Search results for "Reactivity"

showing 10 items of 880 documents

Direct measurement of NO<sub>3</sub> radical reactivity in a boreal forest

2018

Abstract. We present the first direct measurements of NO3 reactivity (or inverse lifetime, s−1) in the Finnish boreal forest. The data were obtained during the IBAIRN campaign (Influence of Biosphere-Atmosphere Interactions on the Reactive Nitrogen budget) which took place in Hyytiälä, Finland during the summer/autumn transition in September 2016. The NO3 reactivity was generally very high with a maximum value of 0.94 s−1 and displayed a strong diel variation with a campaign-averaged nighttime mean value of 0.11 s−1 compared to a daytime value of 0.04 s−1. The highest nighttime NO3 reactivity was accompanied by major depletion of canopy level ozone and was associated with strong temperature…

Forest floorAtmospheric ScienceDaytimeOzone010504 meteorology & atmospheric sciencesReactive nitrogen15. Life on land010501 environmental sciencesSeasonalityAtmospheric sciencesmedicine.disease01 natural sciencesTrace gaschemistry.chemical_compoundchemistry13. Climate actionAtmospheric chemistrymedicineEnvironmental scienceReactivity (chemistry)0105 earth and related environmental sciencesAtmospheric Chemistry and Physics
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Ammonium formate-Pd/C as a new reducing system for 1,2,4-oxadiazoles. Synthesis of guanidine derivatives and reductive rearrangement to quinazolin-4-…

2021

1,2,4-Oxadiazole is a heterocycle with wide reactivity and many useful applications. The reactive O-N bond is usually reduced using molecular hydrogen to obtain amidine derivatives. NH4CO2H-Pd/C is here demonstrated as a new system for the O-N reduction, allowing us to obtain differently substituted acylamidine, acylguanidine and diacylguanidine derivatives. The proposed system is also effective for the achievement of a reductive rearrangement of 5-(2′-aminophenyl)-1,2,4-oxadiazoles into 1-alkylquinazolin-4(1H)-ones. The alkaloid glycosine was also obtained with this method. The obtained compounds were preliminarily tested for their biological activity in terms of their cytotoxicity, induce…

Formatesquinazolin-4-onemedicine.disease_causeGuanidineschemistry.chemical_compoundBiology (General)CytotoxicityAmmonium formateSpectroscopyOxadiazolesMolecular StructureChemistryAlkaloidBiological activityGeneral MedicineComputer Science ApplicationsChemistryOxidation-ReductionPalladiumCell SurvivalQH301-705.5Dipeptidyl Peptidase 4chemistry.chemical_elementAntineoplastic AgentsreductionArticleCatalysisInorganic ChemistryAmidine4-oxadiazolereduction;Cell Line TumorDiabetes MellitusAmmonium formatemedicineHumansHypoglycemic AgentsReactivity (chemistry)Physical and Theoretical ChemistryMolecular BiologyQD1-999QuinazolinonesSettore MED/04 - Patologia GeneralediacylguanidineOrganic Chemistry124-oxadiazolealpha-GlucosidasesacylguanidineSettore CHIM/06 - Chimica OrganicapalladiumCombinatorial chemistryModels ChemicalA549 CellsOxidative stress
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Preparation and reactivity of macrocyclic dienynes

2010

Abstract (1 E ,5 E )-Cyclopentadeca-1,5-dien-3-yne ( 1c ), which represents the first macrocyclic 1,5-dien-3-yne, can be obtained by thermal- or butyllithium-induced fragmentation of the corresponding 1,2,3-selenadiazole 8 . The ( E , E )-dienyne functionality causes a geometrical strain E g , which enhances the reactivity in addition ( 1c → 12 , 13 ) and cycloaddition ( 1c → 10 ) reactions and lowers the isomerization barrier to the unstrained ( E , Z )-configuration 1d ( E g  = 0). A slow process 1c → 1d occurs even at ambient temperatures within several weeks.

Fragmentation (mass spectrometry)Strain (chemistry)StereochemistryChemistryOrganic ChemistryDrug DiscoveryReactivity (chemistry)BiochemistryMedicinal chemistryIsomerizationCycloadditionTetrahedron Letters
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Of Thiols and Disulfides: Methods for Chemoselective Formation of Asymmetric Disulfides in Synthetic Peptides and Polymers.

