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  • 1
    ISSN: 0009-2940
    Keywords: Metallocene complexes, group-4 ; Metallocene cations hydrocarbyl ; Dinuclear complexes main-group ; transition-metal ; Carbometallation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The methylzirconocene cation, employed as the [Cp2ZrCH3(THF)]+BPh4- reagent 1a reacts with (R′C≡C)2SiR2 substrates (6a-d) by means of carbometallation of an alkynyl group to yield the mixed metal ring systems 8a-d, containing both a 1,1-disubstituted μ-alkenyl and an alkynyl bridge between zirconium and silicon (e.g. shown by X-ray crystal structure analyses of complexes 8a and 8c). A similar addition reaction takes place upon treatment of the (butadiene)zirconocene/tris(pentafluorophenyl)-borane 1:1 addition product 9 with (CH3-C≡C)2Si(CH3)2 (6c) to give 10. Here the incipient alkyl zirconocene cation character of the metallocene/borate betaine complex 9 shows up in the alkynyl silane carbometallation reaction.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 1045-1046 
    ISSN: 0009-2940
    Keywords: Planar-tetraccordinate carbon ; μ-Acetylide complex ; μ-Aryl cyanide complex ; Zirconocene cation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The planar-tetracoordinate carbon compound 4 exchanges the bridging μ-(η1-C:η2-C,C)-2-butyne ligand for p-tolunitrile in dichloromethane at 90°C to yield the [μ-(η1-N:η2-C,N)-aryl cyanide]dizirconium cation complex 2a. X-ray diffraction revealed an aza-allenyl-type character of the RCNZr moiety in this thermodynamically favored (μ-nitrile)zirconium cation complex.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 1-3 
    ISSN: 0009-2940
    Keywords: Planar-tetracoordinate carbon atoms ; Metallocene cations methyl ; Metallocene complexes alkynyl group-4 ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The methylhafnocene cation 2a reacts with bispropynylzirco-nocene to give a single regioisomeric planar-tetracoordinate carbon compound (4a) that contains the hafnium atom singly-bonded and the zirconium center η2-coordinated to the bridging μ-(η1-C:η2-C,C-2-butyne) ligand. However, the reaction between the methylzirconocene cation 2b with bis(phenylacetylide)hafnocene (3b) gives the pure regioiso-mer 4b with an opposite relative arrangement of the two group 4 transition metals (the methyl is at the planar-tetra-coordinate carbon atom C2). Complex 4a was characterized by an X-ray crystal structure analysis.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 109 (1997), S. 840-856 
    ISSN: 0044-8249
    Keywords: Anti-van't Hoff/Le Bel-Verbindungen ; Koordinationschemie ; Organometallchemie ; Planar tetrakoordinierter Kohlenstoff ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es ist eine große Herausforderung, Verbindungen mit planar tetrakoordiniertem Kohlenstoff zu synthetisieren, die so stabil sind, daß man sie isolieren und bei Normalbedingungen untersuchen und handhaben kann. Deshalb hat es viele Versuche gegeben, Kohlenwasserstoffgerüste so zu konstruieren, daß sie das tetrakoordinierte Kohlenstoffatom in seiner nichtnatürlichen planaren Koordinationsgeometrie aufnehmen und z. B. durch sterischen Zwang stabil halten könnten. Viel leichter kommt man offenbar zum Ziel, wenn man quadratisch-planar umgebene Kohlenstoffatome elektronisch stabilisiert. Planar tetrakoordinierte Kohlenstoffatome sind sp2-hybridisiert und durch ein Elektronenmangel-σ-System charakterisiert. Das zur σ-Bindungsebene orthogonale p-Orbital ist mit zwei Elektronen besetzt. Daher sind σ-Donor/π-Acceptorsubstituenten, und damit viele Metalle, prinzipiell in der Lage, diese nichtnatürliche Koordinationsgeometrie des tetrakoordinierten Kohlenstoffatoms elektronisch zu stabilisieren. Mittlerweile gibt es gut ausgearbeitete Wege zu sehr stabilen „Anti-van't Hoff/Le Bel-Verbindungen“, bei denen ein planar tetrakoordiniertes Kohlenstoffatom meist durch die gemeinsame Wirkung von zwei direkt gebundenen Metallatomen stabilisiert wird. Das „quadratisch-planar“ umgebene Kohlenstoffatom ist dabei oft Teil eines Doppelbindungssystems. Typische stabilisierende Metallkombinationen sind Zirconium und Aluminium oder Zirconium und Bor. Aber es gibt auch Beispiele mit zwei Übergangsmetallen von der rechten Seite des Periodensystems. Darüber hinaus liegen mittlerweile verläßliche Abschätzungen zur Stabilisierung der planaren Tetrakoordination in solchen Verbindungen vor. Aus theoretischen und experimentellen Untersuchungen ergibt sich, daß in Zr/Zr+-oder Zr/Al-Verbindungen die planare Tetrakoordination des Kohlenstoffatoms ca. 12 bzw. 40 kcal mol-1 günstiger ist als die trigonal-planare Koordination. Quadratisch-planar koordinierter Kohlenstoff ist damit in Organometallverbindungen kein ungewöhnliches Strukturmerkmal mehr und muß häufiger als bisher als eine alternative strukturelle Möglichkeit in Betracht gezogen werden.
    Additional Material: 4 Ill.
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  • 5
    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.
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  • 6
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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