6533b836fe1ef96bd12a1408

RESEARCH PRODUCT

Synthesis of new half sandwich tetrachloro derivatives of molybdenum(V) and tungsten(V). X-ray structures of (C5HPri4)W(CO)3(CH3) and (C5Et5)WCl4

Dolores MoralesHelmut SitzmannMatthias BastianMatthias BastianRinaldo PoliPhilippe Richard

subject

StereochemistryDimerchemistry.chemical_element010402 general chemistryRing (chemistry)01 natural sciencesBiochemistryTungstenInorganic Chemistrychemistry.chemical_compoundCyclopentadienyl complexOrganometallic synthesisMaterials Chemistrymedicine[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryBulky cyclopentadienyl ligandsMolybdenumAqueous solution010405 organic chemistryHydrideOrganic Chemistry0104 chemical sciencesCrystallographychemistryMolybdenumFerricX-ray structureSingle crystalmedicine.drug

description

International audience; The new synthetic intermediates (Ring)MCl4 [Ring=C5HPri4 or 4Cp, M=Mo, 2; Ring=C5Et5 or VCp, M=W, 4, Ring=4Cp, M=W, 6] containing sterically protecting cyclopentadienyl ligands have been synthesized. Along the synthetic pathway to 2, it was found that the treatment of [4CpMo(CO)3]− with an aqueous ferric solution according to the well established Manning procedure affords the hydride compound 4CpMo(CO)3H (1) by hydrolysis rather than the expected neutral dimer by oxidation. Compound 1 could be converted, however, to 2 upon oxidation with PhICl2 in good yields. Compound 4 is shown by a single crystal X-ray analysis to adopt a monomeric four-legged piano stool structure. The precursors to compounds 4 and 6, (Ring)W(CO)3(CH3) (Ring=VCp, 3; 4Cp, 5) have also been characterized, including an X-ray structure for 5.

10.1016/s0022-328x(02)01392-xhttps://hal.archives-ouvertes.fr/hal-03284170/document