Search results for "polymer"

showing 10 items of 10504 documents

A two-dimensional coordination polymer constructed from binuclear copper(II) metalloligands and manganese(II) ions: Synthesis, crystal structure and …

2016

Abstract The self-assembly process between the binuclear [Cu2(HL)(L)]− complex and the manganese(II) ion affords a two-dimensional coordination polymer of formula [Mn{Cu2(HL)(L)}2(H2O)2]n (1) (H3L = 3-hydroxyiminomethylsalicylic acid) where parallel ladder-like motifs of defective double cubanes of bis(phenoxo)dicopper(II) units as rods and anti-syn carboxylato bridges as rungs act as ligands towards tetraaqua-manganese(II) entities through the deprotonated oxime groups. The topology of 1 is compared with the one of another compound, [Mn{Cu2(HL)(L)}2(H2O)4]·4H2O·2DMF (1′) which was obtained in different conditions by Okawa et al. (J. Chem. Soc., Dalton Trans. (2001) 3119). Magnetic suscepti…

010405 organic chemistryStereochemistryCoordination polymerchemistry.chemical_elementCrystal structureManganese010402 general chemistryOxime01 natural sciencesMagnetic susceptibilityCopper0104 chemical sciencesIonInorganic Chemistrychemistry.chemical_compoundCrystallographyDeprotonationchemistryMaterials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
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Helical supramolecular polymerization of C3-symmetric amides and retroamides: on the origin of cooperativity and handedness.

2016

The cooperative supramolecular polymerization of 1 and 2 yields P- or M-type helical aggregates depending on the absolute configuration (S or R) of the stereogenic centres attached to the side chains. The connectivity of the amide group does not affect the handedness of the helical aggregates, but determines a larger cooperativity for retroamides 1.

010405 organic chemistryStereochemistryMetals and AlloysSupramolecular chemistryAbsolute configurationCooperativityGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStereocenterchemistry.chemical_compoundCrystallographychemistryPolymerizationAmideMaterials ChemistryCeramics and CompositesSide chainChemical communications (Cambridge, England)
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Carbon monoxide activation by a molecular aluminium imide: C-O bond cleavage and C-C bond formation

2020

Anionic molecular imide complexes of aluminium are accessible via a rational synthetic approach involving the reactions of organo azides with a potassium aluminyl reagent. In the case of K2 [(NON)Al(NDipp)]2 (NON=4,5-bis(2,6-diisopropylanilido)-2,7-di-tert-butyl-9,9-dimethyl-xanthene; Dipp=2,6-diisopropylphenyl) structural characterization by X-ray crystallography reveals a short Al-N distance, which is thought primarily to be due to the low coordinate nature of the nitrogen centre. The Al-N unit is highly polar, and capable of the activation of relatively inert chemical bonds, such as those found in dihydrogen and carbon monoxide. In the case of CO, uptake of two molecules of the substrate…

010405 organic chemistrySubstrate (chemistry)General Chemistry010402 general chemistry01 natural sciencesIsocyanateCatalysis3. Good health0104 chemical scienceschemistry.chemical_compoundchemistryChemical bondReagentPolymer chemistryMoleculeImideBond cleavageCarbon monoxide
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Electrochemical and spectroelectrochemical studies of β-phosphorylated Zn porphyrins

2013

The electrochemical and spectroelectrochemical properties of two β-phosphorylated Zn porphyrins, [2-diethoxyphosphoryl-5,10,15,20-tetraphenylporphyrinato]zinc (1) and [2-diisopropoxyphosphoryl-5,10,15,20-tetraphenylporphyrinato]zinc (2), are reported in CH 2 Cl 2 and PhCN containing tetrabutylammonium perchlorate (TBAP) or tetrabutylammonium hexafluorophosphate (TBAPF6) as supporting electrolyte. Under certain solution conditions, three one-electron reductions are observed, with the last process being attributed to the product of a chemical reaction following formation of the porphyrin dianion. Two or three oxidations are observed for the same compounds, again depending upon the solution c…

010405 organic chemistrySupporting electrolyteDimerSubstituentchemistry.chemical_elementGeneral ChemistryZinc010402 general chemistryPhotochemistry01 natural sciencesPorphyrinRedox0104 chemical scienceschemistry.chemical_compoundRadical ionchemistryPolymer chemistryTetrabutylammonium hexafluorophosphate[CHIM]Chemical SciencesComputingMilieux_MISCELLANEOUSJournal of Porphyrins and Phthalocyanines
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Synthesis of new terpyridine-like ligands based on triazolopyridines and benzotriazoles

2017

Herein, terpyridine triazole-based analogs bearing benzotriazoles or/and triazolopyridines are prepared via copper catalysis, where the arrangement of the nitrogen atoms is proven to be crucial to the spectroscopic properties of these ligands.

