Search results for "surface"

showing 10 items of 9345 documents

A new experimental protocol for intrazeolite photooxidations. The first product-based estimate of an upper limit for the intrazeolite singlet oxygen …

2002

The intrazeolite photooxidations of several alkenes have been examined in hexane and in perfluorohexane slurries. The ability of perfluorohexane to increase the affinity of alkenes for the interior of the zeolite was documented. The nearly identical reaction rates in the two slurry solvents are attributed to a leveling of the singlet oxygen lifetime by the zeolite framework. A consideration of the rates of the various intrazeolite processes was used to estimate an upper limit for the intrazeolite lifetime of singlet oxygen.

chemistry.chemical_classificationSinglet oxygenGeneral ChemistryPhotochemistryBiochemistryCatalysisCatalysisHexaneReaction ratechemistry.chemical_compoundColloid and Surface ChemistryReaction rate constantHydrocarbonchemistryOrganic chemistryZeolitePerfluorohexaneJournal of the American Chemical Society
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The influence of counterions and hydrophobic moieties on the thermostability of Langmuir-Blodgett multilayers

1994

Abstract Langmuir-Blodgett (LB) multilayers with various counterions and different organic moieties (one- and two-chain fatty acids, polymeric acid) are prepared to investigate on line temperature-dependent structural changes and desorption by small-angle X-ray scattering (SAXS), interference-enhanced reflection and Nomarsky microscopy. On temperature increase a sequence of phase transitions can be observed. A crystalline LB film melts to a fluid phase and eventually desorbs either from droplets or from a homogeneous film. The phase sequence depends on the counterion: nickel stearate and magnesium stearate melt while the layered structure is conserved; SAXS measurements reveal a continuous,…

chemistry.chemical_classificationSmall-angle X-ray scatteringMetals and AlloysSurfaces and InterfacesLangmuir–Blodgett filmSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryChemical engineeringStearatePhase (matter)Materials ChemistryOrganic chemistryThermal stabilityMagnesium stearateStearic acidCounterionThin Solid Films
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Isoreticular two-dimensional magnetic coordination polymers prepared through pre-synthetic ligand functionalization

2018

Chemical functionalization is a powerful approach to tailor the physical and chemical properties of two-dimensional (2D) materials, increase their processability and stability, tune their functionalities and, even, create new 2D materials. This is typically achieved through post-synthetic functionalization by anchoring molecules on the surface of an exfoliated 2D crystal, but it inevitably alters the long-range structural order of the material. Here we present a pre-synthetic approach that allows the isolation of crystalline, robust and magnetic functionalized monolayers of coordination polymers. A series of five isostructural layered magnetic coordination polymers based on Fe(ii) centres a…

chemistry.chemical_classificationSolucions polimèriquesChemistryLigandMagnetismGeneral Chemical EngineeringNanotechnology02 engineering and technologyGeneral ChemistryPolymerCiència dels materials010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesExfoliation joint0104 chemical sciencesMonolayerSurface modificationMoleculeIsostructural0210 nano-technologyNature Chemistry
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Solvent-free ruthenium-catalysed triflate coupling as a convenient method for selective azole-o-C-H monoarylation.

2019

Metal-catalysed ortho-directed C–H functionalization usually faces selectivity issues in the competition between mono- and disubstitution processes. We report herein the ruthenium-catalysed N-directed C–H monoarylation of arylpyrazoles with a selectivity of up to 96% or that generally reaches values above 80%. This selectivity is an effect of solvent-free conditions associated with sulfonate reagents, in the absence of frequently used acidic additives.

chemistry.chemical_classificationSolvent free010405 organic chemistryChemistryOrganic Chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesRutheniumchemistry.chemical_compoundSulfonateReagentSurface modificationAzolePhysical and Theoretical ChemistrySelectivityTrifluoromethanesulfonateOrganicbiomolecular chemistry
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Sorption of Hydrocarbons on Peat, and Possibilities for Using Peat-Based Oil Sorbent for Treatment of Polluted Areas

2017

The growing use and transport of crude oil and oil products has led to an increasing amount of spillages of various scales. In the event of an oil spill, it is important to stop the spill from spreading and to clean up the polluted environment. One of the possible ways of treating the polluted areas is the use of oil sorbents. The sorbents used for collecting oil in case of oil spills are mostly synthetic, which limits the possibilities of their disposal. The aim of our study is to investigate the possible use of peat and its modification products for oil and other hydrocarbon sorption. Peat is a prospective material for oil sorption because it has such advantages as low cost, biodegradabil…

chemistry.chemical_classificationSorbentPeatHydrocarbonchemistrySpecific surface areaEnvironmental chemistryEnvironmental scienceSorptionBiodegradationPorositycomplex mixturesDecompositionLinnaeus Eco-Tech
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Fluorescence excitation and emission spectroscopy on single MEH-PPV chains at low temperature.

