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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1453-1459 
    ISSN: 1434-1948
    Keywords: Group-5 bent metallocene cation complexes ; (Butadiene)tantalocene cation ; (s-trans-η4-Butadiene)metal complex ; Ethene polymerization ; Metallocenes ; Homogeneous catalysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: (Butadiene)TaCp*Cl2 (6) was treated with CpNa to yield (η2-butadiene)TaCp*CpCl (7). Subsequent reaction with [Cp2ZrCH3+][CH3B(C6F5)3-] resulted in transfer of the chloride ligand from tantalum to zirconium with formation of the [(s-trans-η4-butadiene)TaCp*Cp]+ cation [8, with CH3B(C6F5)3- anion]. Complex 8 was characterized spectroscopically and by an X-ray crystal structure analysis. The group-5 [(s-trans-η4-C4H6)TaCp*Cp]+ bent metallocene cation complex 8 reacts with ketones (acetone, adamantanone) to yield the corresponding seven-membered 2-tantalatetrahydrooxepine cation complexes (9, 10). 1-Cyanoadamantane reacts with 8 to yield the 2-tantala-3,6-dihydro-2H-azepine cation system 11. Activation of 8 with methylalumoxane gives an active ethene polymerization catalyst.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: Planar-tetracoordinate carbon ; Dynamic organometallic systems, μ-alkyne complexes ; π-Agostic systems ; Zirconium ; Metallocenes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The benzonitrile hydrozirconation product Cp2ZrCl(N—CHPh) 8 was treated with propynyl lithium to yield the (propynyl)(benzaldimido)ZrCp; complex 9. Subsequent treatment with trityl tetraphenylborate generated [Cp2Zr(C—C—CH3)-BPh-4] that instantaneously added to 9 to eventually form the (μ-aldimido)(μ-η1:η2-hexadiyne)ZrCp2 cation 11. The X-ray crystal structure analysis showed that 11 contains a planar-tetracoordinate carbon atom that is stabilized by forming a three-center-two-electron bond with the two adjacent metal atoms. Similarly, complex 9 reacted with [Cp2Zr(CH3)+CH3B(C6F5)3 1 to yield the planar-tetracoordinate carbon containing (μ-aldimido)(μ-η1:η2-2-butyne) Cp; cation 12. Both complexes 11 and 12 exhibit dynamic NMR spectra due to their rapid reorganization of the dimetallabicyclic frameworks (ΔG* = 10 kcal mol-1) in addition to an anchimerically assisted C—N bond rotation (ΔG* =15 kcal mol-1).
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 28 (1989), S. 397-412 
    ISSN: 0570-0833
    Keywords: Carbene ligands ; Carbene ligands ; Titanium ; Hafnium ; Metallocenes ; Zirconium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The structure and creativity spectrum of transition-metal carbene complexes has been widened significantly by the bent metallocenes of titanium, zirconium, and hafnium. Proceeding from metal carbonyls and reactive (butadiene)-, (aryne)-, or (olefin) MCp2 complexes, many new Fischer-type metaloxycarbene complexes of Zr, Hf, V, Nb, Cr, Mo, W, Mn, Re, Fe, Ru, Os, Co, Ni, and Rh have been synthesized. The incorporation of titanocene, zirconocene, or hafnocene fragments allows new types of carbene complexes to be prepared. For the (alkylidenamido)metallocene complexes , metallocene ylides , and binuclear (μ-alkynyl)metallocene compounds, some metalligand π bonding is indicated. Metallocene complexes with metallaoxirane units, , show similar chemical behavior to that of binuclear (μ-methylene)complexes . The methylene groups of zirconaoxirane complexes, which are derived from carbon monoxide, may be expelled as ethylene by thermally induced CC coupling. With metal hydrides, CH2 transfer with insertion into the metal-hydride bond occurs. In one case, methylene insertion into a metal-carbon bond can even be observed. These reactions of Ti-group metallaoxiranes could be models for postulated intermediates in the Fischer-Tropsch synthesis.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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