Search results for "Group 2 organometallic chemistry"

showing 10 items of 64 documents

The first example of cofacial bis(dipyrrins)

2016

International audience; Two series of cofacial bis(dipyrrins) were prepared and their photophysical properties as well as their bimolecular fluorescence quenching with C-60 were investigated. DFT and TDDFT computations were also performed as a modeling tool to address the nature of the fluorescence state and the possible inter-chromophore interactions. Clearly, there is no evidence for such interactions and the bimolecular quenching of fluorescence, in comparison with mono-dipyrrins, indicates that C-60-bis(dipyrrin) contacts occur from the outside of the "mouth" of the cofacial structure.

010402 general chemistryPhotochemistry01 natural sciences[ CHIM ] Chemical SciencesCatalysisTransition metalexcitation-energiesmolecular-orbital methodsorganometallic compoundsMaterials Chemistry[CHIM]Chemical Sciencessinglet energy transfersdensity-functional theoryvalence basis-setsGroup 2 organometallic chemistryQuenching (fluorescence)010405 organic chemistryChemistryGeneral ChemistryTime-dependent density functional theorytransition-metalsFluorescence0104 chemical scienceslight-harvesting systems2nd-row elementsDensity functional theoryextended basis-sets
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Sequestration of organomettalic compounds by synthetic and naturally occuring polycarboxylate ligands. Binding of monomethylmercury(II) by polyacryli…

2007

The sequestering capacity of synthetic and naturally occurring polycarboxylate ligands towards mono- methylmercury(II) was evaluated by stability quantitative data on the interaction of CH3Hgþ with different molecular weight synthetic polyacrylates (2 and 20 kDa average M.wt) and alginate (70– 100 kDa) extracted from brown algae Macrocystis pyrifera. The influence of ionic medium was evaluated by measurements on the CH3Hgþ-polyacrylate systems in NaNO3 medium at different ionic strengths (0.10, 0.25, 0.50 and 0.75mol Lÿ1), and a Debye–Hu¨ ckel type equation was used for the dependence of complex formation constants on ionic strength. Measurements on the CH3Hgþ - alginate system were carried…

Chemical Health and SafetybiologyChemistryHealth Toxicology and MutagenesisComplex formationIonic bondingmonomethylmercury; sequestration by organic matter; polyacrylic and alginic acidsToxicologybiology.organism_classificationBrown algaemonomethylmercuryBinding abilityType equationpolyacrylic and alginic acidsmonomethylmercury sequestration by organic matter polyacrylic and alginic acids speciation equilibrium analysis complex species formationIonic strengthOrganic chemistrySettore CHIM/01 - Chimica Analiticasequestration by organic matterNuclear chemistryGroup 2 organometallic chemistry
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Stereoselective syntheses of piperidinones and their modification by organometallic coupling reactions

2007

Dehydropiperidinones stereoselectively obtained from N-arabinosyl imines were iodinated at the enaminone structure. Knochel iodine-magnesium exchange afforded Grignard compounds of these piperidinone derivatives which reacted, either directly or after transmetalation to zinc or copper intermediates, with alkyl-, aryl- or acylhalides to give correspondingly substituted piperidinones. Stereoselective conjugate allyl cuprate addition to a thus obtained 5-allyl dehydropiperidinone and ring-closing metathesis of the product gave a hydroquinolinone containing three stereogenic centers.

Chemistry OrganicMolecular ConformationStereoisomerismCrystallography X-RayMetathesisBiochemistryCoupling reactionStereocenterchemistry.chemical_compoundTransmetalationOrganometallic CompoundsOrganic chemistryMagnesiumPhysical and Theoretical ChemistryPiperidonesGroup 2 organometallic chemistryMolecular StructureChemistryArylOrganic ChemistryStereoisomerismZincModels ChemicalStereoselectivityIminesCopperIodineOrg. Biomol. Chem.
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Complexes of organometallic compounds XXVIII. The solution chemistry of bis(acetylacetone)ethylenediimine adducts of organotin(IV) halides

1971

Abstract The nature of methanol solutions of a series of bis(acetylacetone)ethylenediimine adducts of organotin(IV) halides has been studied by electronic and PMR spectroscopy and by osmometry and conductivity. Effectively complete dissociation to the free ligand and solvated organotin(IV) halide moieties is inferred.

