Search results for "assembly"

showing 10 items of 768 documents

Formation of Triple‐Stranded Dinuclear Helicates with Dicatecholimine Ligands: The Influence of Steric Hindrance at the Spacer

2005

A series of new imine-bridged dicatechol ligands 3a–f-H4 with sterically demanding groups at the spacers are used for the formation of titanium(IV) complexes M4[(3)3Ti2]. All three ligands 3a–c-H4 form triple-stranded dinuclear helicates. When the bulky ligands 3a-H4 or 3c-H4 are used with potassium as the countercation, oligomeric or polymeric side products are also observed. The imine-bridged ligand 3e-H4 quantitatively forms helicates M4[(3e)3Ti2] and not a M4L6 tetrahedron as observed with Raymond’s analogous amide-bridged dicatechol ligand 3i-H4. NMR spectroscopic investigations at variable temperature show that ligand 3f-H4, which possesses a spiro fluorenyl group at the central unit …

Inorganic ChemistrySteric effectsChemistryLigandStereochemistryCentral unitSelf-assemblyEuropean Journal of Inorganic Chemistry
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Surface Chemistry Directs the Tunable Assembly of TiO 2 Anatase Nanocubes into Three‐Dimensional Mesocrystals

2019

Inorganic ChemistrySurface (mathematics)ColloidAnatasechemistrychemistry.chemical_elementNanotechnologySelf-assemblyTitaniumEuropean Journal of Inorganic Chemistry
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Facile Synthesis and Self‐Assembly of Zinc (2‐Diethoxyphosphorylethynyl)porphyrins

2019

Inorganic Chemistrychemistrychemistry.chemical_elementHomogeneous catalysisZincSelf-assemblyCombinatorial chemistryEuropean Journal of Inorganic Chemistry
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Molecular-Programmed Self-Assembly of Homo- and Heterometallic Tetranuclear Coordination Compounds: Synthesis, Crystal Structures, and Magnetic Prope…

2009

New homo- and heterobimetallic tetranuclear complexes of formula [Cu4(mpba)(Me4en)4(H2O)4](ClO4)4·3H2O (1), [Cu4(mpba)(Me4en)4(H2O)4](PF6)4·2H2O (2), [Cu4(ppba)(Me4en)4(H2O)4](ClO4)4·2H2O (3), [Cu4(mpba)(dipn)4](ClO4)4·3H2O (4), [Cu4(ppba)(dipn)4](ClO4)4·2H2O (5), and [Cu2Ni2(ppba)(dipn)4(H2O)2](PF6)4 (6) [mpba = N,N′-1,3-phenylenebis(oxamate), ppba = N,N′-1,4-phenylenebis(oxamate), Me4en = N,N,N′,N′-tetramethylethylenediamine, and dipn = dipropylenetriamine] have been synthesized and structurally and magnetically characterized. Complexes 1−6 have been prepared following a molecular-programmed self-assembly method, where a heteropolytopic tetranucleating phenylenedioxamato bridging ligand (…

Inorganic Chemistrychemistry.chemical_classificationCrystallographyChemistryStereochemistryMetal ions in aqueous solutionCationic polymerizationBridging ligandCrystal structureSelf-assemblyPhysical and Theoretical ChemistryCoordination complexInorganic Chemistry
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Cyclophosphazenes as versatile substrates in polymer chemistry

2004

In this article we present the synthesis of new cyclophosphazenes and their use as chain extenders, polymers compatibilizers, and monomers.

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundMonomerchemistryOrganic ChemistryPolymer chemistrySupramolecular chemistryOrganic chemistryPolymerSelf-assemblyBiochemistrySynthesis (chemical) Derivatives NMR spectroscopy
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Interfacial Self-Assembly of Water-Soluble Cationic Porphyrins for the Reduction of Oxygen to Water

2012

Meet at the border: Assembly of the water-soluble cobalt tetrakis(N-methylpyridinium-4-yl)porphyrin [CoTMPyP]4+ at soft interfaces is enhanced and stabilized by its interfacial interaction with the lipophilic anion (C6F5)4B−. The supramolecular structure thus formed (see picture) provides excellent catalytic activity in the four-electron reduction of oxygen.

Inorganic chemistrySupramolecular chemistry2Nd-Harmonic Generationchemistry.chemical_element010402 general chemistryporphyrinsOxygen01 natural sciencesCatalysisMolecular ElectrocatalysisCatalysisinterfacesPolarized Interfacechemistry.chemical_compound[SPI]Engineering Sciences [physics]AggregationPolymer chemistry[CHIM]Chemical Sciencesliquid-liquid interfacesComputingMilieux_MISCELLANEOUS[PHYS]Physics [physics]oxygen reduction reactionDioxygen010405 organic chemistryCationic polymerizationGeneral ChemistryGeneral Medicineself-assemblyPorphyrin3. Good health0104 chemical scienceschemistryTetrathiafulvaleneSelf-assemblyImmiscible Electrolyte-SolutionsCobaltTetrathiafulvalene
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Tetraurea calix[4]arenes with sulfur functions: synthesis, dimerization to capsules, and self-assembly on gold.

