Search results for "Orbit"

showing 10 items of 1104 documents

Theoretical Design of Organic Metals Based on the Phthalocyanine Macrocycle

1990

Phthalocyanine molecular crystals and cofacially linked polymers are well documented as low-dimensional materials that may attain high electrical conductivities. Air-stable conductivities on the order of 1 to 1000 S/cm after partial oxidation by iodine have been reported.1–3 These conductivity studies indicate that the electrical conductivity has very little dependence on the identity of the atom complexed in the cavity, but is strongly dependent on the orientation and spacing of the phthalocyanine rings. A columnar stacking with minimum spacing leads to a maximum interaction between π-molecular orbitals on adjacent rings and promotes the highest conductivity. More effective π-interactions …

chemistry.chemical_classificationMaterials scienceStackingPolymerConductivityConjugated systemPhotochemistrychemistry.chemical_compoundCrystallographychemistryAtomic orbitalElectrical resistivity and conductivityPhthalocyanineMolecule
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Superexchange pathways in oxovanadium(IV) phosphates

1992

Abstract Oxovanadium(IV) phosphates show a diversity of magnetic behaviours that cannot be deduced from their respective structural features only. In part, this is due to the involvement of phosphate bridges in the spin transfer between V(IV) centres, and 31P solid state nuclear magnetic resonance becomes a key tool in determining the exchange mechanisms. The magnetic properties of a wide set of vanadium(IV) containing derivatives can be explained by realizing that a good overlap of the magnetic orbits may be achieved through paths involving phosphorus d orbitals.

chemistry.chemical_classificationMechanical EngineeringMetals and AlloysVanadiumchemistry.chemical_elementOxovanadium IVPhosphatePhysics::Geophysicschemistry.chemical_compoundCrystallographySolid-state nuclear magnetic resonancechemistryAtomic orbitalMechanics of MaterialsSuperexchangeMaterials ChemistrySpin transferInorganic compoundNuclear chemistryJournal of Alloys and Compounds
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On the aromaticity of uracil and its 5-halogeno derivatives as revealed by theoretically derived geometric and magnetic indexes

2020

AbstractThe problem of aromaticity in heterocyclic rings of uracil and its 5-halogenoderivatives (5XU) was analyzed theoretically by calculating modified harmonic oscillator model of aromaticity (HOMA) for Heterocycle Electron Delocalization (HOMHED), nucleus-independent chemical shift parameters (NICS) and the so-called scan experiments, using helium-3 atom as a magnetic probe. The impact of halogen electronegativity on C5 atom’s NBO charges was also investigated. Water, as a polar environment, has a negligible impact on 5XU aromaticity. The most stable diketo tautomer shows a very low aromaticity while the “rare” dihydroxy form (tautomer No 6) is aromatic and resembles benzene. This is in…

chemistry.chemical_classificationNICSDouble bond010405 organic chemistryAromaticityChemical shiftAromaticity010402 general chemistryCondensed Matter PhysicsRing (chemistry)01 natural sciencesTautomer0104 chemical sciences5-halogenouracilElectronegativityCrystallographychemistryAtom3 He NMRHOMAPhysical and Theoretical ChemistryHOMHEDUracilNatural bond orbitalStructural Chemistry
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Polydispersity Effects on Interpenetration in Compressed Brushes

2019

We study the effect of polydispersity on the compression and interpenetration properties of two opposing polymer brushes by numerical self-consistent field approach and by analytical theory. Polydispersity is represented by an experimentally relevant Schulz–Zimm chain-length distribution. We focus on three different polydispersities representing sharp, moderate, and extremely wide chain length distributions and derive approximate analytical expressions for the pressure–separation curves, Π(D). We study the brush interpenetration and quantify it in terms of the overlap integral, Γ, representing the number of interbrush contacts, and interpenetration length, δ. For the case of moderate densit…

chemistry.chemical_classificationPhysicsEquation of statePolymers and PlasticsField (physics)Organic ChemistryDispersity02 engineering and technologyPolymerOrbital overlap010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular physicsVirial theorem0104 chemical sciencesInorganic ChemistryDistribution (mathematics)chemistryMaterials Chemistry0210 nano-technologyScalingMacromolecules
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An ELF analysis of the C–C bond formation step in the N-heterocyclic carbene-catalyzed hydroacylation of unactivated C–C double bonds

2012

The changes in electron-density along the C–C bond-formation step in the N-heterocyclic carbene-catalyzed hydroacylation of unactivated double bonds has been studied by an electron localization function (ELF) analysis at the B3LYP/6-31G** level in order to characterize the reaction mechanism. Analysis of DFT reactivity indices and the natural bond orbital and ELF analysis at the most relevant points of the intrinsic reaction coordinate indicate that the reaction path takes place through a two-stage one-step mechanism with non-polar character. In the first stage a hydrogen atom is transferred from the hydroxyl group of Breslow intermediate 12 to the terminal olefinic carbon atom, to yield a …

chemistry.chemical_classificationReaction mechanismDouble bondStereochemistryGeneral Chemical EngineeringStetter reactionHydroacylationGeneral Chemistrychemistry.chemical_compoundchemistryIntramolecular forceReactivity (chemistry)CarbeneNatural bond orbitalRSC Advances
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The effect of osmo-induced stress on product formation by Zymomonas mobilis on sucrose

