Search results for "Polycyclic Aromatic Hydrocarbons | Hot Paper"

showing 10 items of 32 documents

Isomer effects in fragmentation of Polycyclic Aromatic Hydrocarbons

2015

We have observed significant differences in the fragmentation patterns of isomeric Polycyclic Aromatic Hydrocarbon (PAH) cations following collisions with helium atoms at center-of-mass energies around 100 eV. This is in contrast to the situation at other collision energies or in photo-absorption experiments where isomeric effects are very weak and where the lowest-energy dissociation channels (H- and C2H2-loss) domihate in statistical fragmentation processes. In the 100 eV range, non-statistical fragmentation also competes and is uniquely linked to losses of single carbon atoms (CHx-losses). We find that such CHx-losses are correlated with the ionic ground state energy within a given group…

IONSCollision-induced dissociationIonic bondingPolycyclic aromatic hydrocarbonPhotochemistryANTHRACENE01 natural sciencesDissociation (chemistry)IsomersMOLECULESchemistry.chemical_compoundFragmentation (mass spectrometry)Fragmentation0103 physical sciencesMoleculeCollisionsTANDEM MASS-SPECTROMETRYPolycyclic Aromatic HydrocarbonsPhysical and Theoretical ChemistryCOLLISION-INDUCED DISSOCIATION010303 astronomy & astrophysicsInstrumentationSpectroscopyNon-statistical fragmentationchemistry.chemical_classificationAnthracenePolycyclic Aromatic Hydrocarbons PAHs[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]010401 analytical chemistryCondensed Matter Physics0104 chemical sciencesDIFFERENTIATIONchemistryIONIZATIONCATIONSGROWTH[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Ground stateC14H10International Journal of Mass Spectrometry
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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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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
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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
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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
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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)
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Polycyclic Aromatic Hydrocarbons Phenanthrene and Retene Modify the Action Potential via Multiple Ion Currents in Rainbow Trout Oncorhynchus mykiss C…

2019

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous contaminants in aqueous environments. They affect cardiovascular development and function in fishes. The 3-ring PAH phenanthrene has recently been shown to impair cardiac excitation-contraction coupling by inhibiting Ca2+ and K+ currents in marine warm-water scombrid fishes. To see if similar events take place in a boreal freshwater fish, we studied whether the PAHs phenanthrene and retene (an alkylated phenanthrene) modify the action potential (AP) via effects on Na+ (INa ), Ca2+ (ICaL ), or K+ (IKr , IK1 ) currents in the ventricular myocytes of the rainbow trout (Oncorhynchus mykiss) heart. Electrophysiological characteristics of myo…

PAH-yhdisteetHealth Toxicology and MutagenesiscardiotoxicityAction Potentialstoksikologia010501 environmental sciences01 natural sciences03 medical and health scienceschemistry.chemical_compoundmode of actionEnvironmental ChemistryMyocyteAnimalsaquatic toxicologyMyocytes CardiacPatch clampPolycyclic Aromatic HydrocarbonsMode of actionIon channelkalat030304 developmental biology0105 earth and related environmental sciencesvesistöt0303 health sciencesRetenebiologyPhenanthrenePhenanthrenesAryl hydrocarbon receptorhiilivedytchemistryReceptors Aryl Hydrocarbonpolycyclic aromatic hydrocarbons (PAHs)Oncorhynchus mykissbiology.proteinBiophysicsRainbow troutWater Pollutants ChemicalEnvironmental toxicology and chemistry
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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
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Retene, pyrene and phenanthrene cause distinct molecular-level changes in the cardiac tissue of rainbow trout (Oncorhynchus mykiss) larvae, Part 2 – …

2020

Polycyclic aromatic hydrocarbons (PAHs) are global contaminants of concern. Despite several decades of research, their mechanisms of toxicity are not very well understood. Early life stages of fish are particularly sensitive with the developing cardiac tissue being a main target of PAHs toxicity. The mechanisms of cardiotoxicity of the three widespread model polycyclic aromatic hydrocarbons (PAHs) retene, pyrene and phenanthrene were explored in rainbow trout (Oncorhynchus mykiss) early life stages. Newly hatched larvae were exposed to sublethal doses of each individual PAH causing no detectable morphometric alterations. Changes in the cardiac proteome and metabolome were assessed after 7 o…

Proteomicsbiologiset vaikutuksetEnvironmental Engineering010504 meteorology & atmospheric sciencestoksiinitDevelopmental toxicitycardiotoxicity010501 environmental sciencesmyrkyllisyys01 natural sciencesproteomiikkaTranscriptomechemistry.chemical_compoundMetabolomicsproteomicsMetabolomeEnvironmental ChemistryAnimalsMetabolomicsdevelopmental toxicityaquatic toxicology14. Life underwaterPolycyclic Aromatic HydrocarbonsWaste Management and Disposal0105 earth and related environmental scienceskalatRetenevesistötPyrenesbiologyChemistryPhenanthrenePhenanthrenesAryl hydrocarbon receptorPollutionmetabolomicsekotoksikologiaBiochemistryLarvaOncorhynchus mykisspolycyclic aromatic hydrocarbons (PAHs)biology.proteinPyrenearomaattiset hiilivedytepäpuhtaudet
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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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