Search results for "Acceptor"

showing 10 items of 394 documents

Structural Characterization of Molecular Interface Layers Using Neutron and X-Ray Reflectivity Techniques

1992

Synthetic microstructures used in biological research today include a variety of different systems that serve very diverse purposes and require very different fabrication and characterization techniques. One class of microstructures that is at the boundary between life and materials sciences, and certainly has been associated closer to the latter in the past, is that of molecularly structured planar interface films. In fact, Langmuir-Blodgett (LB) films,1 i.e. molecularly layered films comprised of amphiphatic organic molecules on solid substrates, have been used for many years as model systems for the investigation of molecular interactions between chromophores or donor/ acceptor couples, …

X-ray reflectivityFabricationPlanarMaterials scienceNanotechnologyNeutron reflectometryChromophoreMicrostructureAcceptorCharacterization (materials science)
researchProduct

Experimental and Theoretical Investigations on the Synthesis, Structure, Reactivity, and Bonding of the Stannylene-Iron Complex Bis{{bis(2-tert-butyl…

2000

The pi-(arene)bis(stannylene) complex bis(bis(2-tert-butyl-4,5,6-trimethylphenyl)SnFe(eta6-toluene) (Sn-Fe-Sn, 15) is accessible in high yields by a metal-atom-mediated synthesis between iron atoms, toluene, and the stannylene [bis(2-tert-butyl-4,5,6-trimethylphenyl)Sn](3). Complex 15 has a half-sandwich structure with short Fe -Sn bonds (2.432(1) A) and a trigonal-planar coordination at both the Fe and Sn atoms. The distance between the two Sn centers is 3.56 A. Complex 15 is stable under ambient conditions and displays a pi-arene lability, so far rarely observed for (arene)iron complexes; this leads to an irreversible substitution of the arene and formation of fivefold-coordinated zeroval…

Zerovalent ironLabilityOrganic ChemistryInorganic chemistryChemiechemistry.chemical_elementGeneral ChemistryAcceptorTolueneCatalysisCrystallographychemistry.chemical_compoundchemistryAtomic orbitalMolecular orbitalTinPi backbonding
researchProduct

Selective Stepwise Suzuki Cross-Coupling Reaction for the Modelling of Photosynthetic Donor−Acceptor Systems

2009

A Suzuki reaction performed as a selective stepwise substitution of two boryl groups on a diarylporphyrin precursor is reported for straightforward construction of a porphyrin trimer, modeling photosynthetic donor-acceptor systems.

[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryOrganic ChemistryTrimer010402 general chemistryPhotosynthesisPhotochemistry01 natural sciencesBiochemistryPorphyrinCoupling reaction0104 chemical scienceschemistry.chemical_compounddonor-acceptor systemchemistrySuzuki reaction[ CHIM.ORGA ] Chemical Sciences/Organic chemistryface to faceSuzuki couplingPhysical and Theoretical ChemistryDonor acceptorporphyrinComputingMilieux_MISCELLANEOUSOrganic Letters
researchProduct

Increased electron donor and electron acceptor characters enhance the adhesion between oil droplets and cells of Yarrowia lipolytica as evaluated by …

2003

International audience; The adhesion of methyl ricinoleate droplets to cells of the yeast Yarrowia lipolytica was investigated. A new cytometric method, relying on the double staining of fatty globules with Nile Red and of cells with Calcofluor, enabled us to quantify methyl ricinoleate droplet adhesion to cells precultured on a hydrophilic or on a hydrophobic carbon source. In this last case, droplet adsorption was enhanced and a MATS (microbial adhesion to solvents) test revealed that this increase was due to Lewis acid-base interactions and not to an increase in the hydrophobic properties of the cell surface. These preliminary results demonstrate that the developed cytometric method is p…

