Search results for "Uv-Vi"

showing 10 items of 37 documents

Hydrogen bonding and proton transfer involving the trihydride complexes Cp*M(dppe)H 3 (M = Mo, W) and fluorinated alcohols: the competitive role of t…

2003

International audience; The protonation of complexes Cp*M(dppe)H3 (dppe is ethylenebis(diphenylphosphine), M = Mo (1), W (2)) by a variety of fluorinated alcohols of different acid strength (FCH2CH2OH, CF3CH2OH, (CF3)2CHOH, and (CF3)3COH) was investigated experimentally by the variable temperature spectroscopic methods (IR, NMR) and stopped-flow technique (UV-Vis). The structures of the hydrogen-bonded and proton transfer products were studied by DFT calculations. In agreement with the calculation results, the IR data suggest that the initial hydrogen bond is established with a hydride site for complex 1 and with the metal site for complex 2. However, no intermediate dihydrogen complex foun…

Hydrogen bondingTheoretical studyUv-vis NMR spectroscopyInorganic chemistryTransition metal polyhydridesInfrared spectroscopyProtonation010402 general chemistry01 natural sciencesProton transferMetalchemistry.chemical_compound[CHIM.COOR]Chemical Sciences/Coordination chemistrychemistry.chemical_classificationDiphenylphosphine010405 organic chemistryHydrogen bondChemistryHydrideGeneral Chemistry0104 chemical sciencesCrystallographyAcid strengthvisual_artvisual_art.visual_art_mediumIRDihydrogen complex
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Ethane-Bridged Zinc-Porphyrin Dimers in Langmuir-Shäfer Thin Films: Structural and Spectroscopic Properties

2006

This work reports on the structural and spectroscopic properties of ethane-bridged Zn porphyrin dimers (1) in Langmuir-Scha¨fer (LS) thin films by combining scanning force microscopy (SFM) with film balance, UV-vis absorption, fluorescence, and nanosecond laser flash photolysis measurements. Results show that depending on the surface pressure the Langmuir films of pure 1 can be arranged in two different condensed phases, whereas SFM of the LS films shows characteristic fractal networks constituted by nanoscopic aggregates. The spectral findings agree with a picture in which 1 is apparently present in the anti conformation but aggregated in a sort of H-type structure whose optical features r…

LangmuirPorphyrinsLangmuir-Schaefer filmPhotochemistryporphyrin dimerPorphyrinSurfaces Coatings and Filmscircular dichroismchemistry.chemical_compoundCrystallographychemistryUltrafast laser spectroscopyMaterials ChemistryArachidic acidFlash photolysisPhysical and Theoretical ChemistryAbsorption (chemistry)Thin filmChiralityUV-vis absorptionConformational isomerismfluorescence and nanosecond laser flash photolysis measurements
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Novel Lipophilic Lanthanide Bis-Phthalocyanines Functionalized by Pentadecylphenoxy Groups: Synthesis, Characterization and UV-Photostability

2012

Novel sandwich-type phthalocyanines containing a rare earth metal core (Pr, Nd, Eu-Lu) and macrocycles peripherally substituted by pentadecylphenoxy groups were synthesized using a cardanol-based phthalonitrile precursor and the respective lanthanide acetate. Additionally, the metal free-base analog compound was studied for comparison. The purified reaction products were all found to be thick and viscous substances at room temperature, showing liquid crystalline behavior with a distinct increase in fluidity at ca. 40 ° C. The complexes are readily soluble in chloroalkyl solvents and dissolve fairly well in DMF with some tendency to form aggregates. Besides they are strongly hydrophobic and …

LanthanideIndolesMagnetic Resonance SpectroscopyUltraviolet Rayslanthanide bis-phthalocyaninePharmaceutical ScienceIsoindolesPhotochemistryphotostabilityLanthanoid Series ElementsArticleAnalytical Chemistrylcsh:QD241-441Phthalonitrilechemistry.chemical_compoundUltraviolet visible spectroscopylcsh:Organic chemistrylanthanide bis-phthalocyanines; cardanol; UV-Vis spectroscopy; photostabilityDrug DiscoverycardanolPhysical and Theoretical ChemistryPhotodegradationlanthanide bis-phthalocyaninesDichloromethaneCardanolPhotolysisMolecular StructureOrganic ChemistryUV-Vis spectroscopychemistryChemistry (miscellaneous)Molecular MedicineDimethylformamideAbsorption (chemistry)Molecules
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Hydrogen bond-mediated conjugates involving lanthanide diphthalocyanines and trifluoroacetic acid (Lnpc2@TFA): Structure, photoactivity, and stability

