Search results for "etica"

showing 10 items of 14083 documents

Isophorone on Au/MgO/Ag(001) : Physisorption with Electrostatic Site Selection

2017

We report a computational study of isophorone C9H14O adsorption on a Ag(001)-supported ultrathin MgO film with Au adatoms and clusters employing density functional theory calculations. The calculations show that the keto form of isophorone is more stable than the enol tautomers both in gas phase and on the MgO/Ag(001) surface. The interaction between the keto isophorone and step and terrace sites of MgO/Ag(001) displays long interaction distances, relatively weakly exothermic adsorption energies, lack of charge transfer, and minor changes in the density of states, all of which indicate that the molecule merely physisorbs on the surface. The step sites are energetically preferred adsorption …

ta114Chemistry02 engineering and technology021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesTautomerEnolSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographyGeneral EnergyAdsorptionPhysisorptionisophorone adsorption0103 physical sciencesDensity of statesMoleculeDensity functional theoryPhysical and Theoretical Chemistry010306 general physics0210 nano-technologyta116IsophoroneJournal of Physical Chemistry C
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Theoretical Analysis of the M12Ag32(SR)404– and X@M12Ag32(SR)304– Nanoclusters (M = Au, Ag; X = H, Mn)

2014

We analyze the electronic structure and optical properties of the recently reported, structurally known M12Ag32(SR)304– clusters (M = Au, Ag) by using density functional theory and time-dependent density functional perturbation theory. Effects of the chemical changes in the metal core, charge of the cluster, and nature of the thiolate ligand on the electronic structure and optical absorption are reported. In addition, doping the metal core with a magnetic transition metal atom (Mn) or hydrogen (protons) is discussed. Although all these clusters can be considered as 18-electron superatoms with a shell configuration 1S2 1P6 1D10, we find that the optical spectrum is sensitive to the charge st…

ta114ChemistryDopingnanoclustersElectronic structurechemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNanoclustersMetalCrystallographyGeneral EnergyTransition metalvisual_artAtomCluster (physics)visual_art.visual_art_mediumDensity functional theoryPhysical and Theoretical ChemistryAtomic physicsta116physicsJournal of Physical Chemistry C
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Ultrafast electronic relaxation and vibrational cooling dynamics of Au 144(SC2H4Ph)60 nanocluster probed by transient mid-IR spectroscopy

2014

Energy relaxation dynamics of a gold nanocluster with atomically precise composition, Au144(SC2H4Ph)60, is studied by transient mid-IR spectroscopy. The experiment is designed to simultaneously pro...

ta114ChemistryDynamics (mechanics)Analytical chemistryMolecular physicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyVibrational energy relaxationRelaxation (physics)Transient (oscillation)Physical and Theoretical ChemistrySpectroscopyUltrashort pulseta116The Journal of Physical Chemistry C
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TDDFT Analysis of Optical Properties of Thiol Monolayer-Protected Gold and Intermetallic Silver–Gold Au144(SR)60 and Au84Ag60(SR)60 Clusters

2014

The optical absorption spectra of atomistic model structures for experimentally isolated all-gold Au144(SR)60 and intermetallic Au84Ag60(SR)60 clusters are systematically analyzed from linear-response time-dependent density functional theory (LR-TDDFT) and time-dependent density functional perturbation theory (TD-DFPT) calculations. The computed spectra, utilizing the atomistic model for Au144(SR)60 published by us in 2009, reproduce closely the experimental observations for corresponding isolated compounds, reported previously by Kumara and Dass in 2011. A collective dipole oscillation within the metal cores of the all-gold and intermetallic clusters is formed as response to light in the v…

ta114ChemistryIntermetallicTime-dependent density functional theoryMolecular physicsSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMetalDipoleGeneral Energyvisual_artMonolayervisual_art.visual_art_mediumDensity functional theoryPhysical and Theoretical ChemistrySurface plasmon resonanceAtomic physicsta116The Journal of Physical Chemistry C
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Vibrational Perturbations and Ligand–Layer Coupling in a Single Crystal of Au144(SC2H4Ph)60 Nanocluster

2015

We have determined vibrational signatures and optical gap of the Au144(PET)60 (PET: phenylethylthiol, SC2H4Ph) nanocluster solvated in deuterated dichloromethane (DCM-D2, CD2Cl2) and in a single crystal. For crystals, solid-state (13)C NMR and X-ray diffraction were also measured. A revised value of 2200 cm(-1) (0.27 eV) was obtained for the optical gap in both phases. The vibrational spectra of solvated AU144(PET)60 closely resembles that of neat PET, while the crystalline-state spectrum exhibits significant inhomogeneous spectral broadening, frequency shifts, intensity transfer between vibrational modes, and an increase in the overtone and combination transition intensities. Spectral broa…

ta114ChemistryOvertoneta221Analytical chemistryOvertone bandMolecular physicsHot bandCrystalMolecular vibrationGeneral Materials SciencePhysical and Theoretical ChemistryRotational–vibrational couplingSingle crystalta116Doppler broadeningThe Journal of Physical Chemistry Letters
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Role of Vibrational Dynamics in Electronic Relaxation of Cr(acac)3

