Search results for "Note"

showing 10 items of 10709 documents

Effective conjugation in conjugated polymers with strongly twisted backbones: A case study on fluorinated MEHPPV

2016

Conjugated polymers with strongly twisted backbones, such as MEHPPV with fluorinated vinylene units (F-MEHPPV), demand a redefinition of the all-important ‘effective conjugation length’ ECL, which we extract here by a facile graphical method. In MEHPPV (being essentially planar), the ECL coincides with the ‘maximum conducive chain length’ MCC and extends over about n ≈ 9 repetition units (RU). In F-MEHPPV, the MCC is similarly long with n ≈ 8, but the ECL localizes on just one RU. The strong twist in F-MEHPPV persists in the excited state, broadening the emission spectrum and quenching the fluorescence with reduced radiative and enhanced non-radiative rates.

chemistry.chemical_classificationfluorinated MEHPPVMaterials scienceQuenching (fluorescence)twisted backbones02 engineering and technologyGeneral ChemistryPolymerConjugated system010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesFluorescence0104 chemical sciencesChain lengthPlanarchemistryExcited stateEffective conjugationMaterials ChemistryEmission spectrum0210 nano-technology
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Carbon nanostructures incorporated on methacrylate monoliths for separation of small molecules by nano-liquid chromatography

2018

Abstract Carbon nanostructures have been incorporated to polymethacrylate monoliths to develop novel stationary phases with enhanced separation performance in nano-liquid chromatography (nano-LC). Two incorporation approaches of these nanomaterials in monoliths were investigated. Single-walled carbon nanohorns (SWNHs) were first incorporated to the polymerization mixture, followed by UV initiation. The resulting stationary phases with embedded SWNHs led to an increase in the separation performance of analytes compared to the parent monolith. Alternatively, a two-step photo-grafting approach was also adopted to attach the carbon nanoparticles onto the polymer monolith surface. The effect of …

chemistry.chemical_classificationgeographyMaterials sciencegeography.geographical_feature_categoryScanning electron microscope010401 analytical chemistrychemistry.chemical_element02 engineering and technologyCarbon nanotubePolymer021001 nanoscience & nanotechnologyMethacrylate01 natural sciences0104 chemical sciencesAnalytical Chemistrylaw.inventionNanomaterialschemistryChemical engineeringPolymerizationlawMonolith0210 nano-technologyCarbonSpectroscopyMicrochemical Journal
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MCM-41 silica monoliths with independent control of meso- and macroporosity

2007

Centimetre sized macroporous silica monoliths consisting of MCM-41 have been prepared by a two-step procedure allowing an independent control of the meso- and macro-porosity. In the first step a monolith with a macroporosity tailored between 2 and 20 μm is prepared under acidic medium by a phase separation, named spinodal decomposition, leading to a bicontinuous structure of a silica/polymer phase and a water phase. The monolith is then reacted in an alkaline solution of cetyltrimethyl ammonium to transform the silica skeleton into MCM-41 under conditions which preserve the original morphology and macroporosity of the material. The combination of spinodal decomposition and pseudomorphic tra…

chemistry.chemical_classificationgeographygeography.geographical_feature_categoryMorphology (linguistics)ChromatographySpinodal decomposition[CHIM.MATE]Chemical Sciences/Material chemistry02 engineering and technologyGeneral ChemistryPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical sciencesMCM-41chemistryChemical engineering[ CHIM.MATE ] Chemical Sciences/Material chemistryPhase (matter)Materials Chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Monolith0210 nano-technologyComputingMilieux_MISCELLANEOUSNew Journal of Chemistry
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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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Electrical Behaviour of Heterobimetallic [MM′(EtCS2)4] (MM′=NiPd, NiPt, PdPt) and MM′X-Chain Polymers [PtM(EtCS2)4I] (M=Ni, Pd)

2012

Herein, we report the isolation of new heterobimetallic complexes [Ni0.6Pd1.4ACHTUNGTRENUNG(EtCS2)4] (1), [NiPtACHTUNGTRENUNG(EtCS2)4] (2) and [Pd0.4Pt1.6ACHTUNGTRENUNG(EtCS2)4] (3), which were constructed by using transmetallation procedures. Subsequent oxidation with iodine furnished the MM'X monodimensional chains [Ni0.6Pt1.4ACHTUNGTRENUNG(EtCS2)4I] (4) and [Ni0.1Pd0.3Pt1.6ACHTUNGTRENUNG(EtCS2)4I] (5). The physical properties of these systems were investigated and the chain structures 4 and 5 were found to be reminiscent of the parent [Pt2ACHTUNGTRENUNG(EtCS2)4I] species. However, they were more sensitively dependent on the localised nature of the charge on the Ni ion, which caused spont…

chemistry.chemical_classificationmolecular electronicsOrganic ChemistryNanotechnologyGeneral ChemistryPolymerDFTinorganic polymerCatalysisIonCrystallographyTransmetalationchemistryConduction bandChemistry - A European Journal
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Methyl-Substituted α-Cyclodextrin as Affinity Material for Storage, Separation, and Detection of Trichlorofluoromethane

