Search results for "DFT CALCULATION"

showing 10 items of 81 documents

Structure and vibrational features of the protic ionic liquid 1,8-diazabicyclo[5.4.0]-undec-7-ene-8-ium bis(trifluoromethanesulfonyl)amide, [DBUH][TF…

2022

Abstract The Protic Ionic Liquid (PIL) formed by neutralization of the super-strong base 1,7-diazabicyclo[5.4.0]undec-7-ene (DBU) with the super-strong acid bis(trifluoromethanesulfonyl)-imide (TFSI), indicated as [DBUH][TFSI], has been investigated. Its chemical physical properties and structural features have been explored using a synergy of experimental and computational tools. Molecular Dynamics-rationalised X-ray diffraction patterns highlight the major role played by hydrogen bonding (HB) in affecting morphology in this PIL. A comparison between HB features in this and in related PILs has been presented, on the base of far-IR experiments and DFT analysis. Indications of a weaker HB in…

Hydrogen bondingMaterials scienceProtic Ionic LiquidBase (chemistry)DFT calculationMolecular Dynamics010402 general chemistry01 natural scienceschemistry.chemical_compoundDFT calculation; Far-ir spectroscopy; Hydrogen bonding; Molecular Dynamics; Protic Ionic Liquid; X-ray scatteringPhase (matter)Materials ChemistryFar-ir spectroscopyPhysical and Theoretical ChemistryConformational isomerismSpectroscopychemistry.chemical_classification010405 organic chemistryHydrogen bondX-ray scatteringCondensed Matter PhysicsAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallography18-Diazabicyclo[5.4.0]undec-7-enechemistryAbsorption bandIonic liquidDispersion (chemistry)Journal of Molecular Liquids
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A novel 2,6-bis(benzoxazolyl)phenol macrocyclic chemosensor with enhanced fluorophore properties by photoinduced intramolecular proton transfer

2023

Macrocyclic ligand L, in which a 2,6-bis(2-benzoxazolyl)phenol (bis-HBO) group is incorporated in triethylenetetramine, was designed and synthesized with the aim of creating a chemosensor with high selectivity and specificity for metal cations in an aqueous environment. The availability of several proton acceptors and donors, and amine and phenol hydroxy groups, respectively, affects the keto-enol equilibrium in both the ground and excited states, and the ligand properties show dependence on the pH of the solution. L is fluorescent in the visible range, through an excited-state intramolecular proton transfer (ESIPT) mechanism. The results of an exhaustive characterization of L by spectrosco…

Macrocyclic ligandInorganic ChemistryExcited state intramolecular proton transfer (ESIPT)Settore CHIM/03 - Chimica Generale E InorganicaFluorescence sensorDFT calculationMetal complexeDalton Transactions
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Proton sponge lead halides containing 1D polyoctahedral chains

2021

Hybrid one-dimensional lead halides, containing the protonated 1,8-bis(dimethylamino)naphthalene moiety (C14H19N2, monoprotonated "proton sponge"), were prepared by simple one-pot methods and investigated in terms of crystal structure, morphology, thermal stability and electronic properties. The as-precipitated (C14H19N2)PbBr3 and (C14H19N2)PbI3 species are isostructural and crystallize in the orthorhombic Pbca space group, resulting in 1D crystal phases with ([PbX3](-))(infinity) chains (built by face-sharing [PbX6] octahedra; X = Br, I), among which the (C14H19N2)(+) cations are inserted. The two compounds display complete miscibility in the solid state: both (C14H19N2)PbI2Br and (C14H19N…

Materials science1D-pseudo perovskiteBand gapGeneral ChemistryCrystal structureCondensed Matter PhysicsCrystalhybrid lead halides trimethylsulfoxonium powder diffraction solid solution ionic defectivity periodic DFT calculationsCrystallographyOctahedronPhase (matter)General Materials ScienceOrthorhombic crystal systemThermal stabilityIsostructuralCrystEngComm
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Out-of-plane transport of 1T-TaS2/graphene-based van der Waals heterostructures

2021

Due to their anisotropy, layered materials are excellent candidates for studying the interplay between the in-plane and out-of-plane entanglement in strongly correlated systems. A relevant example is provided by 1T-TaS2, which exhibits a multifaceted electronic and magnetic scenario due to the existence of several charge density wave (CDW) configurations. It includes quantum hidden phases, superconductivity and exotic quantum spin liquid (QSL) states, which are highly dependent on the out-of-plane stacking of the CDW. In this system, the interlayer stacking of the CDW is crucial for the interpretation of the underlying electronic and magnetic phase diagram. Here, thin-layers of 1T-TaS2 are …

