0000000000433388

AUTHOR

C.j. Alarcón

Synthesis, characterization and kinetics of the metallation of the intermediate compound to produce compound · (H2O) from Rh(II) tetraacetate

Abstract Photochemical irradiation of mixtures of [Rh2(μ-O2CCH3)4]·(HOCH3)2 and P(2-(CH3O)C6H4)Ph2 (POMe) in CH2Cl2 solution (1:1 molar ratio) yields quantitatively compound [ Rh 2 (μ- O 2 CCH 3 ) 3 ( O 2 CCH 3 )(η 2 - P (2-( CH 3 O ) C 6 H 4 ) Ph 2 ]·( H 2 O ) (1) containing a POMe acting as a chelating equatorial ( P ) axial ( O ) donor ligand. This compound undergoes intramolecular CH activation reaction at one of the phenyl rings in CHCl3 or CH3COOH/toluene solution at room temperature to form the monometallated compound [ Rh 2 (μ- O 2 CCH 3 ) 3 (μ-( C C 3 H 4 ) P (2-( CH 3 O C 6 H 4 ) Ph )]· ( H 2 O ) ( 2 ). The kinetics of the 1 → bd2 reaction have been studied in acid media (CH3CO…

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Synthesis and crystal structure of {Rh2(O2CCH3)4·P(o-CH3OH6H4)Ph2}2. A novel dirhodium(II) monoadduct with intermolecular μ-oxo interactions

Abstract We have investigated the reaction of dirhodium tetraacetate with the phosphine P( o -CH 3 OH 6 H 4 )Ph 2 (P) under different experimental conditions. From these reactions we have been able to isolate the dirhodium tetraacetate phosphine mono-adduct. The crystal structure shows that in the solid state this compound forms a centrosymmetric dimer of the dimer, {Rh 2 (O 2 CCH 3 ) 4 ·P(0-CH 3 OC 6 H 4 )Ph 2 } 2 , in which we oxygen atom from one acetate group in one Rh 2 (O 2 CCH 3 ) 4 ·P unit is axially coordinating one Rh atom on another Rh 2 (O 2 CCH 3 ) 4 · P unit (Rh⋯) 2.347(3) A intermolecular versus Rh⋯O 2.455(3) A intermolecular), and vice versa. The RhRh bond distance is 2.414…

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