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  • 1
    ISSN: 0009-2940
    Keywords: Diphosphamanganacyclopropanes ; Alkyne insertion ; Alkyne addition ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal-;Containing Heterocycles: Preparation, Properties, Reactions, LXXX.  -  Insertion and Addition Reactions on Diphosphamanganacyclopropanes with Activated AlkynesThe thermally and kinetically stable diphosphamanganabicyclooctadienones 3a  -  e [R2 = tBu: R1 = iPr (a), nPr (b), Ph (c); R2 = Cy: R1 = nPr (d), Ph (e)] are obtained by the reaction of the alkyne (CCO2Me)2 with the diphosphamanganacyclopropanes (OC)4Mn-PR12=PR2 (2a  -  e). Depending on steric factors the formation of 3a  -  e occurs in two different ways. In a first step the alkyne is inserted into the P  -  P bond of 2a  -  e to give the kinetically labile five-membered rings 1a  -  e. Subsequently another alkyne is added to the PR2 and a CO group of 1a  -  e to give 3a  -  e. In an alternative way the alkyne is added first to the PR2 and a CO group of 2a with formation of the diphosphamanganabicyclohexenone 4a. Insertion of a second alkyne into the P  -  P bond of 4a affords the bicyclooctadienone 3a. Compound 2a, 3c, and 4a have been characterized by X-ray structural analyses.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: Ether-phosphanes ; Ruthenium complexes ; Polysiloxane matrices ; CP-MAS NMR ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carrier-Bound Organometallic Complexes, III[1]. - Polysiloxane-Bound (Ether-phosphane)ruthenium(II) Complexes and Their CP-MAS NMR-Spectroscopic CharacterizationThe reaction of the functionalized ether-phosphane ligand CH3O(CH2)2P(Ph)(CH2)3Si(OMe)3 (1c) with Cl2Ru(PPh3)3 (2) and HRuCl(CO)(PPh3)3 (3) results in the formation of the mono-chelated (ether-phosphane)ruthenium(II) complex Cl2Ru(P∼O)2(P∼O) (4c) and the hydride HRuCl(CO)(P∼O)3 (5c) (P∼O: η1-P-coordinated; P∼O: η2-O∼P-coordinated). Compounds 4c and 5c are polycondensated to the corresponding polysiloxane-bound complexes 4c′ and 5c′. 31P-chemical shifts of the immobilized species 4c′ and 5c′ in the solid-state CP-MAS NMR spectra are compared with those of the 31P{1H}-NMR spectra of monomeric complexes 4b, c and 5b, c with the ligands CH3O(CH2)2P(Ph)(CH2)3SiMe3 (1b) and 1c in solution. No change in the structure between the monomeric and polymeric species could be observed. According to 29Si CP-MAS NMR-spectroscopic investigations the polysiloxane chains are connected by ruthenium complexes to a network with favourable properties. The chelated polysiloxane-bound red complex 4c′ adds CO in the solid state to give quantitatively yellow all-trans-Cl2Ru(CO)2(P∼O)2 (6c′). In the presence of carbon monoxide there is an equilibrium between 5c′ and HRuCl(CO)2(P∼O)2 (7c′) which was also found in solution for 5b, c and 7b, c. The reactions indicate that the chemistry of polysiloxane-bound ether-phosphane complexes can well be compared with the chemistry in solution. 31P CP-MAS NMR spectra of the complexes 4c′ and 5c′ are strongly dominated by a chemical shift anisotropy which shows a fingerprint pattern both for monomeric crystalline complexes 4a, 5a [containing ligand Ph2P(CH2)2OCH3 (1a)] and polysiloxane-bound phosphane complexes 4c′ and 5c′.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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