Search results for "Ordination"

showing 10 items of 1367 documents

Cryptand-like anion receptors

2010

The design of supramolecular hosts for anions began with simple diaza bicycles, named katapinands, and has evolved over the last 40 years to a number of elegantly designed receptors capable of binding many different anions. About the same time the term cryptand appeared in reference to another bicyclic compound that was selective for alkaline-earth ions. Since the first report these simple bicycles, a vast arena of hosts has appeared, including acyclic, monocyclic, and other multicyclic supramolecular receptors. Studies of these systems have revealed considerable information about anion coordination chemistry, including the fact that many of these complexes mimic their transition-metal coro…

chemistry.chemical_classificationBicyclic moleculeCovalent bondChemistryStereochemistryCoordination numberCryptandSupramolecular chemistryGeneral ChemistryIonCoordination complexChemical Society Reviews
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Downsizing of Nanocrystals While Retaining Bistable Spin Crossover Properties in Three-Dimensional Hofmann-Type {Fe(pz)[Pt(CN)4]}–Iodine Adducts

2021

Mastering nanostructuration of functional materials into electronic devices is presently an essential task in materials science. This is particularly relevant for spin crossover (SCO) compounds, whose properties are extremely sensitive to size reduction. Indeed, the search for materials displaying strong cooperative hysteretic SCO properties operative at the nanoscale close near room temperature is extremely challenging. In this context, we describe here the synthesis and characterization of 20-30 nm surfactant-free nanocrystals of the FeII Hofmann-type polymer {FeII(pz)[PtII,IVIx(CN)4]} (pz = pyrazine), which affords the first example of a robust three-dimensional coordination polymer, sub…

chemistry.chemical_classificationBistabilityPyrazine010405 organic chemistryCoordination polymerContext (language use)Polymer010402 general chemistry01 natural sciences0104 chemical sciencesCharacterization (materials science)Inorganic ChemistryCrystallographychemistry.chemical_compoundchemistryNanocrystalSpin crossoverPhysical and Theoretical ChemistryInorganic Chemistry
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Group 13 complexes of dipyridylmethane, a forgotten ligand in coordination chemistry.

2015

The reactions of dipyridylmethane (dpma) with group 13 trichlorides were investigated in 1 : 1 and 1 : 2 molar ratios using NMR spectroscopy and X-ray crystallography. With 1 : 1 stoichiometry and Et2O as solvent, reactions employing AlCl3 or GaCl3 gave mixtures of products with the salt [(dpma)2MCl2](+)[MCl4](-) (M = Al, Ga) as the main species. The corresponding reactions in 1 : 2 molar ratio gave similar mixtures but with [(dpma)MCl2](+)[MCl4](-) as the primary product. Pure salts [(dpma)AlCl2](+)[Cl](-) and [(dpma)AlCl2](+)[AlCl4](-) could be obtained by performing the reactions in CH3CN. In the case of InCl3, a neutral monoadduct (dpma)InCl3 formed regardless of the stoichiometry emplo…

chemistry.chemical_classificationBoron groupChemistryLigandStereochemistryligandsdipyridylmethaneMethylene bridgeNuclear magnetic resonance spectroscopyliganditMedicinal chemistrydipyridyylimetaaniCoordination complexInorganic ChemistryBipyridinechemistry.chemical_compoundkoordinaatiokemiaDeprotonationcoordination chemistryReactivity (chemistry)ta116Dalton transactions (Cambridge, England : 2003)
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Studies on coordination compounds vii, chromatographic, thermoanalytical and spectroscopic studies on thermal decomposition of cadmium(II) and lead(I…

1982

On the basis of decomposition temperatures and infrared spectra, cadmium(II) and lead(II) bissalicylaldoximates were considered to havetrans andcis structures, respectively.

chemistry.chemical_classificationCadmiumChemistryThermal decompositionInorganic chemistrychemistry.chemical_elementInfrared spectroscopy010402 general chemistry01 natural sciencesDecomposition010406 physical chemistry0104 chemical sciencesCoordination complexMass spectrumPyrolysisJournal of Thermal Analysis
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Two-step spin crossover behaviour in the chiral one-dimensional coordination polymer [Fe(HAT)(NCS)2]∞

2015

Solvated and unsolvated forms of the complex [Fe(HAT)(NCS)2]∞·(nMeOH) (1) (n = 1.5, 0; HAT = 1,4,5,8,9,12-hexaazatriphenylene) were prepared. The structure of 1·(1.5MeOH), measured at 120 K, showed that this system crystallizes in the homochiral P43 tetragonal space group. The solid is constituted of stacks of one-dimensional coordination polymers running along c-axis. All the FeII centres have the same Λ or Δ conformation and are in the LS state at 120 K. In the range of temperatures 10–300 K the magnetic properties of 1·(1.5MeOH) shows the occurrence of reversible spin crossover behaviour. However, above ca. 310 K complete desolvation of 1·(1.5MeOH) to give 1 was observed from crystal str…

chemistry.chemical_classificationChemistryCoordination polymerGeneral Chemical EngineeringTwo stepEnthalpyGeneral ChemistryCrystal structurePolymerTetragonal crystal systemchemistry.chemical_compoundCrystallographySpin crossoverThermal analysisRSC Advances
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Group 14 Metalloles, Ionic Species and Coordination Compounds

