Search results for "coordination complex"

showing 10 items of 381 documents

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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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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Self-assembly and alterable relaxivity of an organic cation-encapsulated gadolinium-containing polyoxometalate

2012

A new amphiphilic molecule bearing poly(ethylene oxide) (PEO) and quaternary ammonium group, was designed and synthesized to encapsulate paramagnetic Gd(III)-containing polyoxometalate (Gd-POM) through electrostatic interaction for obtaining a water-soluble organic-inorganic hybrid building block based on POM. The yielding organic cation-encapsulated Gd-POM (OCEP-Gd) complex exhibited water-solubility and amphiphility, leading to the spontaneous self-assembly into a regular vesicular structure with PEO chains towards water phase and POM units locating at the middle. The vesicular aggregate which has a regular monolayer structure, was further studied by means of dynamic light scattering, tra…

Magnetic Resonance Spectroscopyanimal structuresAqueous solutionMaterials scienceEthylene oxideStatic ElectricityContrast MediaWaterGadoliniumNanotechnologyTungsten CompoundsInorganic Chemistrychemistry.chemical_compoundX-Ray DiffractionChemical engineeringchemistryDynamic light scatteringCoordination ComplexesTransmission electron microscopyCationsPhase (matter)MonolayerPolyoxometalatesense organsSelf-assemblyDalton Transactions
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m-Carboranylphosphinate as Versatile Building Blocks To Design all Inorganic Coordination Polymers

2017

The first examples of coordination polymers of manganese(II) and a nickel(II) complex with a purely inorganic carboranylphosphinate ligand are reported, together with its exhaustive characterization. X-ray analysis revealed 1D polymeric chains with carboranylphosphinate ligands bridging two manganese(II) centers. The reactivity of polymer 1 with water and Lewis bases has also been studied Thanks to MINECO (CTQ2015-66143-P, CTQ2010-16237 and SEV-2015-0496), Generalitat de Catalunya (2014/SGR/149), and COST CM1302. E.O. who is enrolled in the PhD program of the UAB thanks for FPU grant

Manganese compoundsInorganic chemistrychemistry.chemical_elementManganese010402 general chemistry01 natural sciencesInorganic ChemistryPolymer chemistrycarboranylphosphinatecoordination complexesLewis acids and basesPhysical and Theoretical Chemistryta116polymerschemistry.chemical_classificationQuímica inorgànica010405 organic chemistryLigandPolymerChemistry Inorganic0104 chemical sciencesNickelManganès -- Compostoscoordination polymerschemistrymanganeseInorganic Chemistry
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Isomorphous replacement of MII ions in MII–GdIII dimers (MII = CuII, MnII, NiII, CoII, ZnII): magnetic studies of the products

2011

Complexes [M(II)Gd(III){pyCO(OEt)pyC(OH)(OEt)py}₃](ClO₄)₂·EtOH [M(II) = Cu(II) (1), Mn(II) (2), Ni(II) (3), Co(II) (4) and Zn(II) (5)] crystallize in the monoclinic Cc space group and contain one hexacoordinate M(II) ion and one enneacoordinate Gd(III) ion, bridged by three {pyCO(OEt)pyC(OH)(OEt)py}⁻ ligands. Magnetic susceptibility measurements indicate a ferromagnetic interaction for 1 and antiferromagnetic interactions for 2-4. Using the Ĥ = -JŜ(Gd(III))Ŝ(M(II)) spin Hamiltonian formalism, fits to the magnetic susceptibility data yielded J values of +0.32 cm⁻¹ for 1, -1.7 cm⁻¹ for 2, and -0.22 cm⁻¹ for 3. In complex 4, the orbital contributions of Co(II) precluded the determination of th…

ManganeseChemistryStereochemistryMolecular ConformationHexacoordinateSpin hamiltonianGadoliniumCobaltCrystallography X-RayMagnetic susceptibilityInductive couplingIonInorganic ChemistryMagneticsZincCrystallographyFerromagnetismCoordination ComplexesMetalsNickelAntiferromagnetismDimerizationCopperMonoclinic crystal systemDalton Transactions
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Exploring the Specificity of Rationally Designed Peptides Reconstituted from the Cell-Free Extract of Deinococcus radiodurans toward Mn(II) and Cu(II)

2020

A series of five rationally designed decapeptides [DEHGTAVMLK (DP1), THMVLAKGED (DP2), GTAVMLKDEH (Term-DEH), TMVLDEHAKG (Mid-DEH), and DEHGGGGDEH (Bis-DEH)] have been studied for their interactions with Cu(II) and Mn(II) ions. The peptides, constructed including the most prevalent amino acid content found in the cell-free extract of Deinococcus radiodurans (DR), play a fundamental role in the antioxidant mechanism related to its exceptional radioresistance. Mn(II) ions, in complex with these peptides, are found to be an essential ingredient for the DR protection kit. In this work, a detailed characterization of Cu(II) systems was included, because Cu(II)–peptide complexes have also shown r…

Manganesebiology010405 organic chemistryChemistryStereochemistryDeinococcus radioduransCell free010402 general chemistrybiology.organism_classification01 natural sciencesArticle0104 chemical sciencesInorganic ChemistryCoordination ComplexesDeinococcusPhysical and Theoretical ChemistryOligopeptidesCopperProtein BindingInorganic Chemistry
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Selective targeting of PARP-1 zinc finger recognition domains with Au(III) organometallics

2018

The binding of Au(iii) complexes to the zinc finger domain of the anticancer drug target PARP-1 was studied using a hyphenated mass spectrometry approach combined with quantum mechanics/molecular mechanics (QM/MM) studies. Competition experiments were carried out, whereby each Au complex was exposed to two types of zinc fingers. Notably, the cyclometallated Au-C^N complex was identified as the most selective candidate to disrupt the PARP-1 zinc finger domain, forming distinct adducts compared to the coordination compound Auphen.

