Search results for "Density functional calculation"

showing 10 items of 64 documents

Dicopper(II) metallacyclophanes with photoswitchable oligoacene spacers: a joint experimental and computational study on molecular magnetic photoswit…

2018

Dinuclear copper(II) complexes of the metallacyclophane-type, (nBu4N)4[Cu2(2,6-anba)2] (1) and (nBu4N)4[Cu2(1,5-naba)2]·4H2O (2) with photoactive 2,6-anthracene-(2,6-anba) and 1,5-naphthalenebis(oxamate) (1,5-naba) bridging ligands, are reported. They undergo a thermally reversible, solid-state photomagnetic (ON/OFF) switching between the moderately strong antiferromagnetically coupled dicopper(II) species and the corresponding magnetically uncoupled [4+4] photocycloaddition product. Density functional calculations give further insights on the intramolecular (“pseudo-bimolecular”) photocycloaddition reaction of the two facing 2,6-anthracene or 1,5-naphthalene spacers in this novel family of…

Spintronics010405 organic chemistryChemistryIntermetallicchemistry.chemical_elementOligoacenes010402 general chemistry01 natural sciencesCopper0104 chemical sciencesIonPhotochemical reactivityCrystallographyDensity functional calculationsIntramolecular forceMagnetic propertiesMaterials ChemistryAntiferromagnetismPhotochemical reactivityPhysical and Theoretical ChemistryCopper
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A Hydrogen-Bonded Supramolecular meso-Helix

2003

[EN] A new one-dimensional hydrogen-bonded polymer with a unique meso-helical structure has been prepared from the spontaneous self-assembly in the solid-state of meta-substituted phenylene dioxamic acid diethyl ester monomers. The helical nature of this molecule and its self-complementary character, through intermolecular hydrogen bonding between oxamic acid ester functions, are the two main factors responsible for the crystalline aggregation process, as confirmed by both experimental X-ray crystallographic data and theoretical ab initio calculations.

StereochemistryHydrogen bondOrganic ChemistrySupramolecular chemistryCrystal engineeringCrystal engineeringAmidesHydrogen bondschemistry.chemical_compoundCrystallographyDensity functional calculationsMonomerchemistryAb initio quantum chemistry methodsPhenyleneFISICA APLICADAHelixMoleculePhysical and Theoretical ChemistryHelical structures
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Two new supramolecular architectures of singly phenoxo-bridged copper(II) and doubly phenoxo-bridged manganese(II) complexes derived from an unusual …

2009

International audience; Two new coordination complexes {[(L)Cu2('-L)(NO3)(CH3OH)0.3(H2O)0.7]·NO3}[Cu(L)(NO3)(CH3OH)] (1) and [Mn2(-L)2(H2O)(1-N3)2(CH3OH)] (2) derived from (E)-N-(2-hydroxy-3-methoxybenzylidene)acetohydrazide [LH] have been synthesized. The new potentially tetradentate ONOO donor hydrazone ligand [LH] has shown considerable metal ion selective phenoxo bridging in 1 and 2. It has coordinated copper(II) ions in its tridentate as well as in tetradentate fashion whereas for manganese(II) ions it solely showed its tetradentate character. In 1 the two adjacent pentacoordinate copper(II) centers are connected by a rare single phenoxo linkage of the hydrazone ligand whereas 2 is a d…

StereochemistrySupramolecular chemistrychemistry.chemical_elementManganese010402 general chemistry01 natural sciencesHydrogen bondslaw.inventionIonInorganic ChemistryMetalO ligandslawElectron paramagnetic resonanceBridging ligands010405 organic chemistryChemistryHydrogen bondStructure elucidation[CHIM.MATE]Chemical Sciences/Material chemistryCopper0104 chemical sciencesDensity functional calculationsCrystallographyvisual_artvisual_art.visual_art_mediumHydrazone ligandSupramolecular chemistry
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Synthesis and stereochemical properties of "extended" biphenols bridged by ortho-, meta-, and para-phenylene spacers

