Search results for "Electronic effect"

showing 10 items of 45 documents

A Molecular Electron Density Theory Study of the Role of the Copper Metalation of Azomethine Ylides in [3 + 2] Cycloaddition Reactions.

2018

The copper metalation of azomethine ylides (AYs) in [3 + 2] cycloaddition (32CA) reactions with electron-deficient ethylenes has been studied within the Molecular Electron Density Theory (MEDT) at the MPWB1K/6-311G(d,p) level, in order to shed light on the electronic effect of the metalation in the course of the reaction. Analysis of the Conceptual Density Functional Theory reactivity indices indicates that the metalation of AYs markedly enhances the nucleophilicity of these species given the anionic character of the AY framework. These 32CA reactions take place through stepwise mechanisms characterized by the formation of a molecular complex. Both nonmetalated and metalated 32CA reactions …

010405 organic chemistryChemistryMetalationOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesMedicinal chemistryCycloaddition0104 chemical sciencesNucleophileElectronic effectSingle bondDensity functional theoryReactivity (chemistry)The Journal of organic chemistry
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Modular P-Chirogenic Phosphine-Sulfide Ligands: Clear Evidence for Both Electronic Effect and P-Chirality Driving Enantioselectivity in Palladium-Cat…

2015

Using the ephedrine methodology, modular stereoselective syntheses of a new class of P-chirogenic phosphines bearing a sulfur-chelating arm (P*,S-hybrid ligand) are described. A first series of syntheses based on a Fries-like rearrangement of P-chirogenic phosphinite-boranes, which are prepared from 2-bromobenzyl or 2-bromophenethyl alcohol and are mediated by metal–halide exchange, have been performed. This rearrangement affords phosphine-boranes stereospecifically with an o-hydroxyalkylphenyl substituent. The latter residue is subsequently converted into a sulfur-containing group. In a second series, the stereoselective syntheses were achieved according to a new strategy involving a react…

Allylic rearrangementPhosphinite010405 organic chemistryLigandStereochemistryOrganic ChemistrySubstituentAbsolute configurationchemistry.chemical_element010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryElectronic effectPhysical and Theoretical ChemistryPhosphinePalladiumOrganometallics
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Substituent effect on the redox potential of substituted (aryl)(2-nitrobenzo[ b ]thiophen-3-yl)amines

2001

Abstract The electronic effect of some meta- or para-substituents on the reduction of the title compounds has been investigated. The reversible reduction potential values of these compounds have been evaluated by cyclic voltammetry at a mercury electrode in 0.1 M tetraethylammoniumtetrafluoroborate, dimethylsulfoxide solutions. The substituent effect depends on both its nature and its position. The reduction potential values of the derivatives studied have been correlated with the Hammett substituent constants.

ChemistryArylOrganic ChemistrySubstituentDropping mercury electrodeBiochemistryRedoxMedicinal chemistrychemistry.chemical_compoundorganic electrochemistry substituents effect on thermodynamics redox processesDrug DiscoveryElectronic effectOrganic chemistryCyclic voltammetryTetrahedron
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Structural and electronic contributions to hyperpolarizability in methyl p-hydroxy benzoate

2006

Abstract The single crystals of methyl p-hydroxy benzoate (MPHB) are grown from methanol solution by a low temperature solution growth technique. The SHG efficiency is tested using Q-switched Nd:YAG laser of wavelength λ at 1064 nm, which is approximately 1.2 times that of urea. Vibrational spectral analysis using NIR-FT Raman and FT-IR spectra is carried out to understand the structural and electronic contributions to hyperpolarizability in MPHB. The DFT computations are also performed at B3LYP/6-311G(d,p) level to derive equilibrium geometry, vibrational wavenumbers and intensities. The results of ab initio calculations at HF/6-311G(d,p) level show that the vibrational contribution for th…

ChemistryHydrogen bondOrganic ChemistryIntermolecular forceAnalytical chemistryHyperpolarizabilityAcceptorAnalytical ChemistryInorganic Chemistrysymbols.namesakeAb initio quantum chemistry methodsIntramolecular forcesymbolsElectronic effectPhysical chemistryRaman spectroscopySpectroscopyJournal of Molecular Structure
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Density Functional Theory Study on Propane and Propene Adsorption on Pt(111) and PtSn Alloy Surfaces

2011

Density functional theory calculations were performed to investigate the adsorption of propane, propene, and C and H atoms on Pt and PtSn surfaces employing the revised Perdew–Burke–Ernzerhof (RPBE) and vdW-DF functionals. Propane adsorption was found to be mediated by van der Waals interactions without significant site preference on any of the studied surfaces. The adsorption characteristics of propene are different: On the Pt(111) and Pt3Sn(111) surfaces, propene adsorption is covalent, and the molecule prefers a di-σ site to a π site. Alloying Pt(111) with Sn leads to weaker adsorption owing to geometric and relaxation effects, whereas electronic effects are found to be small. On the PtS…

ChemistryInorganic chemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPropenesymbols.namesakechemistry.chemical_compoundGeneral EnergyAdsorptionPropaneElectronic effectsymbolsPhysical chemistryMoleculeDensity functional theoryDehydrogenationPhysical and Theoretical Chemistryvan der Waals forceta116The Journal of Physical Chemistry C
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Tuning Of Organic Heterojunction Conductivity By The Substituents' Electronic Effects In Phthalocyanines For Ambipolar Gas Sensors

