Search results for "bond"

showing 10 items of 3527 documents

Implicit public debt thresholds: An operational proposal

2020

Abstract Gauging the public debt-to-GDP ratio a country can sustain in the medium-run without putting fiscal sustainability at risk is a question of key relevance for policy-makers. Deviations from a safe level of debt should be watched over in order to take corrective measures. In this paper we make a proposal for an operational characterization of the “prudent debt level”. To do so, we use standard methods based on Vector Autoregressions to compute the probability that the public debt ratio exceeds a given threshold, using the Spanish case as an example. The resulting probabilities are highly and positively correlated with market risk assessment, measured by the spread with respect to the…

EstimationEconomics and Econometrics050208 financemedia_common.quotation_subjectBond05 social sciencesMarket riskOrder (exchange)Debt0502 economics and businessEconometricsEconomicsDebt ratio050207 economicsFiscal sustainabilitymedia_commonComplement (set theory)Journal of Policy Modeling
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[3+2] Cycloaddition reaction of 1H-phosphorinium-3-olate and 1-methylphosphorinium-3-olate with methyl acrylate: A DFT study

2016

Abstract A density functional theory study was performed on the [3+2] cycloaddition (32CA) reaction of 1H-phosphorinium-3-olate and 1-methylphosphorinium-3-olate with methyl acrylate. The thermodynamic and kinetic parameters were analysed by considering the regio- and stereoisomeric pathways in gas phase and solvents. The geometries indicate that the transition states are slightly more advanced and asynchronous in ethanol. Electron localisation function topological analysis of the bonding changes along the most favourable reaction pathway associated with the 32CA reaction of 1H-phosphorinium-3-olate with methyl acrylate indicates that the reaction takes place through a two-stage one-step me…

Ethanol010405 organic chemistryHydrogen bondRegioselectivitychemistry.chemical_element010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciencesBiochemistryNitrogenTransition stateCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistryComputational chemistryDensity functional theoryPhysical and Theoretical ChemistryMethyl acrylateComputational and Theoretical Chemistry
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Metal-bound Nitrate Anion as an Acceptor for Halogen Bonds in mono-Halopyridine-Copper(II) nitrate Complexes

2019

Fifteen n-halopyridine-Cu(NO3)2 complexes (n = 2, 3, 4) obtained from two different solvents, acetonitrile and ethanol, are investigated for C–X···O–N halogen bonds (XBs) in the solid state by single and powder X-ray diffraction. The nitrate anions bind copper(II) via anisobidentate modes and one of three oxygens act as an XB acceptor to halogens on the core pyridine rings. The N-metal coordination activates the electron-deficient π-system and triggers even C2- and C4-chlorines in the corresponding [Cu(2-chloropyridine)2(NO3)2] and [Cu(4-chloropyridine)2(NO3)2(ACN)] complexes to form short C–Cl2/Cl4···O–N halogen bonds. Notably, the C2–Cl2···O–N XBs with a normalized XB distance parameter (…

Ethanol010405 organic chemistryhalogen bondsSolid-stateNitrate anionGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciencesAcceptor3. Good health0104 chemical sciencesMetalchemistry.chemical_compoundchemistryvisual_artPolymer chemistryHalogenCopper(II) nitratevisual_art.visual_art_mediumGeneral Materials ScienceAcetonitrile
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Palladium on pumice: new catalysts for the stereoselective semihydrogenation of alkynes to (Z)-alkenes

2001

Abstract High selectivities (93–99%) and excellent stereoselectivities (>99%) in the semihydrogenation of CC triple bonds were achieved using palladium on pumice with a metal loading of 0.5, 1.5 or 3.0% wt as catalyst. The reactions were carried out in ethanol or tetrahydrofuran with only 2.5% of ethylenediamine allowing a self-terminating semihydrogenation independently on the CC triple bond.

