Search results for "Cubane"

showing 10 items of 34 documents

Two bimetallic layered materials with “Cu4Fe3” defective cubane units: syntheses, structures and magnetic properties of {[CuII(tn)]2[FeII(CN)6]}3·[Na…

2005

Abstract Reactions of the [Fe III (CN) 6 ] 3− anion with the [Cu II (tn)] 2+ ion (tn = 1,3-diaminopropane) afford the compounds {[Cu II (tn)] 2 [Fe II (CN) 6 ]}3·[Na 3 Fe III (CN) 6 ]·12H 2 O (1) and {[Cu n (tn)] 2 [Fe II (CN) 6 ]}·KCl·5H 2 O (2). Despite the differences concerning their asymmetric units, both structures present strong similar features: in both structures, the Cu(II) ion presents a square-base pyramidal CuN 5 environment and each [Fe II (CN) 6 ] 4− anion is linked to six Cu(II) ions through its six N atoms leading to infinite [Cu II (tn)] 2 [Fe II (CN) 6 ] layers which can be viewed as 2-D layered arrangement generated by the defective cubane units Cu 4 Fe 3 involving Fe-CN…

010405 organic chemistryChemistryCoordination polymerMechanical EngineeringInorganic chemistryMetals and AlloysCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesElectronic Optical and Magnetic MaterialsParamagnetismchemistry.chemical_compoundCrystallographyTransition metalMechanics of MaterialsCubaneMaterials ChemistryMoleculeAntiferromagnetismBimetallic stripSynthetic Metals
researchProduct

A carboxylate-bridged NiII8 cluster with a distorted cubane topology: structure, magnetism and density functional studies

2016

Using a dicarboxylate ligand appended with (2-pyridyl)ethylamine unit, a new cluster [NiII8(L4)6(DMF)2(CH3OH)2(H2O)6][ClO4]4·2CH3OH·2CH3CO2C2H5 (1) [L4(2−): 3-[N-{2-(pyridin-2-yl)ethyl}amino]-bis(propionate)] has been synthesized, through ‘coordination-driven self-assembly’. The crystal structure of 1 reveals a centrosymmetric octanuclear carboxylate-bridged nickel(II) tetracation, with a distorted cubane topology. The four crystallographically independent nickel(II) centres differ markedly in their coordination environment. Magnetic studies (2–300 K) reveal that in 1 the net magnetic-exchange is antiferromagnetic. Based on geometric parameters associated with two interacting nickel(II) cen…

010405 organic chemistryMagnetismchemistry.chemical_elementCrystal structure010402 general chemistryTopology01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographyMonatomic ionNickelchemistryFerromagnetismCubaneAntiferromagnetismCarboxylateDalton Transactions
researchProduct

The hetero-cubane structures of the heavy alkali metal tert-amyloxides [MOCMe2Et]4 (M = K, Rb, Cs)

2018

A series of alkali metal (Li–Cs) alkoxides of tert-pentanol (1,1-dimethylpropan-1-ol) have been prepared by reaction of the corresponding metal with the alcohol in n-hexane or n-heptane. The compounds were purified by vacuum sublimation and crystallised in n-hexane to produce crystals suitable for single-crystal X-ray diffraction studies. The structures of the potassium, rubidium, and caesium compounds revealed tetrameric units with additional intra- and intermolecular interactions between the metal atom and alkoxide methyl groups, increasing with the size of the metal involved.

