft terpolymers. For this purpose the synthesis of monoadamantyl-functionalized linear polyglycerols (Ada-linPG) and hyperbranched polyglycerols (Ada-hbPG) as well as poly(ethylene glycol)-block-linear polyglycerol (Ada-PEG-b-linPG) and poly(ethylene glycol)-block-hyperbranched poly(glycerol) (Ada-PEG-b-hbPG) block copolymers was established. Isothermal titration calorimetry (ITC) with β-cyclodextrin revealed a shielding effect of hyperbranched …

chemistry.chemical_classificationPolymers and PlasticsOrganic Chemistrytechnology industry and agricultureSupramolecular chemistryIsothermal titration calorimetryPolymerRaftInorganic Chemistrychemistry.chemical_compoundGraft polymerchemistryPolymer chemistryMaterials ChemistryCopolymerSide chainEthylene glycolMacromolecules
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A Generalized Method for High‐Speed Fluorination of Metal Oxides by Spark Plasma Sintering Yields Ta 3 O 7 F and TaO 2 F with High Photocatalytic Act…

2021

A general method to carry out the fluorination of metal oxides with poly(tetrafluoroethylene) (PTFE, Teflon) waste by spark plasma sintering (SPS) on a minute scale with Teflon is reported. The potential of this new approach is highlighted by the following results. i) The tantalum oxyfluorides Ta3 O7 F and TaO2 F are obtained from plastic scrap without using toxic or caustic chemicals for fluorination. ii) Short reaction times (minutes rather than days) reduce the process time the energy costs by almost three orders of magnitude. iii) The oxyfluorides Ta3 O7 F and TaO2 F are produced in gram amounts of nanoparticles. Their synthesis can be upscaled to the kg range with industrial sintering …

Materials scienceMechanical EngineeringOxygen evolutionTantalumSpark plasma sinteringNanoparticlechemistry.chemical_elementSintering02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryChemical engineeringMechanics of MaterialsPhotocatalysisGeneral Materials ScienceTetrafluoroethylene0210 nano-technologyAdvanced Materials
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Systematical, experimental investigations on LiMgZ (Z= P, As, Sb) wide band gap semiconductors

2011

This work reports on the experimental investigation of the wide band gap compounds LiMgZ (Z = P, As, Sb), which are promising candidates for opto-electronics and anode materials for Lithium batteries. The compounds crystallize in the cubic (C1_b) MgAgAs structure (space group F-43m). The polycrystalline samples were synthesized by solid state reaction methods. X-ray and neutron diffraction measurements show a homogeneous, single-phased samples. The electronic properties were studied using the direct current (DC) method. Additionally UV-VIS diffuse reflectance spectra were recorded in order to investigate the band gap nature. The measurements show that all compounds exhibit semiconducting be…

Condensed Matter - Materials ScienceMaterials scienceAcoustics and UltrasonicsBand gapNeutron diffractionDirect currentWide-bandgap semiconductorAnalytical chemistryMaterials Science (cond-mat.mtrl-sci)FOS: Physical scienceschemistry.chemical_elementCondensed Matter PhysicsSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonchemistryLithiumCrystallite
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Monitoring a Mechanochemical Reaction Reveals the Formation of a New ACC Defect Variant Containing the HCO 3 – Anion Encapsulated by an Amorphous Mat…

2020

Crystal growth &amp; design 20(10), 6831 - 6846 (2020). doi:10.1021/acs.cgd.0c00912

[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesPyrophosphatelaw.inventionchemistry.chemical_compoundlaw[CHIM.CRIS]Chemical Sciences/CristallographyGeneral Materials ScienceCrystallization010405 organic chemistryGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryCondensed Matter PhysicsCondensation reactionPhosphate540Amorphous calcium carbonate0104 chemical sciences3. Good healthAmorphous solidCalcium carbonatechemistryChemical engineering13. Climate actionddc:540Carbonate[SDU.STU.MI]Sciences of the Universe [physics]/Earth Sciences/Mineralogy
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Insights into the In Vitro Formation of Apatite from Mg‐Stabilized Amorphous Calcium Carbonate

2020

Materials sciencechemistry.chemical_elementCalciumCondensed Matter PhysicsApatiteIn vitroAmorphous calcium carbonateElectronic Optical and Magnetic MaterialsAmorphous solidBiomaterialschemistry.chemical_compoundCalcium carbonatechemistryvisual_artElectrochemistryvisual_art.visual_art_mediumNuclear chemistryAdvanced Functional Materials
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Rational Design of Thermoresponsive Microgel Templates with Polydopamine Surface Coating for Microtissue Applications.