2015

Ultrafast energy relaxation of Cr(acac)3 dissolved in tetrachloroethylene (TCE) is studied by time-resolved infrared (TRIR) spectroscopy by using electronic and vibrational excitation. After electronic excitation at 400 or 345 nm, the ground state recovers in two time scales: 15 ps (major pathway) and 800 ps (minor pathway), corresponding to fast electronic transition to the ground state and intermediate trapping on the long-lived (2)E state followed by intersystem crossing (ISC) to the ground state. The quantum yield for the fast recovery of the ground state depends on the excitation wavelength, being higher for 345 nm. Vibrational cooling (VC) occurs on the electronic excited states with …

ta114ChemistryRelaxation (NMR)kinetic modelsQuantum yieldMolecular physicsMolecular electronic transitiontransition metal complexesvibrationsIntersystem crossingComputational chemistryExcited statePhysical and Theoretical ChemistryGround stateSpectroscopyta116ExcitationThe Journal of Physical Chemistry A
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Optical Properties of Monolayer-Protected Aluminum Clusters: Time-Dependent Density Functional Theory Study

2015

We examine the electronic and optical properties of experimentally known monolayer-protected aluminum clusters Al4(C5H5)4, Al50(C5Me5)12, and Al69(N(SiMe3)2)183– using time-dependent density functional theory. By comparing Al4(C5H5)4 and the theoretical Al4(N(SiMe3)2)4 cluster, we observe significant changes in the optical absorption spectra caused by different hybridization between metal core and ligands. Using these initial observations, we explain the calculated spectra of Al50(C5Me5)12 and Al69(N(SiMe3)2)183–. Al50(C5Me5)12 shows a structured spectrum with clear regions of low-intensity core-to-core transitions followed by high-intensity ligand-to-core transitions due to its high symmet…

ta114Chemistrychemistry.chemical_elementTime-dependent density functional theorySpectral lineSymmetry (physics)3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsaluminum clustersMetalCrystallographytime-dependent density functional theoryGeneral EnergyAluminiumvisual_artMonolayervisual_art.visual_art_mediumCluster (physics)Density functional theoryPhysical and Theoretical Chemistryta116Journal of Physical Chemistry C
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A Unified AMBER-Compatible Molecular Mechanics Force Field for Thiolate-Protected Gold Nanoclusters.

2016

We present transferable AMBER-compatible force field parameters for thiolate-protected gold nanoclusters. Five different sized clusters containing both organo-soluble and water-soluble thiolate ligands served as test systems in MD simulations, and parameters were validated against DFT and experimental results. The cluster geometries remain intact during the MD simulations in various solvents, and structural fluctuations and energetics showed agreement with DFT calculations. Experimental diffusion coefficients and crystal structures were also reproduced with sufficient accuracy. The presented parameter set contains the minimum number of cluster-specific parameters enabling the use of these p…

ta114Chemistrythiolate ligands02 engineering and technologyCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular mechanicsForce field (chemistry)0104 chemical sciencesComputer Science ApplicationsNanoclustersComputational chemistryChemical physicsCluster (physics)Physical and Theoretical Chemistry0210 nano-technologyta116gold nanoclustersJournal of chemical theory and computation
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Electronic Structure and Optical Properties of the Intrinsically Chiral 16-Electron Superatom Complex [Au20(PP3)4]4+

2014

The recently solved crystal structure of the [Au20(PP3)4]Cl4 cluster (PP3: tris(2-(diphenylphophino)ethyl)phosphine) is examined using density functional theory (DFT). The Au20 core of the cluster is intrinsically chiral by the arrangement of the Au atoms. This is in contrast to the chirality of thiolate-protected gold clusters, in which the protecting Au-thiolate units are arranged in chiral patterns on achiral cores. We interpret the electronic structure of the [Au20(PP3)4]Cl4 cluster in terms of the superatom complex model. The 16-electron cluster cannot be interpreted as a dimer of 8-electron clusters (which are magic). Instead, a superatomic electron configuration of 1S(2) 1P(6) 1D(6) …

ta114Condensed matter physicsAbsorption spectroscopyChemistrySuperatomCrystal structureElectronic structureCrystallographyCluster (physics)Density functional theoryElectron configurationPhysical and Theoretical ChemistryChirality (chemistry)ta116The Journal of Physical Chemistry A
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Force Distribution Analysis of Mechanochemically Reactive Dimethylcyclobutene

2013

Internal molecular forces can guide chemical reactions, yet are not straightforwardly accessible within a quantum mechanical description of the reacting molecules. Here, we present a force-matching force distribution analysis (FM-FDA) to analyze internal forces in molecules. We simulated the ring opening of trans-3,4-dimethylcyclobutene (tDCB) with on-the-fly semiempirical molecular dynamics. The self-consistent density functional tight binding (SCC-DFTB) method accurately described the force-dependent ring-opening kinetics of tDCB, showing quantitative agreement with both experimental and computational data at higher levels. Mechanical force was applied in two different ways, namely, exter…

ta114CyclobuteneChemistryMolecular ConformationMolecular Dynamics SimulationRing (chemistry)Atomic and Molecular Physics and Optics:Science::Biological sciences::Biophysics [DRNTU]chemistry.chemical_compoundMolecular dynamicsAccelerationTight bindingIsomerismComputational chemistryChemical physicsMechanochemistryQuantum TheoryMoleculeReactivity (chemistry)Physical and Theoretical Chemistryta116CyclobutanesChemPhysChem
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