Search results for "RAMAN"

showing 10 items of 1328 documents

Spectroscopic behaviour of metal–drug complexes. Infrared spectra of Cu(II) complexes with 5-amino-1,3,4-thiadiazole-2-thiol (Hatm)

1997

Abstract The infrared spectra of the drug Hatm and its copper (II) complexes with stoichiometry [Cu(atm) 2 (H 2 O)] and [Cu(Hatm)(HIm) 2 (SO 4 )] are reported and discussed. The Raman spectrum of Hatm is also reported. An assignment of Hatm, HIm, H 2 O and SO 4 modes in the complexes is proposed in comparison with the modes of the free ligands. Important information about the metal–ligand vibrations has been obtained.

chemistry.chemical_classificationchemistry.chemical_elementInfrared spectroscopyPhotochemistryCopperMetalsymbols.namesakechemistryvisual_artsymbolsvisual_art.visual_art_mediumThiolPhysical chemistryRaman spectroscopySpectroscopyStoichiometryVibrational Spectroscopy
researchProduct

Convenient Synthesis of 3-Cinnamoyl-2-styrylchromones: Reinvestigation of the Baker-Venkataraman Rearrangement

2010

An efficient and straightforward, one-pot sequence gives access to highly functionalized 3-cinnamoyl-2-styrylchromones in excellent yields. The low solubility of the target molecules allows convenient isolation. The formation of an α,α-dicinnamoylated acetophenone, as a consequence of a two-fold Baker-Venkataraman sequence, has to be anticipated.

chemistry.chemical_compoundchemistryOne pot reactionOrganic ChemistryBaker–Venkataraman rearrangementMoleculeOrganic chemistrySequence (biology)Physical and Theoretical ChemistrySolubilityCombinatorial chemistryChemical synthesisAcetophenoneEuropean Journal of Organic Chemistry
researchProduct

Non-covalent graphene nanobuds from mono- and tripodal binding motifs.

2017

Graphene nanobuds were prepared via the non-covalent anchoring of C60-based molecules endowed with one or three pyrene units, respectively. TGA, FTIR, UV-Vis and TEM investigations confirmed the formation of nanohybrids. For the two molecular derivatives, striking differences were determined in their interaction with graphene or carbon surfaces by Raman, cyclic voltammetry and molecular mechanics calculations, revealing the important role of pyrene adsorption in modulating the electronic properties of the nanohybrids.

chemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysislaw.inventionsymbols.namesakechemistry.chemical_compoundAdsorptionlawMaterials ChemistryOrganic chemistryMoleculeFourier transform infrared spectroscopyGrapheneMetals and Alloystechnology industry and agricultureQuímica orgánicaGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryCeramics and CompositessymbolsPyreneCyclic voltammetry0210 nano-technologyRaman spectroscopyCarbonChemical communications (Cambridge, England)
researchProduct

Growth, characterization, and high-pressure optical studies of CuWO4

2008

Copper tungstate (CuWO4) crystals grown by the top-seeded solution growth method were characterized by X-ray diffraction, Raman scattering, and optical measurements. CuWO4 has a triclinic structure (P 1¯) with a = 4.709 A, b = 5.845 A, c = 4.884 A, α = 88.3°, β = 92.5°, and γ = 97.2°. It consists of corner-linked CuO6 and WO6 octahedra, the former having a pseudo-tetragonally elongated geometry caused by the Cu2+ Jahn–Teller effect. Fifteen out of the eighteen Raman modes of CuWO4 are reported, discussed, and compared with those of other tungstates. We also determined the indirect band-gap energy of CuWO4 (2.3 eV) and its negative pressure coefficient up to 25 GPa. The pressure evolution of…

chemistry.chemical_elementElectronic structureCrystal structureTriclinic crystal systemCondensed Matter PhysicsCoppersymbols.namesakeCrystallographychemistry.chemical_compoundOctahedronchemistryTungstatesymbolsRaman spectroscopyRaman scatteringHigh Pressure Research
researchProduct

Titanium dioxide in dental enamel as a trace element and its variation with bleaching

