6533b83afe1ef96bd12a7803

RESEARCH PRODUCT

Orthometalation of Tris(3-sodium sulfonatophenyl)phosphine with Dirhodium(II) Acetate

Pascual LahuertaFlorian P. PruchnikElizaveta ShestakovaRadosław StarostaPiotr Smoleński

subject

TrisLigandChemical shiftOrganic ChemistryRing (chemistry)PhotochemistryMedicinal chemistryInorganic ChemistryAcetic acidchemistry.chemical_compoundchemistryMoleculePhysical and Theoretical ChemistryTPPTSPhosphine

description

Tetraacetatodirhodium(II) reacts with tris(3-sodium sulfonatophenyl)phosphine (TPPTS) giving [Rh2(μ-OOCCH3)3{μ-(3-NaO3SC6H3)P(C6H4SO3Na-3)2}(HOOCCH3)]·6H2O (1) and [Rh2(μ-OOCCH3)2{μ-(3-NaO3SC6H3)P(C6H4SO3Na-3)2}2(HOOCCH3)]·12H2O (2). Their structures and properties have been studied by electronic, IR, and 31P{1H}, 1H, 1H{31P}, and 13C{1H} NMR spectroscopies. In compound 1, one of the acetate bridges is replaced by a phosphine ligand, orthometalated via the C2 carbon atom of the phenyl ring. One axial site of the Rh24+ core is occupied by a sulfonato group of the metalated ring and another one by a labile molecule of acetic acid. 1H NMR spectroscopy shows that chemical shifts of the aromatic protons depend on the nature of the axial ligands. Compound 2 contains two orthometalated molecules of TPPTS with a head-to-head structure, and one of these ligands is metalated via the C2 atom and another one via C6.

https://doi.org/10.1021/om9800703