Search results for "Bridging"

showing 10 items of 155 documents

Selective ortho-metallation reaction of the phosphine P(o-ClC6H4)Ph2. Synthesis and crystal structure of [Rh2(μ-O2CCH3)3(μ-(ClC6H3)PPh2(OH2)2]·CHCl3

1993

Abstract From the reaction of [Rh2(O2CCH3)4(MeOH)2] in hot acetic acid with P(o-ClC6H4)Ph2, two monometallated compounds [Rh2(O2CCH3)3(C6H4)P(o-ClC6H4)Ph(HO2CCH3)2] (1), already described, and [Rh2(O2CCH3)3{(ClC6H3)PPh2}(OH2)2] have been isolated. The new compound has been characterized by an X-ray study. It crystallizes in the triclinic space group P1. It contains three acetate groups bridging a Rh24+ unit that has a Rh-Rh bond distance of 2.426(1) A; the fourth bridging ligand is derived from one P(o-ClC6H4)Ph2 metallated in the halogenated ring. The two water molecules occupy the axial coordination sites.

StereochemistryMetalationOrganic ChemistryBridging ligandCrystal structureTriclinic crystal systemBiochemistryMedicinal chemistryInorganic ChemistryBond lengthchemistry.chemical_compoundAcetic acidchemistryMaterials ChemistryCarboxylatePhysical and Theoretical ChemistryPhosphineJournal of Organometallic Chemistry
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Simultaneous substitution of bridging acetate groups and reversible RhC bond cleavage in [Rh2(O2CCH3)3-{(C6H4)PPh2}(HO2CCH3)2] in the presence of CF…

1993

Abstract The reaction of the monometallated compound [Rh2(O2CCH3)3 {(C6H4)PPh2}(HO2CCH3)2] (1) with CF3CO2H at room temperature yields [Rh2(O2CCF3)3{(C6H4)PPh2}(HO2CCF3)2] (3) as the only isolable product. Compound 3 has been characterized by X-ray methods. 3 crystallizes in the space group P21 / n. It contains three trifluoroacetate groups bridging a Rh4+2 unit with a RhRh bond distance of 2.438(1) Ă; the fourth bridging ligand is a triphenylphosphine metallated at one of the ortho positions. Two molecules of trifluoroacetic acid occupy the axial coordination positions. In addition to the substitution of acetate groups, reversible electrophilic RhC bond activation is observed.

StereochemistryOrganic ChemistryBridging ligandCrystal structureBiochemistryInorganic ChemistryBond lengthchemistry.chemical_compoundCrystallographychemistryElectrophileMaterials ChemistryTrifluoroacetic acidCarboxylatePhysical and Theoretical ChemistryTriphenylphosphineBond cleavageJournal of Organometallic Chemistry
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Molecular structure of the compound [Rh2(O2CCH3)3{(C6H4)P(BrC6H4-1,2)(C6H5)} · (HO2CCH3)2].Kinetic study of the exchange reaction of acetate groups w…

1993

Abstract The compound [Rh 2 (O 2 CCH 3 ) 3 {(C 6 H 4 )P(BrC 6 H 4 -1,2) (C 6 H 5 )} · (HO 2 CCH 3 ) 2 ] has been isolated in high yield from the thermal reaction of dirhodium tetraacetate and the phosphine P(BrC 6 H 4 -1,2) (C 6 H 5 ) 2 in acetic acid. The structure of this compound has been determined by X-ray diffraction; it crystallizes in the P 1 (triclinic) space group and contains three acetate groups bridging a Rh 2 4+ unit the RhRh distance being 2.432(1)A; the fourth bridging ligand is an ortho -bromophenyldiphenylphosphine metallated at one of the ortho positions of the unsubstituted phenyl rings. Two molecules of acetic acid occupy the axial coordination positions. Stepwise exch…

