ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    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.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...