Search results for " COMPLEXES"

showing 10 items of 818 documents

Gold nanostars co-coated with the Cu(II) complex of a tetraazamacrocyclic ligand

2015

The twelve-membered tetraazamacrocyclic ligand L1 bears an appended lipoic acid unit, whose disulphide ring is an efficient grafting moiety for the surface of gold nanostars (GNS). The GNS that were used featured a localized surface plasmon resonance (LSPR) absorption at ∼800 nm, i.e. in the near infrared (NIR). We investigated different approaches for coating them with the Cu(2+) complex of L1. While the direct reaction of [CuL1](2+) with as-prepared GNS led to aggregation, an initial coating step with polyethyleneglycol-thiol (PEG-SH) was found to be advantageous. Displacement reactions were carried out on pegylated GNS either with [CuL1](2+), directly generating [Cun(L1@GNS)](2n+), or wi…

LuminescenceLuminescent AgentsMacrocyclic CompoundsGole nanoparticelle Cooper macrocyclesStereochemistryChemistryKineticsMetal NanoparticlesPet imagingSurface Plasmon Resonanceengineering.materialPhotothermal therapyCyclamsInorganic ChemistryCrystallographyTransmetalationCoatingCoordination ComplexesHeterocyclic CompoundsengineeringMoietyGoldSurface plasmon resonanceLuminescenceCopper
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Anticancer Activity, Reduction Mechanism and G-Quadruplex DNA Binding of a Redox-Activated Platinum(IV)–Salphen Complex

2022

Aiming at reducing the unselective cytotoxicity of Pt(II) chemotherapeutics, a great deal of effort has been concentrated into the design of metal-containing drugs with different anticancer mechanisms of action. Inert Pt(IV) prodrugs have been proposed to be a valid alternative as they are activated by reduction directly into the cell releasing active Pt(II) species. On the other hand, a promising strategy for designing metallodrugs is to explore new potential biological targets rather than canonical B-DNA. G-quadruplex nucleic acid, obtained by self-assembly of guanine-rich nucleic acid sequences, has recently been considered an attractive target for anticancer drug design. Therefore, comp…

MDPt(IV) complexesOrganic ChemistryAntineoplastic AgentsDNAGeneral MedicineDFTPt(IV) complexes; G-quadruplex; DFT; MDCatalysisComputer Science ApplicationsG‐quadruplexG-QuadruplexesInorganic ChemistrySettore CHIM/03 - Chimica Generale E InorganicaProdrugsPhysical and Theoretical ChemistryOxidation-ReductionMolecular BiologySpectroscopyPlatinumInternational Journal of Molecular Sciences
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Kinetics of Insulin Aggregation: Disentanglement of Amyloid Fibrillation from Large-Size Cluster Formation

2006

Kinetics of human insulin aggregation has been studied at pH 1.6 and 60 degrees C, when amyloid fibrils are formed. We developed a novel approach based on the analysis of scattered light intensity distribution, which allows distinguishing between small and large size aggregates. By this method, we observed an exponential growth of fibrillar aggregates implying a heterogeneous aggregation mechanism. Also, the apparent lag time observed, correlated with the major increase of thioflavin T fluorescence, has been assigned to the onset of large size cluster formation.

MECHANISMModels MolecularAmyloidAmyloidmedicine.medical_treatmentKineticsBiophysicschemistry.chemical_compoundExponential growthFIBRILSmedicineCluster (physics)HumansInsulinComputer SimulationBenzothiazolesParticle SizeATOMIC-FORCE MICROSCOPYInsulinPATHWAYSProteinsFluorescenceLIGHT-SCATTERINGCrystallographyKineticsThiazoleschemistryModels ChemicalMultiprotein ComplexesBiophysicsThioflavinParticle sizeBETA-PROTEINNUCLEATIONBiophysical Journal
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Antigen-processing machinery breakdown and tumor growth.

2000

Defects in the major histocompatibility complex (MHC) class I antigen-processing machinery (APM) have been described in tumors of different histology. Murine data suggest that defects in the MHC class II APM might also be associated with malignant transformation of human cells. This article describes the pathophysiology of the MHC class I and II APM, reviews APM abnormalities in tumor cells and discusses their role in the escape of tumor cells from in vitro recognition by T cells.

