Search results for "FUNCTIONAL"

showing 10 items of 4822 documents

Bending Carbon Nanoforms for Supramolecular Recognition: A Topological Study on Hemifullerene-Based Aggregates

2018

International audience; Buckybowls have risen as appealing fullerene fragment derivatives. Their intrinsic curvature has been exploited in the generation of host–guest supramolecular assemblies, not only through concave–convex complementarity but also through less-known concave–concave staggered arrangements. Whereas the stabilization of bowl-in-bowl dispositions has been ascribed to efficient π–π forces together with favorable dipole–dipole interactions, a detailed analysis on the forces guiding the formation of the staggered arrangements is missing so far. Herein, we present a thorough theoretical characterization of bowl-in-bowl vs staggered hemifullerene-based homodimers and heterodimer…

Fullerene010405 organic chemistryChemistrySupramolecular chemistrychemistry.chemical_elementBending010402 general chemistry01 natural sciences0104 chemical sciencesCharacterization (materials science)Chemical bondChemical physicsMoleculeDensity functional theory[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryCarbonThe Journal of Physical Chemistry A
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Complexation and Electronic Communication between Corannulene-Based Buckybowls and a Curved Truxene-TTF Donor

2017

Abstract: The association behavior of an electron-donating, bowl-shaped, truxene-based tetrathiafulvalene (truxTTF) with two corannulene-based fullerene fragments, C32H12 and C38H14, is investigated in several solvents. Formation of 1:1 complexes is followed by absorption titrations and complemented by density functional theory (DFT) calculations. The binding constants are in the range logKa=2.9–3.5. DFT calculations reveal that the most stable arrangement is the conformation in which the 1,3-dithiole ring of truxTTF is placed inside the concave cavity of the corannulene derivative. This arrangement is confirmed experimentally by NMR measurements, and implies that a combination of p–p and C…

Fullerene010405 organic chemistryOrganic ChemistrySupramolecular chemistryQuímica orgánicaGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis3. Good health0104 chemical sciencesPhotoexcitationchemistry.chemical_compoundCrystallographychemistryCorannuleneUltrafast laser spectroscopyDensity functional theoryAbsorption (chemistry)Tetrathiafulvalene
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From small to medium and beyond: a pragmatic approach in predicting properties of Ne containing structures

2013

In this study, we outlined a pragmatic approach for structural studies leading to better understanding of polycarbon structures using 21Ne as a nuclear magnetic resonance (NMR) probe. 21Ne NMR parameters of a single neon atom and its dimer were predicted at the CCSD(T) level in combination with large basis sets. At a lower level of theory, an interaction of neon atom with 1,3-cyclopentadiene ring and with five- and six-membered rings in carbazole was studied using the restricted Hartree–Fock (RHF) and density functional theory (DFT) combined with smaller basis sets. The RHF and DFT modelling of neon interaction with nanosized objects were performed on cyclacenes and selected fullerenes.

Fullerene21Ne NMRDimerBiophysicschemistry.chemical_elementRing (chemistry)Molecular physicsDFTNeonchemistry.chemical_compoundComputational chemistrycarbazoleAtomPhysics::Atomic and Molecular ClustersPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryMolecular Biologydispersion interactionsBasis (linear algebra)CarbazolefullerenesCondensed Matter PhysicschemistryDensity functional theorycyclacenesMolecular Physics
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Efficient Modeling of NMR Parameters in Carbon Nanosystems

2015

Rapid growth of nanoscience and nanotechnology requires new and more powerful modeling tools. Efficient theoretical modeling of large molecular systems at the ab initio and Density Functional Theory (DFT) levels of theory depends critically on the size and completeness of the basis set used. The recently designed variants of STO-3G basis set (STO-3Gel, STO-3Gmag), modified to correctly predict electronic and magnetic properties were tested on simple models of pristine and functionalized carbon nanotube (CNT) systems and fullerenes using the B3LYP and VSXC density functionals. Predicted geometries, vibrational properties, and HOMO/LUMO gaps of the model systems, calculated with typical 6-31G…

FullereneBasis (linear algebra)ChemistryIsotropyAb initioNanotechnologyCarbon nanotubeComputer Science Applicationslaw.inventionChemical physicslawPhysics::Atomic and Molecular ClustersDensity functional theoryPhysical and Theoretical ChemistryHOMO/LUMOBasis setJournal of Chemical Theory and Computation
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Modeling21Ne NMR parameters for carbon nanosystems

2013

The potential of nuclear magnetic resonance (NMR) technique in probing the structure of porous systems including carbon nanostructures filled with inert gases is analysed theoretically using accurate calculations of neon ((21) Ne) nuclear magnetic shieldings. The CBS estimates of (21) Ne NMR parameters were performed for single atom, its dimer and neon interacting with acetylene, ethylene and 1,3-cyclopentadiene. Several levels of theory including restricted Hartree-Fock (RHF), Moller-Plesset perturbation theory to the second order (MP2), density functional theory (DFT) with van Voorhis and Scuseria's t-dependent gradient-corrected correlation functional (VSXC), coupled cluster with single …

FullereneDimerchemistry.chemical_elementGeneral ChemistryMolecular physicsNeonchemistry.chemical_compoundCoupled clusterchemistryAcetyleneComputational chemistryAtomGeneral Materials ScienceDensity functional theoryPerturbation theory (quantum mechanics)Magnetic Resonance in Chemistry
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Efficient and accurate modeling of electron photoemission in nanostructures with TDDFT

2017

We derive and extend the time-dependent surface-flux method introduced in [L. Tao, A. Scrinzi, New J. Phys. 14, 013021 (2012)] within a time-dependent density-functional theory (TDDFT) formalism and use it to calculate photoelectron spectra and angular distributions of atoms and molecules when excited by laser pulses. We present other, existing computational TDDFT methods that are suitable for the calculation of electron emission in compact spatial regions, and compare their results. We illustrate the performance of the new method by simulating strong-field ionization of C60 fullerene and discuss final state effects in the orbital reconstruction of planar organic molecules.

