Search results for "Molecule"

showing 10 items of 5162 documents

Hexakis(diethylacetamide)iron(II) hexahalorhenate(IV) ionic salts: X-ray structures and magnetic properties

2015

Two novel Fe<sup>II</sup>-Re<sup>IV</sup> compounds of general formula [Fe<sup>II</sup>(DEA)<inf>6</inf>][Re<sup>IV</sup>X<inf>6</inf>] where DEA = diethylacetamide and X = Cl (1) and Br (2) have been prepared and magnetostructurally characterised. Complexes 1 and 2 are isomorphic ionic salts that crystallise in the trigonal crystal system with space group R(-3). The rhenium(IV) ion in 1 and 2 is six-coordinate with six chloro (1) or bromo (2) ligands building a regular octahedral chromophore. The Fe<sup>II</sup> ion is also six-coordinate, and bonded to six oxygen atoms from six DEA molecules. [Fe<sup&gt…

/dk/atira/pure/subjectarea/asjc/1600/1606/dk/atira/pure/subjectarea/asjc/1600/1604Rhenium(IV) complexes/dk/atira/pure/subjectarea/asjc/2500/2505ChemistryInorganic chemistrySupramolecular chemistryIonic bondingchemistry.chemical_elementDiethylacetamideCrystal structureRheniumIron(II) complexesMagnetic susceptibilityX-ray diffractionInorganic ChemistryCrystallographyOctahedronMagnetic propertiesX-ray crystallographyMaterials ChemistryMoleculePhysical and Theoretical ChemistryPolyhedron
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Thermal- and photo-induced spin crossover in the 1D coordination polymer [Fe(4-tBupy)3][Au(CN)2]2 (4-tBupy = 4-tert-butylpyridine)

2021

Reaction of the unidentate pyridine ligand containing a bulky t-butyl substituent with Fe2+ and [Au(CN)2]− affords a new type of spin crossover (SCO) coordination polymer in the 1D compound [Fe(4-tBupy)3][Au(CN)2]2⋅0.5H2O (1), which is formed by chains of Fe(II) complexes linked through bridging [Au(CN)2]− with three terminal 4-tBupy and one monodentate [Au(CN)2]− ligands completing the octahedral coordination around Fe(II). Longer reaction times led to the minor products [Fe(4-tBupy)2][Au(CN)2]2 (2), which presents a 2D structure more similar to that found in the other SCO compounds based on [Au(CN)2]−, and the 1D compound [Fe(4-tBupy)2(MeOH)][Au(CN)2]2 (3), in which one of the three termi…

010302 applied physicsDenticityCoordination polymerSpin transitionSubstituentGeneral Physics and Astronomy02 engineering and technology021001 nanoscience & nanotechnology01 natural sciences3. Good healthchemistry.chemical_compoundCrystallographyOctahedronchemistrySpin crossoverExcited state0103 physical sciencesMoleculeFísica de l'estat sòlidCompostos de coordinació0210 nano-technologyMaterials
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Exploring the transport properties of equatorially low coordinated erbium single ion magnets

2019

Single-molecule spin transport represents the lower limit of miniaturization of spintronic devices. These experiments, although extremely challenging, are key to understand the magneto-electronic properties of a molecule in a junction. In this context, theoretical screening of new magnetic molecules provides invaluable knowledge before carrying out sophisticated experiments. Herein, we investigate the transport properties of three equatorially low-coordinated erbium single ion magnets with C3v symmetry: Er[N(SiMe3⁠)2⁠]3⁠ (1), Er(btmsm)3⁠ (2) and Er(dbpc)3⁠ (3), where btmsm=bis(trimethylsilyl)methyl and dbpc=2,6-di-tert-butyl-p-cresolate. Our ligand field analysis, based on previous spectros…

