Search results for "Measurements"

showing 10 items of 720 documents

Synthesis of Soluble Donor-Acceptor Double-Cable polymers based on polythiophene and tetracyanoanthraquinodimethane (TCAQ).

2003

[structure: see text] Novel suitably functionalized tetracyanoanthraquinodimethane (TCAQ) derivatives covalently linked to thiophene moieties have been synthesized. The thiophene-based monomers have been chemically polymerized and copolymerized to yield new and soluble donor-acceptor double-cable polymers. The absorption and emission data reveal that the optical properties can be finely tuned by modifying the ratio of monomers in the copolymerization process.

Magnetic Resonance SpectroscopyFotoricettoriPolymersAnthraquinonesThiophenesmacromolecular substancesBiochemistryIndicators and Reagentchemistry.chemical_compoundSpettroscopiaThiophenePolymer chemistryCopolymerThiophenePhysical and Theoretical ChemistryPolymerPolimerichemistry.chemical_classificationOrganic Chemistrytechnology industry and agriculturePolymerSettore CHIM/06 - Chimica OrganicaMonomerchemistryPolymerizationCovalent bondLuminescent MeasurementLuminescent MeasurementsPolythiopheneMolecular MedicineAnthraquinoneIndicators and ReagentsSpectrophotometry UltravioletAbsorption (chemistry)Celle solariSintesi
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Acylated triterpene saponins from Silene jenisseensis

1995

Abstract From the roots of Silene jenisseensis a new trans-p-methoxycinnamoyl triterpene saponin has been isolated along with its cis-p-methoxycinnamoyl isomer as an inseparable mixture. Their structures were established by chemical means and spectroscopic methods including 1D- and 2D-homonuclear and heteronuclear correlation NMR spectroscopy as 3-O-[β- d -galactopyranosyl -(1 → 2)-β- d -glucuronopyranosyl ]-28-O-[β- d -glucopyranosyl -(1 → 2)-α- l - rhamnopyranosyl -(1 → 2)-β- d -4-O-trans-p- methoxycinnamoyl-fucopyranosyl ] quillaic acid and its cis-isomer, respectively. They did not show any activity in the in vitro chemoluminescence granulocytes assay, but exhibited only a weak inhibito…

Magnetic Resonance SpectroscopyStereochemistryAcylationMolecular Sequence DataSaponinCaryophyllaceaePlant ScienceHorticulturePlant RootsBiochemistrylaw.inventionTriterpenelawCarbohydrate ConformationHumansMoleculeMedicine Chinese TraditionalOleanolic AcidMolecular BiologyChemiluminescencechemistry.chemical_classificationPlants MedicinalbiologyChemistryGeneral MedicineNuclear magnetic resonance spectroscopySaponinsbiology.organism_classificationTriterpenesIn vitroCarbohydrate SequenceHeteronuclear moleculeLuminescent MeasurementsGranulocytesPhytochemistry
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Triplet-triplet energy transfer controlled by the donor-acceptor distance in rigidly held palladium-containing cofacial bisporphyrins.

2005

Eleven new complexes, including mono-, heterobi-, and homobimetallic cofacial bisporphyrins, (Pd)H 2 DPS, (M)H 2 DPX, (M)H 2 DPB, (PdZn)DPS, (PdZn)DPX, (Pt) 2 DPX, (M) 2 DPB (M=Pd, Pt), and (Pt)P (DPS 4 - = 4,6-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]dibenzothiophene tetraanion, DPX 4 - = 4,5-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]-9,9-dimethylxanthene tetraanion, DPB 4 - =1,8-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]biphenylene tetraanion, P 2 - = 5-phenyl-2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrin dianion) have been synthesized and characterized. The photophysical properties of the donor (M)P (M=Pd or Pt, P= porphy…

Magnetic Resonance SpectroscopyStereochemistryMetalloporphyrinschemistry.chemical_elementCrystal structureThiophenesTriclinic crystal systemCrystallography X-RayCatalysischemistry.chemical_compoundReaction rate constantPlatinumMolecular StructureOrganic ChemistryFree baseGeneral ChemistryBiphenyleneAcceptorPorphyrinCrystallographyZincchemistryEnergy TransferXanthenesSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationLuminescent MeasurementsSpectrophotometry UltravioletPalladiumPalladiumChemistry (Weinheim an der Bergstrasse, Germany)
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Two polymorphs Ni(II) complexes containing the dicyanamide ligand: syntheses, structures and magnetic properties of {[Ni(meso-CTH)(μ1,5-dca)]ClO4}n a…

2004

Abstract Two polymorphs Ni(II) complexes {[Ni(meso-CTH)(μ1,5-dca)]ClO4}n (1) and [Ni(meso-CTH)][Ni(meso-CTH)(dca)2](ClO4)2 (2) have been obtained in the same synthesis from dicyanamide (dca) and [Ni(meso-CTH)](ClO4)2 and have been characterized by X-ray crystallography and magnetic measurements. Complex 1 is a 1D cationic polymeric zig-zag chain with single end-to-end dca bridges connecting Ni(II) ions in trans positions, whereas in compound 2 coexist two different types of Ni(II) mononuclear units, cationic square-planar and neutral octahedral. Variable-temperature magnetic measurements reveal weak ferromagnetic interactions across the single end-to-end dca bridges in 1, while for 2 the ma…

Magnetic measurements010405 organic chemistryLigandCationic polymerization010402 general chemistry01 natural sciences0104 chemical sciencesIonInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryFerromagnetismOctahedronMaterials ChemistryCyclotetradecanePhysical and Theoretical ChemistryDicyanamideInorganica Chimica Acta
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Adducts of organolead(IV) and organothallium(III) chlorides with N,N′-ethylenebis(salicylideneiminato)nickel(II) and bis(β-mercaptoethylamine)nickel(…

1974

Abstract Novel 1/1 adducts of organolead(IV) and organothallium(III) chlorides with the complexes N,N′-ethylenebis(salicylideneiminato)nickel(II) and bis(β-mercaptoethylamine)nickel(II) have been synthesized. Their configurations have been investigated in the solid state by IR and electronic spectroscopy and by magnetic measurements.

