Search results for "modification"

showing 10 items of 853 documents

HALE-IoT: HArdening LEgacy Internet-of-Things devices by retrofitting defensive firmware modifications and implants

2022

Internet-Of-Things (IoT) devices and their firmware are notorious for their lifelong vulnerabilities. As device infection increases, vendors also fail to release patches at a competitive pace. Despite security in IoT being an active area of research, prior work has mainly focused on vulnerability detection and exploitation, threat modelling, and protocol security. However, these methods are ineffective in preventing attacks against legacy and End-Of-Life devices that are already vulnerable. Current research mainly focuses on implementing and demonstrating the potential of malicious modifications. Hardening emerges as an effective solution to provide IoT devices with an additional layer of d…

IoTfirmware modificationcybersecurityend-of-lifesuojausSSL-proxyHTTPSlegacyfirmwaredefensive techniquesWAFretrofit securityesineiden internettietoturvakyberturvallisuusEOLverkkohyökkäyksetdeviceshaavoittuvuus
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Endfunctional Polymers by Functionalization of Living Cationic Chain Ends with 1,1-Diphenylethylene

1995

Abstract A new functionalization method has been developed for the synthesis of 2,2-diphenylvinyl(DPV)-telechelic polyisobutylene (PIB). First, living carbocationic polymerization (LCCP) of isobutylene (IB) is quantitatively end-quenched with a nonpolymerizable olefin, 1,1-diphenylethylene (DPE). This process yields a mixture of diphenyl substituted vinyl and tertiary chlorine endgroups. Treatment of the resulting polymer with potassium-tert-butoxide (tBuOK) leads to the quantitative formation of DPV-telechelic PIB which is a potential macroinitiator precursor for living anionic polymerizations.

Isobutylenechemistry.chemical_classificationOlefin fiberTelechelic polymerPolymers and PlasticsCationic polymerizationChemical modificationGeneral ChemistryPolymerchemistry.chemical_compoundPolymerizationchemistryPolymer chemistryMaterials ChemistryCeramics and CompositesSurface modificationOrganic chemistryJournal of Macromolecular Science, Part A
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Rapid and Complete Surface Modification with Strain-Promoted Oxidation-Controlled Cyclooctyne-1,2-Quinone Cycloaddition (SPOCQ)

2017

Abstract Strain‐promoted oxidation‐controlled cyclooctyne‐1,2‐quinone cycloaddition (SPOCQ) between functionalized bicyclo[6.1.0]non‐4‐yne (BCN) and surface‐bound quinones revealed an unprecedented 100 % conjugation efficiency. In addition, monitoring by direct analysis in real time mass spectrometry (DART‐MS) revealed the underlying kinetics and activation parameters of this immobilization process in dependence on its microenvironment.

Kinetics02 engineering and technologyMetal-free click chemistry010402 general chemistryMass spectrometry01 natural sciencesCatalysisQuímica de superfíciesVLAGMass spectrometryStrain (chemistry)Bicyclic moleculeChemistryCommunicationOrganic ChemistryGeneral MedicineGeneral ChemistryCyclooctynes021001 nanoscience & nanotechnologyOrganische ChemieSurface chemistryCombinatorial chemistryCommunicationsCycloaddition0104 chemical sciencesQuinoneKineticsSurface modification0210 nano-technologyQuímica orgànicaAngewandte Chemie International Edition
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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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Synthesis, characterization and study of covalently modified triazole LAPONITE® edges

2020

Abstract LAPONITE® (Lap) clay mineral was successful functionalized by triazole groups in a two steps procedure. First, the Lap edges were modified with 3-azidopropyltrimethoxysilane by traditional heating and microwave irradiation. Microwave irradiation allowed us to obtain high loading onto the Lap edges in lower times compared to those obtained through conventional method. Afterwards, the triazole moieties were obtained by reaction between azido functionalized Lap and propargyl alcohol. The successful functionalization of Lap was proved by thermogravimetric analysis, FT-IR spectroscopy, dynamic light scattering and ζ-potential measurements. Finally, the effects of the surface modificatio…

