Search results for "React"

showing 10 items of 9101 documents

Thiol-Stabilized Atomically Precise, Superatomic Silver Nanoparticles for Catalyzing Cycloisomerization of Alkynyl Amines

2018

Abstract Both the electronic and surface structures of metal nanomaterials play critical roles in determining their chemical properties. However, the non-molecular nature of conventional nanoparticles makes it extremely challenging to understand the molecular mechanism behind many of their unique electronic and surface properties. In this work, we report the synthesis, molecular and electronic structures of an atomically precise nanoparticle, [Ag206L72]q (L = thiolate, halide; q = charge). With a four-shell Ag7@Ag32@Ag77@Ag90 Ino-decahedral structure having a nearly perfect D5h symmetry, the metal core of the nanoparticle is co-stabilized by 68 thiolate and 4 halide ligands. Both electroche…

superatomMaterials sciencemetal nanoclustersatomically precise nanoparticlesNanoparticle02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesSilver nanoparticleNanomaterialsCycloisomerizationjalometallitReactivity (chemistry)ta116PlasmonMultidisciplinaryta114Superatom021001 nanoscience & nanotechnologynanocatalysisnobel metal0104 chemical sciencesDensity functional theorynanohiukkaset0210 nano-technologyNational Science Review
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Structural Motifs of Alkali Metal Superbases in Non‐coordinating Solvents

2020

Abstract Lochmann–Schlosser superbases (LSB) are a standard reagent in synthetic chemistry to achieve an exchange of a proton on an organic framework with an alkali metal cation, which in turn can be replaced by a wide range of electrophilic groups. In standard examples, the deprotonating reagent consists of an equimolar mixture of n‐butyllithium and potassium t‐butoxide. However, the nature of the reactive species could not be pinned down either for this composition or for similar mixtures with comparable high reactivity. Despite the poor solubility and the fierce reactivity, some insights into this mixture were achieved by some indirect results, comparison with chemically related systems,…

superbasealkali metalschemistry.chemical_element010402 general chemistry01 natural sciencesChemical synthesisCatalysisReactivity (chemistry)Solubility010405 organic chemistrypotassiumOrganic ChemistrySuperbaseaggregationMinireviewsGeneral ChemistryAlkali metalCombinatorial chemistry0104 chemical scienceschemistrylithiumReagentElectrophileLithiumMinireviewOrganometallic Chemistry | Reviews ShowcaseChemistry – A European Journal
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Ca-48+Bk-249 Fusion Reaction Leading to Element Z=117: Long-Lived alpha-Decaying (270)Db and Discovery of Lr-266

2014

The superheavy element with atomic number Z=117 was produced as an evaporation residue in the 48Ca+249Bk fusion reaction at the gas-filled recoil separator TASCA at GSI Darmstadt, Germany. The radioactive decay of evaporation residues and their α-decay products was studied using a detection setup that allowed measuring decays of single atomic nuclei with half-lives between sub-μs and a few days. Two decay chains comprising seven α decays and a spontaneous fission each were identified and are assigned to the isotope 294117 and its decay products. A hitherto unknown α-decay branch in 270Db (Z=105) was observed, which populated the new isotope 266Lr (Z=103). The identification of the long-live…

superheavy nucleiseparatorgsitascaca-48-inducted reactionsheaviest elements
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Polystyrene-supported organocatalysts for alfa-selenenylation and Michael reactions. A common post-modification approach for catalytic differentiation

2011

Three different resin-supported catalysts have been prepared by using the well established post-modification approach by means of thiol-ene coupling reaction. Two catalysts were tested for the first time in the asymmetric α-selenenylation of propanal, while the third catalyst was used in the Michael addition reaction. While the preliminary results are not encouraging in the case of supported Jørgensen’ catalyst, interesting data have been collected with both for the supported MacMillan and prolyl-prolinol catalysts. In fact, these catalysts displayed good activity and selectivity. A reversed enantioselectivity in the α-selenenylation was observed by changing the polarity of the solvent. Fin…

supported catalystMichael reactionSettore CHIM/06 - Chimica Organicaorganocatalysialfa-selenenylation
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Supramolecular Organocatalysis in Water Mediated by Macrocyclic Compounds