2017

Background Titanium is a less studied trace element in dental enamel. Literature relates an increased Titanium concentration with a decreased enamel crystal domain size, which in turn is related to a higher color value. The aim of our study was to analyze the effect of tooth bleaching agents on its concentration in dental enamel by means of confocal Raman spectroscopy. Material and methods Human teeth were randomly distributed in six experimental groups (n=10) and submitted to different bleaching protocols according to the manufacturer´s instructions. Confocal Raman spectroscopy was carried out in order to identify and quantify the presence of titanium dioxide molecules in enamel prior to a…

chemistry.chemical_elementOdontología01 natural sciences010309 optics03 medical and health sciencessymbols.namesakechemistry.chemical_compound0302 clinical medicinestomatognathic systemwhitening0103 physical sciencesHydrogen peroxideGeneral DentistryTooth Bleaching AgentsEnamel painttitanium dioxidecarbamide peroxideChemistryDental enameltechnology industry and agricultureTrace elementbleaching030206 dentistryHydrogen peroxide:CIENCIAS MÉDICAS [UNESCO]stomatognathic diseasesvisual_artRaman spectroscopyUNESCO::CIENCIAS MÉDICASTitanium dioxidevisual_art.visual_art_mediumsymbolsRaman spectroscopyNuclear chemistryTitaniumJournal of Clinical and Experimental Dentistry
researchProduct

Orientation-Dependent Handedness of Chiral Plasmons on Nanosphere Dimers: How to Turn a Right Hand into a Left Hand

2016

Optical activity, which is used as a discriminator of chiral enantiomers, is demonstrated to be orientation dependent on individual, and nominally achiral, plasmonic nanosphere dimers. Through measurements of their giant Raman optical activity, we demonstrate that L/R-handed enantiomers can be continuously turned into their R/L-handed mirror images without passing through an achiral state. The primitive uniaxial multipolar response, with demonstrable broken parity and time reversal symmetry, reproduces the observations as resonant Raman scattering on plasmons that carry angular momentum. The analysis underscores that chirality does not have a quantitative continuous measure and recognizes t…

chiroptical activityAngular momentumMirror imagePhysics::Optics02 engineering and technology01 natural sciencesMolecular physicssymbols.namesakeOpticsPT invariancemultipolar Raman0103 physical sciencesnonreciprocalElectrical and Electronic Engineering010306 general physicsta116PlasmonPhysicsta114business.industryParity (physics)chiral connectedness021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsT-symmetrysymbolsRaman optical activityRaman optical activity0210 nano-technologyChirality (chemistry)businessRaman scatteringBiotechnologyACS Photonics
researchProduct

Solvated copper(I) hexafluorosilicate π-complexes based on [Cu2(amtd)2]2+ (amtd = 2-allylamino-5-methyl-1,3,4-thiadiazole) dimer

2016

[Cu2(amdt)2]SiF6·C6H6 and [Cu2(amdt)2(H2O)2]SiF6·CH3CN·2H2O (amdt = 2-allylamino-5- methyl-1,3,4-thiadiazole) were obtained by alternating-current electrochemical synthesis, starting from water–acetonitrile–benzene mixtures containing 2-allylamino-5-methyl-1,3,4- thiadiazole and CuSiF6·4H2O. The electrochemical reduction of the saturated copper hexafluorosilicate water solution beneath the neatly poured layer of acetonitrile-benzene amdt solution resulted in the formation of crystalline [Cu2(amdt)2]SiF6·C6H6. The initial stirring of the same mixture before subjecting it to the electrochemical reduction resulted in the formation of [Cu2(amdt)2(H2O)2]SiF6·CH3CN·2H2O. A sluggish hydrolysis of …

computational modelingDimerInorganic chemistrycopper(I) hexafluorosilicateschemistry.chemical_element010402 general chemistry010403 inorganic & nuclear chemistryElectrochemistry01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundHydrolysissymbols.namesakeraman spectroscopyMaterials ChemistryMother liquorPhysical and Theoretical ChemistryAcetonitrileta116heterocyclesOrganic ChemistryCopper0104 chemical scienceschemistrysymbolsPhysical chemistryRaman spectroscopyJournal of Organometallic Chemistry
researchProduct