010405 organic chemistryPotassiumIntermolecular forcechemistry.chemical_element010402 general chemistryAlkali metal01 natural sciences0104 chemical sciencesRubidiumInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryCubaneCaesiumvisual_artAlkoxidevisual_art.visual_art_mediumDalton Transactions
researchProduct

New, Multi‐Dimensional Cu(tn)‐[M(CN) 6 ] n – Cyano‐Bridged, Bimetallic Coordination Materials (M = Fe II , Co III , Cr III and tn = 1,3‐Diaminopropan…

2005

Reaction of the [Fe I I I (CN) 6 ] 3 - anion with [Cu I I (tn)(H 2 O) n ] 2 + (tn = 1,3-diaminopropane) affords the compounds [{Cu I I (tn)} 2 -{Fe I I (CN) 6 }].KCl.5H 2 O (1), [(Cu"(tn))2(Fe"(CN) 6 )].4H 2 O (2), and [{Cu I I (tnH) 2 (H 2 O) 2 }{Fe I I (CN) 6 }].2H 2 O (3). Each iron center in 1 and 2 is linked to six copper(II) ions by six cyanide bridges, while each copper ion is linked to three equivalent iron(II) ions. Despite these resemblances, the two compounds present large structural differences caused by two different orientations of the Cu-NC-Fe bridges: compound 1 has a 2D structure which can be described as successions of "Cu 4 Fe 3 " defective cubane units, while compound 2 …

010405 organic chemistrychemistry.chemical_element13-DiaminopropaneBridging ligandProtonation010402 general chemistry01 natural sciencesCopper0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundParamagnetismCrystallographychemistryCubaneAntiferromagnetismBimetallic stripEuropean Journal of Inorganic Chemistry
researchProduct

Cobalt Clusters with Cubane-Type Topologies Based on Trivacant Polyoxometalate Ligands.

2016

Four novel cobalt-substituted polyoxometalates having cobalt cores exhibiting cubane or dicubane topologies have been synthesized and characterized by IR, elemental analysis, electrochemistry, UV-vis spectroscopy, X-ray single-crystal analysis, and magnetic studies. The tetracobalt(II)-substituted polyoxometalate [Co4(OH)3(H2O)6(PW9O34)](4-) (1) consists of a trilacunary [B-α-PW9O34](9-) unit which accommodates a cubane-like {Co(II)4O4} core. In the heptacobalt(II,III)-containing polyoxometalates [Co7(OH)6(H2O)6(PW9O34)2](9-) (2), [Co7(OH)6(H2O)4(PW9O34)2]n(9n-) (3), and [Co7(OH)6(H2O)6(P2W15O56)2](15-) (4), dicubane-like {Co(II)6Co(III)O8} cores are encapsulated between two heptadentate [B…

010405 organic chemistrychemistry.chemical_elementNanotechnologyType (model theory)010402 general chemistryElectrochemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryCubanePolyoxometalatePhysical and Theoretical ChemistrySpectroscopyCobaltExchange modelInorganic chemistry
researchProduct

Synthesis, structural diversity, inter-conversion and reactivity of Cu(II) complexes of hydroxy-rich molecules

2002

Tetranuclear Cu(II) complexes having linear, cubane and pseudodouble-cubane cores were synthesized using hydroxy-rich molecules possessing amine and imine groups. The products were structurally characterized and were studied for their ability to oxidize catechol as well as for their inter-conversion between mono- and tetra-nuclear complexes.

Absorption SpectraCatecholAbsorption spectroscopyMolecular StructureStereochemistryImineStructural diversityInorganic Chemistrychemistry.chemical_compoundchemistryCubanePolymer chemistryMaterials ChemistryMoleculeAmine gas treatingReactivity (chemistry)CrystallographicPhysical and Theoretical ChemistryIndraStra Global
researchProduct

Stepwise formation of a pentanuclear Ni4Cu heterometallic complex exhibiting a vertex-sharing defective double-cubane core and diphenoxo- and phenoxo…

2013

Sequential reaction of a N5O3 octadentate tripodal ligand with Ni(2+) and subsequently with Cu(2+) and azide ligand afforded the first example of a heterobridged (phenoxo/μ(1,1)-azido) pentanuclear heterometallic (Ni4Cu) compound, which exhibits a centrosymmetric vertex-sharing defective double-cubane structure. The study of the magnetic properties reveals that the compound shows ferromagnetic interaction interactions, leading to an S = 9/2 spin ground state. Density functional theory calculations on the X-ray structure and model compounds predict ferromagnetic interactions through the magnetic exchange pathways involving each couple of metal ions.

