Search results for "FULLERENES"

showing 9 items of 29 documents

Characterizing cavities in model inclusion molecules: a comparative study

1998

We have selected fullerene-60 and -70 cavities as model systems in order to test several methods for characterizing inclusion molecules. The methods are based on different technical foundations such as a square and triangular tessellation of the molecule taken as a unitary sphere, spherical tessellation of the molecular surface, numerical integration of the atomic volumes and surfaces, triangular tessellation of the molecular surface, and a cubic lattice approach to a molecular space. Accurate measures of the molecular volume and surface area have been performed with the pseudo-random Monte Carlo (MCVS) and uniform Monte Carlo (UMCVS) methods. These calculations serve as a reference for the…

Models MolecularFullereneMaterials scienceMonte Carlo methodComputer Graphics and Computer-Aided DesignFractal dimensionCarbonTriangular tilingStandard deviationComputational physicsNumerical integrationComputational chemistryLattice (order)Materials ChemistryMoleculeComputer SimulationFullerenesPhysical and Theoretical ChemistryMonte Carlo MethodAlgorithmsSoftwareSpectroscopyJournal of Molecular Graphics and Modelling
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On novel magnetic probe for fullerene characterization: Theoretical studies on NMR parameters of free and confined in fullerenes HD and H2 molecules

2015

Chemical characterization and separation of individual fullerenes from a raw reaction mixture need new and efficient tools, including rapid spectroscopic techniques. Recent "molecular surgery" synthesis of endohedral complexes of fullerenes with selected atoms and small molecules has opened a new path for experimental and theoretical studies on structural and spectroscopic properties of these molecular systems. Among them are fullerenes with molecular hydrogen confined within a nanoscale cavity. In this work we report on quantum-chemical prediction of nuclear magnetic shielding (and chemical shift) and indirect spin-spin coupling constant in free HD and H2 molecules, as well as models of co…

Models MolecularMagnetic Resonance SpectroscopyFullereneHydrogenchemistry.chemical_element010402 general chemistry01 natural sciencesDFTComputational chemistryHD molecule0103 physical sciencesPhysics::Atomic and Molecular ClustersMaterials ChemistryMoleculeCCSD(T)Physical and Theoretical ChemistrySpectroscopyCoupling constant010304 chemical physicsfullereneBenzeneNuclear magnetic resonance spectroscopyComputer Graphics and Computer-Aided DesignSmall molecule0104 chemical sciencesCoupled clusterModels ChemicalchemistryChemical physicsconstansAnisotropyQuantum TheoryDensity functional theoryFullerenesindirect nuclear spin–spin couplingHydrogenJournal of Molecular Graphics and Modelling
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A self-assembled M8L6 cubic cage that selectively encapsulates large aromatic guests.

2011

Porphyrins cubed: A series of self-assembled M8L6 cubic cages that enclose a volume in excess of 1300 A3 were synthesized (see scheme). The porphyrinic walls of the cubes provide favorable sites for pnp interactions, leading to selectivity between large and chemically similar aromatic guests: three molecules of coronene are incorporated and the higher fullerenes C70nC84 are selectively bound in the presence of

Models MolecularMagnetic Resonance SpectroscopyMolecular StructureCapsulesGeneral ChemistryCrystallography X-RayHydrocarbons AromaticCatalysisCoroneneHigher fullerenesSelf assembledchemistry.chemical_compoundchemistryNickelPolymer chemistryPhysics::Atomic and Molecular ClustersMoleculePolycyclic CompoundsFullerenesCageSelectivityAngewandte Chemie (International ed. in English)
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Stepwise sequential redox potential modulation possible on a single platform.

2011

Step by step: The cluster [3,3'-Co(1,2-C(2)B(9)H(11))(2)](-) is an excellent platform for making a stepwise tunable redox potential system by dehydroiodination. With the addition of up to eight iodine substituents (purple; see picture), there is a fall in the E(1/2)(Co(III)/Co(II)) value from -1.80 V to -0.68 V (vs. Fc(+)/Fc; Fc = ferrocene). A practical application of this tunability has been observed in the growth of polypyrrole.

Models MolecularPolymersInorganic chemistryGeneral MedicineGeneral ChemistryCobaltPolypyrroleCrystallography X-RayElectron transport chainRedoxCatalysisCrystallographychemistry.chemical_compoundFerrocenechemistryModulationOrganometallic CompoundsPyrrolesFullerenesBoranesOxidation-ReductionAngewandte Chemie (International ed. in English)
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Binding Sites, Vibrations and Spin-Lattice Relaxation Times in Europium(II)-Based Metallofullerene Spin Qubits.

2021

Abstract To design molecular spin qubits with enhanced quantum coherence, a control of the coupling between the local vibrations and the spin states is crucial, which could be realized in principle by engineering molecular structures via coordination chemistry. To this end, understanding the underlying structural factors that govern the spin relaxation is a central topic. Here, we report the investigation of the spin dynamics in a series of chemically designed europium(II)‐based endohedral metallofullerenes (EMFs). By introducing a unique structural difference, i. e. metal‐cage binding site, while keeping other molecular parameters constant between different complexes, these manifest the ke…

Spin statesFOS: Physical scienceschemistry.chemical_element010402 general chemistry01 natural sciencesMolecular physicsCatalysischemistry.chemical_compoundVery Important PaperPhysics - Chemical PhysicsPhysics::Atomic and Molecular ClustersPhysics - Atomic and Molecular Clustersspin-vibration couplingQuantumeuropiumSpin-½Chemical Physics (physics.chem-ph)Full Paper010405 organic chemistryChemistryNanotecnologiaOrganic ChemistryRelaxation (NMR)Spin–lattice relaxationfullerenesGeneral ChemistryQuímicaFull Papers0104 chemical sciences3. Good healthQubitMetallofullerenemagnetic propertiesAtomic and Molecular Clusters (physics.atm-clus)Europiumspin qubitsChemistry (Weinheim an der Bergstrasse, Germany)
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Efficient photoinduced electron transfer in a porphyrin tripod-fullerene supramolecular complex via pi-pi interactions in nonpolar media.

