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  • 1
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 933-940 
    ISSN: 0009-2940
    Schlagwort(e): Bis(acyl)1-bridged bimetallic complexes ; Rhenium complexes ; Molybdenum complex ; Ruthenium complex ; Copper complex ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Organometallic Lewis Acids, IL[1]. - Bis(acyl)1-Bridged Heterometallic Complexes of Rhenium, Molybdenum, Ruthenium, and CopperThe reaction of the metalla-β1-diketonate complex [(OC)41-Re[-C(Me)O]2][NMe4] with various organometallic Lewis acids yields the bis(acyl)1-bridged bimetallic complexes (OC)4 -Re[-C(Me)O-]2Re(CO)4 (1), (OC)4Re[-C(Me)O-]2MoCp(CO)2 (2), (OC)4Re[-C(Me)O-]2Ru(η31-C3 H5)(nbd) (nbd=norbor-nadiene) (3), [(OC)4 Re[-C(Me)O-]2Ru(PPh3)2 (CO)2][BF4] (4), and (OC)4 Re[-C(Me)O-]2Cu[-O(Me)C-]2Re(CO)4 (5), respectively. The structures of the compounds 1-5 have been determined by X-ray diffraction. They show different conformations of the six-membered ring Re[-C(Me)O-]2[M]. The molecular structure of complex 1 proves a “flipping” of the acyl ligands.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 0009-2940
    Schlagwort(e): Heterobimetallic complexes ; Iron complexes ; Platinum complexes ; Silyl complexes ; Phosphido bridges ; Hydrido complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Transition Metal Silyl Complexes, 48[1]. - Synthesis of the New Heterobimetallic Dinuclear Silyl Complexes (OC)3(R3Si)-Fe(μ-PR′R″)Pt(1,5-COD)(Fe-Pt), Phosphane Exchange Reactions of (OC)3(R3Si)Fe(μ-PR′R″)Pt(PPh3)2(Fe-Pt), and Preparation of the Dihydrido complexes [(OC)3Fe(μ-PPh2)(μ-H)2Pt(PR3)2][BF4](Fe-Pt)The dinuclear, silyl-substituted complexes (OC)3(R3Si)Fe(μ-PR′r″)Pt(1,5-COD) (1) [μ-PR′R″ = PPh2, PCY2, PHPh; SiR3 = SiPh3, Si(OMe)3] were prepared in high yields by the oxidative addition of the hydrido complexes (OC)3(PHR′R″)Fe(H)-SiR3 to Pt(1,5-COD)2. Upon reaction of (OC)3(R3Si)Fe(μ-PR′R″)Pt(PPh3)2 [μ-PR′R″ = PPh2, PHCy; SiR3 = SiPh3, SiPh2Me, SiPhMeCl, Si(OMe)3] with two equivalents of PR‴3 (PMe3, PBu3, PEt3) or with one equivalent of chelating di-phosphanes (vdpp, dppe, dppm) both PPh3 ligands are displaced, and (OC)3(R3Si)Fe(μ-PR′R″)Pt(PR‴3)2 or (OC)3(R3Si)-Fe(μ-PR′R″)Pt[(PPh2)2X] (X = C=CH2, C2H4, CH2) are formed, respectively. When one equivalent of PMe3 is used, only the PPh3 ligand trans to the μ-PPh2 bridge is substituted, and (OC)3(Ph3Si)Fe(μ-PPh2)Pt(PPh3)(PMe3 is formed. The 1,5-COD ligand in 1 is displaced by P(OR)3 to give (OC)3-(Ph3Si)Fe(μ-PPh2)Pt[P(OR)3]2 (R = Me, Ph). The complexes (OC)3(Ph3Si)Fe(μ-PPh2)Pt(PMe3)2and (OC)3(Ph3Si)Fe(μ-PPh2)Pt[(PPh2)2C=CH2] were characterized by X-ray structure analysis. The short Fe-Si distances [233.0(2) and 235.6(3) pm] and the infrared v(CO) absorptions indicate that the Fe-Pt bonds are quite polar. Protonation of (OC)3(Me2-PhSi)Fe(μPPh2)Pt(PPh3)2 with CF3COOH gives the hydrido-bridged complex [(OC)3(Me2PhSi)Fe(μ-PPh2)(μ-H)Pt-(PPh3)2][O2CCF3]. Upon addition of an excess of HBF4 · Et2O to (OC)3(R3Si)Fe(μ-PPh2)Pt(PPh3)2 (R = Ph, OMe), (OC)3-Si)Fe(μ-PPh2)Pt[Pt[P(OMe)3]2 or (OC)3(Ph2MeSi)Fe(μ-PPh2)-Pt(dppe) R3SiF is split, and the corresponding μ-dihydrido complexes [(OC)3Fe(μ-PPh2)(μ-H)2Pt(PR3)2][BF4] are obtained.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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