2021

Functional microgels provide a versatile basis for synthetic in vitro platforms as alternatives to animal experiments. The tuning of the physical, chemical, and biological properties of synthetic microgels can be achieved by blending suitable polymers and formulating them such to reflect the heterogenous and complex nature of biological tissues. Based on this premise, this paper introduces the development of volume-switchable core-shell microgels as 3D templates to enable cell growth for microtissue applications, using a systematic approach to tune the microgel properties based on a deep conceptual and practical understanding. Microscopic microgel design, such as the tailoring of the microg…

540 Chemistry and allied sciencesMaterials scienceIndolesPolymers and PlasticsPolymersMicrofluidicsBioengineeringNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialsBiological propertyddc:570Materials ChemistryAnimalsNanoscopic scalechemistry.chemical_classificationMicrogelsRational designPolymer021001 nanoscience & nanotechnology0104 chemical sciencesSurface coatingTemplatechemistry540 ChemieSurface modification0210 nano-technologyGelsBiotechnologyMacromolecular bioscience
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Polysiloxane-backbone block copolymers in a one-pot synthesis: a silicone platform for facile functionalization.

2012

Block copolymers consisting exclusively of a silicon-oxygen backbone are synthesized by sequential anionic ring-opening polymerization of different cyclic siloxane monomers. After formation of a poly(dimethylsiloxane) (PDMS) block by butyllithium-initiated polymerization of D3, a functional second block is generated by subsequent addition of tetramethyl tetravinyl cyclotetrasiloxane (D4(V) ), resulting in diblock copolymers comprised a simple PDMS block and a functional poly(methylvinylsiloxane) (PMVS) block. Polymers of varying block length ratios were obtained and characterized. The vinyl groups of the second block can be easily modified with a variety of side chains using hydrosilylation…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsMolecular StructureSiloxanesHydrosilylationOrganic Chemistrytechnology industry and agricultureSiliconesmacromolecular substancesPolymerRing-opening polymerizationPolymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationBlock (telecommunications)Polymer chemistryMaterials ChemistryCopolymerSide chainMacromolecular rapid communications
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Glycine-functionalized copper(ii) hydroxide nanoparticles with high intrinsic superoxide dismutase activity

2017

Superoxide dismutases (SOD) are a group of enzymes that catalyze the dismutation of superoxide (O2−) radicals into molecular oxygen (O2) and H2O2 as a first line of defense against oxidative stress. Here, we show that glycine-functionalized copper(II) hydroxide nanoparticles (Gly-Cu(OH)2 NPs) are functional SOD mimics, whereas bulk Cu(OH)2 is insoluble in water and catalytically inactive. In contrast, Gly-Cu(OH)2 NPs form water-dispersible mesocrystals with a SOD-like activity that is larger than that of their natural CuZn enzyme counterpart. Based on this finding, we devised an application where Gly-Cu(OH)2 NPs were incorporated into cigarette filters. Cigarette smoke contains high concent…

RadicalInorganic chemistryGlycine02 engineering and technology010402 general chemistrymedicine.disease_cause01 natural sciencesSuperoxide dismutasechemistry.chemical_compoundSmokeHydroxidesmedicineHumansGeneral Materials ScienceReactive nitrogen specieschemistry.chemical_classificationCopper(II) hydroxideReactive oxygen speciesbiologySuperoxide DismutaseSuperoxideHydrogen PeroxideTobacco Products021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryA549 Cellsbiology.proteinNanoparticlesHydroxideReactive Oxygen Species0210 nano-technologyCopperOxidative stressNanoscale
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Solid State Fluorination on the Minute Scale: Synthesis of WO 3− x F x with Photocatalytic Activity

