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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 551-558 
    ISSN: 1434-1948
    Keywords: Planar-tetracoordinate carbon ; Zirconocene ; Acetylide complex ; Selective protonation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bis(alkynyl)zirconocene and -hafnocene complexes 4 react with (butadiene)zirconocene or -hafnocene, respectively, to yield the binuclear σ,π-acetylide bridged complexes [(Cp2M)2(μ-C≡C-R)2] 7 (M = Zr, Hf; R = CH3, C2H5, or CH2Ph). The complexes 7 are selectively protonated upon treatment with N,N-dimethylanilinium tetraphenylborate or tetrakis(pentafluorophenyl)borate to yield the dinuclear metallocene cation complexes [(Cp2M1)(μ-RCC1-H)(μ-C≡C-R)M2Cp2+] 13 (M1 = M2 = Zr, a-c; M1 = Zr, M2 = Hf, h; M1 = M2 = Hf, i) that contain a planar-tetracoordinate carbon atom (C1-H) bearing a hydrogen substituent. Complex 13a was characterized by X-ray diffraction. It reveals an agostic interaction of the C1-H moiety with the M2Cp2 unit. The planar-tetracoordinate carbon unit C1-H of 13a exhibits 13C/1H NMRchemical shifts of δ = 161.0 and -0.11 and a coupling constant of 1JCH = 103 Hz. Selective protonation of (μ-alkynyl)bis(group 4 metallocene) complexes containing other additional bridging ligands provides a rather general synthetic entry to planar-tetracoordinate carbon containing complexes of this type: [Cp2M1(μ-C≡C-CH3)(μ-Cl)M2Cp2] (10a-c, M1, M2 = Zr, Hf) and[Cp2M1(μ-C≡C-CH3)(μ-CH3)M2Cp2] (11a,b) selectively add a proton from [(HNMe2Ph)+(BAr4)-] at carbon atom C1 of the acetylide ligand to yield the corresponding “anti-van′t Hoff/LeBel complexes” [Cp2M1(μ-CH3CC1-H)(μ-X)M2Cp2+] (13d-g and k, X = Cl, CH3), respectively.
    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 36 (1997), S. 812-827 
    ISSN: 0570-0833
    Keywords: anti-van't Hoff/LeBel compounds ; coordination modes ; organometallic chemistry ; planar-tetracoordinate carbon ; Anti-van't Hoff/LeBel compounds ; Coordination modes ; Organometallic compounds ; Planar-tetracoordinate carbon ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is a great challenge to synthesize compounds containing planar-tetracoordinate carbon that are stable enough to be isolated, investigated, and handled under ambient conditions. There have therefore been many attempts to construct hydrocarbon frameworks that can incorporate and stabilize tetravalent carbon in this “unnatural” planar coordination geometry, for example, by steric constraints. However, success is apparently more readily achieved if the “square Planar” carbon atom is stabilized electronically. Planar-tetracoordinate carbon is sp2-hybridized and has an electron deficient σ system. The p orbital orthogonal to the bonding plane is occupied by two electrons. Therefore, σ-donor/π-accptor substituents - that is, many metals - are in principle able to stabilize this “unnatural” geometry of tetravalent carbon. Meanwhile, well-established procedures for synthesizing very stable “anti-van't Hoff/LeBel compounds” have been devised, in which the planar-tetracoordinate carbon atom is stabilized, usually by the combined action of two directly bonded metals. In most cases, the square-planar carbon is part of a double bond system. Typical stabilizing metal combinations are Zr/Al or Zr/B, but there are also examples containing two transition metals from the right-hand side of the periodic table. Reliable estimates for the energy of stabilization of square planar carbon in such compounds are now available. Both theoretical and experimental investigations show that square planar carbon atoms that are stabilized by Zr/Zr+ and Zr/Al in dimetallic compounds are favored by about 12 and 40 kcalmol-1, respectively, over the trigonal planar alternatives. Square planar coordinated carbon is thus no longer an unusual feature in organometallic chemistry and must now be more frequently considered as an alternative structural possibility.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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