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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 191-202 
    ISSN: 1434-1948
    Keywords: Polynuclear complexes ; Carbene complexes ; Bridging ligands ; Alkynyl complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The sequential reaction of two equivalents of the dimethylamino(ethynyl)carbene complexes [(CO)5M=C(NMe2)C≡CH] [M = W (1a), Cr (1b)] with two equivalents of nBuLi and one equivalent of a transition metal dichloride, [Cl2M′(Ln)], affords trinuclear biscarbene complexes of the type [(CO)5M=C(NMe2)C≡C-M′(Ln)-C≡CC(NMe)2=M(CO)5] [M′(Ln) = Ni(PEt3)2 (2a, b), Pd(PEt3)2 (3a, b), Pt(PEt3)2 (4a, b), Fe(dmpe)2 (6a), Hg (8a), Ti(η5-C5H5)2 (9a, b)] [dmpe = 1,2-bis(dimethylphosphino)ethane]. Treatment of 1a with equimolar amounts of first nBuLi and then [Cl2M′(Ln)] results in the formation of the monosubstitution products [(CO)5W=C(NMe2)C≡CM′(Ln)] [M′(Ln) = trans-Pd(PEt3)2Cl (5a), trans-Fe(dmpe)2Cl (7a)]. Additionally, the synthesis of the heterobimetallicethynylcarbene complex [(CO)5W=C(NMe2)C≡CPd(PEt3)2C≡CH] (10a), starting from 1a and [ClPd(PEt3)2C≡CH], is described. When three equivalents of 1a are treated, first with three equivalents of nBuLi and then with one equivalent of the trihalides PCl3 or BBr3, the novel tris(ethynylcarbene) complexes [{(CO)5W=C(NMe2)C≡C}3E] [E = B (11a), P (12a)] are obtained. The reaction of four equivalents of 1a,b with four equivalents of nBuLi, followed by addition of one equivalent of a group 14 tetrachloride [M′Cl4], yields the novel tetrakis(ethynylcarbene) complexes [{(CO)5M=C(NMe2)C≡C}4M′] [M′ = Si (13a, b), Ge (14a), Sn (15a, b)]. The complexes 8a, 9a, 12a, and 15a were characterized by X-ray structural analyses. All spectroscopic and structural data suggest that the carbene fragments and the central transition metal or heteroatom in these new bis-, tris-, and tetrakis(ethynylcarbene) complexes interact only weakly.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 1063-1067 
    ISSN: 0009-2940
    Keywords: Heterobimetallic complex ; Carbene complexes ; Bridging ligands ; Coupling reaction ; Alkynes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sequential reaction of the dimethylamino(ethynyl)carbene complex [(CO)5 W=C(NMe2)C≡CH] (1) with nBuLi, CuI and BrC≡CSiMe3 affords the dimethylamino(trimethylsilylbutadiynyl)carbene [(CO)5W=C(NMe2)C≡C—C≡C—SiMe3] (2). Desilylation of 2 with KF/THF/MeOH gives [(CO)5W=C(NMe2)C≡C—C≡CH] (3). The C-stannylated carbene complex [(CO)5W=C(NMe2)C≡C—C≡CSnBu3] (4) is obtained by deprotonation of 3 with nBuLi and subsequent reaction with Bu3SnCl. Pd-catalyzed coupling of complex 4 with [ClRu(CO),Cp] affords the heterobimetallic pentadiynylidene complex [(CO)5W=C(NMe,)C≡C—C≡CRu-(CO)2Cp] (5) The analogous Fe derivative [(CO),W=C(NMe,)C≡C—C≡CFe(CO)2Cp] (6) is obtained by sequential reaction of 3 with nBuLi and [IFe(CO)2Cp] Similarly, treatment of 3 first with nBuLi and then with half an equivalent of HgCl2 affords the novel C4HgC4-bridged biscarbene complex [(CO)3W=C(NMe2)C≡C—C≡CHgC≡C—C≡CC(NMe2)=W(CO)5]( 7 ) All new compounds are stable at room temperature. Spectroscopic data suggest weak interaction of the metal centers in 5 - 7.
    Type of Medium: Electronic Resource
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