Search results for " COMPLEXES"

showing 10 items of 818 documents

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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A novel dimer of oxo-di(acetato)-bridged manganese(III) dimers complex of potential biological significance

2000

[EN] Assembly of the tetranuclear oxomanganese(III) acetato cluster [Mn4O2(O2CMe)(7)(phen)(2)](BF4) from the dinuclear oxo-di(acetato)bridged manganese(III) species [Mn2O(O2CMe)(2)(H2O)(2)(phen)(2)](BF4)(2) . 3H(2)O in aqueous/acetic acid MeOH solution occurs via the new 'dimer of dimers' Mn-III complex [Mn2O(O2CMe)(3)(H2O)(phen)(2)](BF4) . MeOH possesing an unprecedent [Mn-4(mu-O)(2)(mu-O2Me)(4) (mu-(OH2O2CMe)-O-...)(2)] core.

ManganeseAqueous solutionStereochemistryCarboxylato complexesDimerchemistry.chemical_elementCrystal structureManganeseInorganic Chemistrychemistry.chemical_compoundAcetic acidN ligandsO ligandschemistryBiological significanceFISICA APLICADACrystal structuresMaterials ChemistryPhysical and Theoretical ChemistryCluster compounds
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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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Hierarchical Self-Assembly of Halogen-Bonded Block Copolymer Complexes into Upright Cylindrical Domains

2017

Summary Self-assembly of block copolymers into well-defined, ordered arrangements of chemically distinct domains is a reliable strategy for preparing tailored nanostructures. Microphase separation results from the system, minimizing repulsive interactions between dissimilar blocks and maximizing attractive interactions between similar blocks. Supramolecular methods have also achieved this separation by introducing small-molecule additives binding specifically to one block by noncovalent interactions. Here, we use halogen bonding as a supramolecular tool that directs the hierarchical self-assembly of low-molecular-weight perfluorinated molecules and diblock copolymers. Microphase separation …

Materials scienceBlock copolymerGeneral Chemical Engineering116 Chemical sciencesSupramolecular chemistryNanotechnologyblock copolymer02 engineering and technologyhierarchical self-assembly010402 general chemistry01 natural sciencesBiochemistryMicelleArticleSDG9: Industry innovation and infrastructuresupramolecular complexesMaterials ChemistryCopolymerEnvironmental ChemistryNon-covalent interactionsMoleculeLamellar structureta116chemistry.chemical_classificationHalogen bondta114Biochemistry (medical)General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesblock copolymerschemistryChemical engineeringIndustry innovation and infrastructure [SDG9]nanofabricationhalogen bondSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelf-assembly0210 nano-technology
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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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Photoalignment and Surface-Relief-Grating Formation are Efficiently Combined in Low-Molecular-Weight Halogen-Bonded Complexes

2012

It is demonstrated that halogen bonding can be used to construct low-molecular-weight supramolecular complexes with unique light-responsive properties. In particular, halogen bonding drives the formation of a photoresponsive liquid-crystalline complex between a non-mesogenic halogen bond-donor molecule incorporating an azo group, and a non-mesogenic alkoxystilbazole moiety, acting as a halogen bond-acceptor. Upon irradiation with polarized light, the complex exhibits a high degree of photoinduced anisotropy (order parameter of molecular alignment > 0.5). Moreover, efficient photoinduced surface-relief-grating (SRG) formation occurs upon irradiation with a light interference pattern, with…

Materials scienceLightSurface Propertiesta221Supramolecular chemistryPhotochemistrysupramolecular complexeschemistry.chemical_compoundHalogensliquid crystalsLiquid crystalMaterials TestingMoietyMoleculeGeneral Materials Scienceliquid crystalta218Halogen bondta214Azobenzeneta114Mechanical Engineeringself-assemblyMolecular WeightRefractometryazobenzeneAzobenzenechemistryMechanics of Materialshalogen bondingHalogenazobenzene; halogen bonding; liquid crystals; self-assembly; supramolecular complexesSelf-assemblySettore CHIM/07 - Fondamenti Chimici Delle Tecnologiesurface relief gratings
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DNA origami as a nanoscale template for protein assembly

2009

We describe two general approaches to the utilization of DNA origami structures for the assembly of materials. In one approach, DNA origami is used as a prefabricated template for subsequent assembly of materials. In the other, materials are assembled simultaneously with the DNA origami, i.e. the DNA origami technique is used to drive the assembly of materials. Fabrication of complex protein structures is demonstrated by these two approaches. The latter approach has the potential to be extended to the assembly of multiple materials with single attachment chemistry.

Materials scienceMechanical EngineeringBioengineeringNanotechnologyDNAGeneral ChemistryNanostructuresComplex proteinMechanics of MaterialsMultiprotein ComplexesDNA nanotechnologyNanotechnologyDNA origamiGeneral Materials ScienceStreptavidinSelf-assemblyProtein MultimerizationElectrical and Electronic EngineeringNanoscopic scaleNanotechnology
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Macromolecular complexes. Dynamic interactions and electronic processes. Edited byEishun Tsuchida, VCH, Weinheim 1991, vi, 400 pp., hardcover, DM 225…

1991

Materials scienceMechanics of MaterialsMechanical EngineeringPolymer chemistryMacromolecular ComplexesGeneral Materials ScienceAdvanced Materials
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