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  • Inorganic Chemistry  (2)
  • Azatitanacyclobutanes  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 291-299 
    ISSN: 0009-2940
    Keywords: Titanacyclobutane complexes ; Vinylidene intermediates ; Titanium complexes ; MO theory, applied ; Cycloreversion ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Structure and Reactivity of Bis(π-pentamethylcyclopentadienyl)(2-methylidene)titanacyclobutaneThe reaction of vinyllithium with bis(π-pentamethylcyclopentadienyl)titanium dichloride in a molar ratio of 2:1 quantitatively yields the unexpected titanacyclobutane derivative (2) (Cp* = [C5(CH3)5]). The isolated complex 2 has been characterized by spectroscopic methods and by elemental analysis, and its structure has been confirmed by an X-ray structure determination. The chemical reactivity of 2 is characterized by the splitting of the four-membered ring at higher temperatures, forming a titanocene vinylidene fragment {Cp2*Ti = C = CH2} and ethylene. This cycloreversion is confirmed by the fragmentation behavior in the mass spectrometer, and some aspects of it have been studied by Extended Hückel Model calculations.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1003-1013 
    ISSN: 0009-2940
    Keywords: Metallocene complexes, bent ; Titanium complexes ; Vinylidene complexes ; Transition metal complexes ; Heterodinuclear complexes ; Carbene complexes ; Early-Late heterodinuclear complexes ; Metallacycles ; Oxatitanacyclobutane complexes ; Oxatitanacyclopentene complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclic Isomeric Four- and Five-Membered Heterodinculear Carbene Complexes  -  Formed from a Titanocene Vinylidene Fragment and Metal CarbonylsThe four-membered heterodimetallic carbene complexes Cp*2 16 [LnM: Cr(CO)5 (a), Mo(CO)5 (b), W(CO)5 (c), CpRe(CO)2 (f), Mn2(CO)9(g), Re2(CO)9 (h), Fe(CO)4 (i), Rh(acac)(CO) (i)] are easily prepared by trapping the vinylidenetitanocene [Cp*2Ti=C=CH2] fragment 6 with the corresponding metal carbonyls. The vinylidenetitanocene 6 is generated in a favourable manner from Cp*2Ti(CH3)CH=CH2 (13) or Cp * (Fv)TiCH = CH2 (14) [Fv: C5(CH3)4CH2] by a 1,3-H shift (α elimination) at room temperature. The formation of 16 is characterized by a preferred suprafacial [2 + 2] cycloaddition. Starting from Cp*2 (5) or 14 and transition metal carbonyls unexpected isomeric five-membered titanacycles Cp*2 8 [MLn = a-c, MnCp(CO)2 (d), MnCp′(CO)2 (e), f-i] are obtained at higher temperatures (70-100°C). These oxatitanacyclopentenes 8 are formed also upon heating via the kinetic product 16 with high yield, as a result of a 1,2-hydrogen shift, proved for c, g, h. From the spectroscopic data an η1-vinylcarbene structure is deduced, exhibiting a cis- (16) or trans-configurated (8) LnM=C—C=C sequence. An X-ray structure analysis shows the importance of the acyl resonance form in 8a, typically observed for such heterodimetallic carbene complexes. The reversible liberation of the metal carbonyl is a remarkable property of complexes 16 in solution, whereas the thermodynamic product 8 shows the typical properties of Fischer carbene complexes.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 253-256 
    ISSN: 1434-1948
    Keywords: Titanium ; Vinylidene complexes ; [2+2] Cycloaddition ; Metallacycles ; Azatitanacyclobutanes ; Clathrates ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The titanocene vinylidene intermediate [Cp*2Ti=C=CH2] (9) reacted with the carbodiimides R-N=C=N-R [R = p-CH3C6H4 (19a), C6H11 (19b)] to give the N=C-cycloaddition products [Cp*2Ti{-NR-C(=NR)-(C=CH2)-}] [(R = p-CH3C6H4 (20a), C6H11 (20b)]. The X-ray structure of 20a in form of a surprisingly stable n-hexane clathrate is presented. The azatitanacyclobutane [Cp*2Ti{-NPh-C(Ph)(H)-(C=CH2)-}] (22) was formed from the reaction between 9 and benzylidene aniline [PhN=C(Ph)H (21)]. Reactivity studies showed that azatitanacyclobutanes are unreactive upon typical ring-enlargement reactions as observed for other four-membered titanacycles.
    Type of Medium: Electronic Resource
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