Materials scienceBand gapquantum materialsStackingVan der Waals heterostructuresGeneral Physics and AstronomyFOS: Physical sciencescharge-density waves02 engineering and technologyQuantum entanglementDFT calculations01 natural scienceslaw.inventionsymbols.namesakelaw0103 physical sciences11. Sustainability1T-TAS2General Materials Science010306 general physicsMaterialsSuperconductivityCondensed Matter - Materials ScienceCondensed matter physicsGrapheneFermi levelphase-transitionsGeneral EngineeringMaterials Science (cond-mat.mtrl-sci)Conductivitat elèctrica021001 nanoscience & nanotechnology2D materialsstatemodelelectrical propertiestransition-metal dichalcogenidessymbolsQuantum spin liquid0210 nano-technologyCharge density wave
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DFT calculations on subnanometric metal catalysts: a short review on new supported materials

2018

Metal clusters have been used in catalysis for a long time, even in industrial production protocols, and a large number of theoretical and experimental studies aimed at characterizing their structure and reactivity, either when supported or not, are already present in the literature. Nevertheless, in the last years the advances made in the control of the synthesis and stabilization of subnanometric clusters promoted a renewed interest in the field. The shape and size of sub-nanometer clusters are crucial in determining their catalytic activity and selectivity. Moreover, if supported, subnanometric clusters could be highly influenced by the interactions with the support that could affect geo…

Materials scienceDFT calculationSubnanometric metal clusterNanotechnology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciences0104 chemical sciencesCatalysisHeterogeneous catalysiReactivity (chemistry)Metal catalystPhysical and Theoretical Chemistry0210 nano-technologyMetal nanoparticlesMetal clustersElectronic properties
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Spin state, electronic structure and bonding on C-scorpionate [Fe(II)Cl2(tpm)] catalyst: An experimental and computational study

2020

Abstract The Fe(II) spin state in the condensed phase of [Fe(II)Cl2(tpm)] (tpm = [tris(pyrazol-1-yl)methane]; 1) catalyst has been determined through a combined experimental and theoretical investigation of X-Ray Absorption Spectroscopy (XAS) at the FeL2,3-edges and NK-edge. Results indicated that in this phase a mixed singlet/triplet state is plausible. These results have been compared with the already know Fe singlet spin state of the same complex in water solution. A detailed analysis of the electronic structure and bonding mechanism of the catalyst showed that the preference for the low-spin diamagnetic ground state, strongly depends upon the ligands, the bulk solvent and the interactio…

Materials scienceSpin statesDFT calculationHomogeneous catalysis02 engineering and technologyElectronic structure010402 general chemistryDFT calculations01 natural sciencesCatalysisSinglet stateTriplet stateDFT calculations.HOMO/LUMOX-ray absorption spectroscopyC-scorpionate catalystX-ray absorption spectroscopyGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSpin statesC-scorpionate catalyst; DFT calculations; Spin states; X-ray absorption spectroscopySpin statePhysical chemistry0210 nano-technologyGround state
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Ambipolar MoS2 Transistors by Nanoscale Tailoring of Schottky Barrier Using Oxygen Plasma Functionalization

2017

One of the main challenges to exploit molybdenum disulfide (MoS2) potentialities for the next-generation complementary metal oxide semiconductor (CMOS) technology is the realization of p-type or ambipolar field-effect transistors (FETs). Hole transport in MoS2 FETs is typically hampered by the high Schottky barrier height (SBH) for holes at source/drain contacts, due to the Fermi level pinning close to the conduction band. In this work, we show that the SBH of multilayer MoS2 surface can be tailored at nanoscale using soft O-2 plasma treatments. The morphological, chemical, and electrical modifications of MoS2 surface under different plasma conditions were investigated by several microscopi…