2018

In the last decades many efforts have been devoted to design supramolecular organocatalysts able to work in water as the reaction medium. The use of water as solvent provides promising benefits with respect to environmental impact. In this context, macrocyclic compounds played a role of primary importance thanks to their ease of synthesis and their molecular recognition abilities toward the reactants. The aim of this review is to give an overview of the recent advances in the field of supramolecular organocatalysis in water, focusing the attention on calixarene and cyclodextrins derivatives. Calixarenes and cyclodextrins, thanks to their hydrophobic cavities, are able to host selectively th…

supramolecular organocatalysisSupramolecular chemistryContext (language use)Review010402 general chemistry01 natural scienceslcsh:ChemistryHydrophobic effectMolecular recognitionCalixareneHydrophobic effectsupramolecular organocatalysis Water Hydrophobic effect molecular recognition Calixarenes CyclodextrinsCyclodextrins010405 organic chemistryChemistryRegioselectivityWaterGeneral ChemistryCombinatorial chemistry0104 chemical sciencesChemistrylcsh:QD1-999Organic reactionOrganocatalysismolecular recognitionCalixarenes
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UV-VISIBLE LUMINESCENCE OF SILICA NANOPARTICLES

surface reactionspoint defecttime-resolved photoluminescenceSettore FIS/01 - Fisica SperimentaleluminescenceUV laser radiationSilica nanoparticleelectron-phonon coupling
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Control of the Development of Swirling Airflow Dynamics and Its Impact on Biomass Combustion Characteristics

2017

Abstract The development of the swirling flame flow field and gasification/ combustion dynamics at thermo-chemical conversion of biomass pellets has experimentally been studied using a pilot device, which combines a biomass gasifier and combustor by varying the inlet conditions of the fuel-air mixture into the combustor. Experimental modelling of the formation of the cold nonreacting swirling airflow field above the inlet nozzle of the combustor and the upstream flow formation below the inlet nozzle has been carried out to assess the influence of the inlet nozzle diameter, as well primary and secondary air supply rates on the upstream flow formation and air swirl intensity, which is highly …

swirling flow dynamicsWaste managementPhysicsQC1-999020209 energyAirflowGeneral EngineeringEnvironmental engineeringHeat outputGeneral Physics and Astronomymixing of reactantsflame composition02 engineering and technologyheat outputBiomass combustioncombustion of volatiles0202 electrical engineering electronic engineering information engineeringLatvian Journal of Physics and Technical Sciences
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Molecular analysis of lichen-associated bacterial communities.

2006

The bacterial communities associated with 11 different lichen samples (belonging to eight different species) from different habitats were investigated. The culturable aerobic-heterotrophic fraction of the bacterial communities was isolated from nine lichen samples on protein-rich and sugar-rich/N-free media. Thirty-four bacterial isolates were purified and pooled into groups (phylotypes) by analysis of the ribosomal internal transcribed spacer polymorphism. Twenty five phylotypes were identified, each comprising between one and three isolates. One isolate of each phylotype was partially sequenced and the resulting 16S rRNA gene sequences were compared in a phylogenetic analysis. Three gener…

symbiosiSSU rDNAinternal transcribed spacer polymorphismBacteriaBase SequenceLichensbacterial communitieRNA Ribosomal 16SMolecular Sequence DatalichenPolymerase Chain ReactionPhylogenyFEMS microbiology ecology
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Second harmonic ac polarography of strongly adsorbed electroactive species

1981

Abstract The second harmonic ac current is calculated for the case of a quasi-reversible surface redox system: both species are strongly adsorbed according to a Langmuir isotherm and the kinetics of the process are controlled by the electron transfer. The current is measured with a phase-sensitive detector and the variation of the in-phase and quadrature components vs. the frequency leads to the surface rate constant ks. The experimental results obtained for benzo-(c)cinnoline are in good agreement with the theoretical predictions and with the results of impedance measurements. The advantages of the two methods are compared.

symbols.namesakePolarographyElectron transferReaction rate constantAdsorptionChemistryKineticssymbolsAnalytical chemistryLangmuir adsorption modelRedoxElectrical impedanceJournal of Electroanalytical Chemistry and Interfacial Electrochemistry
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Thiophene based imino-pyridyl palladium(II) complexes : Synthesis, molecular structures and Heck coupling reactions

2017

The new compounds (5-methyl-2-thiophene-2-pyridyl(R))imine [R = methyl (L1); R = ethyl (L2)] and (5-bromo-2-thiophene-2-pyridyl(R)imine [R = methyl (L3); R = ethyl (L4)] were successfully synthesized via Schiff base condensation reaction and obtained in good yields. These potential ligands were reacted with [PdCl2(COD)] and [PdClMe(COD)] to give the corresponding complexes [PdCl2(L)] (L = L1-L4; 1–4) and [PdClMe(L)] (L = L1-L4; 5–8). All compounds were characterized by IR, 1H and 13C NMR spectroscopy, elemental analysis and mass spectrometry. The molecular structures of 1, 2, 6 and 8 were confirmed by X-ray crystallography. The complexes were evaluated as catalyst precursors for standard He…

synteesipalladiumheck reactionsimino-pyridylmolecular structures
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