Search results for "Molecular Magnetism"

showing 10 items of 12 documents

Revisiting the thiosemicarbazonecopper(II) reaction with glutathione. Activity against colorectal carcinoma cell lines.

2018

Thiosemicarbazones (TSCs), and their copper derivatives, have been extensively studied mainly due to the potential applications as antitumor compounds. A part of the biological activity of the TSC-CuII complexes rests on their reactivity against cell reductants, as glutathione (GSH). The present paper describes the structure of the [Cu(PTSC)(ONO2)]n compound (1) (HPTSC =pyridine-2-carbaldehyde thiosemicarbazone) and its spectroscopic and magnetic properties. ESI studies performed on the reaction of GSH with 1 and the analogous [{Cu (PTSC*)(ONO2)}2] derivative (2, HPTSC* =pyridine-2-carbaldehyde 4N-methylthiosemicarbazone) show the absence of peaks related with TSC-Cu-GSH species. However GS…

Aparato digestivo-EnfermedadesThiosemicarbazonesSpectrometry Mass Electrospray IonizationColorectal cancerColon carcinoma010402 general chemistryCrystallography X-RayThiosemicarbazone01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundColon carcinomaCell Line TumorSpectroscopy Fourier Transform InfraredmedicineHumansMolecular magnetismDigestive organs-DiseasesMolecular Structure010405 organic chemistryChemistryMyoglobinCytochromes cGlutathioneChemistry Inorganicmedicine.diseaseMolecular biologyGlutathioneQuímica inorgánica0104 chemical sciencesCell cultureDrug Screening Assays AntitumorColorectal NeoplasmsCopperJournal of inorganic biochemistry
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A step further in the comprehension of the magnetic coupling in gadolinium(III)-based carboxylate complexes

2013

Three new gadolinium(III) complexes of formula [Gd4(bta) 3(H2O)16]n·12nH2O (1), [Gd4(bta)3(H2O)12] n·18nH2O (2) and [Gd2(H 2bta)(bta)(H2O)2]n·4nH 2O (3) (H4bta = 1,2,4,5-benzenetetracarboxylic acid) have been synthesized and their structures determined by X-ray diffraction. 1 and 3 are three-dimensional compounds whereas 2 exhibits a two-dimensional structure. The ability of the bta4- to adopt different coordination modes accounts for these high dimensionalities although it precludes a rational structural design. The structures of 1-3 have in common the double oxo-carboxylate bridge between gadolinium(III) ions (μ-O: κ2O,O′) either as a discrete units (1 and 2) or as a chain (3) and one (3)…

DiffractionMetal–organic frameworksStereochemistryGadoliniumchemistry.chemical_elementMagneto–structural correlationsAtmospheric temperature rangeInductive couplingIonInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMaterials ChemistryAntiferromagnetismMetal-organic frameworkCarboxylatePhysical and Theoretical ChemistryMolecular magnetismGadolinium(III)Polyhedron 52: 321-332 (2013)
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Increased conductivity of a hole transport layer due to oxidation by a molecular nanomagnet

2008

Thin film transistors based on polyarylamine poly?N,N?-diphenyl-N,N ?bis?4-hexylphenyl?- ?1,1?biphenyl?-4,4?-diamine ?pTPD? were fabricated using spin coating in order to measure the mobility of pTPD upon oxidation. Partially oxidized pTPD with a molecular magnetic cluster showed an increase in mobility of over two orders of magnitude. A transition in the mobility of pTPD upon doping could also be observed by the presence of a maximum obtained for a given oxidant ratio and subsequent decrease for a higher ratio. Such result agrees well with a previously reported model based on the combined effect of dipolar broadening of the density of states and transport manifold filling. Peer Reviewed

Electron mobilityMaterials scienceOrganic compounds.Analytical chemistryDipolar broadeningGeneral Physics and AstronomySpin coatingHole mobilityElectronic density of statesConductivityOxidacióCompostos orgànicsElectrical resistivity and conductivity:FÍSICA [UNESCO]Molecular clustersOrganic compoundsOxidationDopingElectrical conductivityOxidation.Molecular nanomagnetMolecular magnetic clusterMolecular magnetism Nanostructured materialsSpin coatingDopingUNESCO::FÍSICAElectric conductivity.Thin film transistorsNanostructured materialsConductivitat elèctricaNanomagnet:Enginyeria electrònica::Microelectrònica [Àrees temàtiques de la UPC]Doping ; Electrical conductivity ; Electronic density of states ; Hole mobility ; Molecular clusters ; Molecular magnetism Nanostructured materials ; Organic compounds ; Oxidation ; Spin coating ; Thin film transistorsDensity of statesNanostructured materials.Hole transport layerMaterials nanoestructuratsOrder of magnitude
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Carbonyl Back-Bonding Influencing the Rate of Quantum Tunnelling in a Dysprosium Metallocene Single-Molecule Magnet.

