Search results for "Ryle"

showing 10 items of 138 documents

From anthraquinone to heterocoronene as stable red chromophore

2018

Using the commercially available 1,4,5,8-tetrachloroanthraquinone (1) as starting material, a N-heterocoronene derivative 3 was synthesized via a straightforward two-step reaction. Compound 3 shows a similar photostability as perylene dyes, qualifying it as a promising colorant.

Materials science010405 organic chemistryGeneral ChemistryChromophore010402 general chemistryPhotochemistry01 natural sciencesAnthraquinone0104 chemical scienceschemistry.chemical_compoundchemistryMaterials ChemistryDerivative (chemistry)Perylene
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Diarylethenes in Optically Switchable Organic Light-Emitting Diodes: Direct Investigation of the Reversible Charge Carrier Trapping Process

2021

Advanced optical materials 10, (2021). doi:10.1002/adom.202101116

Materials science67002 engineering and technologyTrapping01 natural sciencesPhotochromismddc:670stimuli-responsive OLEDsOLEDstimuli-responsive OLED010405 organic chemistrybusiness.industry021001 nanoscience & nanotechnologyphotochromismblendAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsdiarylethenesScientific methodOptoelectronicsblendsdiaryletheneCharge carrier0210 nano-technologybusinessF8BT
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Calculation of vibrationally resolved absorption and fluorescence spectra of the rylenes

2020

A generating function method was used to simulate the vibrationally resolved absorption and emission spectra of perylene, terrylene and quaterrylene. This method operates on the basis of adiabatic excitation energies and electronic ground and excited state vibrational frequencies. These parameters were calculated using density functional theory with the PBE0 functional for perylene and terrylene and with the BH-LYP functional for quaterrylene. The vertical excitation energies of the lower excited states were calculated using functionals with differing amounts of Hartree-Fock exchange. The optimal functional for each molecule was chosen by comparing these energies to literature excitation en…

Materials scienceAbsorption spectroscopyNE116 Chemical sciencesGeneral Physics and Astronomy010402 general chemistry01 natural sciences7. Clean energyMolecular physicsSpectral linePOLYCYCLIC AROMATIC-HYDROCARBONSMOLECULESchemistry.chemical_compound0103 physical sciencesPhysics::Atomic and Molecular ClustersEmission spectrumPhysical and Theoretical ChemistryEXCHANGEAbsorption (electromagnetic radiation)010303 astronomy & astrophysicsBASIS-SETSDIFFUSE INTERSTELLAR BANDSPERYLENE C20H12SPECTROSCOPY0104 chemical scienceschemistryExcited stateDensity functional theoryPeryleneExcitationAPPROXIMATIONPhysical Chemistry Chemical Physics
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Perylenetetracarboxylic anhydride as a precursor of fluorescent carbon nanoonion rings

2015

[EN] Thermal annealing at 400 degrees C of perylenetetracarboxylic anhydride in low molecular mass PEG gives rise to the formation of well defined nanoobjects of 2.5 nm height and size distribution from 10 to 65 nm (average 40 nm) after purification of the raw mixture with silicagel chromatography. TEM reveals that the flat nanoobjects are constituted of concentric graphenic rings (0.34 nm interlayer distance). The morphology of the nanoparticles resembles onion rings of nanometric dimensions (nanoonion rings C-NOR). C-NOR particles have an excitation dependent emission with lambda(em) from 430 to 570 nm and a maximum emission quantum yield of 0.49. C-NOR particles can be internalized into …

Materials scienceCell SurvivalPolymerschemistry.chemical_elementNanoparticleQuantum yieldBiocompatible MaterialsPhotochemistryMicroscopy Atomic ForceIn-vitroQUIMICA ORGANICAComplexesEuropiumCell Line TumorSpectroscopy Fourier Transform InfraredOnionsFluorescence microscopeOrganic chemistryHumansFluorescentGeneral Materials ScienceHigh-pressureschemistry.chemical_classificationCarbon nanoonion ringQuantum dotsPolymerFluorescenceCarbonDynamic Light ScatteringHydrocarbonsNanostructuresPhotoluminiscencechemistryMicroscopy FluorescenceQuantum dotBiocompatibilityPerylenetetracarboxylic anhydride.EuropiumCarbon
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Functionalisation of MoS2 2D layers with diarylethene molecules

2021

Functionalisation of two dimensional (2D) materials with stimuli-responsive molecules has been scarcely investigated. Here, MoS2 layers obtained by chemical exfoliation are covalently and non-covalently functionalised using two photoswitchable diarylethene derivatives under their open- and closed-ring isomers. The choice of these light-responsive molecules is based on their excellent thermal irreversibility and fatigue resistance. The characterisation of the resultant molecular/2D heterostructures proves the successful anchoring of the molecules by both approaches as well as the influence that the driving interaction has in the photoswitching behaviour of the diarylethene isomers after thei…

