Search results for "FULLERENES"

showing 10 items of 29 documents

Fused Dibenzo[ a , m ]rubicene: A New Bowl-Shaped Subunit of C 70 Containing Two Pentagons

2016

Total synthetic approaches of fullerenes are the holy grail for organic chemistry. So far, the main attempts have focused on the synthesis of the buckminsterfullerene C60. In contrast, access to subunits of the homologue C70 remains challenging. Here, we demonstrate an efficient bottom-up strategy toward a novel bowl-shaped polycyclic aromatic hydrocarbons (PAH) C34 with two pentagons. This PAH represents a subunit for C70 and of other higher fullerenes. The bowl-shaped structure was unambiguously determined by X-ray crystallography. A bowl-to-bowl inversion for a C70 fragment in solution was investigated by dynamic NMR analysis, showing a bowl-to-bowl inversion energy (ΔG(⧧)) of 16.7 kcal …

Fullerene010405 organic chemistryStereochemistryProtein subunitGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesHigher fullereneschemistry.chemical_compoundColloid and Surface ChemistryBuckminsterfullerenechemistryJournal of the American Chemical Society
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New concepts and applications in macromolecular chemistry of fullerenes

2010

A new classification on the different types of fullerene-containing polymers is presented according to their different properties and applications they exhibit in a variety of fields. Because of their interest and novelty, water-soluble and biodegradable C(60)-polymers are discussed first, followed by polyfullerene-based membranes where unprecedented supramolecular structures are presented. Next are compounds that involve hybrid materials formed from fullerenes and other components such as silica, DNA, and carbon nanotubes (CNTs) where the most recent advances have been achieved. A most relevant topic is still that of C(60)-based donor-acceptor (D-A) polymers. Since their application in pho…

Materials scienceFullereneMacromolecular SubstancesPolymersSupramolecular chemistryNanotechnologyCarbon nanotubeFullerene macromolecules polymers materials chemistry synthesis hybrid materials photovoltaic deviceslaw.inventionlawGeneral Materials Sciencechemistry.chemical_classificationNanotubes CarbonNanowiresPhenyl EthersMechanical EngineeringMolecular electronicsDNAPolymerSettore CHIM/06 - Chimica OrganicaSilicon DioxideSupramolecular polymerschemistryMechanics of MaterialsFullerenesHybrid materialMacromolecule
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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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Chironomus riparius exposure to fullerene-contaminated sediment results in oxidative stress and may impact life cycle parameters

2015

A key component of understanding the potential environmental risks of fullerenes (C60) is their potential effects on benthic invertebrates. Using the sediment dwelling invertebrate Chironomus riparius we explored the effects of acute (12 h and 24 h) and chronic (10 d, 15 d, and 28 d) exposures of sediment associated fullerenes. The aims of this study were to assess the impact of exposure to C60 in the sediment top layer ((0.025, 0.18 and 0.48) C60 mg/cm2) on larval growth, oxidative stress and emergence rates and to quantify larval body burdens in similarly exposed organisms. Oxidative stress localization was observed in the tissues next to the microvilli and exoskeleton through a method fo…

Environmental Engineering010504 meteorology & atmospheric sciencesHealth Toxicology and Mutagenesisved/biology.organism_classification_rank.speciesta1172010501 environmental sciencesBiologymedicine.disease_cause01 natural sciencescarbon nanoparticleChironomidaeArticleecotoxicologyLipid dropletmedicineAnimalsEnvironmental ChemistryEcotoxicologyWaste Management and Disposalta2180105 earth and related environmental sciencesChironomus ripariuschemistry.chemical_classificationReactive oxygen speciesved/biologyEcologySedimentAquatic animalInvertebratesPollutionOxidative StresschemistryBenthic zoneLarvaEnvironmental chemistryFullerenesOxidative stressJournal of Hazardous Materials
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Interaction of C 60 fullerenes with asymmetric and curved lipid membranes: a molecular dynamics study

