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 124 (1991), S. 2197-2201 
    ISSN: 0009-2940
    Keywords: 1,3,2-Diazaborinium Compounds ; Calculations, AM1 ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,3,2-Diazaborinium Compounds  -  New Cationic Boron HeteroarenesThe diazaborinium cation 9 is obtained by the reaction of the vinamidine boron chelate 8 with Et2O - BF3. The cyclic aluminium compound 13 forms with the dichloroboranes RBCl2 (R = Cl, Et, Ph) the cations 15,16a, and 16b. AM1 calculations demonstrate the π interaction of the boron with the nitrogen atoms as well as with the fluoro substituent.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0009-2940
    Keywords: Imidazoles ; Carbenes ; Sulfur Compounds ; Fluorine Compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Imidazole Derivatives, XIXPart XVIII: Ref.[1] .  -  Coordination or reduction? On the Reaction of 1,3-Diisopropyl-4,5-dimethylimidazol-2-ylidene with Sulfur Halides and Sulfur Oxygen Halides Herrn Professor Max Herberhold zum 60. Geburtstag gewidmet.The reaction of 1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene (4, Im) with sulfur halides and sulfur oxygen halides may be described as a coordination (1) or reduction (2) process in respect to the sulfur centre. With SCl2 and SOCl2 the hypervalent sulfur compounds Im · SCl2 (5) and Im · S(O)Cl2 (13) are obtained. The SF2 adduct Im · SF2 (11) is formed on treatment of 5 with AgF. 13 is alkylated by methyl iodide to give the Im · S(Me)OCl2 cation (15). Surprisingly, reduction of the sulfur centre (2) occurs on treatment of 4 with SF4 to form the ImF+SF3- salt 18 containing the new SF3 anion. As expected, the same type of reaction occurs with the sulfuryl halides SO2ClF and SO2F2 to give the fluorosulfites ImCl+-SO2F- (21) and ImF+SO2F- (23). The X-ray structures of 5, 13 and 23 are reported.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 245-250 
    ISSN: 0009-2940
    Keywords: Carbenes ; Organosilicon compounds ; Organotin compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Imidazole Derivatives, XIII. - Carbene Complexes of Silicon and TinHerrn Professor Peter Paetzold zum 60. Geburtstag gewidmet.Stable adducts of the composition L · SiCl4 (2), L · SiR2Cl2 (3,4), and L · SnR2Cl2 (6) are formed by the reaction of the imidazol-2-ylidenes L (1) with the corresponding silicon and tin halides. For L = SiCl4 (2b; L = 1,3-diethyl-4,5-dimethylimidazol-2-ylidene) and L · SnPh2Cl2 (6c; L = 1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene) the monomeric nature of the compounds containing pentacoordinated silicon and tin is established by X-ray structure analyses. The reaction of 1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene (1c) with SnCl2 leads to the formation of the monomeric stannylene complex L · SnCl2 (7c; L = 1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene) whose molecular geometry indicates a week carbon-to-tin donor bond [Sn—C(1) 2.290(5) Å].
    Additional Material: 3 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...