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  • 1
    ISSN: 0009-2940
    Keywords: Tetraphosphorus ligands ; Bond cleavage in P4, stepwise ; Rhodium P4 complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pn Ligands with Maximum Electron-Donor Capacity, 7. - Three-Component Reaction of P4-Phosphorus with [CpxRh(CO)2] in the Presence of [Cr(CO)5THF] or [CpMn(CO)2THF]. - A Method of Studying the Pathway from Tetrahedral P4 to the Planar cyclo-P4 LigandHerrn Professor Gerhard Fritz zum 75. Geburtstag gewidmet.The reaction of P4 with [CpxRh(CO)2] (Cpx = Cp′, Cp′′; Cp′ = η5-C5H4tBu, Cp′′ = η5-C5H3tBu2-1,3) in the presence of [Cr(CO)5THF] leads to [CpxRh(CO)(η1:1-P4){Cr(CO)5}4] (1a, b), [Cp′′Rh(η4-P4){Cr(CO)5}3] (2b), and [Cp′Rh(η4-P4){Cr-(CO)5}4] (3a). In the corresponding reaction with [CpMn-(CO)2THF] no P4 takes part, and [(Cp′′RhCO)(CpMnCO)(μ-CO)2] (4) is formed. An X-ray structure determination of [CpxRh(CO)(η1:1-P4){Cr(CO)5}4] (1) and [Cp′Rh(η4-P4)-{Cr(CO)5}4] (3a) indicates a stepwise (PP) bond cleavage as the transformation pathway from the P4 tetrahedron to the cyclo-P4 ligand by passing a bicyclotetraphosphane. In the cyclo-P4 ligand complex 3a all P atoms are able to coordinate to [Cr(CO)5] groups. However, in [Cp′′Rh(η4-P4){Cr(CO)5}3] (2b) the additional tBu group at the Cpx ligand sterically influences the coordination behavior of the P atoms, and only three of them are able to coordinate to [Cr(CO)5] units. In these syntheses the [Cr(CO)5] moieties promote the reaction and stabilise intermediates along the reaction pathway. Variable-temperature 31P{1H}-NMR measurements indicate for 2b the freezing of the Cp′′ rotation at low temperature and reveals a ΔG≠c (at the coalescence temperature) of 36 kJ mol-1. Surprisingly, in [(Cp′′RhCO)(CpMnCO)(μ-CO)2]-(Rh-Mn) (4) the Cpx ligands are cis-oriented whereas in [(Cp*RhCO)(CpMnCO)(μ-CO)2](Rh-Mn) a trans arrangement is observed. This indicates the unusual behavior of the Cp′′ ligand as a “rod” and not as an “enlarged disk” like Cp* in the crystal lattice of these compounds.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: Carbon dioxide fixation ; 1-Azadiene ligands ; Nickel(0) complexes ; Carboxylation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organometallic CO2 Reservoires from Nickel(0)-1-Azadiene-Type Ligands and Their Reactivity in the Carboxylation of Acetophenone1-Azadiene-type ligands yield with nickel(0) binuclear organometallic compounds of the type [Ni(1-azadiene)n,]2 (n = 1, 2). The structures of the complexes 1 (n = 2, ligand A) and 3 (n = 1, ligand C) have been characterized by X-ray crystallography. 1 is unreactive towards CO2, 3 and similar compounds are able to react with CO2 to give metallacyclic carbamato complexes of Ni(II). In these compounds CO2 is activated and can carboxylate acetophenone to yield benzoylic acid upon protolysis. These reactions mimic biologic conversion reactions of CO2 into organic material by organometallics. - The addition of two moles of the (bpy)Ni(0)-fragment [from (bpy)Ni(COD)] to 3 gives the tetranuclear complex 6. The X-ray analysis of the monomeric model compound (bi-py)Ni(A) (11) shows that only the olefin part is coordinated. 6 and 11 can also react with CO2. Cu(I) complexes with 1-azadiene-type ligands are not reactive towards CO2.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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