2015

Interaction of fullerenes with asymmetric and curved DOPC/DOPS bicelles is studied by means of coarse-grained molecular dynamics simulations. The effects caused by asymmetric lipid composition of the membrane leaflets and the curvature of the membrane are analyzed. It is shown that the aggregates of fullerenes prefer to penetrate into the membrane in the regions of the moderately positive mean curvature. Upon penetration into the hydrophobic core of the membrane fullerenes avoid the regions of the extreme positive or the negative curvature. Fullerenes increase the ordering of lipid tails, which are in direct contact with them, but do not influence other lipids significantly. Our data sugges…

0301 basic medicine[ SDV.BBM.BP ] Life Sciences [q-bio]/Biochemistry Molecular Biology/BiophysicsFullereneLipid BilayersGeneral Physics and AstronomyPhosphatidylserinesModel lipid bilayerMolecular Dynamics SimulationCurvatureQuantitative Biology::Cell BehaviorQuantitative Biology::Subcellular Processes03 medical and health sciencesMolecular dynamicsPhysics::Atomic and Molecular ClustersOrganic chemistryPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSPhysics::Biological PhysicsMean curvatureChemistryPenetration (firestop)[SDV.BBM.BP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Biophysics030104 developmental biologyMembraneMembrane curvatureBiophysicsPhosphatidylcholineslipids (amino acids peptides and proteins)Fullerenes
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Fullerenes(nC60) affect the growth and development of the sediment-dwelling invertebrate Chironomus riparius larvae

2015

Abstract The possible toxicity of nanoparticles (NPs) to aquatic organisms needs to be investigated for chronic effects at low concentrations. Chronic effects of carbon NPs, fullerenesC60, on the midges of Chironomus riparius at different life stages on larvae and adult midges were investigated. Sediment associated fullerenesC60 were studied by 10-day growth and 42-day emergence tests with artificial sediment at nominal concentration ranges 0.0004–80 mg/kg dry weight. The body length decreased in the lower tested concentrations (0.0025–20 mg/kg), but the effect vanished with higher concentrations. Delayed emergence rate observed at 0.5 mg/kg. The observed effects correlated with analyzed se…

MaleGeologic SedimentshiiliHealth Toxicology and Mutagenesista1172ved/biology.organism_classification_rank.speciesPopulationmyrkyllisyysToxicologycarbon nanoparticleChironomidaeToxicologyDry weightAnimalssurviaissääsketeducationta116nanoecotoxicologyInvertebrateChironomus ripariusLarvaeducation.field_of_studyChironomus ripariusved/biologyChemistrySedimentGeneral MedicinePollutionekotoksikologiafullereenitBenthic zonenanotoxicityLarvaEnvironmental chemistryToxicitynanohiukkasetFemaleFullerenesWater Pollutants ChemicalEnvironmental Pollution
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Carbon based nanomaterials for tissue engineering of bone: Building new bone on small black scaffolds: A review.

2019

Graphical abstract

0301 basic medicineScaffoldCarbon nanotubesNanotechnologyCarbon nanotubeReview ArticleBone tissuelaw.inventionNanodiamondsScaffold03 medical and health sciences0302 clinical medicineTissue engineeringlawBone cellmedicineCarbon dotsTissue engineeringlcsh:Science (General)BoneCarbon nanomaterialsComputingMethodologies_COMPUTERGRAPHICSGraphene oxidelcsh:R5-920MultidisciplinaryChemistryRegeneration (biology)030104 developmental biologymedicine.anatomical_structure030220 oncology & carcinogenesisCarbon nanomaterialsFullerenesStem celllcsh:Medicine (General)lcsh:Q1-390Journal of advanced research
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Substrate templating guides the photoinduced reaction of C60on calcite