2008

Fluorescence emission and excitation spectra of single MEH-PPV polymer molecules dispersed in thin PMMA films have been recorded at 1.2 and 20 K. We observe single as well as multichromophore emission in single chain emission spectra, whereby the relative fractions depend on the two different molecular weights (50 and 350 kDa) studied. The molecular weight also affects the distribution of peak emission maxima, which is monomodal (bimodal) for the low (high) molecular weight. The appearance of an additional "red" subpopulation for the high molecular weight sample is attributed to interactions of multiple chromophores from a sufficiently flexible single chain. The comparison of emission spect…

chemistry.chemical_classificationSpectral shape analysisMolecular massAnalytical chemistryAstrophysics::Cosmology and Extragalactic AstrophysicsPolymerChromophoreFluorescenceSurfaces Coatings and FilmschemistryMaterials ChemistryMoleculeEmission spectrumPhysical and Theoretical ChemistryAstrophysics::Galaxy AstrophysicsExcitationThe journal of physical chemistry. B
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Pressure-induced cooperative spin transition in ironII 2D coordination polymers: room-temperature visible spectroscopic study.

2011

For the 2D coordination polymers [Fe(3-Fpy)(2)M(II)(CN)(4)] (M(II) = Ni, Pd, Pt), the pressure-induced spin crossover behavior has been investigated at 298 K by monitoring the distinct optical properties associated with each spin state. Cooperative first-order spin transition characterized by a piezohysteresis loop ca. 0.1 GPa wide was observed for the three derivatives. Application of the mean field regular solution theory has enabled estimation of the cooperative parameter, Γ(p), and the enthalpy, ΔH(HL)(p), associated with the spin transition for each derivative. These values, found in the intervals 6.8-7.9 and 18.6-20.8 kJ mol(-1), respectively, are consistent with those previously repo…

chemistry.chemical_classificationSpin statesCondensed matter physicsEnthalpySpin transitionElastic energyPolymerSurfaces Coatings and FilmschemistryMean field theorySpin crossoverMaterials ChemistryPhysical chemistryPhysical and Theoretical ChemistrySpin-½The journal of physical chemistry. B
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Experimental Investigations and ab Initio Studies on Hexacoordinated Complexes of Dichlorosilane

1998

Dichlorosilane, SiH2Cl2, forms two different kinds of coordination compounds with pyridine and 3-picoline:  the simple adduct trans-SiH2Cl2(L)2 and the ionic complex [SiH2(L)4]Cl2·4CHCl3 (L = pyridine, 3-picoline). The adducts trans-SiH2Cl2(py)2, 1, and trans-SiH2Cl2(3pic)2, 2, form directly from the reaction of bis(dichlorosilyl)methylamine, NMe(SiHCl2)2 with pyridine (py), and 3-picoline (3pic). Reaction of 1 with an excess of pyridine in chloroform yielded [SiH2(py)4]Cl2·4CHCl3, 3. The molecular and crystal structures of 1−3 were investigated by single-crystal X-ray diffraction. The Si atoms of all three compounds are hexacoordinated and lie on centers of inversion. The basic structural …

chemistry.chemical_classificationStereochemistryAb initioDichlorosilaneGeneral ChemistryCrystal structureTriclinic crystal systemBiochemistryCatalysisCoordination complexAdductchemistry.chemical_compoundCrystallographyColloid and Surface ChemistrychemistryPyridineMonoclinic crystal systemJournal of the American Chemical Society
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Consecutive Selective Adsorption of Pentamidine and Phosphate Biomolecules on a Self-Assembled Layer:  Reversible Formation of a Chemically Selective…

1996

In situ ellipsometric film thickness measurements, FT-IR external reflectance spectroscopy, and potentiometric measurements indicated that the amphiphile pentamidine (PAM), a bisbenzamidine, associated by self-assembly with a preformed self-assembled monolayer of a mercaptoalkanoic acid on gold. The structural properties of PAM and the nature of the substrate were ideal for the formation of a densely packed monolayer. This process was fully reversible, as demonstrated by changing the pH of the surrounding medium. Thus, disassembly−reassembly occurred when the pH was cycled between 8.7 and 3. The bilayer structure, featuring a positively charged amidinium surface, was subsequently used for s…

chemistry.chemical_classificationStereochemistryBilayerBiomoleculeSubstrate (chemistry)PhosphatePhotochemistryAnalytical Chemistrychemistry.chemical_compoundchemistrySelective adsorptionMonolayerAmphiphileSurface chargeAnalytical Chemistry
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Postsynthetic Approach for the Rational Design of Chiral Ferroelectric Metal–Organic Frameworks

2017

International audience; Ferroelectrics (FEs) are materials of paramount importance with a wide diversity of applications. Herein, we propose a postsynthetic methodology for the smart implementation of ferroelectricity in chiral metal−organic frameworks (MOFs): following a single-crystal to single-crystal cation metathesis, the Ca2+ counterions of a preformed chiral MOF of formula Ca6II{CuII24[(S,S)-hismox]12(OH2)3}·212H2O (1), where hismox is a chiral ligand derived from the natural amino acid l-histidine, are replaced by CH3NH3+. The resulting compound, (CH3NH3)12{CuII24[(S,S)-hismox]12(OH2)3}·178H2O (2), retains the polar space group of 1 and is ferroelectric below 260 K. These results op…

chemistry.chemical_classificationStereochemistryChiral ligandRational design02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyMetathesis01 natural sciencesBiochemistryFerroelectricityCatalysis0104 chemical sciencesCrystallographyColloid and Surface Chemistrychemistry[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Metal-organic frameworkCounterion0210 nano-technology
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