[SDV.BIO]Life Sciences [q-bio]/BiotechnologyMESH : Microscopy FluorescenceYarrowiaElectron donorMESH: Flow CytometryMESH: Microscopy Fluorescencechemistry.chemical_compoundMESH: Microscopy ConfocalMESH : Fatty AcidsMESH : Electron Transportchemistry.chemical_classification0303 health sciencesMicroscopyMicroscopy ConfocalbiologyFatty AcidsMESH : OilsAdhesivenessAdhesionElectron acceptorFlow CytometryMESH: Fatty AcidsBiochemistryConfocalMESH: OilsGeneral Agricultural and Biological SciencesRicinoleic AcidsMESH : AdhesivenessMESH : YarrowiaMESH : Flow CytometryFluorescenceElectron Transport03 medical and health sciencesAdsorptionMESH : AdsorptionMESH : Microscopy ConfocalMESH: Electron Transport030304 developmental biology030306 microbiologyNile red[ SDV.BIO ] Life Sciences [q-bio]/BiotechnologyYarrowiaGeneral Chemistrybiology.organism_classificationYeastMESH: Ricinoleic AcidschemistryMicroscopy FluorescenceMESH : Ricinoleic AcidsOil dropletBiophysicsMESH: AdhesivenessMESH: YarrowiaAdsorptionMESH: AdsorptionOils
researchProduct

Tackling Performance Challenges in Organic Photovoltaics: An Overview about Compatibilizers

2020

Organic Photovoltaics (OPVs) based on Bulk Heterojunction (BHJ) blends are a mature technology. Having started their intensive development two decades ago, their low cost, processability and flexibility rapidly funneled the interest of the scientific community, searching for new solutions to expand solar photovoltaics market and promote sustainable development. However, their robust implementation is hampered by some issues, concerning the choice of the donor/acceptor materials, the device thermal/photo-stability, and, last but not least, their morphology. Indeed, the morphological profile of BHJs has a strong impact over charge generation, collection, and recombination processes; control o…

additiveOrganic solar cellComputer sciencePharmaceutical ScienceMature technologymixing interfaceReviewcompatibilizersdonor/acceptor interfaceAnalytical Chemistrylcsh:QD241-441lcsh:Organic chemistryPhotovoltaicsDrug DiscoverySolar Energycompatibilizermorphology modulatorPhysical and Theoretical ChemistrySustainable developmentFlexibility (engineering)morphology modulatorsbusiness.industryOrganic Chemistrybulk heterojunctionEngineering physicsCharge generationModels ChemicalChemistry (miscellaneous)mixing interfacesMolecular Medicineadditivesorganic photovoltaicsbusiness
researchProduct

Enrichment of amino acids by supported liquid membrane extraction using Aliquat 336 as a carrier

1998

Abstract The possible application of Aliquat 336 (trioctylmethyl ammonium chloride) as a carrier for liquid membrane extraction of amino acids was investigated. The extraction is performed from an aqueous donor phase with pH > 11 to an acceptor phase containing a salt solution through a supported liquid membrane with Aliquat 336 as a carrier in the membrane to facilitate amino acid transport. Counter-coupled transport of chloride anions from the acceptor phase to the donor phase is the driving force of the mass transfer in this system. The extraction efficiency depends on the donor phase pH, the carrier concentration in the liquid membrane, the composition of the acceptor phase and the hydr…

amino acidsChromatographyAqueous solutionBiochemistry (medical)Clinical BiochemistryExtraction (chemistry)Aliquat 336Aliquat 336BiochemistryAcceptorAnalytical Chemistrychemistry.chemical_compoundMembranechemistryLiquid–liquid extractionPhase (matter)ElectrochemistryextractionAmmonium chloridesupported liquid membraneSpectroscopyAnalytical Letters
researchProduct

Singlet and triplet energy transfers in tetra-(meso-truxene)zinc(II)- and tetra-(meso-tritruxene)zinc(II) porphyrin and porphyrin-free base dendrimer…