StereochemistryOrganic ChemistryBridging ligandProtonationBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundAcetic acidReaction rate constantchemistryYield (chemistry)Materials ChemistryCarboxylatePhysical and Theoretical ChemistryTriphenylphosphinePhosphineJournal of Organometallic Chemistry
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Structural and magnetic characterization of the tridimensional network [Fe(HCO2)3]n·nHCO2H

2013

In this work we report the structural and magnetic characterization of a new three-dimensional porous metal–organic framework (MOF) based on iron(III) and the formate anion, [Fe(HCO2)3]n·nHCO2H (1), which was obtained by solvothermal synthesis. The tridimensional structure crystallizes in the trigonal space group Rc and is formed by highly regular octahedral Fe(OHCO)6 units. These units contain six equal Fe–O distances, with angles slightly different from 90° or 180°. The packing of 1 corresponds to a 3D covalent network defined by face sharing between the parallelepipeds, which are formed by the interactions of Fe(OHCO)6 units through formate ligands, thus generating a 41263 topology. This…

StereochemistrySolvothermal synthesisBridging ligandGeneral ChemistryCatalysischemistry.chemical_compoundCrystallographyMagnetizationchemistryFerromagnetismNetwork covalent bondingMaterials ChemistryAntiferromagnetismFormateSpin cantingNew Journal of Chemistry
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Two new supramolecular architectures of singly phenoxo-bridged copper(II) and doubly phenoxo-bridged manganese(II) complexes derived from an unusual …

2009

International audience; Two new coordination complexes {[(L)Cu2('-L)(NO3)(CH3OH)0.3(H2O)0.7]·NO3}[Cu(L)(NO3)(CH3OH)] (1) and [Mn2(-L)2(H2O)(1-N3)2(CH3OH)] (2) derived from (E)-N-(2-hydroxy-3-methoxybenzylidene)acetohydrazide [LH] have been synthesized. The new potentially tetradentate ONOO donor hydrazone ligand [LH] has shown considerable metal ion selective phenoxo bridging in 1 and 2. It has coordinated copper(II) ions in its tridentate as well as in tetradentate fashion whereas for manganese(II) ions it solely showed its tetradentate character. In 1 the two adjacent pentacoordinate copper(II) centers are connected by a rare single phenoxo linkage of the hydrazone ligand whereas 2 is a d…

StereochemistrySupramolecular chemistrychemistry.chemical_elementManganese010402 general chemistry01 natural sciencesHydrogen bondslaw.inventionIonInorganic ChemistryMetalO ligandslawElectron paramagnetic resonanceBridging ligands010405 organic chemistryChemistryHydrogen bondStructure elucidation[CHIM.MATE]Chemical Sciences/Material chemistryCopper0104 chemical sciencesDensity functional calculationsCrystallographyvisual_artvisual_art.visual_art_mediumHydrazone ligandSupramolecular chemistry
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Synthesis, crystal structures and magnetic properties of single and double cyanide-bridged bimetallic Fe2(III)Cu(II) zigzag chains.

2004

The bimetallic complexes [[Fe(III)(phen)(CN)4]2Cu(II)(H2O)2].4H2O (1), [[Fe(III)(phen)(CN)4]2Cu(II)].H2O (2) and [[Fe(III)(bipy)(CN)4]2Cu(II)].2H2O (3) and [[Fe(III)(bipy)(CN)4]2Cu(II)(H2O)2].4H2O (4) (phen = 1,10-phenanthroline and bipy = 2,2'-bipyridine) have been prepared and the structures of 1-3 determined by X-ray diffraction. The structure of 1 is made up of neutral cyanide-bridged Fe(III)-Cu(II) zigzag chains of formula [[Fe(III)(phen)(CN)4]2Cu(II)(H2O)2] and uncoordinated water molecules with the [Fe(phen)(CN)4]- entity acting as a bis-monodentate bridging ligand toward two trans-diaquacopper(II) units through two of its four cyanide groups in cis positions. The structure of 2 can …

