Search results for "chemical science"

showing 10 items of 9771 documents

Molecular Mechanisms of the Blockage of Glioblastoma Motility

2021

Glioblastoma (GBM) is the most common and lethal brain tumor. GBM has a remarkable degree of motility and is able to infiltrate the healthy brain. In order to perform a rationale-based drug-repositioning study, we have used known inhibitors of two small Rho GTPases, Rac1 and Cdc42, which are upregulated in GBM and are involved in the signaling processes underlying the orchestration of the cytoskeleton and cellular motility. The selected inhibitors (R-ketorolac and ML141 for Cdc42 and R-ketorolac and EHT 1864 for Rac1) have been successfully employed to reduce the infiltration propensity of GBM in live cell imaging studies. Complementarily, all-atom simulations have elucidated the molecular …

rac1 GTP-Binding Proteinrho GTP-Binding ProteinsGeneral Chemical EngineeringBrain tumorMotilityRAC1CDC42Library and Information SciencesBiologySettore BIO/09 - FisiologiaMicrotubules01 natural sciencesDownregulation and upregulationLive cell imaging0103 physical sciencesmedicineHumanscdc42 GTP-Binding Protein010304 chemical physicsDrug discoveryCancerGeneral Chemistrymedicine.disease0104 chemical sciencesComputer Science Applications010404 medicinal & biomolecular chemistrySettore CHIM/03 - Chimica Generale E InorganicaCancer researchGlioblastomaJournal of Chemical Information and Modeling
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Strongly Coupled Coherent Phonons in Single-Layer MoS 2

2019

We present a transient absorption setup combining broadband detection over the visible-UV range with high temporal resolution ($\sim$20fs) which is ideally suited to trigger and detect vibrational coherences in different classes of materials. We generate and detect coherent phonons (CPs) in single layer (1L) MoS$_2$, as a representative semiconducting 1L-transition metal dichalcogenide (TMD), where the confined dynamical interaction between excitons and phonons is unexplored. The coherent oscillatory motion of the out-of-plane $A'_{1}$ phonons, triggered by the ultrashort laser pulses, dynamically modulates the excitonic resonances on a timescale of few tens fs. We observe an enhancement by…

ramanspectroscopyPhononExcitonGeneral Physics and AstronomyFOS: Physical sciences02 engineering and technologyApplied Physics (physics.app-ph)thz phonons010402 general chemistry01 natural sciencesMolecular physicssymbols.namesakephotoinduced bandgap renormalizationtransient absorption spectroscopyUltrafast laser spectroscopyMesoscale and Nanoscale Physics (cond-mat.mes-hall)General Materials Sciencepulsesexciton−phonon interactionPhysicsab initio calculationCondensed Matter - Materials ScienceCondensed Matter - Mesoscale and Nanoscale Physicstransition metal dichalcogenidesgrapheneGeneral Engineeringmonolayer mos2ResonanceMaterials Science (cond-mat.mtrl-sci)excitationmonodynamicsPhysics - Applied Physics021001 nanoscience & nanotechnology0104 chemical sciencesAmplitudeOrders of magnitude (time)coherent phononsexciton-phonon interactionsymbols0210 nano-technologyRaman spectroscopyExcitationACS Nano
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Proton reduction by phosphinidene-capped triiron clusters

2021

Bis(phosphinidene)-capped triiron carbonyl clusters, including electron rich derivatives formed by substitution with chelating diphosphines, have been prepared and examined as proton reduction catalysts. Treatment of the known cluster [Fe3(CO)9(µ3-PPh)2] (1) with various diphosphines in refluxing THF (for 5, refluxing toluene) afforded the new clusters [Fe3(CO)7(µ3-PPh)2(κ2-dppb)] (2), [Fe3(CO)7(µ3-PPh)2(κ2-dppv)] (3), [Fe3(CO)7(µ3-PPh)2(κ2-dppe)] (4) and [Fe3(CO)7(µ3-PPh)2(µ-κ2-dppf)] (5) in moderate yields, together with small amounts of the corresponding [Fe3(CO)8(µ3-PPh)2(κ1-Ph2PxPPh2)] cluster (x = -C4H6-, -C2H2-, -C2H4-, -C3H6-, -C5H4FeC5H4-). The molecular structures of complexes 3 a…

rautaphosphinidine010402 general chemistryElectrochemistry01 natural sciencesBiochemistryMedicinal chemistryRedoxproton reductionDFTCatalysisInorganic Chemistrychemistry.chemical_compoundkatalyytitelektrokatalyysiDiphosphinesMaterials ChemistryCluster (physics)electrocatalysisPhysical and Theoretical Chemistryfosfori010405 organic chemistryLigandOrganic ChemistrytiheysfunktionaaliteoriakompleksiyhdisteettriironToluene0104 chemical scienceschemistryPhosphinidene
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Proteins in Ionic Liquids: Reactions, Applications, and Futures