LAPONITE® Covalent modification Triazole moieties HydrogelThermogravimetric analysisMaterials scienceTriazole020101 civil engineeringGeology02 engineering and technologySettore CHIM/06 - Chimica OrganicaPropargyl alcohol021001 nanoscience & nanotechnology0201 civil engineeringlaw.inventionchemistry.chemical_compoundchemistryChemical engineeringDynamic light scatteringOptical microscopeGeochemistry and PetrologylawCovalent bondSurface modification0210 nano-technologySpectroscopySettore CHIM/02 - Chimica Fisica
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Large eddy simulation of inertial particles dispersion in a turbulent gas-particle channel flow bounded by rough walls

2020

The purpose of this paper is to understand the capability and consistency of large eddy simulation (LES) in Eulerian–Lagrangian studies aimed at predicting inertial particle dispersion in turbulent wall-bounded flows, in the absence of ad hoc closure models in the Lagrangian equations of particle motion. The degree of improvement granted by LES models is object of debate, in terms of both accurate prediction of particle accumulation and local particle segregation; therefore, we assessed the accuracy in the prediction of the particle velocity statistics by comparison against direct numerical simulation (DNS) of a finer computational mesh, under both one-way and two-way coupling regimes. We p…

Lagrange multipliersLagrangian equationsParticle statisticsParticle statisticsVelocity controlComputational MechanicsDirect numerical simulationWall flow Accurate prediction02 engineering and technology01 natural sciencesReynolds numberSettore ICAR/01 - Idraulica010305 fluids & plasmasPhysics::Fluid Dynamicssymbols.namesake0203 mechanical engineeringEquations of motion0103 physical sciencesParticle velocityDispersionsPhysicsTurbulence modificationTurbulenceMechanical EngineeringLarge eddy simulationTwo phase flowReynolds numberMechanicsTurbulent wall-bounded flows Segregation (metallography)Open-channel flow020303 mechanical engineering & transportsParticle accumulationQuay wallssymbolsParticle segregationParticleForecastingParticle velocitiesLarge eddy simulationActa Mechanica
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Interface-Assisted Sign Inversion of Magnetoresistance in Spin Valves Based on Novel Lanthanide Quinoline Molecules

2018

Molecules are proposed to be an efficient medium to host spin-polarized carriers, due to their weak spin relaxation mechanisms. While relatively long spin lifetimes are measured in molecular devices, the most promising route toward device functionalization is to use the chemical versatility of molecules to achieve a deterministic control and manipulation of the electron spin. Here, by combining magnetotransport experiments with element-specific X-ray absorption spectroscopy, this study shows the ability of molecules to modify spin-dependent properties at the interface level via metal–molecule hybridization pathways. In particular, it is described how the formation of hybrid states determine…

LanthanideMaterials scienceCondensed matter physicsMagnetoresistanceSpin polarizationAbsorption spectroscopySpin valve02 engineering and technology021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesElectronic Optical and Magnetic MaterialsBiomaterials0103 physical sciencesElectrochemistryMoleculeSurface modificationCondensed Matter::Strongly Correlated Electrons010306 general physics0210 nano-technologySpin (physics)Materials
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Chemisorption of Atomically Precise 42-Carbon Graphene Quantum Dots on Metal Oxide Films Greatly Accelerates Interfacial Electron Transfer

2019

Graphene quantum dots (GQDs) are emerging as environmentally friendly, low-cost, and highly tunable building blocks in solar energy conversion architectures, such as solar (fuel) cells. Specifically, GQDs constitute a promising alternative for organometallic dyes in sensitized oxide systems. Current sensitized solar cells employing atomically precise GQDs are based on physisorbed sensitizers, with typically limited efficiencies. Chemisorption has been pointed out as a solution to boost photoconversion efficiencies, by allowing improved control over sensitizer surface coverage and sensitizer-oxide coupling strength. Here, employing time-resolved THz spectroscopy, we demonstrate that chemisor…

LetterMaterials scienceGrapheneOxidechemistry.chemical_elementNanotechnology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionchemistry.chemical_compoundElectron transferchemistryQuantum dotlawChemisorptionSurface modificationGeneral Materials SciencePhysical and Theoretical Chemistry0210 nano-technologyMesoporous materialCarbonThe Journal of Physical Chemistry Letters
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eNOS S-nitrosylates β-actin on Cys374 and regulates PKC-θ at the immune synapse by impairing actin binding to profilin-1.

