Search results for "Paramagnetic organometallics"

showing 2 items of 2 documents

Comparative chemistry of 18-electron Mo(II) and 17-electron Mo(III) compounds containing only carbon-based ligands

1998

International audience; The chemical reactivity of various kinetically stable isomers of compound CpMo(η3-C3H5)(η4-C4H6), 1, and its oxidation product [1]+, as well as the bis-allyl Mo(III) complex CpMo(η3-C3H5)2, 2, and the bis-diene Mo(II) complex [CpMo(η4-C4H6)2]+, 3, is reviewed. The inertness toward isomerization processes of the allyl and butadiene ligands in the Mo(II) complexes has allowed a study of the relative reactivity toward both electrophilic and nucleophilic addition processes as a function of coordination mode. The dependence of various reaction pathways on the metal oxidation state has also been investigated. Of particular interest is the discovery that the electronically …

Allyl ligands010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisInorganic ChemistryMetalButadiene polymerizationOxidation stateMaterials ChemistryOrganic chemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryReactivity (chemistry)Physical and Theoretical ChemistryButadiene dimerizationMolybdenumNucleophilic addition010405 organic chemistryChemistry0104 chemical sciencesvisual_artElectrophilevisual_art.visual_art_mediumParamagnetic organometallicsReactivity of coordinated ligandsIsomerizationCoordination Chemistry Reviews
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Half-sandwich molybdenum(III) compounds containing diazadiene ligands and their use in the controlled radical polymerization of styrene

2002

Abstract The reaction of CpMoCl2 with diazadiene ligands RNCHCHNR (R2dad) affords the corresponding paramagnetic complexes CpMoCl2(R2dad) (R=Ph, 1; p-Tol, 2; C6H3Pr2i-2,6, 3; and Pri, 4). All compounds have been characterized by EPR spectroscopy and have been investigated by cyclic voltammetry. They display one-electron oxidation and reduction processes, these being reversible or irreversible depending on the nature of R. The irreversibility of the reduction wave is due to a chemical follow-up process which consists of chloride loss from the reduced product. This phenomenon is suppressed in the presence of excess chloride in solution. An X-ray structure of 3 verifies the mononuclear na…

Nitroxide mediated radical polymerizationRadical polymerization010402 general chemistryPhotochemistry01 natural sciencesBiochemistryChlorideStyreneInorganic ChemistryLiving free-radical polymerizationchemistry.chemical_compoundCyclopentadienyl complexPolymer chemistryMaterials Chemistrymedicine[CHIM.COOR]Chemical Sciences/Coordination chemistryCyclopentadienylPhysical and Theoretical ChemistryControlled radical polymerizationMolybdenumDiazadiene ligands010405 organic chemistryChemistryOrganic Chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymersCobalt-mediated radical polymerizationPolymerizationParamagnetic organometallicsmedicine.drugJournal of Organometallic Chemistry
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