2019

Biopolymer processing and handling is greatly facilitated by the use of ionic liquids, given the increased solubility, and in some cases, structural stability imparted to these molecules. Focussing on proteins, we highlight here not just the key drivers behind protein-ionic liquid interactions that facilitate these functionalities, but address relevant current and potential applications of protein-ionic liquid interactions, including areas of future interest.

reactionsenzymesNanotechnology02 engineering and technologyReviewengineering.material010402 general chemistry01 natural sciencesphysico-chemical relationshipsENG - Sustainable Process Technologieslcsh:Chemistryionic liquidschemistry.chemical_compoundBeacon - Green Chemicalsmolecular organizationMoleculeSolubilityintermolecular interactionsChemistryIntermolecular forceGeneral Chemistry021001 nanoscience & nanotechnologyproteins0104 chemical sciencesChemistrylcsh:QD1-999Ionic liquidengineeringBiopolymerCurrent (fluid)0210 nano-technologyFutures contractFrontiers in Chemistry
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Polysubstituted ferrocenes as tunable redox mediators

2018

A series of four ferrocenyl ester compounds, 1-methoxycarbonyl- (1), 1,1’-bis(methoxycarbonyl)- (2), 1,1’,3-tris(methoxycarbonyl)- (3) and 1,1’,3,3’-tetrakis(methoxycarbonyl)ferrocene (4), has been studied with respect to their potential use as redox mediators. The impact of the number and position of ester groups present in 1–4 on the electrochemical potential E1/2 is correlated with the sum of Hammett constants. The 1/1+–4/4+ redox couples are chemically stable under the conditions of electrolysis as demonstrated by IR and UV–vis spectroelectrochemical methods. The energies of the C=O stretching vibrations of the ester moieties and the energies of the UV–vis absorptions of 1–4 and 1+–4+ c…

redox mediator010402 general chemistryElectrosynthesis01 natural sciencesMedicinal chemistryRedoxFull Research Paperlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryRedox titrationparamagnetic NMR spectroscopylcsh:ScienceElectrochemical potential010405 organic chemistryChemistryChemical shiftOrganic Chemistryferrocenespectroelectrochemistrycyclic voltammetry0104 chemical sciencesChemistryFerroceneProton NMRlcsh:QCyclic voltammetryBeilstein Journal of Organic Chemistry
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Self-assembly of square planar rhodium carbonyl complexes with 4,4-disubstituted-2,2′-bipyridine ligands

2020

The impact of non-covalent interactions and reaction conditions on formation and self-assembly of ionic pairs of Rh complexes with 4,4’-disubstituted bipyridine ligands ([Rh(L1)(CO)2][Rh(CO)2Cl2])n (1), [Rh(L1)2Cl2][Rh(CO)2Cl2] (2), ([Rh(L1)(CO)2][Rh(CO)2Cl2][Rh(L1)(CO)2]n([Rh(CO)2(Cl)2])n) (3), ([Rh(L2)CO2] [Rh(CO)2Cl2])n∙EtOH (4), ([Rh(L2)(CO)2])n ([Rh(CO)2Cl2])n (5) (L1 = 4,4’-dimethyl-2,2’-bipyridine, L2 = 4,4’-diamine-2,2’-bipyridine) have been studied. Packing of square planar Rh complexes favor formation of one-dimensional chains. In structure 1, the polymeric chain is formed by the alternating cationic [Rh(L1)(CO)2]+ and the anionic [Rh(CO)2Cl2]- units leading to a neutral pseudo li…

reductive carbonylationchemistry.chemical_elementIonic bonding02 engineering and technology010402 general chemistry01 natural sciences22'-BipyridineRhodiumchemistry.chemical_compoundBipyridineGeneral Materials Sciencemetallophilicitychemistry.chemical_classificationLigandHydrogen bondCationic polymerizationcarbonylGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesCrystallographybipyridinechemistryrhodiumCounterion0210 nano-technologySolid State Sciences
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Potential-assisted deposition of mixed alkanethiol self-assembled monolayers

