6533b7cefe1ef96bd1257a9e
RESEARCH PRODUCT
Exploring reactivity of a bis-sulfonium zirconocene-ate dimer: synthesis of various zwitterionic phosphonium anionic zirconocene complexes
Esteban OrtegaPhilippe MeunierNadine PirioPhilippe Richardsubject
SulfoniumDimer010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryInorganic ChemistryBenzaldehydechemistry.chemical_compoundChalcogenanionic zirconoceneMaterials ChemistryOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryReactivity (chemistry)PhosphoniumPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSBicyclic molecule010405 organic chemistrysulfoniumOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryzirconocene-atephosphoniumCycloaddition3. Good health0104 chemical scienceschemistrychalcogenszwitterionic complexesdescription
Abstract Formal [3+2] cycloaddition reactions between the bis-sulfonium zirconocene-ate dimer 1a and methylpropiolate, benzaldehyde and carbon disulfide afforded stable zwitterionic phosphonium zirconocene-ate complexes 2–4, respectively, with two orthocondensed five-membered heterocycles. X-ray crystal structure of 4 has been determined. Elemental chalcogens (S, Se, Te) gave rise also to a new variety of five-coordinate zirconium(IV) complexes (5–7) by a formal [3+1] cycloaddition reaction. In these bicyclic zirconates, sulfur is included in a five-membered ring while the second chalcogen is in a four-membered one.
year | journal | country | edition | language |
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2007-10-01 |