2019

The isocarbonyl-ligated metallocene coordination polymers [Cp*2M(μ-OC)W(Cp)(CO)(μ-CO)]∞ were synthesized with M = Gd (1, L = THF) and Dy (2, no L). In a zero direct-current field, the dysprosium version 2 was found to be a single-molecule magnet (SMM), with analysis of the dynamic magnetic susceptibility data revealing that the axial metallocene coordination environment leads to a large anisotropy barrier of 557(18) cm–1 and a fast quantum-tunnelling rate of ∼3.7 ms. Theoretical analysis of two truncated versions of 2, [Cp*2Dy{(μ-OC)W(Cp)(CO)2}2]− (2a), and [Cp*2Dy(OC)2]+ (2b), in which the effects of electron correlation outside the 4f orbital space were studied, revealed that tungsten-to-…

Electronic correlation010405 organic chemistrymolecular magnetismchemistry.chemical_element010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryMagnetDysprosiumPhysical chemistrySingle-molecule magnetPhysical and Theoretical Chemistrysingle-molecule magnetsMetalloceneQuantum tunnellingPi backbondingInorganic chemistry
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Unveiling the Effect of Magnetic Noise in the Coherence of Single-Molecule Quantum Processors.

2019

Quantum bits (qubits) constitute the most elementary building-blocks of any quantum technology, where information is stored and processed in the form of quantum superpositions between discrete energy levels. In particular, the fabrication of quantum processors is a key long-term goal that will allow us conducting specific tasks much more efficiently than the most powerful classical computers can do. Motivated by recent experiments in which three addressable spin qubits are defined on a potential single-molecule quantum processor, namely the [Gd(H2O)P5W30O110]12− polyoxometalate, we investigate the decohering effect of magnetic noise on the encoded quantum information. Our state-of-the-art m…

Quantum decoherenceDephasingmolecular magnetism02 engineering and technology010402 general chemistry01 natural scienceslcsh:Chemistryquantum algorithmQuantum mechanicspolyoxometalateQuantum informationdecoherenceQuantumscalabilityQuantum computerOriginal ResearchPhysicsmolecular spin qubitsGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesQuantum technologyChemistrymolecular nanomagnetlcsh:QD1-999Qubitcoordination chemistryQuantum algorithm0210 nano-technologyFrontiers in chemistry
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Magnetic properties of vanadium(IV)-based extended systems: [(VO)3(μ-PO4)2(2,2′-bpy)(μ-OH2)]*1/3H2O and (VO)2H4P2O9

2013

International audience; The magnetic properties of [(VO)3(μ-PO4)2(2,2′-bpy)(μ-OH2)]1/3H2O (1) and (VO)2H4P2O9 (2), a tubular and a layered vanadium(IV) phosphates containing triply oxido bridged VIV dimers, are analyzed considering the Bleaney-Bowers S = 1/2 dimer model. In compound 1 the presence of an additional VIV connected with the VIV dimers through μ1,2-PO43− bridges is described with a Curie-Weiss type correction. This model reproduces the magnetic properties of compound 1 with g = 1.956, Jdim = −102.1 cm−1, θ = −0.4 cm−1 and Nα = 278 × 10−6 emu mol−1. In compound 2, the presence of a small percentage of paramagnetic impurity has to be considered to account for the divergence of χm …

StereochemistryDimermolecular magnetismVanadiumchemistry.chemical_elementVPO02 engineering and technology010402 general chemistry01 natural sciencesDFTInorganic ChemistryParamagnetismchemistry.chemical_compoundImpurityhybrid materialsMaterials ChemistryAntiferromagnetismPhysical and Theoretical Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographyMonomerchemistrySuperexchangevanadium0210 nano-technologyHybrid material
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Multiproperty complexes of 4d and 4f metal ions based on biomolecules: from fundamental research to potential applications