FullereneFOS: Physical sciences02 engineering and technologyElectron01 natural sciences7. Clean energySettore FIS/03 - Fisica Della MateriaSpectral linelaw.inventionlawPhysics - Chemical PhysicsIonization0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics - Atomic and Molecular Clusters010306 general physicsChemical Physics (physics.chem-ph)PhysicsAtoms in moleculesTime-dependent density functional theory021001 nanoscience & nanotechnologyCondensed Matter PhysicsLaserElectronic Optical and Magnetic MaterialsExcited stateAtomic physicsAtomic and Molecular Clusters (physics.atm-clus)0210 nano-technologyComputational Methods
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Carbon Nanotubes Conjugated with Triazole-Based Tetrathiafulvalene-Type Receptors for C60 Recognition

2019

Fullerene receptors prepared by a twofold CuI -catalyzed azide-alkyne cycloaddition (CuAAC) reaction with -extended tetrathiafulvalene (exTTF) have been covalently linked to singlewalled carbon nanotubes (SWCNTs) and multi-walled carbon nanotubes (MWCNTs). The nanoconjugates obtained were characterized by several analytical, spectroscopic and microscopic techniques (TEM, FTIR, Raman, TGA and XPS), and evaluated as C60 receptors by UV-Vis spectroscopy. The complexation between the exTTF-triazole receptor in the free state and C60 was also studied by UV-Vis and 1 H NMR titrations, and compared with analogous triazole-based tweezer-type receptors containing the electron-acceptor 11,11,12,12-t…

FullereneFULLERENEShost-guest interactionsTriazoleCarbon nanotubeCOMMUNICATIONConjugated systemHOSTS010402 general chemistry01 natural scienceslaw.inventionchemistry.chemical_compoundsymbols.namesakeTCAQAZIDESlawCHEMISTRYAROMATICITYPHOTOINDUCED ELECTRON-TRANSFERcarbon nanotubes010405 organic chemistryCOMPLEXATIONQuímica orgánicaAromaticityEXTTFGeneral Chemistrypi-extended tetrathiafulvalenes0104 chemical sciencesCrystallographychemistrydensity functional calculationssymbolsDensity functional theoryRaman spectroscopyTetrathiafulvalene
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Locally convex quasi *-algebras with sufficiently many *-representations

2012

AbstractThe main aim of this paper is the investigation of conditions under which a locally convex quasi ⁎-algebra (A[τ],A0) attains sufficiently many (τ,tw)-continuous ⁎-representations in L†(D,H), to separate its points. Having achieved this, a usual notion of bounded elements on A[τ] rises. On the other hand, a natural order exists on (A[τ],A0) related to the topology τ, that also leads to a kind of bounded elements, which we call “order bounded”. What is important is that under certain conditions the latter notion of boundedness coincides with the usual one. Several nice properties of order bounded elements are extracted that enrich the structure of locally convex quasi ⁎-algebras.

Fully representable quasi .-algebraApplied MathematicsBounded elementStructure (category theory)Regular polygonQuasi ⁎-algebraCombinatoricsFully representable quasi ⁎-algebraSettore MAT/05 - Analisi MatematicaBounded functionQuasi *-algebraOrder (group theory)Representable linear functionalAnalysisTopology (chemistry)Mathematics
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Understanding light-driven H 2 evolution through the electronic tuning of aminopyridine cobalt complexes

2017

A new family of cobalt complexes with the general formula [CoII(OTf)2(Y,XPyMetacn)] (1R,Y,XPyMetacn ¼ 1-[(4-X-3,5-Y-2-pyridyl)methyl]-4,7-dimethyl-1,4,7-triazacyclononane, (X ¼ CN (1CN), CO2Et (1CO2Et), Cl (1Cl), H(1H), NMe2 (1NMe2)) where (Y ¼ H, and X ¼ OMe when Y ¼ Me (1DMM)) is reported. We found that the electronic tuning of the Y,XPyMetacn ligand not only has an impact on the electronic and structural properties of the metal center, but also allows for a systematic water-reduction-catalytic control. In particular, the increase of the electron-withdrawing character of the pyridine moiety promotes a 20-fold enhancement of the catalytic outcome. By UV-Vis spectroscopy, luminescence quenc…

Funcional de densitat Teoria delQuenching (fluorescence)010405 organic chemistryLigandchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciences54Catalysis3. Good health0104 chemical sciencesCatalysisCrystallographyCatàlisiCatalytic cyclechemistryUltrafast laser spectroscopyLuminescenceSpectroscopyCobaltDensity functionalsChemical Science
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Principal components for multivariate spatiotemporal functional data

2014

Multivariate spatio-temporal data consist of a three way array with two dimensions’ domains both structured, temporally and spatially; think for example to a set of different pollutant levels recorded for a month/year at different sites. In this kind of dataset we can recognize time series along one dimension, spatial series along another and multivariate data along the third dimension. Statistical techniques aiming at handling huge amounts of information are very important in this context and classical dimension reduction techniques, such as Principal Components, are relevant, allowing to compress the information without much loss. Although time series, as well as spatial series, are recor…

Functional Data Analysis Functional Principal Component Analysis Multivariate Multidimensional DataSettore SECS-S/01 - Statistica
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