Search results for "FULLERENE"

showing 10 items of 197 documents

Design, synthesis and photovoltaic properties of [60]fullerene based molecular materials

2005

Abstract The possibility to use new organic semiconductor materials, in place of silicon wafers, in the fabrication of photovoltaic devices on substrates offer the prospect of lower manufacturing costs, particularly for large area applications. Thus, one of the most promising areas in fullerene research involves its potential application, mixed with conjugated polymers, in mimicking photosynthesis and in the related solar energy conversion. The tendency to phase segregation in blends of C60 derivatives and conjugated polymers has to be optimized to improve both charge photogeneration and transport in photovoltaic devices. In order to optimize device performances, a great deal of work has be…

chemistry.chemical_classificationFullereneFabricationMaterials scienceOrganic solar cellPhotovoltaic systemphotovoltaic devicesBioengineeringNanotechnologyPolymerSettore CHIM/06 - Chimica OrganicaConjugated systemBiomaterialsOrganic semiconductorchemistryMechanics of Materialsfullerene derivativesWafer
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Understanding the affinity of bis-exTTF macrocyclic receptors towards fullerene recognition

2019

A new series of fullerene receptors based on exTTF macrocycles with alkyl ether chains of increasing length is reported. The novel macrocyclic receptors are able to favourably interact with fullerene C60 through a synergistic combination of π–π, CH⋯π and n⋯π noncovalent interactions. We identify that the highest affinity towards C60 recognition is achieved for the host with the tightest fit; that is, the smallest receptor with a cavity large enough to host the buckyball inside (log Ka = 5.2 in chlorobenzene at 298 K). However, besides this expected observation, theoretical calculations evidence that the most stable self-assembling configuration corresponds for all the receptors to an outsid…

chemistry.chemical_classificationFullereneGeneral Physics and Astronomy02 engineering and technologySynergistic combination010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences3. Good health0104 chemical sciencesAlkyl etherchemistry.chemical_compoundCrystallographychemistryChlorobenzeneNon-covalent interactionsPhysical and Theoretical Chemistry0210 nano-technologyReceptorPhysical Chemistry Chemical Physics
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Fullerene-Containing Polymers: An Overview

2009

chemistry.chemical_classificationFullereneMaterials sciencePolymer sciencechemistryFullerene Polymers MacromoleculesPolymerSettore CHIM/06 - Chimica OrganicaMacromolecule
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Synthesis of a Fullerene Derivative of Benzo[18]crown-6 byDiels-Alder Reaction: Complexation Ability, Amphiphilic Properties, and X-Ray Crystal Struc…

1993

A fullerene derivative 1 of benzo[18]crown-6 was obtained by Diels-Alder addition of fullerene[60](C60) to the ortho-quinodimethane prepared in situ from 4,5-bis(bromomethyl)benzo[18]crown-6 (3) with Bu4NI in toluene. Extraction experiments show that the complexation of K+ ions strongly increases the solubility of 1 in protic solvents like MeOH. Using Langmuir-Blodgett techniques, monolayers of the highly amphiphilic fullerene-derived crown ether 1 and its K+ ion complex were prepared. An X-ray crystal structure was obtained from a benzene clathrate of comparison compound 2, synthesized by Diels-Alder reaction of C60 with the ortho-quinodimethane derived from 1,2-bis(bromomethyl)-4,5-dimeth…

chemistry.chemical_classificationFullereneOrganic Chemistry18-Crown-6Crystal structureBiochemistryTolueneCatalysisInclusion compoundInorganic Chemistrychemistry.chemical_compoundBuckminsterfullerenechemistryDrug DiscoveryPolymer chemistryOrganic chemistryPhysical and Theoretical ChemistryCrown etherDerivative (chemistry)Helvetica Chimica Acta
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Electronic communication through pi-conjugated wires in covalently linked porphyrin/C60 ensembles

2005

Novel photo- and electroactive triads, in which pi-conjugated p-phenylenevinylene oligomers (oPPVs) of different length are connected to a photoexcited-state electron donor (i.e., zinc tetraphenylporphyrin) and an electron acceptor (i.e., C(60)), were designed, synthesized, and tested as electron-transfer model systems. A detailed physicochemical investigation, concentrating mainly on long-range charge separation and charge recombination and kinetics, revealed small attenuation factors beta of 0.03+/-0.005 A(-1). Energy matching between the HOMO levels of C(60) and oPPVs emerged as a key parameter for supporting molecular-wire-like behavior: It favors rapid and efficient electron or hole in…

chemistry.chemical_classificationFullereneOrganic ChemistryElectron donorGeneral ChemistrySettore CHIM/06 - Chimica OrganicaElectron acceptorConjugated systemPhotochemistryPorphyrinCatalysisElectron transferMolecular wirechemistry.chemical_compoundchemistryCovalent bondFullerene derivatives
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Solution-processed bi-layer polythiophene–fullerene organic solar cells