010302 applied physicsLigand field theoryMaterials scienceCondensed Matter - Mesoscale and Nanoscale PhysicsSpintronicschemistry.chemical_elementFOS: Physical sciences02 engineering and technology021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesElectronic Optical and Magnetic MaterialsMagnetic fieldErbiumchemistryChemical physicsMagnet0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)MiniaturizationMolecule0210 nano-technologyGround state
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Theoretical insights on the importance of anchoring vs molecular geometry in magnetic molecules acting as junctions

2019

The anchoring of the molecule to an electrode is known to be a key factor in single-molecule spintronics experiments. Likewise, a relaxation down to the most stable geometry is a critical step in theoretical simulations of transport through single-molecule junctions. Herein we present a set of calculations designed to analyze and compare the effect of different anchoring points and the effect of perturbations in the molecular geometry and interelectrode distance. As model system we chose the [V($\alpha$-C$_3$S$_5$)$_3$]$^{2-}$ complex connecting two Au(111) electrodes in a slightly compressed geometry. In our calculations, the attachment happens through an S-Au bond, a common anchoring stra…

010302 applied physicsMaterials scienceCondensed Matter - Mesoscale and Nanoscale PhysicsSpintronicsRelaxation (NMR)AnchoringConductanceFOS: Physical sciences02 engineering and technology021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesElectronic Optical and Magnetic MaterialsMolecular geometryChemical physicsPosition (vector)0103 physical sciencesElectrodeMesoscale and Nanoscale Physics (cond-mat.mes-hall)Molecule0210 nano-technology
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Luminescence properties of chlorine molecules in glassy SiO 2 and optical fibre waveguides

2017

The support from Latvian Research Program IMIS 2, project “Photonics and materials for photonics” is acknowledged. K.K. was partially supported by the Collaborative Research Project of Materials and Structures Laboratory, Tokyo Institute of Technology. The publication costs of this article were covered by the Estonian Academy of Sciences and the University of Tartu.

010302 applied physicsMaterials scienceOptical fiberbusiness.industryGeneral Engineeringphotonicschemistry.chemical_elementoptical fibresamorphous SiO202 engineering and technology021001 nanoscience & nanotechnology01 natural scienceslaw.inventionCl2 impuritieschemistrylaw0103 physical sciencesChlorineluminescence:NATURAL SCIENCES:Physics [Research Subject Categories]MoleculeOptoelectronics0210 nano-technologyLuminescencebusinessProceedings of the Estonian Academy of Sciences
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Effects of water removal on the structure and spin-crossover in an anilato-based compound

2021

The crucial role played by a crystallization water molecule in the spin crossover (SCO) temperature and its hysteresis is described and discussed in compound [NBu4][Fe(bpp)2][Cr(C6O4Br2)3]⋅2.5H2O (1), where bpp = 2,6-bis(pyrazol-3-yl)pyridine and (C6O4Br2)2− = dianion of the 3,6-dibromo-2,5-dihydroxy-1,4-benzoquinone. The compound has isolated [Fe(bpp)2]2+ cations surrounded by chiral [Cr(C6O4Br2)3]3− anions, NBu4+ cations, and a water molecule H-bonded to one of the non-coordinated N–H groups of one bpp ligand. This complex shows a gradual almost complete two-step spin transition centered at ca. 180 and 100 K with no hysteresis. The loss of the water molecules results in a phase transition…

010302 applied physicsPhase transitionMaterials scienceSpin transitionGeneral Physics and Astronomy02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesLIESSTCrystallographychemistry.chemical_compoundchemistrySpin crossoverExcited statePhase (matter)0103 physical sciencesPyridineMolecule0210 nano-technologyJournal of Applied Physics
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High-frequency EPR study on Cu4Cu- and Co4Co-metallacrown complexes

2019

Abstract High-frequency/high-field electron paramagnetic resonance studies on two homonuclear 12-MC-4 metallacrown complexes Cu4Cu and Co4Co are presented. For Cu4Cu, our data imply axial-type g-anisotropy with g x = 2.03 ± 0.01 , g y = 2.04 ± 0.01 , and g z = 2.23 ± 0.01 , yielding g = 2.10 ± 0.02 . No significant zero field splitting (ZFS) of the ground state mode is observed. In Co4Co, we find a m S = ± 3 / 2 ground state with g = 2.66 . The data suggest large anisotropy D of negative sign.