2018

Abstract The severely ozone‐depleting trichlorofluoromethane is still appearing in several recycling processes or industrial applications. A simple and selective supramolecular complex formation of per‐methylated α‐cyclodextrin (1) with the highly volatile trichlorofluoromethane (2) is reported. This interaction moreover leads to thermally stable crystals. Per‐methylated α‐cyclodextrin is successfully exploited as a reversible and selective adsorption material for liquid and airborne trichlorofluoromethane as well as an affinity material for the chemical sensing and detection of this particular volatile organic component.

chemistry.chemical_classificationoptical sensorsCyclodextrinTrichlorofluoromethaneCFC‐11CommunicationComplex formationSupramolecular chemistrymacromolecular substances02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryCommunicationssupramolecular chemistry0104 chemical scienceschemistry.chemical_compoundcyclodextrinchemistrySelective adsorptiontrichlorofluoromethaneOrganic component0210 nano-technologyGlobal Challenges
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How do different surface modification strategies affect the properties of MnO nanoparticles for biomedical applications? Comparison of PEGylated and …

2011

ABSTRACTMnO nanoparticles (NPs) were surface functionalized by two different approaches, (1) using a dopamine-poly(ethylene glycol) (PEG) (DA-PEG) ligand and (2) by encapsulation within a thin silica shell applying a novel approach. Both MnO@DA-PEG and MnO@SiO2 NPs exhibited excellent long-term stability in physiological solutions. In addition, the cytotoxic potential of both materials was comparatively low. Furthermore, owing to the magnetic properties of MnO NPs, both MnO@DA-PEG and MnO@SiO2 lead to a shortening of the longitudinal relaxation time T1 in MRI. In comparison to the PEGylated MnO NPs, the presence of a thin silica shell led to a greater stability of the MnO core itself by pre…

chemistry.chemical_compoundAqueous solutionMaterials sciencechemistryChemical engineeringPEG ratioSurface modificationNanoparticleNanotechnologyLeaching (metallurgy)Ethylene glycolLongitudinal Relaxation TimeIonMRS Proceedings
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ChemInform Abstract: Multi-Arm 1,2,3-Thiadiazole Systems.

2010

Benzene derivatives 2a–c with 6, 4, and 3 side chains bearing terminal 1,2,3-thiadiazole rings, respectively, have been prepared. Alkaline cleavage of 2a–c led to the corresponding alkynethiolates 6a–c, which were trapped by electrophiles such as benzyl bromide or iodomethane. The method provides an alternative to the thermal or photochemical cleavage of 1,2,3-thiadiazoles to thioketenes, which react further with nucleophiles.

chemistry.chemical_compoundBenzyl bromideNucleophileChemistryElectrophileBenzene derivativesSide chainNanotechnologyGeneral MedicineCleavage (embryo)Medicinal chemistryChemInform
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Synthetic and Biological Applications of Fluorous Reagents as Phase Tags

2011

The search for new and better techniques for the purification of organic compounds has made the recent emergence of fluorous chemistry in the field of organic synthesis possible. Using fluorous reagents as phase tags allows for the access of different synthetic routes, and this has been translated into a time reduction and higher simplicity compared to standard, nonfluorous procedures. The synthesis in fluorous phase of target molecules can be pursued in a parallel or combinatorial manner in order to access chemical libraries with structural and/or stereochemical diversity. The preparation of radiolabeled molecules also benefits from the advantages of fluorous synthesis. Finally, biochemica…

chemistry.chemical_compoundChemistryPhase (matter)ReagentNanotechnologyOrganic synthesisFluorous chemistryCombinatorial chemistry
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Titelbild: Cyanide-Bridged Iron(III)–Cobalt(II) Double Zigzag Ferromagnetic Chains: Two New Molecular Magnetic Nanowires (Angew. Chem. 13/2003)

2003

chemistry.chemical_compoundCrystallographyMaterials scienceZigzagchemistryFerromagnetismCyanidechemistry.chemical_elementNanotechnologyGeneral MedicineMagnetic nanowiresCobaltAngewandte Chemie
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