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  • 1
    Electronic Resource
    Electronic Resource
    Synthese, Kristallstruktur und fluktuierendes Verhalten von cis-Cl2Ru(CO)(P∽O)(P^O) mit cis-ständigen (Ether-Phosphan)-LigandenHerrn Professor Wolfgang Beck zum 60. Geburtstag gewidmet. (1992)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1363-1367 
    Details
    ISSN: 0009-2940
    Keywords: Ruthenium(II) complexes ; Ether phosphanes ; Fluxional behavior ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis, Crystal Structure, and Fluxional Behavior of cis-Cl2Ru(CO)(P∽O)(P^O) with cis-Positioned (Ether-Phosphane) LigandsReaction of the ether-phosphane ligands 2a-c with Cl2Ru-(PPh3)3 (1) results in the formation of the bis(chelate) complexes trans-Cl2Ru(P^O)2 (3a-c) (P∽O = η1-P-coordinated; Pb̂O = η2-O,P-coordinated). With CO both Ru-O bonds are cleaved to give all-trans-Cl2Ru(CO)2(P∽O)2 (4a-c). The mono(chelate) complexes 5a-c are obtained from stoichiometric amounts of 3a-c and 4a-c. Upon heating the kinetically controlled products 5a-c are transformed into the thermodynamically more stable isomers cis-Cl2Ru(CO)(P∽O)(P^O) (6a-c). Both 5a-c and 6a-c show fluxional behavior. The higher coalescence temperatures and estimated ΔG≠ values of 6a-c (75, 67, and 70°C, respectively) compared to 5a-c (55, 0, and -10°C, respectively) indicate different exchange mechanisms for 5 and 6. According to an X-ray structure analysis, 6b crystallizes in the monoclinic space group P21/c with Z = 4. The action of CO on 6a-c affords the cis,cis,trans complexes 7a-c.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19921250609
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  • 2
    Electronic Resource
    Electronic Resource
    Ein einfacher Weg zur Herstellung von Alkylpalladium-Verbindungen durch Pd—O-Bindungs-Spaltung in kationischen Bis(ether-phosphan)palladium(II)1-Komplexen mit Grignard-ReagenzienHerrn Professor Heinrich Nöth zum 65. Geburtstag gewidmet. (1993)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1347-1353 
    Details
    ISSN: 0009-2940
    Keywords: Palladium complexes, alkyl-and acyl- ; Ether phosphanes ; Fluxional behavior ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A Simple Method for the Preparation of Alkylpalladium Compounds by Pd—O Bond Cleavage in Cationic Bis(etherphosphane)palladium(II) Complexes with Grignard ReagentsHerrn Professor Heinrich Nöth zum 65. Geburtstag gewidmet.The bis(chelate) complexes [Pd(P∩O)2][ClO4]2 (3a - e) react with methylmagnesium chloride with a concomitant cleavage of two weak Pd—O bonds to give the methyl complexes trans1-ClPd(P∼O)2(CH3) (4a - e) (P ∼ O; η1-P1-coordinated; P∩O: η21-O, P1-chelated; Scheme 1). Diffusion of pentane into the reaction mixture of 4a-e in the presence of the formed magnesium salts yields the cationic complexes trans-[Ch3Pd(P∼O)1-(P∩O)][ClO4] (6a, c). The reaction of 3a-e with benzylmagnesium chloride affords the cationic benzyl complexes cis-[PhCh2Pd(P∼O)(P∩O)][ClO4] (8a-e) in which only one Pd—O bond has been cleaved. In the presence of carbon monoxide 4a-e adn 6a, c are transformed into the corresponding acyl complexes CH3C(O)Pd(P∼O)2Cl (5a-e and [CH3C(O)Pd-(P∼O)(P∩O)][ClO4] (7a, c). Whereas at 183 K variable-temperature 31P{1H}1-NMR measurements of 6a, c, 7a, c indicate a non-rigid behavior of the two differently bound ether-phosphanes, the dynamic process is frozen out for 8a-e. By a lineshape analysis of the spectra the thermodynamic parameters ΔG≢, ΔH≢, and ΔS≢ are obtained. According to a crystal structure analysis 3d and 6c crystallize in the monoclinic space group P21/c with Z=4.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19931260613