MHC class IIAntigen PresentationProteasome Endopeptidase ComplexbiologyAntigen processingImmunologyAntigen presentationHistocompatibility Antigens Class IHistocompatibility Antigens Class IIATP-binding cassette transporterMajor histocompatibility complexIn vitroMalignant transformationCysteine EndopeptidasesATP Binding Cassette Transporter Subfamily B Member 3Multienzyme ComplexesNeoplasmsMHC class IImmunologybiology.proteinCancer researchAnimalsHumansATP-Binding Cassette TransportersImmunology today
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Coordination networks incorporating halogen-bond donor sites and azobenzene groups

2016

Two Zn coordination networks, {[Zn(1)(Py)2]2(2-propanol)}n (3) and {[Zn(1)2(Bipy)2](DMF)2}n (4), incorporating halogen-bond (XB) donor sites and azobenzene groups have been synthesized and fully characterized. Obtaining 3 and 4 confirms that it is possible to use a ligand wherein its coordination bond acceptor sites and XB donor sites are on the same molecular scaffold (i.e., an aromatic ring) without interfering with each other. We demonstrate that XBs play a fundamental role in the architectures and properties of the obtained coordination networks. In 3, XBs promote the formation of 2D supramolecular layers, which, by overlapping each other, allow the incorporation of 2-propanol as a gues…

MOF Supramolecular Chemistry Halogen Bonding AzobenzeneStereochemistry116 Chemical sciencesSupramolecular chemistry02 engineering and technology010402 general chemistryRing (chemistry)01 natural sciencesIUPAC RECOMMENDATIONS 2013chemistry.chemical_compoundMETAL-ORGANIC FRAMEWORKSdell'Università e della RicercaCHEMISTRYTO-CRYSTAL ISOMERIZATIONMinistero dell'IstruzioneMoleculeGeneral Materials Scienceta215SUPRAMOLECULAR SYNTHESISHalogen bondMETAL-ORGANIC FRAMEWORKS; IUPAC RECOMMENDATIONS 2013; TO-CRYSTAL ISOMERIZATION; SUPRAMOLECULAR SYNTHESIS; VISIBLE-LIGHT; POLYMERS; FLUOROAZOBENZENES; COCRYSTALS; COMPLEXES; CHEMISTRYLigandChemistryFLUOROAZOBENZENESMinistero dell'Istruzione dell'Università e della RicercaGeneral ChemistryCOCRYSTALS021001 nanoscience & nanotechnologyCondensed Matter PhysicsAcceptor0104 chemical sciencesCrystallographyAzobenzeneMIURMetal-organic frameworkCOMPLEXESSettore CHIM/07 - Fondamenti Chimici Delle TecnologieVISIBLE-LIGHTPOLYMERS0210 nano-technology
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Holmium(III) Single-Ion Magnet for Cryomagnetic Refrigeration Based on an MRI Contrast Agent Derivative

2021

The coexistence of field-induced blockage of the magnetization and significant magnetocaloric effects in the low-temperature region occurs in a mononuclear holmium(III) diethylenetriamine-N,N,N′,N″,N″-pentaacetate complex, whose gadolinium(III) analogue is a commercial MRI contrast agent. Both properties make it a suitable candidate for cryogenic magnetic refrigeration, thus enlarging the variety of applications of this simple class of multifunctional molecular nanomagnets.

MRI contrast agentGadoliniumCommunicationMagnetic PhenomenaRefrigerationchemistry.chemical_elementPentetic AcidInorganic ChemistryCold TemperatureMagnetizationchemistry.chemical_compoundHolmiumNuclear magnetic resonancechemistryCoordination ComplexesRefrigerationMagnetMagnetic refrigerationMagnetsPhysical and Theoretical ChemistryHolmiumDerivative (chemistry)Inorganic Chemistry
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New Magnetic Thin Film Hybrid Materials Built by the Incorporation of Octanickel(II)-oxamato Clusters Between Clay Mineral Platelets

2011

We report on a new method based on the combination of Langmuir-Schaefer deposition with self-assembly to insert highly anisotropic Ni(8) molecules in a hybrid organic-inorganic nanostructure. Spectroscopic, crystallographic, and magnetic data prove the successful insertion of the guest cationic molecule between templating clay platelets. These results open a new route toward the highly controlled fabrication of tailored functional organic-inorganic nanomaterials.