EthanolOrganic Chemistrychemistry.chemical_elementEthylenediamineTriple bondBiochemistryCatalysischemistry.chemical_compoundchemistryPumiceDrug DiscoveryPolymer chemistryStereoselectivityTetrahydrofuranPalladiumTetrahedron Letters
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ChemInform Abstract: Palladium on Pumice: New Catalysts for the Stereoselective Semihydrogenation of Alkynes to (Z)-Alkenes.

2010

Abstract High selectivities (93–99%) and excellent stereoselectivities (>99%) in the semihydrogenation of CC triple bonds were achieved using palladium on pumice with a metal loading of 0.5, 1.5 or 3.0% wt as catalyst. The reactions were carried out in ethanol or tetrahydrofuran with only 2.5% of ethylenediamine allowing a self-terminating semihydrogenation independently on the CC triple bond.

Ethanolchemistry.chemical_elementEthylenediamineGeneral MedicineTriple bondCatalysischemistry.chemical_compoundchemistryPumicePolymer chemistryOrganic chemistryStereoselectivityTetrahydrofuranPalladiumChemInform
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Reactions at Interfaces: Oxygenation of n-Butyl Ligands Anchored on Silica Surfaces with Methyl(trifluoromethyl)dioxirane

2011

The oxygenation of n-butyl and n-butoxy chains bonded to silica with methyl(trifluoromethyl)dioxirane (1) revealed the ability of the silica matrix to release electron density toward the reacting C(2)-H σ-bond through the Si-C(1) and Si-O(1) σ-bonds connecting the alkyl chain to the surface (silicon β-effect). The silica surface impedes neither the alkyl chain adopting the conformation required for the silicon β-effect nor dioxirane 1 approaching the reactive C(2) methylene group. Reaction regioselectivity is insensitive to changes in the solvation of the reacting system, the location of organic ligands on the silica surface, and the H-bonding character of the silica surface. Reaction rates…

Ethylene OxideTrimethylsilylSiliconSurface PropertiesMolecular Conformationchemistry.chemical_elementChemistry Techniques SyntheticPhotochemistryReaction ratechemistry.chemical_compoundDioxiraneMethyleneAlkylchemistry.chemical_classificationTrifluoromethylOrganic ChemistryRegioselectivityEstersHydrogen BondingStereoisomerismSilicon DioxideOxygenSolutionsKineticschemistryButanesOxidation-ReductionThe Journal of Organic Chemistry
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[N⋅⋅⋅I+⋅⋅⋅N] Halogen-Bonded Dimeric Capsules from Tetrakis(3-pyridyl)ethylene Cavitands

2016

Two [N⋅⋅⋅I+⋅⋅⋅N] halogen-bonded dimeric capsules using tetrakis(3-pyridyl)ethylene cavitands with different lower rim alkyl chains are synthesized and analyzed in solution and the gas phase. These first examples of symmetrical dimeric capsules making use of the iodonium ion (I+) as the main connecting module are characterized by 1H NMR spectroscopy, diffusion ordered NMR spectroscopy (DOSY), electrospray ionization mass spectrometry (ESI-MS), and ion mobility-mass spectrometry (TW-IMS) experiments. The synthesis and effective halogen-bonded dimerization proceeds through analogous dimeric capsules with [N⋅⋅⋅Ag+⋅⋅⋅N] binding motifs as the intermediates as evidenced by the X-ray structures of …

EthyleneElectrospray ionizationhalogen bonds010402 general chemistryMass spectrometry01 natural sciencesCatalysiscavitandsIonchemistry.chemical_compoundPolymer chemistryOrganic chemistrySpectroscopyta116Alkylmass spectrometrychemistry.chemical_classificationta114010405 organic chemistrydimeric capsulesGeneral MedicineGeneral ChemistryNuclear magnetic resonance spectroscopy0104 chemical scienceschemistryHalogenhalonium ionsANGEWANDTE CHEMIE
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The carbenoid-type reactivity of simplest nitrile imine from a molecular electron density theory perspective