2018

In protein or peptide chemistry, thiols are frequently chosen as a chemical entity for chemoselective modification reactions. Although it is a well-established methodology to address cysteines and homocysteines in aqueous media to form S-C bonds, possibilities for the chemoselective formation of asymmetric disulfides have been less approached. Focusing on bioreversibility in conjugation chemistry, the formation of disulfide bonds is highly desirable for the attachment of thiol-containing bioactive agents to proteins or in cross-linking reactions, because disulfide bonds can combine stability in blood with degradability inside cells. In this Concept article, recent approaches in the field of…

Free RadicalsPolymersPeptide02 engineering and technologyConjugated system010402 general chemistryMicroscopy Atomic Force01 natural sciencesCatalysisPolymerizationReactivity (chemistry)DisulfidesSulfhydryl CompoundsProtecting groupSolid-Phase Synthesis Techniqueschemistry.chemical_classificationAqueous mediumOrganic ChemistryGeneral ChemistryPolymer021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryThiolQuantum TheorySelf-assembly0210 nano-technologyPeptidesChemistry (Weinheim an der Bergstrasse, Germany)
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Non-conventional methods and media for the activation and manipulation of carbon nanoforms

2013

Very often, chemical transformations require tedious and long procedures, which, sometimes, can be avoided using alternative methods and media. New protocols, enabling us to save time and solvents, allow us also to explore new reaction profiles. This Tutorial Review focuses on the physical and chemical behavior of carbon nanoforms, CNFs (fullerenes, nanotubes, nanohorns, graphene, etc.) when non-conventional methods and techniques, such as microwave irradiation, mechano-chemistry or highly ionizing radiations are employed. In addition, the reactivity of CNFs in non-conventional media such as water, fluorinated solvents, supercritical fluids, or ionic liquids is also discussed.

FullereneNanotubes Nanohorns Synthesis Microwave chemistry Ionic Liquidschemistry.chemical_elementIonic LiquidsNanotechnologylaw.inventionchemistry.chemical_compoundlawReactivity (chemistry)MicrowavesAlternative methodsGrapheneNanotubes Carboncarbon nanoforms non-conventional techniquesnon-conventional techniquesWaterGeneral ChemistrySettore CHIM/06 - Chimica OrganicaSupercritical fluidCarbonNanostructureschemistryGamma RaysIonic liquidMicrowave irradiationSolventsGraphitecarbon nanoformsCarbon
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Synthesis of Enaminones-Based Benzo[d]imidazole Scaffold: Characterization and Molecular Insight Structure

2020

(E)-1-(1H-Benzo[d]imidazol-2-yl)-3-(dimethylamino)prop-2-en-1-one 2 was synthesized by one-pot synthesis protocol of 2-acetyl benzo[d]imidazole with dimethylformamide dimethylacetal (DMF-DMA) in xylene at 140 &deg

General Chemical EngineeringAcetylacetoneChemical structure010402 general chemistry01 natural sciencesDFTInorganic Chemistrychemistry.chemical_compound<i>β</i>-enaminonelcsh:QD901-999ImidazoleMoleculeGeneral Materials ScienceReactivity (chemistry)β-enaminoneorgaaniset yhdisteetkemiallinen synteesi010405 organic chemistrytiheysfunktionaaliteoriabenzo[<i>d</i>]imidazoleHirshfeld analysiskiteetCondensed Matter Physics0104 chemical sciencesCrystallographyDMF-DMAchemistrybenzo[d]imidazoleOrthorhombic crystal systemlcsh:CrystallographyDerivative (chemistry)Monoclinic crystal systemCrystals
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BODIPY dyes functionalized with 2-(2-dimethylaminophenyl)ethanol moieties as selective OFF–ON fluorescent chemodosimeters for the nerve agent mimics …

2014

[EN] Two OFF-ON fluorescent chemodosimeters based on a BODIPY core for the detection of nerve agent mimics have been synthesized. Their reactivity towards diethylcyanophosphonate (DCNP) and diisopropylfluorophosphate (DFP) has been tested in organic and aqueous phase. These chemodosimeters selectively detect the nerve agent mimics with good LODs. The chemodosimeters hold their sensing properties on solid supports, allowing the preparation of a hand held sensing kit. The sensing in solid-liquid phase has been demonstrated. The X-ray structure of compound 2 has been resolved.