2007

Various calix[4]arene derivatives, fixed in the cone conformation by decylether groups and functionalized at their wide rim by urea residues, were synthesized. In two compounds (4f,g) sulfur functions were attached to the urea groups via different spacers in order to allow binding to metal surfaces. While they exist as single molecules in polar solvents, tetraurea calix[4]arenes of this type (4) combine to form dimeric capsules in aprotic, apolar solvents. A solvent molecule is usually included in such a capsule, if no guest with a higher affinity is present. In the presence of an equimolar amount of the tetratosylurea 5, the exclusive formation of heterodimers, consisting of one molecule o…

Inorganic chemistrySupramolecular chemistryBiochemistryMass SpectrometryMetalchemistry.chemical_compoundElectrolytesPhenolsCationsPolymer chemistryElectrochemistryMoleculeUreaFerrous CompoundsPhysical and Theoretical ChemistryDichloromethaneMethylene ChlorideChloroformOrganic ChemistrySurface Plasmon ResonanceSolutionschemistryModels ChemicalSolubilityvisual_artProton NMRvisual_art.visual_art_mediumSolventsNanoparticlesSelf-assemblyChloroformGoldCyclic voltammetryCalixarenesDimerizationSulfurOrganicbiomolecular chemistry
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Anion template effect and the polymerization degree

2005

Two 2D (M1 and M2) and one 1D (M3) metal‐organic frameworks (MOFs) have been prepared from pyridine functionalized tetradentate ligand tetrakis(nicotinoxymethyl)methane TNM with silver tetrafluoroborate, nickel chloride, and copper hexafluorophosphate. M1 manifests a previously unpresented mode of 4,4 threefold parallel interpenetration for 2D MOFs. Large channels (vdW diameter 9.4 Å) through eclipsed 2D layers of M2 were observed. While the open space percentage in the noninterpenetrated M2 was 38.0 %, the triple interpenetration of the sheets of M1 reduced the void to 10.8 %. With the same ligand and a similar, weakly coordinating anion as that in M1, the structure M3 was rendered one‐dim…

Inorganic chemistrychemistry.chemical_elementCrystal engineeringSelf-assemblyTransition metalsCrystal engineeringSilver tetrafluoroborateZeolite analoguesInorganic ChemistryNickelCrystallographychemistry.chemical_compoundN ligandschemistryPolymerizationTransition metalHexafluorophosphatePyridineSelf-assemblyEuropean Journal of Inorganic Chemistry
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Il perimetro variabile dell’insindacabilità dei Consiglieri regionali: la vis politica delle decisioni “strategiche” per l’economia regionale. Nota a…

2022

La sentenza n. 90 del 2022 della Corte costituzionale risolve un conflitto di attribuzioni fra Stato e Regione Valle d’Aosta originato dalla sentenza della sezione giurisdizionale III centrale della Corte dei conti (la nr. 350 del 2021) di condanna per responsabilità da danno erariale nei confronti di diversi Consiglieri della Regione per aver deliberato un atto amministrativo concernente un’operazione di rifinanziamento del Casinò di Saint-Vincent. A differenza dei criteri precedentemente seguiti per definire l’ambito di applicazione dell’insindacabilità dei Consiglieri regionali nell’ipotesi di deliberazioni consiliari relative ad atti non legislativi (cfr. spec. Corte cost. nn. 69 e 70 d…

Insindacabilità (fondamento)Political DirectionSettore IUS/09 - Istituzioni Di Diritto PubblicoNon legislative actPolitical ActCourt of Auditors (Jurisdiction)Insindacabilità (ambito di applicazione)atto politicoRegional Assemblyindirizzo politicoIrresponsibility (foundation)Constitutional conflicts of powers between State and RegionConsiglio Regionalegiurisdizione Corte dei ContiSettore IUS/08 - Diritto CostituzionaleIrresponsibility (Field of application)Conflitto d’attribuzioni Stato-Regioniatti non legislative
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Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self-Assemble in the Presence of Europium(III) Ions: Reversible t…

2020

[EN] Hybrid nanostructures with switchable and reversible "blue-red-green" emission were efficiently synthesized. These nanostructures comprise polyhedral oligomeric silsesquioxanes (POSS) that behave as a nanocage that can be functionalized with terpyridine-based organic ligands, which can be easily complexed with europium (III) ions. The complexes were characterized by UV-Vis and fluorescence spectroscopy and their stoichiometry was also confirmed by H-1 NMR spectroscopy. In the presence of the Eu(III) ions, the octafunctionalized nanocages self-assemble to form 3D architectures that display an intense red-emission, especially in the solid state. The presence of an alkenyl group bridging …

IsomerizationNanostructureMaterials scienceLuminescenceSilsesquioxanesSelf assemblechemistry.chemical_element010402 general chemistry01 natural sciencesisomerizationIonchemistry.chemical_compoundQUIMICA ORGANICAEuropiumPolymer chemistryluminescenceeuropium010405 organic chemistryself-assemblyGeneral ChemistrySelf-assemblySilsesquioxane0104 chemical sciencessilsesquioxaneschemistrySelf-assemblyLuminescenceEuropiumIsomerization
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