2020

The interaction between lanthanide diphthalocyanine complexes, LnPc2 (Ln = Nd, Sm, Eu, Gd, Yb, Lu

LanthanideTFA conjugatePharmaceutical Science010402 general chemistryPhotochemistryphotostability01 natural sciencessinglet oxygenAnalytical Chemistrylcsh:QD241-441lanthanide diphthalocyanineschemistry.chemical_compoundUV-Vis spectralcsh:Organic chemistryTFA conjugatesDrug DiscoveryTrifluoroacetic acidMoleculePhysical and Theoretical Chemistrylanthanide diphthalocyanine010405 organic chemistryHydrogen bondSinglet oxygenOrganic Chemistryphoton upconversionChromophore0104 chemical scienceschemistryChemistry (miscellaneous)PhthalocyanineMolecular MedicineDensity functional theoryMolecules
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Spectroscopic characterization of non-covalent CuPc-GO system. Experiment and theory

2019

Abstract In this study we report on UV-vis, IR and Raman studies of non-covalent copper phthalocyanine (CuPc) – flake graphene oxide (GO) complex in water and in the solid phase. Experimental results were supported by molecular modeling of structure, electronic and vibrational parameters for free CuPc and its 1 : 1 complexes with water, benzene, phenol, neutral and deprotonated benzoic acid. HOMO-LUMO gaps for these complexes were calculated and compared with data derived from the absorption edge of Q-band in the recorded UV-vis spectra for free CuPc and its adduct with GO in water. Small but non-negligible changes in position of spectral bands observed as result of CuPc interaction with GO…

Materials scienceNon-covalent complexOxidechemistry.chemical_elementMolecular modeling02 engineering and technology010402 general chemistry01 natural sciencesSpectral lineEglaw.inventionchemistry.chemical_compoundsymbols.namesakelawGeneral Materials ScienceBenzeneGrapheneCuPc-GOUV-VIS021001 nanoscience & nanotechnologyCondensed Matter PhysicsCopper0104 chemical scienceschemistryAbsorption edgeRaman spectroscopysymbolsIRPhysical chemistryDensity functional theory0210 nano-technologyRaman spectroscopyMaterials Chemistry and Physics
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Reaction of 3-Amino-1,2,4-Triazole with Diethyl Phosphite and Triethyl Orthoformate: Acid-Base Properties and Antiosteoporotic Activities of the Prod…

2017

The reaction of diethyl phosphite with triethyl orthoformate and a primary amine followed by hydrolysis is presented, and the reaction was suitable for the preparation of (aminomethylene)bisphosphonates. 3-Amino-1,2,4-triazole was chosen as an interesting substrate for this reaction because it possesses multiple groups that can serve as the amino component in the reaction-namely, the side-chain and triazole amines. This substrate readily forms 1,2,4-triazolyl-3-yl-aminomethylenebisphosphonic acid (compound 1) as a major product, along with N-ethylated bisphosphonates as side products. The in vitro antiproliferative effects of the synthesized aminomethylenebisphosphonic acids against J774E m…

Models Molecularorganophosphorus chemistryPhosphitesBase (chemistry)FormatesTriazoleMolecular ConformationPharmaceutical ScienceOsteoclastsApoptosis010402 general chemistry01 natural sciencesAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundHydrolysisMicelcsh:Organic chemistryCell Line TumorDrug DiscoveryOrganic chemistryAnimals3-Amino-124-triazolePhysical and Theoretical Chemistrycrystallographychemistry.chemical_classificationBone Density Conservation AgentsDiphosphonates010405 organic chemistryChemistryCommunicationOrganic ChemistrySubstrate (chemistry)Triazolesthree-component reactionTriethyl orthoformateUV-Vis spectroscopyMagnetic Resonance Imaging0104 chemical sciencesP-containing drugstriazoleChemistry (miscellaneous)potentiometryaminomethylenebisphosponatesMolecular Medicineanti-proliferative activityAmine gas treatingpH-titrationbisphosphonic acidsMolecules (Basel, Switzerland)
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Use of Spectroscopic Techniques to Monitor Changes in Food Quality during Application of Natural Preservatives: A Review

2020

Publisher's version (útgefin grein)