Magnetic measurementsChemistryOrganic ChemistryInorganic chemistrySolid-statechemistry.chemical_elementBiochemistryElectron spectroscopyAdductInorganic ChemistryNickelPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Complexes of organometallic compounds

1974

Abstract Novel 1/1 adducts have been obtained from the complex N , N ′-ethylenebis(salicylideneiminato)nickel(II) (NiSalen) with di- and mono-organotin(IV) chlorides, and their solid state configuration investigated by Mossbauer , IR and electronic spectroscopy and magnetic measurements. In coordinated NiSalen the square planar structure is maintained around Ni II , and the coordination to tin involves three-coordinate phenolic oxygens. The environment of Sn IV is judged to be octahedral in both types of compounds. A trans -R 2 , cis -Cl 2 configuration is advanced for R 2 SnCl 2 NiSalen.

Magnetic measurementsChemistryOrganic ChemistryInorganic chemistrychemistry.chemical_elementBiochemistryMedicinal chemistryElectron spectroscopyAdductInorganic ChemistryNickelOctahedronMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryTinGroup 2 organometallic chemistryJournal of Organometallic Chemistry
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Synthesis, crystal structure and magnetic properties of a novel heterobimetallic rhenium(IV)-dysprosium(III) chain.

2015

The use of the mononuclear rhenium(IV) precursor [ReBr5 (H2 pydc)](-) (H2 pydc=3,5-pyridinedicarboxylic acid) as a metalloligand towards dysprosium(III) afforded the first heterobimetallic Re(IV) -Dy(III) complex. Crystal structures and static and dynamic magnetic properties of both rhenium-containing species are reported herein. The 5d-4f compound shows an extended 1D structure and the AC magnetic measurements reveal frequency dependence at low temperature suggesting slow relaxation of the magnetization.

Magnetic measurementsChemistryOrganic ChemistryRelaxation (NMR)Inorganic chemistrychemistry.chemical_elementGeneral ChemistryFrequency dependenceCrystal structureRheniumCatalysisMagnetizationCrystallographyChain (algebraic topology)DysprosiumChemistry (Weinheim an der Bergstrasse, Germany)
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Magneto-structural correlations in dirhenium(iv) complexes possessing magnetic pathways with even or odd numbers of atoms

2017

The employment of pyrazine (pyz), pyrimidine (pym) and s-triazine (triz) ligands in ReIV chemistry leads to the isolation of a family of complexes of general formula (NBu4)2[(ReX5)2(μ-L)] (L = pyz, X = Cl (1) or Br (2); L = pym, X = Br (3); L = triz, X = Br (4)). 1-4 are dinuclear compounds where two pentahalorhenium(iv) fragments are connected by bidentate pyz, pym and triz ligands. Variable-temperature magnetic measurements, in combination with detailed theoretical studies, uncover the underlying magneto-structural correlation whereby the nature of the exchange between the metal ions is dictated by the number of intervening atoms. That is, the spin-polarization mechanism present dictates …

Magnetic measurementsDenticityPyrazinePyrimidine010405 organic chemistryChemistryStereochemistryLigandMetal ions in aqueous solution010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundFerromagnetismAntiferromagnetismDalton Transactions
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Pressure and Thermally Induced Spin Crossover in a 2D Iron(II) Coordination Polymer {Fe[bipy(ttr)2]}n

2021

Using magnetic measurements and UV -visible spectroscopy we have studied the pressure influence on the spin crossover (SCO) properties of the 2D Fe (II) coordination polymer formulated {Fe[bipy(ttr) 2 ]} n . At variable temperature and fixed pressure, we have measured the magnetic property of this compound. Under different pressures and at room temperature, the visible spectroscopy has been observed. The magnetic experiment displays a two-step spin crossover behavior under pressure. The visible spectroscopic measurements at room temperature show a spin crossover with an asymmetric hysteresis at 0.4GPa.

Magnetic measurementsMaterials scienceCoordination polymerAnalytical chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundHysteresisUltraviolet visible spectroscopychemistrySpin crossover0210 nano-technology2021 5th IEEE Electron Devices Technology & Manufacturing Conference (EDTM)
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Studying the reduction of graphene oxide with magnetic measurements

2019

Abstract The reduction of graphene oxide is one of the most facile methods to fabricate a large amount of graphene. The reduction rate is generally examined by various spectroscopic techniques, but each technique is applied for different purposes. Herein, we demonstrate the correlation between spectroscopic results and magnetic data, which plays an important role in determining the quality of reduced graphene oxides. The magnetic signals are related with the carbon-oxygen functional groups analyzed by spectroscopic tools. Especially, highly reduced sample exhibits the diamagnetic property similar to graphene-like materials. This report can provide an insight to determine the reduction rate …

Magnetic measurementsMaterials scienceGrapheneReduction rateOxideNanotechnology02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionReduction (complexity)chemistry.chemical_compoundchemistrylawDiamagnetismGeneral Materials Science0210 nano-technologyCarbon
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