MULTIPLET STRUCTURENanostructureFabricationNICKELCationic polymerizationchemistry.chemical_elementNanotechnologyCrystal structureDINICKEL(II) COMPLEXESNanomaterialsMOLECULESNickelchemistryMoleculeCRYSTAL-STRUCTURECOREGeneral Materials ScienceVACANCY LEVELSPhysical and Theoretical ChemistryHybrid materialSPIN-EXCHANGEThe Journal of Physical Chemistry Letters
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Magnetic exchange interactions in the heteropoly complexes [M4(H2O)2(PW9O34)2]10− [M=Co(II) and Cu(II)]

1990

The magnetic properties of the heteropolyanions [M4(H2O)2(PW9O34)2]10− [M=Co(II) and Cu(II)] down to 4 K are reported. Their individual heteropoly molecules contain a rhomblike arrangement formed by four coplanar MO6 octahedra sharing edges. The magnetic properties support an intramolecular ferromagnetic exchange in the Co(II) tetramer, and antiferromagnetic exchange in the Cu(II) tetramer. These behaviors are discussed assuming anisotropic exchange in the Co(II) compound, and Heisenberg exchange in the Cu(II) compound. Carlos.Gomez@uv.es

Magnetic PropertiesExchange InteractionsGeneral Physics and AstronomyCopper ComplexesAntiferromagnetismTetramerVery Low TemperatureAntiferromagnetismMoleculeAnisotropy:FÍSICA::Química física [UNESCO]Cobalt Complexes ; Copper Complexes ; Heteropolyanions ; Magnetic Properties ; Exchange Interactions ; Ferromagnetism ; Antiferromagnetism ; Anisotropy ; Heisenberg Model ; Ultralow Temperature ; Very Low TemperatureCondensed matter physicsChemistryHeisenberg modelUltralow TemperatureUNESCO::FÍSICA::Química físicaCrystallographyOctahedronFerromagnetismIntramolecular forceFerromagnetismHeisenberg ModelAnisotropyCobalt ComplexesHeteropolyanions
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Circumdatin H, a new inhibitor of mitochondrial NADH oxidase, from Aspergillus ochraceus

2005

Circumdatin H (1), a new alkaloid from the culture broth of Aspergillus ochraceus, has been isolated, together with a known circumdatin, circumdatin E (2) and other known compounds: flavacol (3) and stephacidin A (4). The structure of 1 was established on the basis of chemical and spectral evidence. All of these alkaloids showed biological activity as inhibitors of the mammalian mitochondrial respiratory chain.

Magnetic Resonance SpectroscopyChemical PhenomenaSpectrophotometry InfraredStereochemistryCircumdatin HMass SpectrometryElectron Transportchemistry.chemical_compoundMultienzyme ComplexesDrug Discoveryheterocyclic compoundsNADH NADPH OxidoreductasesEnzyme InhibitorsPharmacologyAspergillus ochraceusBenzodiazepinonesbiologyChemistry PhysicalAlkaloidStephacidinBiological activityGeneral Medicinebiology.organism_classificationMitochondriaCircumdatin EMitochondrial respiratory chainchemistryBiochemistryFermentationNADH oxidaseSpectrophotometry UltravioletAspergillus ochraceus
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Methylresorcinarene: a reaction vessel to control the coordination geometry of copper(II) in pyridine N-oxide copper(II) complexes

2015

Pyridine and 2-picolinic acid N-oxides form 2 : 2 and 2 : 1 ligand : metal (L : M) discrete L2M2 and polymeric complexes with CuCl2 and Cu(NO3)2, respectively, with copper(ii) salts. The N-oxides also form 1 : 1 host-guest complexes with methylresorcinarene. In combination, the three components form a unique 2 : 2 : 1 host-ligand-metal complex. The methylresorcinarene acts as a reaction vessel/protecting group to control the coordination of copper(ii) from cis-see-saw to trans-square planar, and from octahedral to square planar coordination geometry. These processes were studied in solution and in the solid state via(1)H NMR spectroscopy and single crystal X-ray diffraction.

Magnetic Resonance SpectroscopyPyridinesmethylresorcinareneInorganic chemistrychemistry.chemical_elementPyridine-N-oxideNuclear magnetic resonance spectroscopyCopperInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryOctahedronX-Ray DiffractionCoordination ComplexesPyridinecopper complexesCalixarenesProtecting groupSingle crystalta116CopperCoordination geometryDalton Transactions
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