010302 applied physicsPhysicsCondensed Matter - Materials ScienceCondensed Matter - Mesoscale and Nanoscale PhysicsMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciences02 engineering and technologyZero field splitting021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesHomonuclear moleculeElectronic Optical and Magnetic Materialslaw.inventionlawMesoscale and Nanoscale Physics (cond-mat.mes-hall)0103 physical sciencesAtomic physics0210 nano-technologyGround stateElectron paramagnetic resonanceAnisotropyMetallacrownJournal of Magnetism and Magnetic Materials
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On the ‘expanded local mode’ approach applied to the methane molecule: isotopic substitution CH2D2←CH4

2011

On the basis of a compilation of the ‘expanded local mode’ model and the general isotopic substitution theory, sets of simple analytical relations between different spectroscopic parameters (harmonic frequencies, ωλ, anharmonic coefficients, x λμ, ro-vibrational coefficients, , different kinds of Fermi- and Coriolis-type interaction parameters) of the CH2D2 molecule are derived. All of them are expressed as simple functions of a few initial spectroscopic parameters of the mother, CH4, molecule. Test calculations with the derived isotopic relations show that, in spite of a total absence of initial information about the CH2D2 species, the numerical results of the calculations have a very good…

010304 chemical physicsBasis (linear algebra)ChemistrySubstitution (logic)AnharmonicityBiophysicsThermodynamics010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesComputational chemistryAb initio quantum chemistry methodsSimple (abstract algebra)Simple function0103 physical sciencesMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryMolecular BiologyFermi Gamma-ray Space TelescopeMolecular Physics
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Structural, electronic and energetic effects in heterocyclic fluorene derivatives fused with a fulvene unit

2019

Abstract A set of 36 heterocyclic (B, N and O) fluorene (C) derivatives fused in nine ways with fulvene ring have been analyzed by means of different local aromaticity criteria. Molecular geometry of analyzed compounds were optimized at B3LYP/6-311++G(2d,2p) level of theory. The evaluation of the local aromaticity has been carried out through the use of the geometry-based harmonic oscillator model of aromaticity (HOMA) and the magnetism-based zz‐component of the nucleus independent chemical shifts calculated 1 A above the ring center (NICS1zz) indices as well as one aromaticity index derived from the Quantum Theory Atoms in Molecules (QTAIM), i.e. the para-delocalization index (PDI). Additi…

010304 chemical physicsChemical shiftAtoms in moleculesHeterocyclic fluorene derivativesHOMO-LUMO energy gapsAromaticityFluoreneFulvene010402 general chemistryCondensed Matter PhysicsKinetic energyRing (chemistry)01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundCrystallographyMolecular geometrychemistry0103 physical sciencesPhysical and Theoretical ChemistryFulveneAromaticity indexesComputational and Theoretical Chemistry
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Hydrogen bonding interaction of N5H with water: A first principle calculations

2019

Abstract The cyclopentazol (N5H) and its anion counterpart (N5–) have been studied extensively over the years and detected in the gas phase as well as in solution recently. In the present investigation, an attempt has been made to understand the interaction with water molecule using first principle calculations. Nature of interactions have been studied using both energy decomposition analysis and atoms in molecule (AIM) theory calculations. Further, the strength of non-covalent interactions were analysed using IGMplots.

010304 chemical physicsChemistryHydrogen bond010402 general chemistryCondensed Matter PhysicsDecomposition analysis01 natural sciencesBiochemistry0104 chemical sciencesGas phaseIonChemical physics0103 physical sciencesFirst principleMolecule[CHIM]Chemical SciencesPhysical and Theoretical Chemistry
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