Search results for "Photophysics | Hot Paper"

showing 10 items of 28 documents

Towards Atomically Precise Supported Catalysts from Monolayer‐Protected Clusters: The Critical Role of the Support

2020

Abstract Controlling the size and uniformity of metal clusters with atomic precision is essential for fine‐tuning their catalytic properties, however for clusters deposited on supports, such control is challenging. Here, by combining X‐ray absorption spectroscopy and density functional theory calculations, it is shown that supports play a crucial role in the evolution of monolayer‐protected clusters into catalysts. Based on the acidic nature of the support, cluster‐support interactions lead either to fragmentation of the cluster into isolated Au–ligand species or ligand‐free metallic Au0 clusters. On Lewis acidic supports that bind metals strongly, the latter transformation occurs while pre…

010402 general chemistry01 natural sciencesgold clustersNanomaterials | Hot PaperCatalysiskultaCatalysisNanomaterialsmonolayer-protected clustersMetalklusteritnoncovalent interactionskatalyytitMonolayerCluster (physics)Non-covalent interactionschemistry.chemical_classificationX-ray absorption spectroscopyFull Paper010405 organic chemistryOrganic ChemistryX-ray absorption spectroscopyGeneral ChemistryFull Papersgold0104 chemical sciencesX-Ray Absorption SpectroscopychemistryChemical physicsvisual_artdensity functional calculationsvisual_art.visual_art_mediumDensity functional theorynanohiukkasetcluster-support interactionChemistry (Weinheim an Der Bergstrasse, Germany)
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Synthesis, Thermal, and Optical Properties of Tris(5‐aryl‐1,3,4‐oxadiazol‐2‐yl)‐1,3,5‐triazines, New Star‐Shaped Fluorescent Discotic Liquid Crystals

2019

Abstract The synthesis of tris(aryloxadiazolyl)triazines (TOTs), C 3‐symmetrical star‐shaped mesogenes with a 1,3,5‐triazine center, 5‐phenyl‐1,3,4‐oxadiazole arms, and various peripheral alkoxy side chains is reported. Threefold Huisgen reaction on a central triazine tricarboxylic acid and suitable aryltetrazoles yields the title compounds. Selected analogues with a benzene center are included in this study and allow for an evaluation of the impact of the central unit on the physical properties. Thermal (differential scanning calorimetry, DSC; polarization optical microscopy, POM), optical (UV/Vis, fluorescence), electric (time of flight, TOF), and structural (single crystal; wide‐angle X‐…

540 Chemistry and allied sciencessolvatochromism010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundliquid crystalsDifferential scanning calorimetryLiquid crystalSide chainTriazineheterocyclesFull Paper010405 organic chemistryDiscotic liquid crystalOrganic ChemistrySolvatochromismLiquid Crystals | Hot PaperGeneral ChemistryFull PapersX-ray scattering0104 chemical sciencesCrystallographychemistry540 ChemieAlkoxy groupfluorescenceSingle crystalChemistry – A European Journal
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Filling the Gap in the Metallacrown Family: The 9‐MC‐3 Chromium Metallacrown

2021

Abstract In this work, we report on a long‐sought missing complex in the metallacrown family. We synthesized and characterized the novel chromium metallacrown (MC) complex {CrIII(μ 2‐piv)3[9‐MCCr(III)N(shi)‐3](morph)3}⋅MeOH (in which shi3−=salicyl hydroxamate, piv=pivalate, and morph=morpholine). The MC with a 9‐MC‐3 cavity of kinetically inert chromium(III) ions was synthesized by a solvothermal reaction. Magnetization measurements reveal a high spin ground state.

9-MC-3540 Chemistry and allied sciencesCluster Compounds | Hot PaperCommunicationOrganic Chemistrykinetic stabilityStructural integritychemistry.chemical_elementGeneral ChemistrySolvothermal reactionCatalysisCommunicationsIonmetallacrownMagnetizationCrystallographyChromiumchemistry.chemical_compoundstructural integritychemistry540 ChemieMorpholinechromiumGround stateMetallacrownChemistry (Weinheim an Der Bergstrasse, Germany)
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Influencing the Self‐Sorting Behavior of [2.2]Paracyclophane‐Based Ligands by Introducing Isostructural Binding Motifs

