Search results for " Spectroscopy"

showing 10 items of 6851 documents

A Click Chemistry-Based “Grafting Through” Approach to the Synthesis of a Biorelevant Polymer Brush

2011

A new biorelevant polymer brush showing a polybenzofulvene backbone was synthesized by a ‘‘grafting through’’ approach based on click chemistry and spontaneous polymerization reactions. The easy polymerization of the relatively complex monomer (6-MOEG-9-TM-BF3k) suggests the existence of a particularly efficient recognition process capable of pre-organizing the monomer molecules for the spontaneous polymerization. 13C-NMR spectroscopy as well as UV-vis and fluorescence spectroscopy suggested for poly-6-MOEG-9-TM-BF3k the features of a vinyl (1,2) p-stacked polymer. The new polybenzofulvene derivative was found to interact with water at room temperature to give clear water solutions, but TEM…

chemistry.chemical_classificationpolymer brushPolymers and PlasticsOrganic ChemistryBioengineeringPolymerPolymer brushCell morphologyBiochemistryFluorescence spectroscopyNMRchemistry.chemical_compoundMonomerchemistryChemical engineeringPolymerizationPolymer chemistryclick chemistryClick chemistryMacromolecule
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Structural characterization of U(VI) surface complexes on kaolinite in the presence of humic acid using EXAFS spectroscopy.

2007

To determine the influence of humic acid (HA), pH, and presence of atmospheric CO2 on the sorption of U(VI) onto kaolinite, the structure of the surface complexes was studied by U L III-edge extended X-ray absorption fine structure (EXAFS) spectroscopy. The best fits to the experimental EXAFS data were obtained by including two uranium coordination shells with two axial (O ax) and five equatorial (O eq) oxygen atoms at 1.77+/-0.02 and 2.34+/-0.02 A, respectively, and two coordination shells with one Al/Si atom each at 3.1 and 3.3 A. As in the case of the binary system U(VI)-kaolinite, uranium forms inner-sphere surface complexes by edge sharing with aluminum octahedra and/or silicon tetrahe…

chemistry.chemical_classificationsorptionkaoliniteExtended X-ray absorption fine structureAnalytical chemistrySorptionhumic acidSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsEXAFSColloid and Surface ChemistryAdsorptionchemistryX-ray photoelectron spectroscopyuranium(VI)XPSHumic acidKaoliniteAbsorption (chemistry)surface complexesSpectroscopyJournal of colloid and interface science
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Recognition of Viologen Derivatives in Water by N-Alkyl Ammonium Resorcinarene Chlorides

2017

Three water-soluble N-alkyl ammonium resorcinarene chlorides decorated with terminal hydroxyl groups at the lower rims were synthesized and characterized. The receptors were decorated at the upper rim with either terminal hydroxyl, rigid cyclohexyl, or flexible benzyl groups. The binding affinities of these receptors toward three viologen derivatives, two of which possess an acetylmethyl group attached to one of the pyridine nitrogens, in water were investigated via 1H NMR spectroscopy, fluorescence spectroscopy, and isothermal titration calorimetry (ITC). ITC quantification of the binding process gave association constants of up to 103 M–1. Analyses reveal a spontaneous binding process whi…

chemistry.chemical_classificationta114010405 organic chemistryOrganic ChemistryEnthalpyIsothermal titration calorimetryViologenResorcinarene010402 general chemistry01 natural sciencesviologen derivativesFluorescence spectroscopy0104 chemical scienceschemistry.chemical_compoundN-alkyl ammonium resorcinarene chlorideschemistryPyridinePolymer chemistrymedicineOrganic chemistryAmmoniumta116Alkylmedicine.drugJOURNAL OF ORGANIC CHEMISTRY
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Synthesis and thermal decomposition studies of homo- and heteroleptic tin(iv) thiolates and dithiocarbamates: molecular precursors for tin sulfides

2002

The syntheses and X-ray structures of novel heteroleptic thiolate/dithiocarbamate derivatives (Et2NCS2)2(RS)2Sn (R = Cy, CH2CF3) have been examined and their thermal decompositions compared with those of selected tin(II) and tin(IV) dithiocarbamates. The heteroleptic species decompose to SnS by initial elimination of RSSR to afford (Et2NCS2)2Sn and subsequent loss of [Et2NC(S)]2S. In contrast, (Et2NCS2)4Sn decomposes via [(Et2NCS2)2SnS]2, whose structure has been determined, and finally to SnS2 by sequential elimination of [Et2NC(S)]2S. The two families of compounds, (R2NCS2)4Sn and (Et2NCS2)2(RS)2Sn, thus provide single-source materials for bulk SnS2 and SnS, respectively, by virtue of the…

chemistry.chemical_classificationtin thiolatesMössbauer spectroscopyChemistryInorganic chemistryThermal decompositionSolid-statechemistry.chemical_elementGeneral ChemistryCrystal structureChemical vapor depositionMedicinal chemistryDecompositionchemical vapor depositionSettore CHIM/03 - Chimica Generale E InorganicaTinDithiocarbamateX-ray crystallographyJournal of the Chemical Society, Dalton Transactions
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Binding and Fluorescent Sensing of Dicarboxylates by a Bis(calix[4]pyrrole)-Substituted BODIPY Dye