General Chemical EngineeringBiological Warfare Agentschemistry.chemical_compoundOrganophosphorus HydrolasemedicineOrganic chemistryReactivity (chemistry)Nerve agentEthanolDmmp DetectionQUIMICA INORGANICAOptical-PropertiesAqueous two-phase systemGeneral ChemistryCombinatorial chemistryFluorescenceElectrochemical gas sensorchemistryAcetylcholinesteraseSpectroscopic PropertiesBODIPYPhotonic CrystalBiosensorElectrochemical SensorDerivativesBiosensormedicine.drugRSC Adv.
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Selective photooxidation of ortho-substituted benzyl alcohols and the catalytic role of ortho-methoxybenzaldehyde

2016

It has been recently reported by Palmisano et al. (2015) [1] that the oxidation of 2-methoxybenzyl alcohol (2-MBA) to 2-methoxybenzaldehyde (2-MBAD) proceeds in water under near-UV light with an unexpected catalytic effect of 2-MBAD. In order to investigate the catalytic role of aldehyde in photolytic oxidation of ortho-substituted benzyl alcohols (OSBAs), reactivity runs were carried out with 2-methylbenzyl alcohol (2-MeBA), 2-nitrobenzyl alcohol (2-NBA), 2-hydroxybenzyl alcohol (2-HBA) and 2-chlorobenzyl alcohol (2-CIBA) in the absence and in the presence of their corresponding aldehyde. None of those alcohols showed a measurable oxidation rate even in the presence of their aldehydes but …

General Chemical EngineeringGeneral Physics and AstronomyAlcohol2-MethoxybenzaldehydeHomogeneous photocatalysi010402 general chemistry01 natural sciencesAldehydeCatalysisFerulic acidPhysics and Astronomy (all)chemistry.chemical_compoundBenzyl alcoholOrganic chemistryChemical Engineering (all)Reactivity (chemistry)chemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria Chimica010405 organic chemistryChemistryChemistry (all)General Chemistry0104 chemical sciencesAutocatalytic photooxidationAlcohol oxidationPhotocatalysis2-Methoxybenzaldehyde; Autocatalytic photooxidation; Benzyl alcohols; Homogeneous photocatalysis; Chemistry (all); Chemical Engineering (all); Physics and Astronomy (all)Selectivity
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Cobalt complex based on cyclam for reversible binding of nitric oxide

2008

We report the synthesis and theoretical calculations of nitrosyl cobalt complexes based on saturated tetraazamacrocycle for the reversible binding of nitric oxide (NO). Density-functional theory provides a rigorous theoretical framework for analysing, interpreting and investigating important parameters in order to further tune the properties of these complexes to the target application. We focus on understanding the stability of complexes in methanol solution as well as their reactivity and stability evolution in the presence of NO, O2 and higher nitrogen oxides intermediates. Calculations have been used to explore appropriate combinations of different macrocycles, metal centres and ligands…

General Chemical EngineeringInorganic chemistryInfrared spectroscopychemistry.chemical_element010402 general chemistry01 natural sciencesNitric oxideCoordination complexMetalchemistry.chemical_compoundComputational chemistrynitric oxideCyclamGeneral Materials ScienceReactivity (chemistry)[CHIM.COOR]Chemical Sciences/Coordination chemistryinfrared spectroscopyComputingMilieux_MISCELLANEOUSchemistry.chemical_classification010405 organic chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryGeneral Chemistrycobalt complexesCondensed Matter Physics0104 chemical sciencesmolecular modellingchemistryModeling and Simulationvisual_artvisual_art.visual_art_mediumcoordination chemistryMethanolCobaltInformation Systems
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Synthesis of dimethyl carbonate in supercritical carbon dioxide

2006

The reactivity of carbon dioxide with methanol to form dimethyl carbonate was studied in the presence of the n-butylmethoxytin compounds n-Bu3SnOCH3, n-Bu2Sn(OCH3)2 , and [n-Bu2(CH3O)Sn]2 O. The reaction occurred under solventless conditions at 423 K and was produced by an increase in CO2 pressure. This beneficial effect is primarily attributed to phase behavior. The mass transfer under liquid-vapor biphasic conditions was not limiting when the system reached the supercritical state for a CO2 pressure higher than 16 MPa. Under these conditions, CO2 acted as a reactant and a solvent.

General Chemical EngineeringInorganic chemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural scienceschemistry.chemical_compoundSupercritical carbon dioxidesupercritical carbon dioxide[ CHIM.OTHE ] Chemical Sciences/OtherTin(IV) compoundsdimethyl carbonateReactivity (chemistry)lcsh:Chemical engineeringComputingMilieux_MISCELLANEOUSElectrochemical reduction of carbon dioxideSupercritical water oxidationSupercritical carbon dioxide010405 organic chemistrylcsh:TP155-156[ CHIM.INOR ] Chemical Sciences/Inorganic chemistrySupercritical fluid0104 chemical scienceschemistry13. Climate actionDimethyl carbonateCarbon dioxidetin(IV) compoundsMethanolDimethyl carbonate[CHIM.OTHE]Chemical Sciences/OtherBrazilian Journal of Chemical Engineering
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