2000

The intensification of biosynthesis of fructooligosaccharides in the presence of high salt concentrations was observed during sucrose (10%) fermentation by Zymomonas mobilis 113S. A 0.6 M NaCl concentration led to an increase of oligosaccharide productivity by 3.5-fold. Sorbitol formation was increased in the presence of 0.16 M NaCl and was inhibited at highest salt concentrations. In a medium with high (65%, w/w) sucrose content the salts gave inhibitory effects on fructooligosaccharide production by lyophilised Z. mobilis cells. Influence of salts on gluconic acid and sorbitol formation under these conditions was studied. The ratio of oligosaccharides and gluconic acid productivity (Qolig…

chemistry.chemical_classificationSucroseZymomonasSucrosebiologyOsmotic shockFructooligosaccharideOligosaccharidesGeneral MedicineSodium ChlorideOligosaccharidebiology.organism_classificationMicrobiologyZymomonas mobilischemistry.chemical_compoundchemistryBiochemistryOsmotic PressureGluconic acidSorbitolFermentationSorbitolFood scienceFood ScienceInternational Journal of Food Microbiology
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Soluble Complexes of Cobalt Oxide Fragments Bring the Unique CO2 Photoreduction Activity of a Bulk Material into the Flexible Domain of Molecular Sci…

2021

The deposition of metal oxides is essential to the fabrication of numerous multicomponent solid-state devices and catalysts. However, the reproducible formation of homogeneous metal oxide films or of nanoparticle dispersions at solid interfaces remains an ongoing challenge. Here we report that molecular hexaniobate cluster anion complexes of structurally and electronically distinct fragments of cubic-spinel and monoclinic Co3O4 can serve as tractable yet well-defined functional analogues of bulk cobalt oxide. Notably, the energies of the highest-occupied and lowest-unoccupied molecular orbitals (HOMO and LUMO) of the molecular complexes, 1, closely match the valence- and conduction-band (VB…

chemistry.chemical_classificationValence (chemistry)OxideNanoparticle02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyTin oxidePhotochemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCoordination complexchemistry.chemical_compoundColloid and Surface ChemistrychemistryMolecular orbital0210 nano-technologyCobalt oxideHOMO/LUMOJournal of the American Chemical Society
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Oxotris(oxalato)niobate(V) as counterion in cobalt(II) spin-crossover systems

2016

Abstract This work is devoted to the investigation of the thermally induced spin-crossover behavior from a high-spin state (HS, S = 3/2) at higher temperatures to a low-spin phase (LS, S = 1/2) at lower temperatures of the six-coordinate cobalt(II) complex in the compound [Co(terpy)2]3[NbO(C2O4)3]2·3CH​3OH·4H2O (2). The crystal structure of 2 together with that of its counterion as tetraphenylarsonium(V) salt (AsPh4)3[NbO(C2O4)3]·9H2O (1) are also included. The spin-crossover process was followed by the thermal variation of the χMT product between 2.0 and 400 K under the warming mode, with the LS configuration being achieved at T ⩽ 200 K and the LS → HS interconversion being incomplete at 4…

chemistry.chemical_classificationZeeman effect010405 organic chemistryChemistryInorganic chemistrychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciences0104 chemical scienceslaw.inventionInorganic Chemistrysymbols.namesakelawSpin crossoverMaterials ChemistrysymbolsPhysical chemistryElectron configurationPhysical and Theoretical ChemistryCounterionElectron paramagnetic resonanceCobaltNatural bond orbitalPolyhedron
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Synthesis and Characterization of Extended Bis(terpyridine)ruthenium Amino Acids

2009

(Oligopyridine)ruthenium(II) complexes have been widely used in dye sensitized solar cells and other sophisticated optical devices due to their outstanding photophysical properties and their chemical stability. Herein, we describe the longitudinal extension of our previously reported bis(terpyridine)ruthenium(II) amino acid [Ru(tpy–NH2)(tpy–COOH)]2+ (tpy = 4′-substituted 2,2′:6′,2″-terpyridine) by insertion of para-phenylene spacers –C6H4– between the terpyridine and the functional groups. The influence of the para-phenylene spacer on the absorption and emission properties is investigated using UV/Vis absorption and emission spectroscopy and is discussed within a qualitative molecular orbit…

chemistry.chemical_classificationchemistry.chemical_elementPhotochemistryRutheniumAmino acidInorganic ChemistryDye-sensitized solar cellchemistry.chemical_compoundchemistryPolymer chemistryMolecular orbitalChemical stabilityEmission spectrumAbsorption (chemistry)TerpyridineZeitschrift für anorganische und allgemeine Chemie
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Synthesis, molecular structure, spectroscopic properties and stability of (Z)-N-methyl-C-2,4,6-trimethylphenylnitrone.

2015

Abstract New N-methyl-C-2,4,6-trimethylphenylnitrone 1 has been synthesized starting from N-methylhydroxylamine and mesitaldehyde. The product was fully characterized using different spectroscopic techniques; FTIR, NMR, UV–Vis, high resolution mass spectrometry and X-ray diffraction. The relative stability and percent of population of its two possible isomers (E and Z) were calculated using the B3LYP/6-311++G(d,p) method in gas phase and in solution. In agreement with the X-ray results, it was found that Z-isomer is the most stable one in both gas phase and solution. The molecular geometry, vibrational frequencies, gauge-including atomic orbital (GIAO), and chemical shift values were also c…

chemistry.chemical_classificationeducation.field_of_studyspectroscopynitronesPopulationAnalytical chemistryAtomic and Molecular Physics and OpticsAnalytical ChemistryNitroneMolecular geometryAtomic orbitalchemistryPolarizabilityMoleculeHypsochromic shifteducationInstrumentationta116Natural bond orbitalSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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