2009

A series of isomeric biphenols based on para- (1), meta- (2), and ortho- (3) terphenyl backbones was synthesized. Suzuki cross-coupling methodology was employed for the construction of the terphenyl backbone of their methyl-protected precursors (respectively 8, 13, and 16). Using K2CO3 as the base, the best reaction conditions involved DMF at 100 °C as solvent. Anhydrous conditions greatly improved the yields of the sterically crowded systems (particularly 16). ortho-Terphenyls 3 and 16 exist as mixtures of syn/anti atropisomers in solution. Compound 16 crystallizes in the anti-in form. DFT calculations at the B3LYP/6-311+G(d,p) level indicate that for both compounds the anti-in form is mor…

Steric effectsAtropisomer010405 organic chemistryChemistryStereochemistryOrganic ChemistryContext (language use)010402 general chemistry01 natural sciencesMedicinal chemistryChemical synthesisAtropisomerism0104 chemical sciences[SHS]Humanities and Social SciencesSolventchemistry.chemical_compoundDensity functional calculationsSuzuki reactionPhenyleneTerphenyl[ SHS ] Humanities and Social SciencesCross-couplingBiarylsPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS
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Analytical chemistry on many-center chiral compounds based on vibrational circular dichroism: Absolute configuration assignments and determination of…

2019

The absolute configuration of a chiral molecule is key to its biological activity. Being able to find out what this configuration is, is thus crucial for a wide range of applications. The difficulties associated with such a determination steeply rise as the number of chiral centers in a given compound becomes larger. Concurrently, it becomes increasingly more challenging to determine the levels and identity of potential stereochemical contaminants in a given sample with one and the same technique, leading in practice to extensive and laborious efforts employing multiple analytical techniques. Here, experimental and theoretical studies based on Vibrational Circular Dichroism (VCD) are presen…

Vibrational optical activity02 engineering and technologyCenter (group theory)01 natural sciencesBiochemistrySpectral lineAnalytical ChemistrySynthetic drugsSDG 3 - Good Health and Well-beingComputational chemistryStereochemistryEnvironmental ChemistryAbsolute configurationSpectroscopyFELIX Condensed Matter PhysicsChemistryDiastereomeric impurity levelsPharmaceutics010401 analytical chemistryAbsolute configurationDiastereomer021001 nanoscience & nanotechnology0104 chemical sciencesDensity functional calculationVibrational circular dichroism/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being0210 nano-technologyDensity functional calculation
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Recent Developments in the Chiral Brønsted Acid-catalyzed Allylboration Reaction with Polyfunctionalized Substrates

2016

Asymmetric allylboration has played a central role in organic synthesis ever since the pioneering work by Hoffman and Brown, having found applications in the total synthesis of many natural products. A new dawn for this 40 year-old reaction occurred with the beginning of the new century when the first catalytic asymmetric methods came into play. In less than one decade, several methodologies, able to achieve the desired homoallylic alcohols with ee ranges in the high 90s, were developed. Among them, in the present account, we will disclose our contribution to the development of the chiral binolphosphoric-derived BrOnsted acid-catalyzed allylboration of aldehydes originally reported by Antil…

chemistry.chemical_classification010405 organic chemistryChemistryGeneral Chemical Engineeringasymmetric allylborationTotal synthesisGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryAldehyde0104 chemical sciencesCatalysischiral BrOnsted acid catalysischemistry.chemical_compounddensity functional calculationsMaterials ChemistryOrganic chemistryOrganic synthesisdiversity-oriented synthesisBrønsted–Lowry acid–base theoryallylic compoundsThe Chemical Record
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C2-Symmetric Ferrocene-Bis(ureido)peptides : Synthesis, Conformation and Solid-State Structure