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  • 3
    Electronic Resource
    Electronic Resource
    η1-P- und η2-OP-gebundene (Ether-phosphan)osmium(II)-Komplexe und ihre gegenseitige Umwandlung (1992)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 541-550 
    Details
    ISSN: 0009-2940
    Keywords: Ether phosphanes ; Osmium(II) complexes ; Conversion ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: η1-P- and η2-OP-Bonded (Ether-Phosphane)Osmium(II) Complexes and their Mutual ConversionReactions of cis-Br2Os(CO)4 with the (ether-phosphane) ligands 2a-f results in the formation of the cis,cis,trans-complexes Br2Os(CO)2(P ∼ O)2 (3a-f). 3b crystallizes in the mono-clinic space group P21/c with Z = 4. Irradiation of 3a-f leads to the cleavage of a further CO group and the formation of an Os—O bond to give the mono(chelate) complexes Br2Os(CO)-(PO) PO (5a-f), with one of the O,P ligands being bidentate. 5a-f exist as mixtures of different trans-P (A,B) and cis-P isomers (C-G). Dependent on the fact that a reversible cis/trans equilibrium or an irreversible trans → cis transformation is possible or that no trans-P isomers are present at any temperature, 5a-f may be classified in three categories. Inter-conversion of the isomers A-G results from dissociation of the η1-P coordinated ether-phosphane and concomitant occurrence of the 16e- species Br2Os(CO)(PO) (8). From temperature-dependent 31P{1H}-NMR spectroscopic investigations the temperature for the reversible opening of the metal-oxygen contact is determined. The reversible opening leads to the complexes Br2Os(CO)(PO)2 (9) with a vacant coordination site depending on the Os-O bonding strength. 5a-f react with CO to give all-trans-Br2Os(CO)2(PO)2 (4a-f). The action of the ether-phosphanes 2a-f on OsBr2(PPh3)4 (7) affords the bis(chelate) complexes Br2Os(PO)2 (6a-f) which add carbon monoxide to form all-trans-4a-f.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19921250303
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  • 4
    Electronic Resource
    Electronic Resource
    (Ether-phosphan)eisen(II)1-Komplexe mit den Koordinationszahlen Vier, Fünf und Sechs (1993)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 889-893 
    Details
    ISSN: 0009-2940
    Keywords: Iron(II) complexes ; Ether phosphanes ; Coordination numbers ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: (Ether-phosphane)iron(II) Complexes with the Coordination Numbers Four, Five, and SixPhotolysis of cis,cis,trans1-Br2(OC)2 Fe(P∑O)2 (1a, b) [O,P=Ph2PCH2CH2OCH3 (a), Ph2PCH2C4H7O (b)] results in the formation of the iron(II) complexes Br2Fe(P∼O)2 (2a), [BrFe-(P∩O)(μ1-Br)]2 (4b), and [trans1-Br2Fe(P∩O)(μ1-CO)]2 (5a) with the coordination numbers four, five, and six, respectively. 2a crystallizes in the triclinic space group P\documentclass{article}\pagestyle{empty}\begin{document}$\bar{1}$\end{document} with Z=2 and has two monodentated O,P functions (P∼O: η1-P1-coordinated; P∩O:η2-O,P1-coordinated). The dimeric complex 4b with two O∩P-chelated ligands crystallizes in the orthorhombic space group Pbca with Z=4. 2a and 4b, which react under CO pressure to give the starting complexes 1a, b, are also accessible from the ether-phosphanes 3a, b and anhydrous FeBr2.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19931260406
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