Search results for "Hot Paper"

showing 10 items of 30 documents

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)
researchProduct

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
researchProduct

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)
researchProduct

Inhibition Mechanism of SARS‐CoV‐2 Main Protease with Ketone‐Based Inhibitors Unveiled by Multiscale Simulations: Insights for Improved Designs**

2021

Abstract We present the results of classical and QM/MM simulations for the inhibition of SARS‐CoV‐2 3CL protease by a hydroxymethylketone inhibitor, PF‐00835231. In the noncovalent complex the carbonyl oxygen atom of the warhead is placed in the oxyanion hole formed by residues 143 to 145, while P1–P3 groups are accommodated in the active site with interactions similar to those observed for the peptide substrate. According to alchemical free energy calculations, the P1′ hydroxymethyl group also contributes to the binding free energy. Covalent inhibition of the enzyme is triggered by the proton transfer from Cys145 to His41. This step is followed by the nucleophilic attack of the Sγ atom on …

KetoneMolecular modelStereochemistrySubstituentMolecular Dynamics SimulationSARS‐CoV‐2 Inhibitors | Hot PaperCatalysisQM/MM3CL proteasechemistry.chemical_compoundCatalytic DomaininhibitorsHumansHydroxymethylProtease InhibitorsCoronavirus 3C ProteasesResearch Articleschemistry.chemical_classificationPF-00835231Binding SitesbiologySARS-CoV-2molecular modelingActive siteCOVID-19General ChemistryGeneral MedicineKetonesCOVID-19 Drug TreatmentKineticschemistryCovalent bondDrug Designbiology.proteinThermodynamicsOxyanion holeResearch ArticleAngewandte Chemie
researchProduct

Strain-Promoted Cycloaddition of Cyclopropenes with o-Quinones : A Rapid Click Reaction

2018

Abstract Novel click reactions are of continued interest in fields as diverse as bio‐conjugation, polymer science and surface chemistry. Qualification as a proper “click” reaction requires stringent criteria, including fast kinetics and high conversion, to be met. Herein, we report a novel strain‐promoted cycloaddition between cyclopropenes and o‐quinones in solution and on a surface. We demonstrate the “click character” of the reaction in solution and on surfaces for both monolayer and polymer brush functionalization.

KineticsClick Chemistry | Hot Paper010402 general chemistryPolymer brushO quinones01 natural sciencesCatalysisReaccions químiquesMonolayerotorhinolaryngologic diseasesMetal-free click reactionsVLAGchemistry.chemical_classificationMonolayersMass spectrometry010405 organic chemistryChemistryCommunicationOrganic ChemistryGeneral MedicineGeneral ChemistryPolymerCombinatorial chemistryOrganische ChemieCycloadditionCommunications0104 chemical sciencesKineticsClick chemistrySurface modificationPolymer brushesQuímica orgànicahuman activitiesAngewandte Chemie - International Edition
researchProduct

Multiple Decay Mechanisms and 2D-UV Spectroscopic Fingerprints of Singlet Excited Solvated Adenine-Uracil Monophosphate

2016

The decay channels of singlet excited adenine uracil monophosphate (ApU) in water are studied with CASPT2//CASSCF:MM potential energy calculations and simulation of the 2D-UV spectroscopic fingerprints with the aim of elucidating the role of the different electronic states of the stacked conformer in the excited state dynamics. The adenine 1La state can decay without a barrier to a conical intersection with the ground state. In contrast, the adenine 1Lb and uracil S(U) states have minima that are separated from the intersections by sizeable barriers. Depending on the backbone conformation, the CT state can undergo inter-base hydrogen transfer and decay to the ground state through a conical …

Models Molecularmolecular electronicsChemistry MultidisciplinaryMolecular electronicsphotophysic2-DIMENSIONAL ELECTRONIC SPECTROSCOPYSTATE DYNAMICSBASE-STACKINGPhotochemistry01 natural sciences[CHIM] Chemical SciencesNUCLEIC-ACIDSQuímica quànticaEspectrofotometriaConformational isomerismComputingMilieux_MISCELLANEOUSphotophysics010304 chemical physicsFull PaperHydrogen bondChemistryChemistry (all)Full PapersMolecular spectroscopy[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryChemistryFOURIER-TRANSFORM SPECTROSCOPYSpectrophotometryExcited statePhysical Sciences1ST-PRINCIPLES SIMULATION03 Chemical SciencesGround stateUridine MonophosphateQuantum chemistryEspectroscòpia molecularmolecular electronic010402 general chemistryMolecular physicsCatalysisUltraviolet visible spectroscopy0103 physical sciencesPhotophysics | Hot Paper[CHIM]Chemical SciencesSinglet stateUV/Vis spectroscopyULTRAFAST INTERNAL-CONVERSIONSpectroscopyLIGHT-HARVESTING COMPLEXab initio calculationScience & Technologyab initio calculationsOrganic ChemistryGeneral ChemistryDNAConical intersectionDNA FingerprintingAdenosine Monophosphate0104 chemical sciences[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryAB-INITIO SIMULATIONSElectrònica molecularMOLECULAR-DYNAMICSSpectrophotometry Ultraviolet
researchProduct