2017

The actin cytoskeleton coordinates the organization of signaling microclusters at the immune synapse (IS); however, the mechanisms involved remain poorly understood. We show here that nitric oxide (NO) generated by endothelial nitric oxide synthase (eNOS) controls the coalescence of protein kinase C-¿ (PKC-¿) at the central supramolecular activation cluster (c-SMAC) of the IS. eNOS translocated with the Golgi to the IS and partially colocalized with F-actin around the c-SMAC. This resulted in reduced actin polymerization and centripetal retrograde flow of ß-actin and PKC-¿ from the lamellipodium-like distal (d)-SMAC, promoting PKC-¿ activation. Furthermore, eNOS-derived NO S-nitrosylated ß-…

Life Sciences & Biomedicine - Other Topics0301 basic medicinePOLARIZATIONIMMUNOLOGICAL SYNAPSEImmunological SynapsesT-LymphocytesPROTEINGolgi ApparatusCYTOSKELETONRetrograde FlowBiochemistryARP2/3 COMPLEXT-CELL-ACTIVATIONProfilinsWhite Blood CellsContractile ProteinsFluorescence MicroscopyAnimal CellsMedicine and Health SciencesPseudopodiaBiology (General)Post-Translational ModificationCells CulturedProtein Kinase CMicroscopyT CellsGeneral NeuroscienceLight MicroscopyNeurochemistryRecombinant Proteins3. Good healthIsoenzymesPOLYMERIZATIONProtein TransportCell ProcessesRNA InterferenceCellular TypesNeurochemicalsGeneral Agricultural and Biological SciencesLife Sciences & BiomedicineResearch ArticleBiochemistry & Molecular BiologyNitric Oxide Synthase Type IIIQH301-705.5Imaging TechniquesRecombinant Fusion ProteinsImmune CellsImmunologyLibrary scienceAntigen-Presenting Cellsmacromolecular substancesBiologyNitric OxideResearch and Analysis MethodsGeneral Biochemistry Genetics and Molecular BiologyCell Line03 medical and health sciencesFluorescence ImagingHumansCysteineNITRIC-OXIDE SYNTHASEBiologyScience & TechnologyBlood CellsRECEPTORGeneral Immunology and MicrobiologyBiology and Life SciencesProteinsCell BiologyActinsS-NitrosylationEnzyme ActivationLuminescent ProteinsCytoskeletal Proteins030104 developmental biologyAmino Acid SubstitutionRETROGRADE FLOWProtein Kinase C-thetaMutationProtein Processing Post-TranslationalNeuroscienceActin PolymerizationPLoS biology
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Fluoride-induced modulation of ionic transport in asymmetric nanopores functionalized with “caged” fluorescein moieties

2016

[EN] We demonstrate experimentally and theoretically a nanofluidic fluoride sensing device based on a single conical pore functionalized with "caged" fluorescein moieties. The nanopore functionalization is based on an amine-terminated fluorescein whose phenolic hydroxyl groups are protected with tert-butyldiphenylsilyl (TBDPS) moieties. The protected fluorescein (Fcn-TBDPS-NH2) molecules are then immobilized on the nanopore surface via carbodiimide coupling chemistry. Exposure to fluoride ions removes the uncharged TBDPS moieties due to the fluoride-promoted cleavage of the silicon-oxygen bond, leading to the generation of negatively charged groups on the fluorescein moieties immobilized on…

Life sciences; biologyReaction stepAnalytical chemistryHalideIonic bonding02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundNanoporechemistryddc:570FISICA APLICADASurface modificationMoleculeGeneral Materials ScienceFluorescein0210 nano-technologyFluorideNanoscale
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