2009

1 Introduction 2 Synthesis 3 Organic Chemical Properties of Group 14 Metalloles 4 Polymeric Silole-Containing π-Conjugated Systems 5 Ionic Species and Coordination Compounds 6 Addendum 7 Conclusion 8 Acknowledgements Keywords: five-membered heterocyclic dienes; heterocyclopentadienes - heteroles or metalloles; group 14 metalloles, ionic species and coordination compounds; gas-phase pyrolysis of silacyclopent-3-enes; organometallic dihalide reaction with dilithio reagent; group 14 metalloles; HOMO stabilization; polymeric silole-containing pi-conjugated systems

chemistry.chemical_classificationChemistryGroup (periodic table)ReagentOrganic chemistryIonic bondingPyrolysisCoordination complex
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Synthesis, Structural, Magnetic and Thermal Characterization of {[Cu(bipy)] 2 (μ‐HP 2 O 7 )(μ‐Cl)}·H 2 O

2008

Copper(II) hydroxide reacts with 2,2′-bipyridine (bipy) and sodium pyrophosphate in a 2:2:1 stoichiometric ratio under ambient conditions at pH 1.6 in water. The resulting neutral dinuclear CuII complex features a bridging set containing bridging monoprotonated pyrophosphate and a monoatomic chloro bridge (making this the first pyrophosphate bridged coordination complex containing an alternate, additional halide bridge between the metal centers). Single-crystal X-ray diffraction studies revealed the complex to be {[Cu(bipy)]2(μ-HP2O7)(μ-Cl)}·H2O. The structure consists of a dimeric copper(II) system with each metal ion in a square pyramidal geometry. The asymmetric [Cu(bipy)]2+ units are br…

chemistry.chemical_classificationChemistryHydrogen bondInorganic chemistryProtonationPyrophosphateMagnetic susceptibilitySquare pyramidal molecular geometryCoordination complexInorganic Chemistrychemistry.chemical_compoundCrystallographyIntramolecular forceMoleculeEuropean Journal of Inorganic Chemistry
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Syntheses, crystal structures and magnetic properties of tricyanomethanide-containing bis(2-pyrimidylcarbonyl)amidate copper(II) complexes

2008

Abstract Three new copper(II) complexes of formulae [Cu(bpcam)(tcm)(H2O)] · 2H2O (1), [Cu(bpcam)(tcm)(H2O)] (2) and [Cu(bpcam)(tcm)]n (3) [bpcam = bis(2-pyrimidylcarbonyl)amidate and tcm = tricyanomethanide] have been prepared and their structures determined by single crystal X-ray diffraction. Complexes 1 and 2 are mononuclear species where each copper atom is five-coordinated in a somewhat distorted square pyramidal environment with a tridentate bpcam ligand and a terminally bound tcm group building the basal plane and a water molecule in the apical position. Compound 3 is a uniform copper(II) chain where the [Cu(bpcam)]+ units are connected through single μ-1,5-tcm bridges which link one…

chemistry.chemical_classificationChemistryMagnetismchemistry.chemical_elementCrystal structureMagnetic susceptibilityCopperSquare pyramidal molecular geometryCoordination complexInorganic ChemistryCrystallographyMaterials ChemistryMoleculePhysical and Theoretical ChemistrySingle crystalPolyhedron
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Helicate Extension as a Route to Molecular Wires

2008

We describe the preparation of a helicate containing four closely spaced, linearly arrayed copper(I) ions. This product may be prepared either directly by mixing copper(I) with a set of precursor amine and aldehyde subcomponents, or indirectly through the dimerization of a dicopper(I) helicate upon addition of 1,2-phenylenediamine. A notable feature of this helicate is that its length is not limited by the lengths of its precursor subcomponents: each of the two ligands wrapped around the four copper(I) centers contains one diamine, two dialdehyde, and two monoamine residues. This work thus paves the way for the preparation of longer oligo- and polymeric structures. DFT calculations and elec…

chemistry.chemical_classificationChemistryOrganic ChemistryInorganic chemistryDynamic covalent chemistrychemistry.chemical_elementGeneral ChemistryElectrochemistryCopperCatalysisCoordination complexMolecular wirechemistry.chemical_compoundDelocalized electronCrystallographyDiamineddc:540Self-assemblyChemistry - A European Journal
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Synthesis and Coordination Chemistry of Lower Rim Cavitand Ligands

2001

chemistry.chemical_classificationChemistryOrganic ChemistryPolymer chemistryOrganic chemistryCavitandSelf-assemblyPhysical and Theoretical ChemistryCoordination complexEuropean Journal of Organic Chemistry
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