2020

BiomaterialsMaterials scienceScale (ratio)Chemical engineeringElectrochemistrySolid-statePhotocatalysisCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsAdvanced Functional Materials
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Hydrogen Bonding in Amorphous Alkaline Earth Carbonates

2018

Amorphous intermediates play a crucial role during the crystallization of alkaline earth carbonates. We synthesized amorphous carbonates of magnesium, calcium, strontium, and barium from methanolic solution. The local environment of water and the strength of hydrogen bonding in these hydrated modifications were probed with Fourier transform IR spectroscopy,

inorganic chemicalsmusculoskeletal diseasesStrontiumAlkaline earth metalHydrogen bondMagnesiumInorganic chemistrychemistry.chemical_elementBarium02 engineering and technologyCalcium010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionAmorphous solidInorganic ChemistrychemistrylawPhysical and Theoretical ChemistryCrystallization0210 nano-technologyInorganic Chemistry
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Magneli-type tungsten oxide nanorods as catalysts for the selective oxidation of organic sulfides

2021

Selective oxidation of thioethers is an important reaction to obtain sulfoxides as synthetic intermediates for applications in the chemical industry, medicinal chemistry and biology or the destruction of warfare agents. The reduced Magneli-type tungsten oxide WO3−x possesses a unique oxidase-like activity which facilitates the oxidation of thioethers to the corresponding sulfoxides. More than 90% of the model system methylphenylsulfide could be converted to the sulfoxide with a selectivity of 98% at room temperature within 30 minutes, whereas oxidation to the corresponding sulfone was on a time scale of days. The concentration of the catalyst had a significant impact on the reaction rate. R…

OxidesSulfoxideCombinatorial chemistryDecompositionTungstenNanomaterial-based catalystSulfoneCatalysisInorganic ChemistryReaction ratechemistry.chemical_compoundchemistryHydrogen peroxideSelectivityDalton Transactions
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Calcium Sulfate Nanoparticles with Unusual Dispersibility in Organic Solvents for Transparent Film Processing

2018

Calcium sulfate is one of the most important construction materials. Today it is employed as high-performance compound in medical applications and cement mixtures. We report a synthesis for calcium sulfate nanoparticles with outstanding dispersibility properties in organic solvents without further functionalization. The nanoparticles (amorphous with small γ-anhydrite crystallites, 5–50 nm particle size) form long-term stable dispersions in acetone without any sign of precipitation. 1H NMR spectroscopic techniques and Fourier-transform infrared spectroscopy (FTIR) reveal absorbed 2-propanol on the particle surfaces that induce the unusual dispersibility. Adding water to the nanoparticle disp…

Materials sciencePrecipitation (chemistry)NanoparticleInfrared spectroscopy02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical scienceslaw.inventionBassaniteChemical engineeringlawElectrochemistryParticleGeneral Materials ScienceCrystalliteCrystallizationFourier transform infrared spectroscopy0210 nano-technologySpectroscopyLangmuir
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Mixed Ligand Shell Formation upon Catechol Ligand Adsorption on Hydrophobic TiO2 Nanoparticles

2019

Modifying the surfaces of metal oxide nanoparticles (NPs) with monolayers of ligands provides a simple and direct method to generate multifunctional coatings by altering their surface properties. T...

CatecholChemistryLigandTio2 nanoparticlesShell (structure)02 engineering and technologySurfaces and InterfacesMetal oxide nanoparticlesMixed ligand010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundAdsorptionChemical engineeringMonolayerElectrochemistryGeneral Materials Science0210 nano-technologySpectroscopyLangmuir
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(1-Adamantyl)methyl glycidyl ether: a versatile building block for living polymerization.

