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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 479-488 
    ISSN: 0009-2940
    Keywords: Heterobimetallic complexes ; Carbene complexes ; Alkynes ; Coupling reaction ; Bridging ligands ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sequential reaction of the dimethylamino(trimethylsilylethylnyl)carbene complexes [(CO)5M'=C(NMe2)C≡CSiMe3] [M' = W (1a)] with KF/THFMeOH, nBuLi and transition metal halides, [XMLn], affords heterobimetallic propynyliden complexes of the type [(CO)5M'=C(N-Me2)C≡CMLn] [MLn = Ni(PPh3) Cp (4a, b). Ni(PMe2Ph)2- {Mes) (Mes=2,4,6-C6H2Me3) (5a), Rh(CO)(PPh3)2 (6a), Fe(CO)2Cp (7a,b)]. In contrast, reaction of 1a with MeLi · LiBr and [IFe(CO)2Cp] yields the novel N-metallated complex [(CO)5W=C{N(ME)Fe(CO)2Cp}C≡CSiMe3] (8a). The complexes [(CO)5M'=C(NMe2)C≡CMLn=Fe(CO)2Cp (7a, b), Ru(CO)2Cp (10a,b), Ru(CO)(PPh3)Cp (11a), Mn(CO)5 (12a), Re(CO)5 (13a)] are accessible by Pd-catalyzed coupling of the C-stannylated carbene complexes [(CO)5M'=C-(NMe2)C≡CSnBu3] (9a, b) with [XMLn]. The related monomethylaminocarbene complexes [(CO)5M'=C(NHMe)C≡ CSnBu3] (16a, b), obtained by stannylation of [(C))5M'=C(NHMe)C=CH] (15a, B) with Bu3SnNEt2, react with [IFe(CO)2Cp] to give the bimetallic complexes [(CO)5M'=C(NHMe)C≡CFe(CO)2Cp] (17a, b). The complexes 4a, 5a, 7a and 10a were characterized by X-ray structural analysis. The spectroscopic and structural data suggest that the two metal centers in 4-7, 10-13, and 17 interact only weakly.
    Additional Material: 4 Ill.
    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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  • 3
    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.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 1225-1234 
    ISSN: 1434-1948
    Keywords: Vinylidene complexes ; Cyclobutenylidene complexes ; Bridging ligands ; Cycloadditions ; Cross-coupling ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pentacarbonyl(dimethylvinylidene)chromium, [(CO)5Cr=C=CMe2] (1), reacts with the butadiynyl complexes [Cp(CO)2FeC≡CC≡CR] [2; R = SiMe3 (a), nBu (b), Ph (c)] and [Cp(CO)(PPh3)FeC≡CC≡CSiMe3] (3a) by regiospecific cycloaddition of the Cα≡Cβ bond of the butadiynyl complexes to the C=C bond of 1 to form the 1,3-heterobinuclear cyclobutenylidene complexes 4a-c and 5a with an alkynyl substituent at C-2 of the bridging ring. Desilylation of the 2-C≡CSiMe3 substituent in 4a and 5a with tetrabutylammonium fluoride affords the 2-C≡CH-substituted complexes 6 and 7. Complex 4a reacts with HNMe2 and HN(CH2)5 by substitution of NR2 for the 3-Fe(CO)2Cp fragment to form the corresponding 3-aminocyclobutenylidene complexes 10 and 11. Sequential reactions of 4a with [nBu4N]F and nBu3SnNEt2 give the trinuclear 2-C≡CSnnBu3-substituted complex 12. Coupling of 12 with C6H4I2-p yields the 2-C≡CC6H4I-p-substituted complex 13. Coupling of 7 with C6H4I2-p yields a mixture of the mono-coupling product 14 and the tetranuclear C≡C-C6H4-C≡C-bridged bis(cyclobutenylidene) complex 15. Coupling of 7 with trans-[(Et3P)2MCl2] in the presence of CuI/[Pd(PPh3)4] gives the trinuclear 2-C≡C-M(PEt3)2X-substituted complexes 16 (M = Pd, × = I) and 17 (M = Pt, × = Cl). The spectroscopic data as well as the results of the X-ray-structural analysis of 5a indicate strong electronic communication between the metal centers. In the solid state, 5a exhibits a “butterfly” conformation.
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