ChemistryAcetylacetoneOrganic ChemistryHalideBiochemistryDissociation (chemistry)AdductInorganic Chemistrychemistry.chemical_compoundOsmometerPolymer chemistryMaterials ChemistryOrganic chemistryMethanolPhysical and Theoretical ChemistrySpectroscopyGroup 2 organometallic chemistryJournal of Organometallic Chemistry
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Hybrid Materials Formed by Two Molecular Networks. Towards Multiproperty Materials

1999

Abstract The possibilities offered by hybrid materials formed by two molecular networks in the context of the molecular magnets are illustrated. Molecule-based layered magnets are used as anionic hosts for electroactive molecules, with the aim of obtaining multiproperty materials exhibiting in addition to the cooperative magnetism other interesting properties according to the nature of the inserted molecules. In particular, hybrid molecular compounds containing molecular species giving rise to paramagnetic, conducting, or bi-stable properties are reported.

ChemistryMagnetismInorganic chemistryContext (language use)equipment and suppliesCondensed Matter PhysicsParamagnetismMolecular networkChemical physicsMagnetMoleculeHybrid materialhuman activitiesGroup 2 organometallic chemistry
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Complexes of organometallic compounds. L. The correlation between 119Sn mössbauer isomer shifts and calculated partial charges on tin in adducts of t…

1981

Abstract The relationship between Mossbauer isomer shifts, δ, and atomic charges on tin, QSn has been studied for homologous series RnSnhal4−n· L2 [ n = 0−3; L2 = donor atoms of 1, 2-bis(dipheylphosphino)ethane, N, N′-ethylenebes(salicylideneimine) and N, N′-ethylenbes(acetylacetoneimine)] and Snhal4· 2PR3. Semiempirical values of QSn have been calculated by two methods based on the concept of orbital electronegativity equalization upon bond formation. Linear correlations δ/QSn are obtained, which can be function of the coordination number of the metal atom, for terms of the series characterized by different orbital electronegativities of atoms directly bound to tin. Deviations occur for ad…

Coordination numberInorganic chemistrychemistry.chemical_elementInorganic ChemistryElectronegativityHomologous serieschemistry.chemical_compoundPartial chargeCrystallographychemistryAtomMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryTinGroup 2 organometallic chemistryInorganica Chimica Acta
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Nonbonded Indirect Nuclear Spin–Spin Couplings (J Couplings “Through-Space”) for Structural Determination in Small Organic and Organometallic Species

2013

Abstract Spin–spin coupling constant J provides decisive data for organic compound characterization. This electron-mediated coupling is usually taught as transmitted between covalently bonded magnetic atoms. However, this physical interaction between nuclear spins is much more complex than that with regard to chemical bonding concept. Independent experimental and theoretical studies related to small organic and organometallic species (molecular mass below 2000 g mol − 1 ) have highlighted the existence of J couplings operating via clearly nonbonded interactions and known as “through-space” couplings. Interactions of this type are frequently reported and couplings involving 19  F, 13 C, 77 S…

Coupling constantCouplingChemical bondSpinsHydrogen bondComputational chemistryChemistrySpin (physics)Characterization (materials science)Group 2 organometallic chemistry
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Preparation and structure of the 17-electron (η5-C5R5)Mo(OH)2(dppe) (R=Me, Et) organometallic compounds containing two gem-terminal hydroxide ligands

2000

International audience; Oxidation of (η5-C5R5)MoH3(dppe) (R=Me, Et) by Cp2Fe+ in wet THF leads to the formation of the corresponding (η5-C5R5)Mo(OH)2(dppe). These compounds show a low-potential reversible oxidation wave. The structure of the C5Et5 complex has been confirmed by X-ray diffraction methods: triclinic; space group ; a=11.030(1); b=12.533(1); c=16.241 (1) Å; α=68.585(7); β=75.197(5); γ=83.991(7)°; V=2020.6(3) Å3; Z=2; Dcalc=1.324 g cm−3, μ(Mo–Kα)=0.441 mm−1; R1=0.0325; wR2=0.0875 for 415 parameters and 6823 independent reflections [Rint=0.0177] with I=2σ(I). The molecule shows a four-legged piano-stool geometry with two terminal OH ligands in a relative trans configuration. The c…