Materials Chemistry2506 Metals and AlloysStereochemistryPoly ADP ribose polymeraseSurfaces Coatings and FilmCeramics and Composite010402 general chemistryMass spectrometry01 natural sciencesMolecular mechanicsCatalysisCoordination complexAdductCatalysiMaterials Chemistrychemistry.chemical_classificationZinc finger010405 organic chemistryElectronic Optical and Magnetic MaterialChemistry (all)Metals and AlloysGeneral ChemistryAnticancer drug0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistrySettore CHIM/03 - Chimica Generale E InorganicaCeramics and Composites2506
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Rational Design of Copper(II)-Uracil Nanoprocessed Coordination Polymers to Improve Their Cytotoxic Activity in Biological Media

2021

This work is focused on the rational structural design of two isostructural Cu(II) nano-coordination polymers (NCPs) with uracil-1-acetic acid (UAcOH) (CP1n) and 5-fluorouracil-1-acetic acid (CP2n). Suitable single crystals for ꭕ-ray diffraction studies of CP1 and CP2 were prepared under hydrothermal conditions, enabling their structural determination as 1D-CP ladder-like polymeric structures. The control of the synthetic parameters allows their processability into water colloids based on nanoplates (CP1n and CP2n). These NCPs are stable in water at physiological pHs for long periods. However, interestingly, CP1n is chemically altered in culture media. These transformations provoke the part…

Materials scienceCell SurvivalPolymersCytotoxicitychemistry.chemical_elementAntineoplastic Agentschemistry.chemical_compoundHydrolysisBiological mediaCoordination ComplexesCell Line TumorMoietyHumansGeneral Materials Science5-fluorouracilIsostructuralCytotoxicityUracilchemistry.chemical_classificationReactive oxygen speciesRational designUracilQuímicaCombinatorial chemistryCopperCoordination polymerschemistryNano-coordination polymersReactive Oxygen SpeciesCopper
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A novel 2D coordination network built from hexacopper(i)-iodide clusters and cagelike aminophosphine blocks for reversible “turn-on” sensing of anili…

2018

A new copper(I) coordination polymer [Cu6(μ3-I)6(μ3-PTAO)2]n (1) was prepared from copper(I) iodide and 1,3,5-triaza-7-phosphaadamantane-7-oxide (PTAO). The crystal structure of 1 reveals an intricate 2D coordination network constructed from the hexacopper(I)-iodide [Cu6(μ3-I)6] cluster units with the 4M6-1 topology interlinked by the μ3-PTAO spacers. An overall 2D layer network can be simplified to a binodal 3,6-connected net with the kgd topology. A derived 1@paper material was prepared by impregnating compound 1 onto a filter paper. Detailed investigation of the luminescence properties for 1 and 1@paper in the solid state revealed a remarkable ability of both materials to sense aniline m…

Materials scienceCoordination polymerIodideCrystal structure010402 general chemistryPhotochemistry01 natural scienceschemistry.chemical_compoundAnilineluminescenceMaterials ChemistryMoleculecoordination complexespolymeeritta116polymerschemistry.chemical_classificationBinodal010405 organic chemistryluminesenssikompleksiyhdisteetGeneral Chemistry0104 chemical sciencesCrystallographychemistryNaked eyeLuminescenceJournal of Materials Chemistry C
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Pressure effect investigations on spin-crossover coordination compounds

2018

International audience; The piezochromic properties of spin-crossover complexes have been recognized for a long time, with increasing pressure favouring the low spin state due to its smaller volume and therefore shifting the spin equilibrium towards higher temperatures and accelerating the relaxation at a given temperature. However, the interpretation and quantification of pressure-induced changes have been several times compromised by the relatively poor and incomplete spectral and structural information provided by the detection methods or due to the experimental difficulties related to the need for hydrostatic conditions at low temperatures. The present review is therefore primarily focu…

Materials scienceSpin statesGeneral Chemical Engineering02 engineering and technology010402 general chemistry01 natural scienceslaw.inventionCoordination complexlawSpin crossoverQD[CHIM.COOR]Chemical Sciences/Coordination chemistryHigh-pressure chemistrySpin-½chemistry.chemical_classificationRelaxation (NMR)General Chemistry021001 nanoscience & nanotechnologySpin crossover0104 chemical sciencesVolume (thermodynamics)chemistryChemical physicsHydrostatic equilibrium0210 nano-technologyPressure generation
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