2014

cited By 7; International audience; A substrate-guided photochemical reaction of C60 fullerenes on calcite, a bulk insulator, investigated by non-contact atomic force microscopy is presented. The success of the covalent linkage is evident from a shortening of the intermolecular distances, which is clearly expressed by the disappearance of the moiré pattern. Furthermore, UV/Vis spectroscopy and mass spectrometry measurements carried out on thick films demonstrate the ability of our setup for initiating the photoinduced reaction. The irradiation of C60 results in well-oriented covalently linked domains. The orientation of these domains is dictated by the lattice dimensions of the underlying c…

Fullerenescanning probe microscopysurface chemistry02 engineering and technologyMicroscopy Atomic Force010402 general chemistry01 natural sciencesChemical reaction530CatalysisCalcium CarbonateScanning probe microscopychemistry.chemical_compoundSpectroscopyCalcite[PHYS]Physics [physics]Spectrum AnalysisIntermolecular forcefullerenesGeneral Chemistrycovalent networksself-assemblyPhotochemical Processes021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographychemistryChemical physicsCovalent bondSelf-assembly0210 nano-technology
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Face-to-face held Pacman type porphyrin-fullerene dyads: design, synthesis, charge transfer interactions and photophysical studies

2008

Pacman-type face-to-face zinc-porphyrin-fullerene dyads have been newly synthesized and studied. Owing to the close proximity of the donor and acceptor entities, strong pi-pi intramolecular interactions between the porphyrin and fullerene entities resulted in modulating the spectral and electrochemical properties of the dyads. New absorption and emission bands that correspond to the charge-transfer interactions were observed in the near-IR region. Time-resolved transient absorption studies revealed efficient photoinduced electron transfer from the singlet excited porphyrin to the fullerene entity. The rate constants for photoinduced electron transfer are analyzed in terms of the Marcus theo…

Models MolecularFullereneMagnetic Resonance SpectroscopyPorphyrinsTime FactorsPhotochemistryporphyrinoids010402 general chemistryPhotochemistry01 natural sciencesCatalysisPhotoinduced electron transferElectron Transportchemistry.chemical_compoundElectron transfer[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganometallic CompoundsComputingMilieux_MISCELLANEOUSphotosynthesisMolecular Structure010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistrycharge transferfullerenesGeneral Chemistryelectron transferAcceptorPorphyrin0104 chemical sciencesMarcus theoryZincSpectrometry FluorescenceModels ChemicalExcited stateIntramolecular forceSpectrophotometry UltravioletDimerization
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Weighting non-covalent forces in the molecular recognition of C60. Relevance of concave–convex complementarity

2008

The relative contributions of several weak intermolecular forces to the overall stability of the complexes formed between structurally related receptors and [60]fullerene are compared, revealing a discernible contribution from concave–convex complementarity. Viruela Martin, Pedro Manuel, Pedro.M.Viruela@uv.es ; Viruela Martin, Rafael, Rafael.Viruela@uv.es ; Orti Guillen, Enrique, Enrique.Orti@uv.es

FULLERENESUNESCO::QUÍMICANon covalentBUILDING-BLOCK12-TETRACYANO-9:QUÍMICA [UNESCO]CatalysisMolecular recognitionCHEMISTRYSYSTEMSMaterials ChemistryUNESCO::QUÍMICA::Química orgánicaCARBON NANORINGSChemistryCARBON NANORINGS; BUILDING-BLOCK; FULLERENES; 11111212-TETRACYANO-910-ANTHRAQUINODIMETHANE; COMPLEXATION; DERIVATIVES; RECEPTORS; CHEMISTRY; SYSTEMSCOMPLEXATIONDERIVATIVESIntermolecular force:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysRegular polygonMolecular recognition ; Concave-convex ; Stability ; C60 ; Intermolecular forcesGeneral ChemistrySettore CHIM/06 - Chimica Organica11Intermolecular forcesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsWeighting12Concave-convexbody regionsRECEPTORSC60CrystallographyChemical physicsComplementarity (molecular biology)10-ANTHRAQUINODIMETHANECeramics and CompositesMolecular recognitionStability
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