Low-Temperature Miniemulsion-Based Routes for Synthesis of Metal Oxides.

2020

Abstract The use of miniemulsions containing chemical precursors in the disperse phase is a versatile method to produce nanoparticles and nanostructures of different chemical nature, including not only polymers, but also a variety of inorganic materials. This Minireview focuses on materials in which nanostructures of metal oxides are synthesized in processes that involve the miniemulsion technique in any of the steps. This includes in the first place those approaches in which the spaces provided by nanodroplets are directly used to confine precipitation reactions that lead eventually to oxides. On the other hand, miniemulsions can also be used to form functionalized polymer nanoparticles th…

NanostructurecrystallizationminiemulsioninorganicOxideNanoparticleNanotechnologyMiniemulsions | Hot Paper010402 general chemistry01 natural sciencesCatalysislaw.inventionMetalchemistry.chemical_compoundlawPhase (matter)Crystallizationchemistry.chemical_classification010405 organic chemistryOrganic ChemistryMinireviewsGeneral ChemistryPolymer0104 chemical sciencesMiniemulsionchemistryvisual_artconfinementvisual_art.visual_art_mediumMinireviewoxideChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Chemically Fueled Volume Phase Transition of Polyacid Microgels

2021

Abstract Microgels are soft colloids that show responsive behavior and are easy to functionalize for applications. They are considered key components for future smart colloidal material systems. However, so far microgel systems have almost exclusively been studied in classical responsive switching settings using external triggers, while internally organized, autonomous control mechanisms as found in supramolecular chemistry and DNA nanotechnology relying on fuel‐driven out‐of‐equilibrium concepts have not been implemented into microgel systems. Here, we introduce chemically fueled transient volume phase transitions (VPTs) for poly(methacrylic acid) (PMAA) microgels, where the collapsed hydr…

Phase transition540 Chemistry and allied sciencesMaterials scienceSupramolecular chemistry010402 general chemistrydissipative self-assembly01 natural sciencesnonequilibrium processesCatalysismicrogelschemistry.chemical_compoundColloidMicrogels | Hot PaperDNA nanotechnologyfuelsAutonomous controlResearch Articlespolymerschemistry.chemical_classification010405 organic chemistryMaterial systemGeneral ChemistryPolymerGeneral Medicine0104 chemical sciencesChemical engineeringMethacrylic acidchemistry540 ChemieResearch ArticleAngewandte Chemie
researchProduct

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)
researchProduct

Amphiphilic Polyphenylene Dendron Conjugates for Surface Remodeling of Adenovirus 5

2020

Abstract Amphiphilic surface groups play an important role in many biological processes. The synthesis of amphiphilic polyphenylene dendrimer branches (dendrons), providing alternating hydrophilic and lipophilic surface groups and one reactive ethynyl group at the core is reported. The amphiphilic surface groups serve as biorecognition units that bind to the surface of adenovirus 5 (Ad5), which is a common vector in gene therapy. The Ad5/dendron complexes showed high gene transduction efficiencies in coxsackie‐adenovirus receptor (CAR)‐negative cells. Moreover, the dendrons offer incorporation of new functions at the dendron core by in situ post‐modifications, even when bound to the Ad5 sur…

Surface (mathematics)DendrimersCell SurvivalPolymersSurface PropertiesvirusesProtein CoronaCHO CellsGene delivery010402 general chemistry01 natural sciencesCatalysisAdenoviridaeTransduction (genetics)CricetulusCricetinaeDendrimerAmphiphilegene technologyAnimalsvirusesResearch ArticlesamphiphilesCycloaddition Reaction010405 organic chemistryChemistryBlood ProteinsGeneral MedicineGeneral ChemistryDendrimers | Hot PaperCombinatorial chemistryproteins0104 chemical sciencesLiposomesHydrophobic and Hydrophilic InteractionsBlood streamResearch ArticleProtein BindingConjugateAngewandte Chemie International Edition
researchProduct