Hydroxide complexeschemistry.chemical_elementHalf-sandwich complexesElectronTriclinic crystal system010402 general chemistry01 natural sciencesBiochemistrylaw.inventionInorganic Chemistrychemistry.chemical_compoundTrans configurationlawOxidationMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryElectron paramagnetic resonanceGroup 2 organometallic chemistryMolybdenum010405 organic chemistryOrganic ChemistryHydride complexes0104 chemical sciencesCrystallographychemistryMolybdenumHydroxide
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Selective opening of nanoscopic capped mesoporous inorganic materials with nerve agent simulants; an application to design chromo-fluorogenic probes.

2011

A hybrid nanoscopic capped mesoporous material, that is selectively opened in the presence of nerve agent simulants, has been prepared and used as a probe for the chromo-fluorogenic detection of these chemicals. © 2011 The Royal Society of Chemistry.

INGENIERIA DE LA CONSTRUCCIONMaterials scienceSilicon dioxideSomanNanotechnologyCatalysisArticleMolecular hybridizationchemistry.chemical_compoundQUIMICA ORGANICAMCM-41QUIMICA ANALITICAMaterials ChemistrymedicineOrganometallic CompoundsNanotechnologyChemical Warfare AgentsNanoscopic scaleTabunGroup 2 organometallic chemistryNerve agentFluorescent DyesSelective openingChemical warfare agentQUIMICA INORGANICAMetals and AlloysHydrogen BondingGeneral ChemistrySilicon DioxideSarinMcm 41Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesDrug determinationInorganic materialsColorimetryMesoporous materialControlled studyPorositymedicine.drugChemical communications (Cambridge, England)
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Novel mixed-valence Cu compounds formed by Cu(II) dimers with double oximato bridges: in situ formation of anionic layer [Cu2(SCN)3]n(n-).

2013

Two new N3O donor ketoxime Schiff bases (HL(1) and HL(2)) have been synthesized by condensing N,N-dimethylethylenediamine with diacetylmonoxime and benzilmonoxime, respectively in a 1:1 ratio. Reaction of Cu(ClO4)2·6H2O with HL(1) resulted in a discrete oximato-bridged dinuclear Cu(II) complex [Cu2(L(1))2(H2O)2](ClO4)2 (1). The same reaction in presence of NaSCN affords the complex {[Cu(II)2(L(1))2][Cu(I)4(μ(1,3)-SCN)4(μ(1,1,3)-SCN)2]}n (2), where partial Cu(II)→Cu(I) reduction is observed. In 2, arrays of [Cu(II)2(L(1))2](2+) cationic units are inserted in between 2D {[Cu(I)4(SCN)6](2-)}n layers and connected via μ(1,1,3)-SCN(-) links, thus forming a 3D network. On the other hand, reaction…

In situAnionsModels MolecularStereochemistryAnionchemistry.chemical_elementInfrared spectroscopy010402 general chemistryCrystallography X-RayAnions; Copper; Crystallography X-Ray; Dimerization; Models Molecular; Molecular Structure; Organometallic Compounds; Oximes; Thiocyanates01 natural sciencesInorganic ChemistryOximeModelsOximes[CHIM.CRIS]Chemical Sciences/CristallographyOrganometallic CompoundsMolecule[CHIM]Chemical SciencesGroup 2 organometallic chemistryOrganometallic CompoundCrystallographyValence (chemistry)Molecular Structure010405 organic chemistryCationic polymerizationMolecular[CHIM.MATE]Chemical Sciences/Material chemistryCopper0104 chemical sciencesCrystallographychemistryX-RaySingle crystalDimerizationCopperThiocyanatesDalton transactions (Cambridge, England : 2003)
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