6533b86efe1ef96bd12cc05b
RESEARCH PRODUCT
Preparation of trichloro- and tribromocyclopentadienyltungsten(IV)
Rinaldo PoliRaymund C. TorralbaHaley BlackburnHeinz-bernhard KraatzJames C. Fettingersubject
Stereochemistrychemistry.chemical_element010402 general chemistryRing (chemistry)01 natural sciencesBiochemistryMedicinal chemistryCO-free compoundsTungstenAdductInorganic ChemistryParamagnetismchemistry.chemical_compoundMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistryLigandOrganic ChemistryDecarbonylationMetal–metal bondsToluene0104 chemical sciences3. Good healthDiamagnetismchemistryMolybdenumX-ray structuresdescription
International audience; The thermal decarbonylation of (Ring)WX3(CO)2 in refluxing toluene has led to the preparation of the CO-free compounds [(Ring)WX3]2 [Ring=η5-C5H5 (Cp) and X=Cl (1a) or Br (1b); Ring=η5-C5H4Me (Cp′), X=Cl (2a) or Br (2b); Ring=η5-C5Me5 (Cp*), X=Cl (3)]. The NMR properties of these molecules are consistent with diamagnetism and thereby indicate a different structure from that of the paramagnetic molybdenum analogues. Compounds 1a and 2a react with dppe to afford mononuclear 18-electron adducts, (Ring)WCl3(dppe) (Ring=Cp (4) or Cp′ (5)). The X-ray structure of 5 shows a pseudo-fac-octahedral geometry with the dppe ligand occupying two equatorial (e.g. cis relative to Cp′) coordination sites. The X-ray structure of two by-products of the synthetic processes are also reported, e.g. Cp′3W3Cl3(μ2-Cl)2(μ3-O) (6) and [Cp*WCl3]2(μ-O) (7).
year | journal | country | edition | language |
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2000-01-01 | Journal of Organometallic Chemistry |