010405 organic chemistryTriazolechemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCopperCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryOrganic chemistryTerpyridineNew Journal of Chemistry
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Catalytic activity of biscobalt porphyrin-corrole dyads toward the reduction of dioxygen

2009

A series of biscobalt cofacial porphyrin-corrole dyads bearing mesityl substituents at the meso positions of the corrole ring were investigated as to their electrochemistry, spectroelectrochemistry, and CO binding properties in nonaqueous media and then applied to the surface of a graphite electrode and tested as electrocatalysts for the reduction of dioxygen to water or hydrogen peroxide in air-saturated aqueous solutions containing 1 M HClO(4). The catalytic reduction of O(2) with the same dyads was also investigated in the homogeneous phase using 1,1'-dimethylferrocene as a reductant in PhCN containing HClO(4). The examined compounds are represented as (PMes(2)CY)Co(2), where P = a porph…

010405 organic chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry010402 general chemistryElectrocatalystPhotochemistry01 natural sciencesPorphyrin0104 chemical sciencesCatalysisInorganic Chemistrychemistry.chemical_compoundElectron transferchemistrycorrolePolymer chemistryelectrocatalyst[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryCyclic voltammetryCorroleRotating disk electrodeVoltammetryporphyrinComputingMilieux_MISCELLANEOUSreduction of dioxygen
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Mono-DMSO ligated cobalt nitrophenylcorroles: electrochemical and spectral characterization

2018

Four mono-DMSO ligated cobalt corroles with one or three meso-nitrophenyl substituents on the macrocycle were synthesized and investigated as to their electrochemical and spectroscopic properties in CH2Cl2 and DMSO. Comparisons are made between redox reactions of the five-coordinate DMSO adducts in the current study and earlier examined five- and six-coordinate cobalt corroles with pyridine axial ligands which were characterized in a variety of nonaqueous electrochemical solvents. The binding of carbon monoxide (CO) is also investigated.

010405 organic chemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesRedoxCatalysis0104 chemical sciencesAdductchemistry.chemical_compoundchemistryPyridinePolymer chemistryMaterials ChemistryCobaltCarbon monoxideNew Journal of Chemistry
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A reinvestigation of compound CpMo(PMe3)2(CH3)2: Alkylation by single electron transfer and radical addition?

2001

International audience; The synthesis of the half-sandwich molybdenum(III) diphosphine dimethyl complex CpMo(PMe3)2(CH3)2 has been reinvestigated. The compound was obtained from the corresponding dichloro complex CpMo(PMe3)2Cl2 and methyllithium at low temperatures and isolated as a crystalline product by conducting all operations at temperatures lower than −10 °C. The complex is thermally unstable at room temperature but has been fully characterised by EPR spectroscopy, cyclic voltammetry and X-ray diffraction. The formation reaction is retarded by excess phosphine. On the basis of this and other related observations, a mechanism involving phosphine pre-dissociation followed by single elec…

010405 organic chemistrychemistry.chemical_elementGeneral ChemistryAlkylation010402 general chemistryPhotochemistry01 natural sciences0104 chemical scienceslaw.inventionSingle electronchemistry.chemical_compoundchemistrylawMolybdenumPolymer chemistryMethyllithium[CHIM.COOR]Chemical Sciences/Coordination chemistryCyclic voltammetryElectron paramagnetic resonancePhosphine
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Superiority of Optimized Portfolios to Naive Diversification: Fact or Fiction?

2017

Abstract DeMiguel, Garlappi, and Uppal (2009) conducted a highly influential study where they demonstrated that none of the optimized portfolios consistently outperformed the naive diversification. This result triggered a heated debate within the academic community on whether portfolio optimization adds value. Nowadays several studies claim to defend the value of portfolio optimization. The commonality in all these studies is that various portfolio optimization methods are implemented using the datasets generously provided by Kenneth French and the performance is measured by means of the Sharpe ratio. This paper aims to provide a cautionary note regarding the use of Kenneth French datasets …

010407 polymers050208 financeActuarial scienceLow-volatility anomalyComputer scienceSharpe ratio05 social sciencesDiversification (finance)01 natural sciences0104 chemical sciencesReplicating portfolio0502 economics and businessValue (economics)EconometricsEconomicsAcademic communityData libraryPost-modern portfolio theoryPortfolio optimizationFinanceSSRN Electronic Journal
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Optimal Dynamic Portfolio Risk Management

2016

Numerous econometric studies report that financial asset volatilities and correlations are time-varying and predictable. Over the past decade, this knowledge has stimulated increasing interest in various dynamic portfolio risk control techniques. The two basic types of risk control techniques are: risk control across assets and risk control over time. At present, the two types of risk control techniques are not implemented simultaneously. There has been surprisingly little theoretical study of optimal dynamic portfolio risk management. In this paper, the author fills this gap in the literature by formulating and solving the multi-period portfolio choice problem. In terms of dynamic portfoli…

010407 polymersEconomics and EconometricsApplication portfolio managementComputer scienceFinancial assetControl (management)Diversification (finance)01 natural sciencesSpectral risk measureAccounting0502 economics and businessEconomicsEconometricsCapital asset pricing modelChoice problemModern portfolio theoryRisk managementActuarial science050208 financebusiness.industry05 social sciencesGeneral Business Management and AccountingPortfolio risk0104 chemical sciencesReplicating portfolioRisk ControlPortfolioPortfolio optimizationbusinessFinanceThe Journal of Portfolio Management
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