2010

A novel porphyrin tripod (TPZn(3)) was synthesized via "click chemistry". Three porphyrin moieties of TPZn(3) are geometrically close and linked by a flexible linker. The electron-transfer oxidation of TPZn(3) results in intramolecular pi-dimer formation between porphyrin moieties as indicated by electrochemical, vis-NIR, and ESR measurements. The cyclic voltammogram of TPZn(3) exhibited stepwise one-electron oxidation processes of three porphyrin moieties in the range from 0.58 to 0.73 V (vs SCE in CH(2)Cl(2)). When TPZn(3) was oxidized by tris(2,2'-bipyridyl)-ruthenium(III) ([Ru(bpy)(3)](3+)), the oxidized species (TPZn(3))(n+) (0n/= 3) exhibited a charge resonance band in the NIR region …

dyadFullerenePorphyrinsMacromolecular SubstancesPhotochemistrySupramolecular chemistrycharge-separated state010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisPhotoinduced electron transferchemistry.chemical_compoundColloid and Surface Chemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryMoleculeComputingMilieux_MISCELLANEOUSMolecular Structure[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryTripod (photography)reaction center mimicryGeneral ChemistryPorphyrin0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryZincchemistryIntramolecular forceclick chemistry[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryClick chemistryQuantum TheoryFullerenesporphyrinOxidation-ReductionJournal of the American Chemical Society
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A Tunable, Fullerene‐Based Molecular Amplifier for Vibrational Circular Dichroism

2019

Abstract Vibrational circular dichroism (VCD) studies are reported on a chiral compound in which a fullerene C60 moiety is used as an electron acceptor and local VCD amplifier for an alanine‐based peptide chain. Four redox states are investigated in this study, of which three are reduced species that possess low‐lying electronic states as confirmed by UV/Vis spectroelectrochemistry. VCD measurements in combination with (TD)DFT calculations are used to investigate (i) how the low‐lying electronic states of the reduced species modulate the amplification of VCD signals, (ii) how this amplification depends on the distance between oscillator and amplifier, and (iii) how the spatial extent of the…

endocrine systemFullerenechirality010402 general chemistry01 natural sciencesRedoxCatalysisAnalytical ChemistryElectronic statesMoietychemistry.chemical_classificationFull Paper010405 organic chemistryAmplifierOrganic ChemistryfullerenesspectroelectrochemistryGeneral ChemistryFull PapersElectron acceptorvibrational circular dichroism0104 chemical sciencesCrystallographychemistrydensity functional calculationsVibrational circular dichroismChirality (chemistry)Chemistry – A European Journal
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Conjugation with carbon nanotubes improves the performance of mesoporous silicon as Li-ion battery anode

2020

Carbon nanotubes can be utilized in several ways to enhance the performance of silicon-based anodes. In the present work, thermally carbonized mesoporous silicon (TCPSi) microparticles and single-walled carbon nanotubes (CNTs) are conjugated to create a hybrid material that performs as the Li-ion battery anode better than the physical mixture of TCPSi and CNTs. It is found out that the way the conjugation is done has an essential role in the performance of the anode. The conjugation should be made between negatively charged TCPSi and positively charged CNTs. Based on the electrochemical experiments it is concluded that the positive charges, i.e., excess amine groups of the hybrid material i…

energy science and technologyEnergy storageElectronic properties and materialspiibatteriesenergy storageEnergy science and technologyelektroditlcsh:RlitiumioniakutCarbon nanotubes and fullereneslcsh:MedicineArticleBatteriescarbon nanotubes and fullereneslcsh:Qelectronic properties and materialsnanoputketlcsh:SciencekomposiititScientific Reports
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Theoretical and computational studies of magnetic anisotropy and exchange coupling in molecular systems

2018

The field of molecular magnetism studies the magnetic properties of molecular systems as opposed to conventional metal-based magnets. The high chemical modifiability of the constituting molecules makes such materials highly versatile, and the small size of the building blocks leads to the rise of various quantum mechanical phenomena, such as tunneling and entanglement. These phenomena can then be further utilized in the construction of nanoscale quantum devices. This dissertation describes computational and theoretical studies in the field of molecular magnetism using state-of-the-art quantum chemical methods based on ab initio multireference approaches and broken symmetry density functional t…

organic magnetsmagnetic anisotropymagneettiset ominaisuudetCASPT2tiheysfunktionaaliteoriamolecular magnetismexchange interactionmolekyylitkompleksiyhdisteetorganometalliyhdisteetCASSCFDFTspin-orbit couplingquantum chemistrybroken symmetry DFTkvanttikemiaendohedral metallo-fullereneslanthanidessingle-molecule magnetsmagnetismiNEVPT2orgaaniset yhdisteet
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