2014

(1-Adamantyl)methyl glycidyl ether (AdaGE) is introduced as a versatile monomer for oxyanionic polymerization, enabling controlled incorporation of adamantyl moieties in aliphatic polyethers. Via copolymerization with ethoxyethyl glycidyl ether (EEGE) and subsequent cleavage of the acetal protection groups of EEGE, hydrophilic linear polyglycerols with an adjustable amount of pendant adamantyl moieties are obtained. The adamantyl unit permits control over thermal properties and solubility profile of these polymers (LCST). Additionally, AdaGE is utilized as a termination agent in carbanionic polymerization, affording adamantyl-terminated polymers. Using these structures as macroinitiators fo…

chemistry.chemical_classificationGlycerolMaterials sciencePolymers and PlasticsEthylene oxidePolymersOrganic ChemistryAcetalAdamantanePolymerPolymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryAmphiphileMaterials ChemistryCopolymerLiving polymerizationOrganic chemistryEpoxy CompoundsHydrophobic and Hydrophilic InteractionsMacromolecular rapid communications
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Batch-to-Melt Conversion Kinetics in Sodium Aluminosilicate Batches Using Different Alumina Raw Materials

2016

The batch-to-melt conversion in batches of sand, soda ash and corundum (C), alumina spinel (A), boehmite (B), or gibbsite (G) as Al2O3 carrier are studied using thermal analysis, X-ray diffraction, and 27Al nuclear magnetic resonance spectroscopy. Laboratory-scaled batches are either heated continuously or quenched from 1600°C in a series of increasing dwell times. The results show that the conversion from the raw materials to the fresh melt proceeds in two kinetic stages. During the first stage (3–5 min), fast conversion of nearly 95% by mass occurs and the conversion coefficient increases in the order G < C ≈ A < B. The second stage is controlled by the slow dissolution of intermediate cr…

010302 applied physicsBoehmiteMaterials scienceSpinelAnalytical chemistryMineralogyCorundum02 engineering and technologyengineering.material021001 nanoscience & nanotechnology01 natural sciencesCristobalitechemistry.chemical_compoundchemistry0103 physical sciencesengineeringGeneral Materials Science0210 nano-technologyThermal analysisDissolutionGibbsiteSodium aluminosilicateInternational Journal of Applied Glass Science
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High-speed solid state fluorination of Nb2O5 yields NbO2F and Nb3O7F with photocatalytic activity for oxygen evolution from water

2021

Solid state reactions are slow because the diffusion of atoms or ions through the reactant, intermediate and crystalline product phases is the rate-limiting step. This requires days or even weeks of high temperature treatment, and consumption of large amounts of energy. We employed spark-plasma sintering, an engineering technique that is used for high-speed consolidation of powders with a pulsed electric current passing through the sample to carry out the fluorination of niobium oxide in minute intervals. The approach saves time and large amounts of waste energy. Moreover, it allows the preparation of fluorinated niobium oxides on a gram scale using poly(tetrafluoroethylene) (®Teflon) scrap…

Inorganic ChemistryPhotocurrentMaterials sciencechemistryChemical engineeringDiffusionNiobiumOxygen evolutionPhotocatalysischemistry.chemical_elementSpark plasma sinteringNiobium oxideSinteringDalton Transactions
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CCDC 1455868: Experimental Crystal Structure Determination

2016

Related Article: Philipp Benrath, Maximilian Kaiser, Thomas Limbach, Mihail Mondeshki and Jan Klett|2016|Angew.Chem.,Int.Ed.|55|10886|doi:10.1002/anie.201602792

pentakis(mu-t-butoxy)-tris(mu-neopentyl)-tetra-lithium-tetra-potassiumSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 1455867: Experimental Crystal Structure Determination

2016

Related Article: Philipp Benrath, Maximilian Kaiser, Thomas Limbach, Mihail Mondeshki and Jan Klett|2016|Angew.Chem.,Int.Ed.|55|10886|doi:10.1002/anie.201602792

Space GroupCrystallographytetrakis(mu-t-butoxy)-tris(mu-neopentyl)-tetra-lithium-tri-potassium tris(mu-t-butoxy)-tetrakis(mu-neopentyl)-tetra-lithium-tri-potassiumCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct