Search results for "FULLERENE"

showing 10 items of 197 documents

Characterization of Interaction Between Humic Acids and Buckminsterfullerene Using Flourescene Spectroscopy

2017

The interaction between buckminsterfullerene C60 and humic acids (HA) of different origins was compared using fluorescence spectroscopy as a function of pH, humic acid concentration, ionic strength. Binding constants between fullerene and humic acids were calculated. It can be suggested that the complexation was driven by hydrophobic interactions depending on the properties of the interacting compounds. Hydrophobic interaction model as indicated by linear Stern-Volmer plots and high Kd values is characterizing the interaction between buckminsterfullerene C60 and humic acids The results of this study support the development of an understanding of the fate of nanomaterials in the environment …

chemistry.chemical_compoundBuckminsterfullereneComputational chemistryChemistrySpectroscopycomplex mixturesCharacterization (materials science)Linnaeus Eco-Tech
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Single and Multiple Additions of Dibenzoylmethane onto Buckminsterfullerene (Eur. J. Org. Chem. 35/2013)

2013

chemistry.chemical_compoundBuckminsterfullereneFullerenechemistryDibenzoylmethaneComputational chemistryOrganic ChemistryOrganic chemistryPhysical and Theoretical ChemistryMass spectrometryEuropean Journal of Organic Chemistry
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Concave Tetrathiafulvalene-Type Donors as Supramolecular Partners for Fullerenes

2007

The cap fits! A new class of concave π-extended tetrathiafulvalene (TTF) derivatives, truxene-TTFs, were prepared and characterized, and their self-assembly with fullerenes was investigated (see picture). Truxene-TTFs represent the first example of TTF-related electron donors that serve, without chemical modification, as monotopic receptors for fullerenes in solution. (Chemical Equation Presented). © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.

chemistry.chemical_compoundCrystallographyFullerenechemistryStereochemistrySupramolecular chemistryChemical modificationGeneral ChemistrySelf-assemblyGeneral MedicineChemical equationCatalysisTetrathiafulvaleneAngewandte Chemie
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Investigation of Charge-Transfer Interactions Induced by Encapsulating Fullerene in a Mesoporous Tetrathiafulvalene-Based Metal-Organic Framework

2019

<p>The design of Metal-Organic Frameworks (MOFs) incorporating electroactive guest molecules in the pores has become a subject of great interest in order to install additional electrical functionalities within the framework while maintaining porosity. In this direction, understanding the charge-transfer (CT) process between the framework and the guest molecules is crucial towards the design of new electroactive MOFs. Herein, we present the encapsulation of fullerenes (C<sub>60</sub>) in a mesoporous tetrathiafulvalene(TTF)-based MOF. The CT process between the electron-acceptor C<sub>60 </sub>guest and the electron-donor TTF ligand is studied in detail by means…

chemistry.chemical_compoundMaterials scienceFullerenechemistryMoleculeMetal-organic frameworkNanotechnologySorptionDensity functional theoryMesoporous materialPorosityTetrathiafulvalene
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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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Organocatalytic Alcohol Oxidation Catalyzed by Recyclable TEMPO-functionalized [60]fullerene

2014

fullerene alcohol oxidation 2266-Tetramethylpiperidine 1-oxyl (TEMPO)
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C60-TEMPO-IL hybrid: “release and catch” organocatalyst for the oxidation of alcohols

2014

fullerene ionic liquids alcohol oxidation 2266-tetramethylpiperidine 1-oxyl
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Carbon nanotube azafullerene peapods and their electronic transport properties

2008

memoryazafullerenefullereenithiilicarbon nanotube
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