2021

Abstract Exploiting organic heterojunction effects in electrical devices are an important strategy to improve the electrical conductivity, which can be utilized into improving the conductometric gas sensors performances. In this endeavor, the present article reports fabrication of organic heterostructures in a bilayer device configuration incorporating octa-substituted nickel phthalocyanines (NiPc) and radical lutetium bis-phthalocyanine (LuPc2) and investigates their sensing properties towards NH3 vapor. NiPc having hexyl sulfanyl, hexyl sulfonyl and p-carboxyphenoxy moieties are synthesized, which electronic effects are electron donating, accepting and moderate accepting, respectively, al…

Conductometric TransducerMaterials science02 engineering and technologyConductivity010402 general chemistryPhotochemistry01 natural scienceschemistry.chemical_compoundAmmoniaSulfanylMaterials ChemistryElectronic effect[CHIM]Chemical SciencesElectrical and Electronic EngineeringInstrumentationComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationAmbipolar diffusionBilayerMetals and AlloysPhthalocyanineHeterojunctionElectron acceptor021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMolecular materialschemistryHeterojunctionCyclic voltammetryGas sensor0210 nano-technology
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Study of the complex formation between the [Cu(bpca)]+ secondary building unit and the aromatic N donors 2,3,5,6-tetra(2-pyridyl)pyrazine (tppz) and …

2017

Two new complexes of the formula [{Cu(bpca)}2(μ-tppz)](NO3)2·5H2O (1) and [Cu(bpca)(H2O)(ClO4)(μ-bpp)Cu(bpca)(H2O)2]ClO4·H2O (2) [tppz = 2,3,5,6-tetra(2-pyridyl)pyrazine and bpp = 1,3-bis(4-pyridyl)propane] have been prepared by the reaction of the [Cu(bpca)]+ [Hbpca = bis(2-pyridylcarbonyl)imide] building block and the tppz and bpp N donors. An unusual coordination mode of the tppz ligand was observed in 1, which functions as a bis(bidentate) ligand to two copper(II) atoms each coordinated to a nitrogen atom of the pyrazine moiety and a pyridyl nitrogen atom. This compound presents a layered structure of alternating anionic (ca. 1.6 A) and cationic (ca. 10 A) slices, providing the opportun…

DenticityPyrazine010405 organic chemistryInorganic chemistrySupramolecular chemistryGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundPerchlorateCrystallographychemistryElectronic effectMoleculeMoietyGeneral Materials ScienceImideCrystEngComm
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A small spherical liquid: A DFT molecular dynamics study of WAu12

2009

The finite-temperature dynamics of WAu12, incorporating both electronic and structural effects, is studied using a density-functional-based Born-Oppenheimer molecular dynamics method. Molecular dynamics simulations for monomolecular WAu12 suggest a surface-melting-type behaviour of the angular degrees of freedom between 366 and 512 K. Thermally averaged electron density-of-states of WAu12 are compared to the experimental photoelectron spectra of WAu12(-).

Electron densityPhotoemission spectroscopyChemistryDynamics (mechanics)General Physics and AstronomyElectron010402 general chemistry7. Clean energy01 natural sciencesSpectral line0104 chemical sciencesMolecular dynamicsChemical physics0103 physical sciencesDensity of statesElectronic effectPhysical chemistryPhysical and Theoretical Chemistry010306 general physicsPhysical Chemistry Chemical Physics
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Oligothienoacenes versus oligothiophenes: Impact of ring fusion on the optical properties

2010

The impact of backbone rigidity on the optical properties of thiophene-based compounds is studied by analyzing in detail the geometrical, electronic, optical and vibronic features of a family of oligothienoacenes (nnTAs) in comparison to non-fused α-oligothiophenes (nnTs) by means of quantum-chemical calculations. Ring fusion in nnTAs provokes a greater conjugation in the ground state. However, the change in the bond length alternation upon electronic excitation is very similar in both systems, which is also reflected in a similar evolution of the first optical transition energy with increasing oligomer size. Larger transition energies in nnTAsvs.nnTs arise from an electronic effect rather …

FusionChemistryGeneral Physics and AstronomyMolecular physicsCrystallographychemistry.chemical_compoundRigidity (electromagnetism)Normal modeElectronic effectThiophenePhysical and Theoretical ChemistryGround stateMirror symmetryExcitation
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The electronic substituent influence on the thermally allowed electrocyclic interconversion cyclobutene/butadiene. A MNDO study

1984

The effects of donor/acceptor substitution on the conrotatory cyclobutene/butadiene interconversion have not yet been experimentally studied. MNDO Synchronous Transit/MINIMAX calculations for all possible combinations of NH2/NH3 + 3 groups at the fissile single bond reveal very large substituent effects on the opening reactions and reverse cyclisations. Diamino(1b/2b), diammonio-(1c/2c) and amino-ammonio-substitutions (1d/2d) change the activation energy of the reference ring opening reaction (1a →2a) from 49.9 kcal/mol to 34.7, 29.8 and 26.0 kcal/mol, respectively. This rate enhancement parallels the monotone shift of the transition state pathcoordinate towards the cyclobutenes. Relative t…

Hammond's postulateElectrocyclic reactionCyclobuteneSubstituentMNDOPhotochemistrychemistry.chemical_compoundchemistryComputational chemistryElectronic effectSingle bondChiropracticsPhysical and Theoretical ChemistryConrotatory and disrotatoryTheoretica Chimica Acta
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