Stereochemistrychemistry.chemical_elementBridging ligandCrystal structureCopperlaw.inventionInorganic ChemistryCrystallographychemistrylawMoleculeDensity functional theoryCrystallizationBimetallic stripCritical fieldDalton transactions (Cambridge, England : 2003)
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Ligand effects on the dimensionality of oxamato-bridged mixed-metal open-framework magnets

2012

Increasing dimensionality [from 2D (1) to 3D (2)] and T(C) [from 10 (1) to 20 K (2)] in two new oxamato-bridged heterobimetallic Mn(II)(2)Cu(II)(3) open-frameworks result from the steric hindrance provided by the different alkyl substituents of the N-phenyloxamate bridging ligands.

Steric effectschemistry.chemical_classificationBridging (networking)Mixed metalChemistryLigandStereochemistryMetals and AlloysGeneral ChemistryOpen frameworkCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyMagnetMaterials ChemistryCeramics and CompositesAlkylCurse of dimensionalityChemical Communications
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Sodium Adsorption on the TiO2110 Surface an XAFS Structural Study

2005

The adsorption site of sodium atoms deposited onto a clean TiO2(110) surface has been determined by EXAFS. The best result is obtained for an 'in-between' site where the sodium is bound to two bridging oxygen atoms at 2.25 A and one in-plane one at 2.40 A in full agreement with DFT calculations. At higher coverage the site becomes a hollow site where Na is equidistant to the three oxygen atoms at 2.30 A.

Surface (mathematics)Materials scienceExtended X-ray absorption fine structureSodiumchemistry.chemical_elementCondensed Matter PhysicsAtomic and Molecular Physics and OpticsX-ray absorption fine structureBridging oxygenOxygen atomAdsorptionchemistryPhysical chemistryEquidistantMathematical PhysicsPhysica Scripta
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Luminescence of the surface nonbridging oxygen hole center in silica: Spectral and decay properties

2008

We investigated the red luminescence in a porous film of silica nanoparticles, originating from surface nonbridging oxygen hole centers. The excitation spectrum was measured from 1.8 to 8.0 eV by a tunable laser system and a synchrotron radiation source; this spectrum evidences a peak at 2.0 eV, nearly overlapping with the emission, and an ultraviolet broadband with peaks at 4.8 and 6.0 eV. The emission is characterized by a spectrum with two subbands split by 0.07 eV, its decay occurs with lifetime longer than 30 microsec and undergoes a thermal quenching by a factor aboout 2 with increasing temperature from 10 to 290 K. The optical characteristics of surface and bulk centers are discussed…

Surface (mathematics)Materials sciencebusiness.industryTime resolved luminescenceOptoelectronicsdefects nanoparticles luminescence time resolved measurements silicaCenter (algebra and category theory)Condensed Matter PhysicsbusinessLuminescencePorous mediumElectronic Optical and Magnetic MaterialsNonbridging oxygen
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Facilitating organisational learning through teamwork-based knowledge management: evidence from Spain

2015

[EN] In the context of organisational learning optimisation through knowledge management policies, it is essential to pay careful attention to teamwork design and dynamics. Having these ideas in mind, the aim of our paper is to empirically study whether a number of knowledge management policies related to team design and dynamics facilitate organisational learning processes across the different ontological levels (individual, group, and organisational-institutional). Hence, we propose a model linking teamwork-design based on knowledge management policies (including the sub-dimensions of team composition, team bonding, and team bridging) and organisational learning. We test this model in a s…

Teamwork designKnowledge managementInstitutional learningmedia_common.quotation_subjectKnowledge managementTeam bridgingTeam effectivenessPsychological safetyContext (language use)ModellingEducationTeamsManagement of Technology and InnovationTeam bondingTeam compositionOrganisational learningmedia_commonTeam compositionTeamworkTeam creativitybusiness.industryTeamwork dynamicsCreativityTeam autonomyIndividual learningTeam learningSpainGroup learningORGANIZACION DE EMPRESASbusinessPsychologyAutonomy
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