2023

El trabajo desarrollado en esta Tesis se enmarca en el campo de la Química de Coordinación y el Magnetismo Molecular, vectores base para el desarrollo de múltiples aplicaciones en Nanomedicina y Nanotecnología. El estudio de los compuestos de coordinación tiene una larga historia que se remonta a principios del siglo XIX, con notables contribuciones de químicos como Berzelius y Jørgensen. Esta rama de la química se centra en la comprensión de las propiedades de unión de los ligandos (moléculas o aniones donadores de electrones) a los iones metálicos. Las teorías de Alfred Werner sobre la coordinación de iones metálicos a principios del siglo XX marcaron un hito importante en este campo. El …

antitumoral activityapplicationsUNESCO::QUÍMICAmolecular magnetismcontrast agentbiosensorbiomoleculesSMMelectrochemistrymagnetismcoordination chemistrydysprosiumgadoliniumruthenium
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Coordination chemistry on surfaces through vapor phase processing: smart molecular/graphene heterostructures based on spin-crossover complexes and 2D…

2023

Los compuestos de coordinación están últimamente focalizando la atención de los investigadores en el campo de la nanociencia. Particular interés están generando aquellos compuestos con propiedades magnéticas de cara a su integración a la nanoescala en ramas como la electrónica y/o la espintrónica moleculares. Sin embargo, para su uso real en dispositivos destinados a estas aplicaciones, su procesabilidad es un requisito indispensable. En el marco de esta necesidad, la presente tesis doctoral se ha destinado al estudio del procesado sobre superficies mediante técnicas de fase gas de dos tipos distintos de compuestos de coordinación. Por tanto, el trabajo se ha dividido en dos partes. La prim…

chemistry on surfacesspin-crossoverUNESCO::QUÍMICAsublimable moleculesmolecular magnetismcoordination complexessmart heterostructurestwo-dimensional materialslayered coordination polymerschemical vapor deposition
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Communication between iron(II) building blocks in cooperative spin transition phenomena

2003

[EN] In the present article we discuss the cooperative nature of the spin crossover phenomenon in iron(II) complexes, providing a perspective of the state of the art in this area. The first aspect we discuss is the role of the intermolecular interactions, more precisely the ¿-interactions, in mononuclear complexes. We show that by playing with the nature of the ligands, aliphatic, aromatic, or extended aromatic, it is possible to create stronger cohesive forces and receive a more cooperative response from the compound. In the next step the singular family of bipyrimidine-bridged iron(II) dinuclear compounds is presented as the simplest example of polynuclear spin crossover complexes exhibit…

genetic structuresStereochemistryChemistryIntermolecular forceSupramolecular chemistrySpin transitionSpin transitionIron(II) complexesInorganic ChemistryChemical physicsSpin crossoverFISICA APLICADAIntramolecular forceMaterials ChemistryMolecular magnetismPhysical and Theoretical ChemistrySupramolecular chemistryTopology (chemistry)Curse of dimensionalityCoordination Chemistry Reviews
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Strong Exchange Coupling in a Trimetallic Radical-Bridged Cobalt(II)-Hexaazatrinaphthylene Complex.

2016

Reducing hexaazatrinaphthylene (HAN) with potassium in the presence of 18-c-6 produces [{K(18-c-6)}HAN], which contains the S=1/2 radical [HAN](.-) . The [HAN](.-) radical can be transferred to the cobalt(II) amide [Co{N(SiMe3 )2 }2 ], forming [K(18-c-6)][(HAN){Co(N'')2 }3 ]; magnetic measurements on this compound reveal an S=4 spin system with strong cobalt-ligand antiferromagnetic exchange and J≈-290 cm(-1) (-2 J formalism). In contrast, the Co(II) centres in the unreduced analogue [(HAN){Co(N'')2 }3 ] are weakly coupled (J≈-4.4 cm(-1) ). The finding that [HAN](.-) can be synthesized as a stable salt and transferred to cobalt introduces potential new routes to magnetic materials based on …

hexaazatrinaphthyleneCommunicationmagnetismnon-innocent ligandsradicalsMolecular MagnetismcobaltCommunicationsAngewandte Chemie (International ed. in English)
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