Materials scienceHeterojunction02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesExfoliation joint0104 chemical sciencesElectrònica molecularFatigue resistancechemistry.chemical_compoundDiarylethenechemistryCovalent bondMaterials ChemistryMolecule0210 nano-technologyMaterialsLayer (electronics)Journal of Materials Chemistry C
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Molecular semiconductor-doped insulator (MSDI) heterojunctions: Oligothiophene/bisphtalocyanine (LuPc2) and perylene/bisphthalocyanine as new structu…

2010

Abstract The combination of a sexithiophene and a perylene diimide derivatives, as p-type and n-type materials, respectively, used as sub-layers, to an intrinsic semiconductor, namely the lutetium bisphthalocyanine, allows to obtain a new transducer for gas sensing. These transducers were called molecular semiconductor-doped insulator (MSDI) heterojunctions, were recently designed and reported, but with only phthalocyanines as active materials. p-Type material leads to MSDIs that exhibit a positive response to ozone and a negative response to ammonia, whereas MSDIs prepared from n-type material exhibit a positive response to ammonia and negative response to ozone. The remarkable point is th…

Materials scienceIntrinsic semiconductorbusiness.industryDopingMetals and Alloyschemistry.chemical_elementHeterojunctionInsulator (electricity)Condensed Matter PhysicsLutetiumSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundTransducerchemistryDiimideMaterials ChemistryOptoelectronicsElectrical and Electronic EngineeringbusinessInstrumentationPeryleneSensors and Actuators B: Chemical
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Light-responsive hybrid material based on luminescent core-shell quantum dots and steroidal organogel

2016

We report the synthesis of a smart novel hybrid with reversible photoswitchable luminescence properties modulated by light. The combination of a low molecular weight organogelator (LMOG) and CdSe/ZnS core-shell semiconductor nanoparticles capped with trioctylphosphine oxide ligands produces a luminescent, stable and transparent material. Modulation of the luminescence properties was successfully achieved using a diarylethene photochromic compound, with good resistance to fatigue ca. 22 cycles. Interestingly, the morphology of the organogel fibers was preserved in the hybrid, while a partial luminescence quenching of the nanoparticle was observed. This material could have implication for on-…

Materials scienceOrganogelNanoparticleNanotechnology02 engineering and technology010402 general chemistry01 natural sciences//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundPhotochromismPhotoswitchableDiaryletheneQuantum DotsMaterials Chemistry//purl.org/becyt/ford/1.4 [https]Quenching (fluorescence)Otras Ciencias QuímicasCiencias QuímicasGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryChemical engineeringQuantum dot0210 nano-technologyHybrid materialLuminescenceTrioctylphosphine oxideCIENCIAS NATURALES Y EXACTAS
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Noncovalent Functionalization and Passivation of Black Phosphorus with Optimized Perylene Diimides for Hybrid Field Effect Transistors

2020

Amongst the different existing methods to passivate black phosphorus (BP) from environmental degradation, the noncovalent functionalization with perylene diimides (PDI) has been postulated as one of the most promising routes because it allows preserving its electronic properties. This work describes the noncovalent functionalization and outstanding environmental protection of BP with tailor made PDI having peri-amide aromatic side chains, which include phenyl and naphthyl groups, exhibiting a significantly increased molecule-BP interaction. These results are rationalized by density functional theory (DFT) calculations showing that the adsorption energies are mainly governed by van der Waals…

Materials sciencePassivation010405 organic chemistryMechanical EngineeringNanotechnology02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesBlack phosphorus0104 chemical scienceschemistry.chemical_compoundchemistryMechanics of Materialsddc:540Surface modificationField-effect transistor0210 nano-technologyMaterialsPerylene
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Monolayer black phosphorus by sequential wetchemical surface oxidation

2018

We report a straightforward chemical methodology for controlling the thickness of black phosphorus flakes down to the monolayer limit by layer-by-layer oxidation and thinning, using water as solubilizing agent.

Materials sciencePassivationGeneral Chemical EngineeringFOS: Physical sciencesApplied Physics (physics.app-ph)02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundDiimideMonolayerChemical Engineering (all)MaterialsChemistry (all)food and beveragesPhysics - Applied PhysicsQuímicaGeneral ChemistryChromophore021001 nanoscience & nanotechnology0104 chemical sciencesChemistrychemistryChemical engineeringIonic liquidddc:540Surface modificationChemistry (all); Chemical Engineering (all)0210 nano-technologyLayer (electronics)Perylene
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Photodynamics at the CdSe Quantum Dot–Perylene Diimide Interface: Unraveling the Excitation Energy and Electron Transfer Pathways

2021

Excitation energy and charge transfer processes in perylene diimide dye–CdSe quantum dot complexes have been studied by femtosecond transient absorption spectroscopy. After excitation of the quantu...

Materials sciencePhysics::Optics02 engineering and technologyCondensed Matter::Mesoscopic Systems and Quantum Hall Effect010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundElectron transferGeneral EnergychemistryQuantum dotChemical physicsDiimideFemtosecondUltrafast laser spectroscopyPhysics::Atomic and Molecular ClustersPhysical and Theoretical Chemistry0210 nano-technologySpectroscopyPeryleneExcitationThe Journal of Physical Chemistry C
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