2009

The extension of peptide derivatives of ferrocene-1,1'-dicarboxylic acid by formal insertion of NH units between ferrocene and peptide strands results in ferrocene-bis(ureido)-peptides. Experimentally, alanine and dialanine methyl esters were attached to the 1- and 1'-position of 1,1'-diiso-cyanoferrocene to give the corresponding bis(ureido)peptide derivatives 3 and 4. The conformation of 3 has been determined in the solid state by X-ray crystallography. In solution the preferred conformation of 3 and 4 has been elucidated by NMR, IR and CD spectroscopy in concert with DFT calculations. The secondary structure of ferrocene―bis(ureido)peptides 3 and 4 is determined by double bifurcated intr…

chemistry.chemical_classificationAlanineCircular dichroismStereochemistryHydrogen bondPeptideInorganic Chemistrychemistry.chemical_compoundDicarboxylic acidFerrocenechemistryIntramolecular forceconformation analysis; density functional calculations; hydrogen bonds; metallocenes; peptidesProtein secondary structure
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A DFT study of the molecular mechanisms of the nucleophilic addition of ester-derived lithium enolates and silyl ketene acetals to nitrones: Effects …

2006

9 pages, 6 schemes, 3 figures, 2 tables.

chemistry.chemical_classificationNucleophilic additionSilylationReaction mechanismsOrganic ChemistryKeteneEnolatesMedicinal chemistryCycloadditionNitroneLewis acid catalysischemistry.chemical_compoundDensity functional calculationsAcetalsNucleophilechemistryOrganic chemistryLewis acids and basesPhysical and Theoretical ChemistryNucleophilic addition
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B-DNA Structure and Stability as Function of Nucleic Acid Composition. Dispersion-Corrected DFT Study of Dinucleoside-Monophosphate Single and Double…

2013

actions of the sugar-phosphate skeleton with water; (6) hydrophobic interactions of the DNA cylindrical core, made up by the hydrogen-bonded and stacked nitrogen bases, with the water solvent. Recently, there has been increasing effort in developing and applying quantum chemical methods able to reproduce the structure of native B-DNA and to correctly describe the energy involved in the intrastrand and interstrand noncovalent interactions between the nucleotide monomers. This topic has been approached by both wave function methods and density functional theory. [2] Water solvent and sodium counterions also play an important role in the formation and relative stabilization of the double-helic…

chemistry.chemical_classificationStereochemistryChemistryBase pairHydrogen bondStackingGeneral ChemistryCrystal structureFull Papersstacking interactionsNucleobaseHydrophobic effectCrystallographyDNA structuresSettore CHIM/03 - Chimica Generale E Inorganicadensity functional calculationshydrogen bondsNon-covalent interactionsDNA DFT calculations structure stabilityDensity functional theoryWatson–Crick base pairsTheoretical ChemistryGeneralLiterature_REFERENCE(e.g.dictionariesencyclopediasglossaries)
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Advanced descriptors for long-range noncovalent interactions between SARS-CoV-2 spikes and polymer surfaces.

2021

The recent pandemic triggered numerous societal efforts aimed to control and limit the spread of SARS-CoV-2. One of these aspects is related on how the virion interacts with inanimate surfaces, which might be the source of secondary infection. Although recent works address the adsorption of the spike protein on surfaces, there is no information concerning the long-range interactions between spike and surfaces, experimented by the virion when is dispersed in the droplet before its possible adsorption. Some descriptors, namely the interaction potentials per single protein and global potentials, were calculated in this work. These descriptors, evaluated for the closed and open states of the sp…

chemistry.chemical_classificationclosed and open structuresDensity Functional calculationsSecondary infectionIonic bondingFiltration and SeparationPolymerArticleAnalytical Chemistrychemistry.chemical_compoundAdsorptionPolylactic acidchemistryChemical physicsCovalent bondlong-range interaction potential energiesPolyethylene terephthalateNon-covalent interactionssurface affinity descriptorsSARS-CoV-2 spike proteinsMolecular Mechanics and Dynamics simulationsSeparation and purification technology
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