PreservativeantioxidantPhysiologyClinical Biochemistryedible filmsReview01 natural sciencesBiochemistryRamanmedia_common2. Zero hungerPhysicsFood preservation04 agricultural and veterinary sciences040401 food scienceEdible filmsAndoxunarefniEssential oilsFlúrljómunMatvælifluorescenceAntioxidant2301 Química Analíticamedia_common.quotation_subjectessential oils ; fluorescence ; UV-Vis spectroscopy ; Fourier transform infrared ; Raman ; edible films ; shelf-life ; antioxidant ; antimicrobialShelf lifeNatural (archaeology)FluorescenceLitrófsgreining0404 agricultural biotechnologyFourier transform infrared3309.13 Conservación de AlimentosQuality (business)Molecular Biologyessential oilsShelf-lifeConsumer demand010401 analytical chemistrylcsh:RM1-9503309.90 Microbiología de AlimentosCell BiologyBiopreservationUV-Vis spectroscopy0104 chemical sciencesshelf-lifelcsh:Therapeutics. PharmacologyantimicrobialAntimicrobialBiochemical engineeringFood qualityAntioxidants
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Is Acetaldehyde a substance of abuse? Evidence from a free-access, three-bottle choice paradigm

2012

At present, neuroscience literature dealing with Acetaldehyde (ACD), ethanol first metabolite, as a drug of abuse, reported conditioned taste aversion paradigm and conditioned place preference, following ICV or i.p. administration. No reports exist on ACD oral self-administration probably because of its high volatility. For this reason, this pilot study was aimed at the evaluation of ACD concentration in aqueous solutions, and consequently to the rat drinking behaviour when acetaldehyde was presented in a free-access paradigm together with water and a sweet solution. Preliminarly we investigated the loss of ACD content in aqueous standard solutions. For the investigation of ACD concentratio…

Settore CHIM/09 - Farmaceutico Tecnologico ApplicativoSettore BIO/14 - FarmacologiaAcetaldehyde Addiction Three bottle choice UV-Vis Analysis
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Boron doping of silicon rich carbides: Electrical properties

2013

Boron doped multilayers based on silicon carbide/silicon rich carbide, aimed at the formation of silicon nanodots for photovoltaic applications, are studied. X-ray diffraction confirms the formation of crystallized Si and 3C-SiC nanodomains. Fourier Transform Infrared spectroscopy indicates the occurrence of remarkable interdiffusion between adjacent layers. However, the investigated material retains memory of the initial dopant distribution. Electrical measurements suggest the presence of an unintentional dopant impurity in the intrinsic SiC matrix. The overall volume concentration of nanodots is determined by optical simulation and is shown not to contribute to lateral conduction. Remarka…

Silicon nanodotMaterials scienceSiliconSilicon dioxideBoron dopingInorganic chemistrychemistry.chemical_elementSilicon carbide02 engineering and technologySettore ING-INF/01 - Elettronica7. Clean energy01 natural sciencesSettore FIS/03 - Fisica Della MateriaCarbidechemistry.chemical_compoundUV-vis reflection and transmittanceMultilayer0103 physical sciencesSilicon carbideGeneral Materials ScienceElectrical measurementsSilicon rich carbide010302 applied physicsDopantbusiness.industryMechanical EngineeringDopingFourier transform infrared spectroscopySilica021001 nanoscience & nanotechnologyCondensed Matter PhysicsSilicon richOptical propertieElectrical transportchemistryMechanics of MaterialsUV-vis reflection and transmittance Doping (additives)Boron-dopingOptoelectronicsElectric propertieNanodot0210 nano-technologybusinessX ray diffraction Boron carbideMaterials Science and Engineering: B
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Synthesis, UV/vis, FT-IR and Mössbauer spectroscopic characterization and molecular structure of the Bis[4-(2-aminoethyl)morpholine](tetrakis(4-metox…

2016

International audience; The synthesis, the UV-visible, FT-IR and Mossbauer spectroscopy and the crystal structure characterizations of the bis[4-(2-Aminoethyl)morpholine]tetrakis(4-metoxyphenyl)porphy-rinato)iron(II) complex are described. The title compound crystallizes in the triclinic, space group P-1, with a = 11.1253(4) angstrom, b = 11.2379(4) angstrom, c = 11.5488(4) angstrom, alpha = 72.304(2)degrees, beta = 86.002(2)degrees gamma = 72.066(2)degrees, V = 1308.28(8) angstrom(3), Z = 1. The Mossbauer data are consistent with an iron(II) low-spin (S = 0) porphyin species. The spin-state is confirmed by the value of the average equatorial iron-nitrogen pyrrole distance (Fe-Np = 1.988(2)…

Supramolecular chemistry02 engineering and technologyCrystal structureTriclinic crystal system010402 general chemistryspin01 natural sciencesUV-visible[ CHIM ] Chemical SciencesAnalytical ChemistryInorganic ChemistryMossbauerchemistry.chemical_compoundMorpholineMössbauer spectroscopy[CHIM]Chemical SciencesSpectroscopyPyrroleHydrogen bondOrganic Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesX-ray diffractionCrystallographychemistryIron porphyrin complexX-ray crystallography0210 nano-technologycrystal-structures
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