Polymorphism and versatile solvate formation of thiophanate-methyl

2009

The polymorphism of a fungicide, thiophanate-methyl (TM), was investigated with conventional solvent screening methods. Two polymorphs, the thermodynamically most stable form I and the less stable form II, were found. TM was also found to crystallize as a plethora of different solvates which produced mostly form II upon desolvation. The structures of form I and form II and the fourteen discovered solvates were solved by single crystal X-ray diffraction. The most stable forms were further characterized by powder diffraction, thermoanalytical (TG/DTA, DSC and thermomicroscopy) and spectroscopic (IR, Raman, ¹³C CP/MAS NMR) methods. peerReviewed

crystal formChemistrypolymorfiaGeneral ChemistryCondensed Matter PhysicssolvaattipolymorphismSolventCrystallographysymbols.namesakekidemuotosolvatePolymorphism (materials science)symbolsScreening methodThiophanate-methylGeneral Materials ScienceDesolvationRaman spectroscopySingle crystalPowder diffractionCrystEngComm
researchProduct

The first copper(I)-olefin complexes bearing a 1,3,4-oxadiazole core: Alternating-current electrochemical crystallization, X-ray experiment and DFT s…

2017

By means of alternating-current electrochemical technique, four new π-complexes, namely [Cu2(C11H10N2OS)2Br1.91Cl0.09] (1), [Cu(C11H10N2OS)NO3] (2), [Cu2(C11H10N2OS)2(H2O)2](BF4)2 (3) and [Cu2(C11H10N2OS)2(H2O)2](ClO4)2 (4), were obtained using copper(II) salts and the 2-(allylthio)-5-phenyl-1,3,4-oxadiazole (C11H10N2OS) ligand. The metal and halogen centers in 1 form Cu2X2 dimers; the N-atom from the oxadiazole ring and the Cdouble bond; length as m-dashC bond of the allyl group from the same ligand complete the copper coordination environment, giving [Cu(C11H10N2OS)X]2 isolated fragments. The ligand plays the same chelating role in 2, whereas the O (NO3) atom occupies the third position i…

crystal structure3Stereochemistry1chemistry.chemical_elementOxadiazolekupariCrystal structure134-oxadiazole derivatives4-oxadiazole derivatives010402 general chemistryElectrochemistryRing (chemistry)DFT01 natural sciencesolefinpi-complexInorganic ChemistryMetalchemistry.chemical_compoundraman spectroscopyMaterials ChemistryMoleculePhysical and Theoretical Chemistryta116010405 organic chemistryLigandac-electrochemical techniquekompleksiyhdisteetCoppercopper(I)0104 chemical sciencesCrystallographychemistryvisual_artvisual_art.visual_art_mediumPolyhedron
researchProduct

Synthesis and self-assembly of a PEGylated-graphene aerogel

2016

Abstract In the frame of this work, we present, for the first time, the synthesis and self-assembly of an aerogel built by graphene oxide-polyethylene glycol. The synthetic route involves at first the coupling of GO with an amino-terminated polyethylene glycol sample by carbodiimide in aqueous environment, and the subsequent conversion of the hydrogel achieved into an aerogel via freeze-drying. The 3D PEGylated graphene-based aerogel, characterized by spectroscopic, morphological, structural and mechanical analyses, displays an ultralight and highly porous (99.7%) network and possesses high mechanical properties together with a good biocompatibility.

del-assemblyMaterials sciencesynthesisBiocompatibility02 engineering and technologyPolyethylene glycol010402 general chemistry01 natural scienceslaw.inventionchemistry.chemical_compoundEngineering (all)lawHighly porousB.Stress/strain curveD.Raman spectroscopycharacterizationComposite materialGraphene oxideCarbodiimidePEGylated-grapheneAqueous solutionGraphenetechnology industry and agricultureGeneral EngineeringAerogel021001 nanoscience & nanotechnologyB.Porosity/void0104 chemical scienceschemistryCeramics and CompositesSelf-assembly0210 nano-technologyA.Functional compositeComposites Science and Technology
researchProduct