2013

A bis(calix[4]pyrrole)-substituted BODIPY ditopic receptor 1 has been synthesised and characterised. The binding and sensing properties of 1 towards several aliphatic and aromatic dicarboxylates have been evaluated by using UV/Vis fluorescence and 1H NMR spectroscopy. The receptor strongly binds linear α,ω-dicarboxylates of appropriate lengths (C9 and C10) by acting as a cleft. For all dicarboxylates, the binding event is detected by a bathochromic shift in the UV/Vis spectra of the receptor and by strong quenching of its fluorescence.

chemistry.chemical_compound1h nmr spectroscopyQuenching (fluorescence)chemistryOrganic ChemistryBathochromic shiftmacromolecular substancesVis spectraPhysical and Theoretical ChemistryBODIPYPhotochemistryFluorescencePyrroleEuropean Journal of Organic Chemistry
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Optical Absorption of Zinc Selenide Doped with Cobalt (Zn1-xCoxSe) under Hydrostatic Pressure

2000

Optical absorption of the diluted magnetic semiconductor Zn 1-x Co x Se (x = 0.02) has been measured at room temperature under hydrostatic pressure up to 14 GPa in a membrane diamond-anvil cell. We found two absorption features: (i) an absorption structure in the energy range 1.5 to 1.8 eV, with a negligible pressure shift (i.e. (0.45 ± 0.05) meV/GPa) which we have identified as the Co 2+ (3d 7 ) internal transition 4 A 2 (F) → 4 T 1 (P) and (ii) an onset in the energy range 2 to 2.7 eV which redshifts with pressure (dE/dP = (-8.1 ± 0.6) meV/GPa). We have attributed such absorption edge to charge transfer between the ZnSe valence band and the Co 2+ (3d 7 ) levels. On the assumption that tho…

chemistry.chemical_compoundAbsorption spectroscopyAbsorption edgeChemistryHydrostatic pressureDopingAnalytical chemistryZinc selenideMagnetic semiconductorCondensed Matter PhysicsAbsorption (electromagnetic radiation)Diamond anvil cellElectronic Optical and Magnetic Materialsphysica status solidi (a)
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Absorption spectrum of the f(A1g) ← X(Eg), a(F2g) electronic transition of OsF6

1997

Abstract The absorption spectrum of the visible band of OsF 6 has been recorded using a commercial spectrophotometer. The first vibronic assignments for this band have been realized using the analogy with the d ← X transition of IrF 6 . Some vibronic parameter values are derived.

chemistry.chemical_compoundAbsorption spectroscopyChemistryVisible bandVibronic spectroscopyAtomic physicsOsmium hexafluorideInstrumentationSpectroscopyAtomic and Molecular Physics and OpticsMolecular electronic transitionAnalytical ChemistrySpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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Erweiterte Konjugation in unsymmetrischen Stilbenylsquarainen

1998

Extended Conjugation in Stilbenylsquaraines Unsymmetrical 1-aryl-3-stilbenylsquaraines 2a–e and 1,3-bis(stilbenyl)squaraines 3a–c were prepared by CC coupling reactions of the corresponding substituted arenes with derivatives of squaric acid (Schemes 2 and 3). Dialkylamino and alkoxy groups enhance the solubility of these dyes and enlarge the intramolecular charge transfer of these donor–acceptor–donor systems. The extended conjugation of the stilbene units – in comparison with arene building blocks – leads to significant bathochromic shifts in the Vis/NIR absorption spectra.

chemistry.chemical_compoundAbsorption spectroscopychemistryIntramolecular forceBathochromic shiftAlkoxy groupSquaric acidSolubilityPhotochemistryMedicinal chemistryCoupling reactionJournal f�r Praktische Chemie/Chemiker-Zeitung
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Polycondensed nitrogen heterocycles. Part19. Pyrrolo[1,2-f]phenanthridines by pschorr-type cyclization brought about by hypophosphorous acid

1986

Pyrrolo[1,2-f]phenanthridines were prepared in good yields by the diazotization in acetic acid of the amines la,b and subsequent treatment with hypophosphorous acid. The necessity for hypophosphorous acid in the reaction was demonstrated.

chemistry.chemical_compoundAcetic acidHypophosphorous acidchemistryOrganic ChemistryOrganic chemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopyNitrogenJournal of Heterocyclic Chemistry
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Rotational State Change of Acetonitrile Vapor on MCM-41 upon Capillary Condensation with the aid of Time-Correlation Function Analysis of IR Spectros…

2000

The infrared spectra of adsorbed acetonitrile on MCM-41 (porewidth = 3.2 nm) were measured at 303 K. In the CN stretching ν2 region, two bands were observed at 2265 cm− 1 and 2254 cm− 1, assigned to hydrogen-bonded molecules on surface hydroxyls of MCM-41, and physisorbed molecules in mesopores, respectively. We designate here the 2265 cm− 1 band as the ν2α band and the 2254 cm− 1 band as the ν2β band. The bandwidth of the fundamental transition ν2fβ, was obtained by removing the overlap with hot band transitions of the same mode, ν2α band, and other modes by least-squares fitting. Before capillary condensation, the relaxation time τ obtained from the bandwidth of the ν2fβ band was smaller …

chemistry.chemical_compoundAdsorptionCapillary condensationMCM-41chemistryAnalytical chemistryInfrared spectroscopyMoleculeMesoporous materialAcetonitrileHot band
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