2019

Abstract The [3 + 2] cycloaddition (32CA) reactions of the simplest nitrile imine with ethylene and electrophilic dicyanoethylene have been studied within the Molecular Electron Density Theory (MEDT) with the aim of characterising its reactivity. Topological analysis of the electron localisation function of NI shows that it has a carbenoid structure. The activation energy of the 32CA reaction of the simplest nitrile imine with dicyanoethylene is 5.6 kcal mol−1 lower than that involving ethylene, in agreement with the high polar character of the former reaction. Bonding Evolution Theory accounts for the cb-type reactivity of nitrile imine. Along the more favourable ortho regioisomeric path a…

EthyleneNitrile010405 organic chemistryOrganic ChemistryImine010402 general chemistry01 natural sciencesBiochemistryCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistryDrug DiscoveryPolymer chemistryElectrophileSingle bondReactivity (chemistry)CarbenoidTetrahedron
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Grafting of Hindered Phenol Groups onto Ethylene/α-Olefin Copolymer by Nitroxide Radical Coupling

2017

The covalent immobilization of hindered phenol groups, with potential antioxidant activity, onto an ethylene/α-olefin (EOC) copolymer was carried out by the nitroxide radical coupling (NRC) reaction performed in the melt with a peroxide and the 3,5-di-tert-butyl-4-hydroxybenzoyl-2,2,6,6-tetramethylpiperidine-1-oxyl radical (BHB-T). Functionalized EOC (EOC-g-(BHB-T)) was exposed to photo- and thermo-oxidation. By comparison with some model compounds bearing the (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) moiety or the hindered phenol unit, it was observed that the grafted BHB-T could effectively help the stabilization of the polymer matrix both under photo- and thermo-oxidation. In addit…

EthylenePolymers and Plastics02 engineering and technology010402 general chemistry01 natural sciencesPeroxideArticlelcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistrynitroxide radical couplingPolymer chemistryCopolymerMoietyantioxidant covalent immobilizationchemistry.chemical_classificationOlefin fiberhindered phenol moietyChemistry (all)General ChemistryPolymer021001 nanoscience & nanotechnologyGrafting0104 chemical scienceschemistryCovalent bondantioxidant covalent immobilization; nitroxide radical coupling; hindered phenol moiety; HAS-NOR antioxidant0210 nano-technologyHAS-NOR antioxidantPolymers
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A glimpse of the limits of the European economic governance through the legislative and jurisprudential route of the "after-Weimar" German "economic …

2020

El objetivo de esta investigación es reconstruir los límites de la gestión de las finanzas públicas en la Unión Monetaria Europea, utilizando la perspectiva del camino de la "constitución económica" alemana posterior a Weimar. El proceso federativo de la UE no presenta las mismas características legales de ningún otro, incluido el alemán. Sin embargo, algunos problemas son necesariamente similares y similares soluciones se pueden encontrar. En consecuencia, esto documento se centra en la sucesión de reformas en la governance económica europea desde 2008 analizando, en particular, el tema de compartir las obligaciones de la deuda a nivel europeo, esto a través del diálogo entre el Bundesverf…

European levelWeimarconstitución económicamedia_common.quotation_subjectfederative processSH1_12BundesverfassungsgerichtGermanEconomicaproceso federativoDebtPolitical scienceJurisprudence. Philosophy and theory of lawmedia_commonEMU:CIENCIAS JURÍDICAS [UNESCO]EurobondsConstitutionK201-487EMU Weimar "economic constitution" federative process Bundesverfassungsgericht Eurobonds taxationSH1_5Economic governanceLegislaturelanguage.human_languageUemPhilosophyimpuestosUNESCO::CIENCIAS JURÍDICASPolitical economy"economic constitution"languageEuropean monetary uniontaxationUem Weimar constitución económica proceso federativo Bundesverfassungsgericht Eurobonds impuestosLaw
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