2020

Abstract Two isostructural ligands with either nitrile (Lnit) or isonitrile (Liso) moieties directly connected to a [2.2]paracyclophane backbone with pseudo‐meta substitution pattern have been synthesized. The ligand itself (Lnit) or its precursors (Liso) were resolved by HPLC on a chiral stationary phase and the absolute configuration of the isolated enantiomers was assigned by XRD analysis and/or by comparison of quantum‐chemical simulated and experimental electronic circular dichroism (ECD) spectra. Surprisingly, the resulting metallosupramolecular aggregates formed in solution upon coordination of [(dppp)Pd(OTf)2] differ in their composition: whereas Lnit forms dinuclear complexes, Liso…

Circular dichroismNitrileSupramolecular chemistry010402 general chemistry01 natural sciencesCatalysisself-sortingsupramolecular chemistrychemistry.chemical_compoundIsostructuralFull Paper010405 organic chemistryLigandOrganic ChemistryAbsolute configurationGeneral ChemistryNuclear magnetic resonance spectroscopyself-assemblyFull Papers0104 chemical sciencesCrystallographychemistrynitrile ligandsEnantiomerSupramolecular Chemistry | Hot Paperisonitrile ligandsChemistry (Weinheim an Der Bergstrasse, Germany)
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Reactivity of Nickel(II) Porphyrins in oCVD Processes—Polymerisation, Intramolecular Cyclisation and Chlorination

2019

Abstract Oxidative chemical vapour deposition of (5,15‐diphenylporphyrinato)nickel(II) (NiDPP) with iron(III) chloride as oxidant yielded a conjugated poly(metalloporphyrin) as a highly coloured thin film, which is potentially useful for optoelectronic applications. This study clarified the reactive sites of the porphyrin monomer NiDPP by HRMS, UV/Vis/NIR spectroscopy, cyclic voltammetry and EPR spectroscopy in combination with quantum chemical calculations. Unsubstituted meso positions are essential for successful polymerisation, as demonstrated by varying the porphyrin meso substituent pattern from di‐ to tri‐ and tetraphenyl substitution. DFT calculations support the proposed radical oxi…

Conjugated systemporphyrins010402 general chemistryPhotochemistry01 natural sciencesCatalysischemical vapor depositionnickelchemistry.chemical_compoundReactivity (chemistry)Full Paper010405 organic chemistryOrganic ChemistryRegioselectivityGeneral ChemistryFull PapersPorphyrin0104 chemical sciencesMonomerthin filmschemistryPolymerizationpolymerizationChemical Vapor Deposition | Hot PaperOxidative coupling of methaneCyclic voltammetryChemistry – A European Journal
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Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups

2019

Abstract We herein present a metal‐free, electrosynthetic method that enables the direct dehydrogenative coupling reactions of phenols carrying electron‐withdrawing groups for the first time. The reactions are easy to conduct and scalable, as they are carried out in undivided cells and obviate the necessity for additional supporting electrolyte. As such, this conversion is efficient, practical, and thereby environmentally friendly, as production of waste is minimized. The method features a broad substrate scope, and a variety of functional groups are tolerated, providing easy access to precursors for novel polydentate ligands and even heterocycles such as dibenzofurans.

Denticityoxidation010405 organic chemistryChemistrySupporting electrolyteCommunicationC−C couplingoxygen heterocyclesSubstrate (chemistry)General Chemistry010402 general chemistryElectrochemistry01 natural sciencesEnvironmentally friendlyCombinatorial chemistryCommunicationsCatalysisCoupling reaction0104 chemical scienceschemistry.chemical_compoundElectrochemistry | Hot Paperelectrochemistrycross-couplingPolar effectPhenolsAngewandte Chemie International Edition
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A Next‐Generation Air‐Stable Palladium(I) Dimer Enables Olefin Migration and Selective C−C Coupling in Air

2020

Abstract We report a new air‐stable PdI dimer, [Pd(μ‐I)(PCy2 tBu)]2, which triggers E‐selective olefin migration to enamides and styrene derivatives in the presence of multiple functional groups and with complete tolerance of air. The same dimer also triggers extremely rapid C−C coupling (alkylation and arylation) at room temperature in a modular and triply selective fashion of aromatic C−Br, C−OTf/OFs, and C−Cl bonds in poly(pseudo)halogenated arenes, displaying superior activity over previous PdI dimer generations for substrates that bear substituents ortho to C−OTf.