Materials scienceambipolar transistorsSchottky barrierDFT calculationNanotechnology02 engineering and technologyDFT calculations01 natural scienceschemistry.chemical_compoundX-ray photoelectron spectroscopy0103 physical sciencesScanning transmission electron microscopyGeneral Materials ScienceSchottky barrierMolybdenum disulfide010302 applied physicsAmbipolar diffusionElectron energy loss spectroscopyConductive atomic force microscopy021001 nanoscience & nanotechnologyconductive atomic force microscopyatomic resolution STEMchemistryambipolar transistorSurface modificationMaterials Science (all)0210 nano-technologyMoS2
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Adducts of free-base meso-tetraarylporphyrins with trihaloacetic acids: Structure and photostability

2020

Abstract Four diverse meso-tetraarylporphyrins in the form of diprotonated adducts with trifluoro-, trichloro-, tribromoacetic acids and acetic acid were investigated in benzene solution. Despite similar structural distortion of the chromophore system due to protonation, the respective adducts demonstrated different photostability when exposed to UV irradiation. The trifluoro- and trichloroacetic adducts, and the acetic acid one, showed some common features both molecular and in the mechanism of photodegradation. However, the tribromo-derivative decayed according to a different kinetic scheme, revealing a considerable impact of the bromine atoms upon the pyrrole units of the porphyrin macro…

Meso-tetraarylporphyrinsSinglet oxygenGeneral Chemical EngineeringGeneral Physics and AstronomyFree baseProtonation02 engineering and technologyGeneral ChemistryChromophore010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryDFT calculations01 natural sciencesPorphyrinTrihaloacetic acids0104 chemical sciencesAdductPorphyrin protonationchemistry.chemical_compoundAcetic acidchemistry0210 nano-technologyPhotodegradationPyrroleJournal of Photochemistry and Photobiology A-Chemistry
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Reaction between Indazole and Pd-Bound Isocyanides-A Theoretical Mechanistic Study

2018

The mechanism of the addition of indazole (Ind)&mdash

Models Molecular3003Activation of small moleculesIndazolesisocyanideIsocyanidePharmaceutical ScienceDFT calculationProtonation010402 general chemistryDFT calculationsactivation of small molecule01 natural sciencesMedicinal chemistryArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundDeprotonationNucleophilelcsh:Organic chemistryTheoreticalModelsDrug DiscoveryNitrilesPhysical and Theoretical ChemistryMechanical PhenomenaIndazoleNucleophilic additionCyanidesMolecular Structure010405 organic chemistrynitrileDrug Discovery3003 Pharmaceutical ScienceOrganic ChemistryRegioselectivityMolecularIsocyanidesModels TheoreticalTautomer0104 chemical sciencesnucleophilic additionchemistryChemistry (miscellaneous)Settore CHIM/03 - Chimica Generale E InorganicaMolecular Medicinereaction mechanismActivation of small molecules; DFT calculations; Isocyanides; Nitriles; Nucleophilic addition; Reaction mechanism; Cyanides; Indazoles; Models Molecular; Molecular Structure; Palladium; Mechanical Phenomena; Models Theoretical; Analytical Chemistry; Chemistry (miscellaneous); Molecular Medicine; 3003; Drug Discovery3003 Pharmaceutical Science; Physical and Theoretical Chemistry; Organic ChemistryPalladium
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Conformational properties of N-acetyl-L-alanine N',N'-dimethylamide

2004

Ab initio/DFT analysis of the conformational properties of free Ac-Ala-NMe(2) (N-acetyl-L-alanine-N',N'-dimethylamide) in terms of the N-H.O, N-H.N, C-H.O hydrogen bonds and C(delta+) = O(delta-) dipole attractions was performed. The Ala residue combined with the C-terminal tertiary amide prefers an extended conformation and that characteristic of the (i + 1)th position of the betaVIb turn. These can be easily remodelled into a structure compatible with the (i + 1)th position of the betaII/betaVIa turn. The residue has also the potential to adopt the conformation accommodated at both central positions of the betaIII/betaIII' turn or the (i + 1)th position of the betaI/beta'I turn.

Models MolecularAlkylationProtein ConformationStereochemistryMolecular ConformationAb initioCalorimetryN-acetyl-L-alanineGeneral Biochemistry Genetics and Molecular Biologyab initio/DFT calculationschemistry.chemical_compoundResidue (chemistry)AmideN-alkylpeptidesPeptide designAlanineHydrogen bondN′N′-dimethylamidesAmidesβ-turnsDipoleCrystallographyAlanine derivativechemistryThermodynamicsPeptidesActa Biochimica Polonica
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