AzidesMagnetic Resonance SpectroscopyMolecular StructureChemistryStereochemistryMetal ions in aqueous solutionStereoisomerismCrystallography X-RayLigandsVertex (geometry)Inorganic Chemistrychemistry.chemical_compoundCrystallographyFerromagnetismCubaneCoordination ComplexesNickelTripodal ligandQuantum TheoryDensity functional theoryAzidePhysical and Theoretical ChemistryGround stateCopperInorganic chemistry
researchProduct

Luminescent P-Chirogenic Copper Clusters

2013

P-chirogenic clusters of the cubanes [Cu4I4L4] (L = chiral phosphine) were prepared from (+)- and (-)-ephedrine with L = (S)- or (R)-(R)(Ph)(i-Pr)P (with R = CH3 (seven steps) or C17H35 (10 steps)) with e.e. up to 96%. The X-ray structure of [Cu4I4((R)-(CH3)(Ph)(i-Pr)P)4] confirmed the cubane structure with average Cu···Cu and Cu···I distances of 2.954 and 2.696 Å, respectively. The cubane structure of the corresponding [Cu4I4((S)-(CH3)(Ph)(i-Pr)P)4] was established by the comparison of the X-ray powder diffraction patterns, and the opposite optical activity of the (S)- and (R)-ligand-containing clusters was confirmed by circular dichroism spectroscopy. Small-angle X-ray scattering patterns…

Circular dichroismchemistry.chemical_elementCopperInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryCubaneExcited stateEmission spectrumPhysical and Theoretical ChemistryLuminescencePhosphinePowder diffractionInorganic Chemistry
researchProduct

[(Pyridylcarbonyl)pyridyl]triazolopyridines, Useful Ligands for the Construction of Polynuclear Coordination Compounds – Synthesis, Crystal Structure…

2007

A new tetranuclear cubane Cu4O4 complex has been synthesised from assembly of CuII ions and the polydentate ligand (pyridin-2-yl){6-([1,2,3]triazolo[1,5-a]pyridin-3-yl)pyridin-2-yl}methanone. Crystallographic analysis indicates that the Cu4O4 unit has an S4 symmetry. The magnetic properties have been analysed using the H = –2Σi,jJijSiSj spin Hamiltonian. Two distinct coupling constants, 2J1,3 = –37.4 cm–1 and 2J1,2 = –2.6 cm–1, obtained from the fitting of the experimental data have been rationalised on the basis of a density functional study of magnetostructural correlations in cubane complexes containing the Cu4O4 core. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)

Coupling constantchemistry.chemical_classificationDenticityLigandStereochemistrychemistry.chemical_elementCrystal structureCopperIonCoordination complexInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryCubaneEuropean Journal of Inorganic Chemistry
researchProduct

Novel Bimetallic-Dicyanamide Extended Two- and Three-Dimensional Networks through [Cu(rac-CTH)]2+ Cation Templation

2009

Reaction of [Cu(rac-CTH)]2+ with dicyanamide and Mn2+ or Fe2+ produces three bimetallic extended structures. Complexes 1 and 2, both obtained in the same reaction pot, consist of two different (4,4) two-dimensional (2D) layers, with the [Cu(rac-CTH)(dca)]+ cations noncoordinated and coordinated to the Mn(μ1,5-dca) network for 1 and 2, respectively (rac-CTH = racemic-5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane). Complex 2 shows an unusual monodentate coordination mode through the central amide nitrogen of the dca ligand which is first reported for a polynuclear complex. The structure of 3 consists of a three-dimensional network which can be described as a stacking of layers m…

Denticity010405 organic chemistryChemistryLigandStereochemistryStackingGeneral ChemistryCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciences3. Good healthchemistry.chemical_compoundCrystallographyCubaneAmideGeneral Materials ScienceDicyanamideBimetallic stripCrystal Growth & Design
researchProduct