2010

Abstract Preparation of self-assembled monolayers (SAMs) usually involves passive incubation. The recently developed potential-assisted deposition is indeed more selective as well as 100-fold faster than passive adsorption, thereby enhancing the reproducibility of the monolayer deposition. This article aims to identify the electrodeposition conditions necessary to prepare mixed alkanethiol SAMs on gold surface. Parameters such as concentrations in solution, electrode polarization and deposition time were examined for two chain lengths, C 3 (mercaptopropionic acid, MPA) and C 18 (octadecanethiol, ODT). The kinetics and composition of the SAMs were systematically characterized by reductive st…

reductive desorptionGeneral Chemical EngineeringAnalytical chemistry02 engineering and technology010402 general chemistry01 natural sciencesAdsorptionEllipsometryDesorption[ CHIM.OTHE ] Chemical Sciences/OtherMonolayerDeposition (phase transition)oxidative adsorptionSurface plasmon resonanceComputingMilieux_MISCELLANEOUSChemistrySelf-assembled monolayer021001 nanoscience & nanotechnologybinary SAMs0104 chemical scienceselectrochemistrySelf-assembly0210 nano-technology[CHIM.OTHE]Chemical Sciences/Othersurface plasmon resonanceellipsometry
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Synthesis, Electrochemistry, and Photophysics of Aza-BODIPY Porphyrin Dyes

2016

International audience; The synthesis of dyad and triad aza-BODIPY-porphyrin systems in two steps starting from an aryl-substituted aza-BODIPY chromophore is described. The properties of the resulting aza-BODIPY-porphyrin conjugates have been extensively investigated by means of electrochemistry, spectroelectrochemistry, and absorption/emission spectroscopy. Fluorescence measurements have revealed a dramatic loss of luminescence intensity, mainly due to competitive energy transfer and photoinduced electron transfer involving charge separation followed by recombination.

resonance energy-transferporphyrinoidstetraarylazadipyrromethenes010402 general chemistryPhotochemistryElectrochemistry01 natural sciences7. Clean energy[ CHIM ] Chemical SciencesCatalysisFluorescence spectroscopyPhotoinduced electron transfersinglet oxygentransfersphotoinduced electron-transferphotoinduced electron transferchemistry.chemical_compoundgeneration[CHIM]Chemical Scienceselectrogenerated chemiluminescencespectroscopic propertiespolyadsAbsorption (electromagnetic radiation)aza-BODIPYs010405 organic chemistryfullereneOrganic ChemistryGeneral ChemistryChromophorefluorescence spectroscopyPorphyrinFluorescence0104 chemical sciences3. Good healthchemistryelectrochemistryderivativesLuminescence
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Phytochemical investigation of the needles of Abies nebrodensis (Lojac.) Mattei

2019

Abies nebrodensis (Lojac.) Mattei (Pinaceae) is a species living in a very small population only in a confined area of Sicily. In this study, the dichloromethane extract of the leaves was analyzed. Apart from three already known metabolites namely dehydroabietic acid; maltol; and rheosmin, previously detected in other species of Abies, a lanostane derivative was isolated. Its chemical structure was elucidated by means of extensive spectroscopic methods.

rheosminAbies nebrodensiChemical structurePopulationMaltolPlant Science01 natural sciencesBiochemistryLanostaneAnalytical ChemistrySettore BIO/01 - Botanica Generalechemistry.chemical_compoundOrganic chemistrySettore BIO/15 - Biologia FarmaceuticaAbies nebrodensiseducationeducation.field_of_studymaltolbiology010405 organic chemistrySettore BIO/02 - Botanica SistematicaOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classification0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryPhytochemicalPinaceaedehydroabietic acidlanostaneDerivative (chemistry)
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Synthesis and biological evaluation of novel peptidomimetics as rhodesain inhibitors

2016

Novel rhodesain inhibitors were developed by combining an enantiomerically pure 3-bromoisoxazoline warhead with a 1,4-benzodiazepine scaffold as specific recognition moiety. All compounds were proven to inhibit rhodesain with Ki values in the low-micromolar range. Their activity towards rhodesain was found to be coupled to an in vitro antitrypanosomal activity, with IC50 values ranging from the mid-micromolar to a low-micromolar value for the most active rhodesain inhibitor (R,S,S)-3. All compounds showed a good selectivity against the target enzyme since all of them were proven to be poor inhibitors of human cathepsin L. Novel rhodesain inhibitors were developed by combining an enantiomeri…

rhodesainPharmacologychemistry.chemical_classificationCathepsinPeptidomimetic010405 organic chemistryChemistryPeptidomimeticProton Magnetic Resonance SpectroscopyenPeptidomimetics; rhodesain; trypanosomaGeneral Medicine01 natural sciencesCombinatorial chemistryIn vitro0104 chemical sciencesCysteine Endopeptidases010404 medicinal & biomolecular chemistryEnzymeDrug DiscoveryIc50 valuesMoietyPeptidomimeticsCarbon-13 Magnetic Resonance SpectroscopytrypanosomaBiological evaluationJournal of Enzyme Inhibition and Medicinal Chemistry
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