Dimerchemistry.chemical_elementHomogeneous catalysisAlkylationmigration010402 general chemistry01 natural sciencesolefinCatalysisStyreneCatalysischemistry.chemical_compoundkatalyytitPolymer chemistryChemoselectivityOlefin fiber010405 organic chemistryCommunicationC−C couplingGeneral MedicineGeneral Chemistrypalladiumhomogeneous catalysisCommunications3. Good health0104 chemical scienceschemistrychemoselectivitykatalyysiddc:540Homogeneous Catalysis | Hot Paperolefin migrationPalladiumAngewandte Chemie International Edition
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Selective and Scalable Electrosynthesis of 2H-2-(Aryl)-benzo[d]-1,2,3-triazoles and Their N-Oxides by Using Leaded Bronze Cathodes.

2020

Abstract Electrosynthesis of 2H‐2‐(aryl)benzo[d]‐1,2,3‐triazoles and their N‐oxides from 2‐nitroazobenzene derivatives is reported. The electrolysis is conducted in a very simple undivided cell under constant current conditions with a leaded bronze cathode and a glassy carbon anode. The product distribution between 2H‐2‐(aryl)benzo[d]‐1,2,3‐triazoles and their N‐oxides can be guided by simply controlling the current density and the amount of the charge applied. The reaction tolerates several sensitive functional groups in reductive electrochemistry. The usefulness and the applicability of the synthetic method is demonstrated by a formal synthesis of an antiviral compound.

Green chemistry540 Chemistry and allied sciencesazo compoundsreductionGlassy carbon010402 general chemistryElectrosynthesisElectrochemistry01 natural sciencesCatalysislaw.inventionchemistry.chemical_compoundlawsustainable chemistryElectrolysis010405 organic chemistryChemistryArylCommunicationOrganic ChemistryGeneral ChemistryCombinatorial chemistryCathodeCommunications0104 chemical sciencesAnodeElectrochemistry | Hot Paperelectrochemistry540 Chemienitrogen heterocyclesChemistry (Weinheim an der Bergstrasse, Germany)
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Singlet‐Contrast Magnetic Resonance Imaging: Unlocking Hyperpolarization with Metabolism

2020

Abstract Hyperpolarization‐enhanced magnetic resonance imaging can be used to study biomolecular processes in the body, but typically requires nuclei such as 13C, 15N, or 129Xe due to their long spin‐polarization lifetimes and the absence of a proton‐background signal from water and fat in the images. Here we present a novel type of 1H imaging, in which hyperpolarized spin order is locked in a nonmagnetic long‐lived correlated (singlet) state, and is only liberated for imaging by a specific biochemical reaction. In this work we produce hyperpolarized fumarate via chemical reaction of a precursor molecule with para‐enriched hydrogen gas, and the proton singlet order in fumarate is released a…

Hydrogenchemistry.chemical_elementHyperpolarization; MRI; Metabolism; NMRparahydrogensinglet order010402 general chemistrySpin isomers of hydrogen01 natural sciencesChemical reactionCatalysisNuclear magnetic resonancemedicineMoleculeSinglet stateHyperpolarization (physics)Research Articlesmedicine.diagnostic_test010405 organic chemistryChemistryMagnetic resonance imagingMagnetic Resonance Imaging | Hot PaperGeneral ChemistryMetabolism540NMR0104 chemical sciencesHyperpolarizationMetabolismddc:540Research ArticleMRI
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124I Radiolabeling of a AuIII‐NHC Complex for In Vivo Biodistribution Studies†

2020

Abstract AuIII complexes with N‐heterocyclic carbene (NHC) ligands have shown remarkable potential as anticancer agents, yet their fate in vivo has not been thoroughly examined and understood. Reported herein is the synthesis of new AuIII‐NHC complexes by direct oxidation with radioactive [124I]I2 as a valuable strategy to monitor the in vivo biodistribution of this class of compounds using positron emission tomography (PET). While in vitro analyses provide direct evidence for the importance of AuIII‐to‐AuI reduction to achieve full anticancer activity, in vivo studies reveal that a fraction of the AuIII‐NHC prodrug is not immediately reduced after administration but able to reach the major…

Imaging Agents | Hot Paperpositron emission tomography010405 organic chemistryChemistryGeneral ChemistryProdrug010402 general chemistryanticancer01 natural sciencesCombinatorial chemistryCatalysisIn vitro3. Good health0104 chemical sciencesIn vivoIn vivo biodistributionSettore CHIM/03 - Chimica Generale E InorganicametallodrugsN-heterocyclic carbenesanticancer; metallodrugs; N-heterocyclic carbenes; positron emission tomography; radiochemistryradiochemistryResearch ArticlesResearch ArticleAngewandte Chemie (International Ed. in English)
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