2011

The synthesis, optical properties, and energy transfer features of four dendrimers composed of meso-tetrasubstituted zinc(II) porphyrin (ZnP) or a free base (P) central core, where the substituents are four truxene (Tru) or four tritruxene dendrons (TriTru), TruP, TriTruP, TruZnP, and TriTruZnP, are reported. Selective excitation of the truxene donors results in a photoinduced singlet energy transfer from the truxenes to the porphyrin acceptor. The rates for singlet energy transfer (k(ET)), evaluated from the change in the fluorescence lifetime of the donors (Tru and TriTru) in the presence and absence of the acceptor (P or ZnP) for TruP, TruZnP, TriTruP, and TriTruZnP, are 5.9, 1.2, 0.87, …

biologyChemistryFree basechemistry.chemical_elementZincbiology.organism_classificationPhotochemistryFluorescencePorphyrinAcceptorInorganic Chemistrychemistry.chemical_compoundDendrimerTetraSinglet statePhysical and Theoretical ChemistryInorganic chemistry
researchProduct

Pseudo-Planar Organic Heterojunctions by Sequential Printing of Quasi-Miscible Inks

2021

This work deals with the interfacial mixing mechanism of picoliter (pL)-scale droplets produced by sequential inkjet printing of organic-based inks onto ITO/PET surfaces at a moderately high Weber number (~101). Differently from solution dispensing processes at a high Bond number such as spin coating, the deposition by inkjet printing is strictly controlled by droplet velocity, ink viscosity, and surface tension. In particular, this study considers the interfacial mixing of droplets containing the most investigated donor/acceptor couple for organic solar cells, i.e., poly(3-hexylthiophene) (P3HT) and (6,6)-phenyl-C61-butyric acid methyl ester (PCBM), showing how low-viscosity and low-surfac…

bisolvent dropletsSpin coatinginkjet printingMaterials scienceFabricationOrganic solar cellHeterojunctionSurfaces and InterfacesEngineering (General). Civil engineering (General)AcceptorPolymer solar celldroplet mixingSurfaces Coatings and FilmsSurface tensionChemical engineeringpseudo-planar heterojunctionsMaterials ChemistryWeber numberTA1-2040Coatings
researchProduct

Water-Tolerant Trifloaluminate Ionic Liquids: New and Unique Lewis Acidic Catalysts for the Synthesis of Chromane

2018

The first example of triflometallate ionic liquids, named in analogy to chlorometallate ionic liquids, is reported. Trifloaluminate ionic liquids, synthesised from 1-alkyl-3-methylimidazolium triflates and aluminium triflate, were characterised by multinuclear NMR spectroscopy and FT-IR spectroscopy, revealing the existence of oligonuclear, multiply-charged trifloaluminate anions, with multiple bridging triflate modes. Acceptor numbers were determined to quantify their Lewis acidity, rendering trifloaluminate ionic liquids as medium-strength Lewis acids (AN = ca. 65). Used as acidic catalysts in the cycloaddition of 2,4-dimethylphenol and isoprene (molar ratio 2:1) to prepare chromane, trif…

carbon nanotubes010405 organic chemistrymetal triflatesGeneral ChemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciencesAcceptor0104 chemical sciencesCatalysislcsh:ChemistryChemistrychemistry.chemical_compoundchromanelcsh:QD1-999chemistrytrifloaluminate ionic liquidsPolymer chemistryIonic liquidChromaneLewis acids and basesSILPTrifluoromethanesulfonateIsopreneOriginal Research
researchProduct

Relationship between Electron Affinity and Half-Wave Reduction Potential: A Theoretical Study on Cyclic Electron-Acceptor Compounds.

2016

A high-level ab initio protocol to compute accurate electron affinities and half-wave reduction potentials is presented and applied for a series of electron-acceptor compounds with potential interest in organic electronics and redox flow batteries. The comprehensive comparison between the theoretical and experimental electron affinities not only proves the reliability of the theoretical G3(MP2) approach employed but also calls into question certain experimental measurements, which need to be revised. By using the thermodynamic cycle for the one-electron attachment reaction A+e- →A- , theoretical estimates for the first half-wave reduction potential have been computed along the series of ele…

chemistry.chemical_classification010304 chemical physicsChemistryAb initioSolvationElectronElectron acceptor010402 general chemistry01 natural sciencesRedoxAtomic and Molecular Physics and Optics0104 chemical sciencesReduction (complexity)Ab initio quantum chemistry methodsComputational chemistryChemical physicsElectron affinity0103 physical sciencesPhysical and Theoretical ChemistryChemphyschem : a European journal of chemical physics and physical chemistry
researchProduct