2013

An ionic polymer based on a polythiophene backbone with appended imidazolium moieties was successfully implemented as a donor material in fully solution-processed efficient bi-layer solar cells prepared by the low impact meniscus coating technique. High fill factors and device reproducibility were obtained, even for ultrathin polymer layers, indicating excellent film formation properties and good compatibility with solution processing techniques. The possibility of smooth counter ion exchange, allowing solubility modification and efficiency tuning, enables exploration of new functionalities and other device architectures.

chemistry.chemical_classificationMaterials scienceFullereneOrganic solar cellGeneral Chemical EngineeringIonic bondingNanotechnologyGeneral ChemistryPolymerengineering.materialchemistry.chemical_compoundchemistryCoatingengineeringPolythiopheneSolubilityCounterionRSC Advances
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Main-Chain and Side-Chain C60-Polymers

2009

chemistry.chemical_classificationMaterials sciencechemistryPolymer scienceChain (algebraic topology)Fullerene Polymers SynthesisSide chainPolymerSettore CHIM/06 - Chimica Organica
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Quinonoid π-extended tetrathiafulvalenes (TTFs)

2001

Publisher Summary Tetrathiafulvalene (TTF) is a fascinating planar πelectron-donor molecule with a broad range of potential applications. TTF and its derivatives play an important role in the field of organic conductors forming charge-transfer (CT) complexes and radical cation salts (Bechgaard salts) with a huge variety of electron-acceptor molecules and anions in the search for electrically conducting and superconducting materials. The chapter focuses on highly π-extended electron donors with p-quinodimethane structures as interesting precursors of materials with non-conventional properties. The first dimeric examples of π-extended TTF derivatives connected through an oxygen atom are also …

chemistry.chemical_classificationchemistry.chemical_compoundCrystallographyFullerenechemistryRadical ionCovalent bondStereochemistryMoietyMoleculeConjugated systemElectron acceptorTetrathiafulvalene
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ChemInform Abstract: Synthesis of a Fullerene Derivative of Benzo(18)crown-6 by Diels-Alder Reaction: Complexation Ability, Amphiphilic Properties, a…

2010

A fullerene derivative 1 of benzo[18]crown-6 was obtained by Diels-Alder addition of fullerene[60](C60) to the ortho-quinodimethane prepared in situ from 4,5-bis(bromomethyl)benzo[18]crown-6 (3) with Bu4NI in toluene. Extraction experiments show that the complexation of K+ ions strongly increases the solubility of 1 in protic solvents like MeOH. Using Langmuir-Blodgett techniques, monolayers of the highly amphiphilic fullerene-derived crown ether 1 and its K+ ion complex were prepared. An X-ray crystal structure was obtained from a benzene clathrate of comparison compound 2, synthesized by Diels-Alder reaction of C60 with the ortho-quinodimethane derived from 1,2-bis(bromomethyl)-4,5-dimeth…

chemistry.chemical_classificationchemistry.chemical_compoundFullerenechemistry18-Crown-6Polymer chemistryGeneral MedicineCrystal structureBenzeneTolueneDerivative (chemistry)Crown etherDiels–Alder reactionChemInform
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Photovoltaic effect in bulk heterojunction system with glass forming indandione derivative DMABI-6Ph

2018

The aim of the work is to evaluate possible use of 2-[[4-(bis(2-trityloxyethyl)amino)phenyl]methylene]indane-1,3-dione (DMABI-6Ph) as light absorbing material for solar cells. DMABI-6Ph is a perspective material due to its good photoelectrical, thermal and chemical properties. The main advantage of DMABI-6Ph is its ability to form amorphous films by wet-casting methods thus allowing using the compound in organic solar cells made from solution. For now most popular materials for solution processable solar cells are polymer P3HT and fullerene derivative PCBM, but lot of investigations are in the field of new low molecular weight materials to replace the polymer. Photoelectrical measurements w…

chemistry.chemical_classificationglass forming structureFullereneMaterials scienceOrganic solar cellOpen-circuit voltage020209 energybulk heterojunction02 engineering and technologyPolymerPhotovoltaic effect021001 nanoscience & nanotechnology7. Clean energyPolymer solar cellpower conversion efficiencyAmorphous solidchemistryChemical engineeringElectron affinity:NATURAL SCIENCES:Physics [Research Subject Categories]0202 electrical engineering electronic engineering information engineeringenergy levels0210 nano-technologyindandione groupEnergy Procedia
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