4.1 Article

Synthesis and Characterization of Cp*Be-F-Al(ORF)3

Journal

ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
Volume 641, Issue 3-4, Pages 655-659

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/zaac.201400476

Keywords

Cyclopentadienyl; Beryllium; Weakly coordinating anion; Lewis acids; Density functional calculations

Funding

  1. University of Freiburg
  2. FRIAS
  3. ERC in the project UniChem.
  4. DFG in the Normalverfahren
  5. Fonds der Chemischen Industrie

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The reaction of Ag[Al(ORF)(4)] [R-F = C(CF3)(3)] with Cp*Be-Br was investigated. With the less basic CH2Cl2 as solvent, redox chemistry prevailed, elemental silver and the pentamethylcyclopentenyl cation (Cp*H-2(+)) formed. However, upon changing to the more -basic solvents fluorobenzene and o-difluorobenzene, the silver metathesis reaction went smooth and produced intermediately the [Cp*Be](+) cation and AgBr. However, the very strong Lewis acid [Cp*Be](+) activated one of the 36 equivalent C-F bonds of the [Al(ORF)(4)](-) anion and finally formed two stable crystalline compounds containing the Cp*Be-F-Al(ORF)(3) molecule, which includes a [F-Al(ORF)(3)](-) anion coordinated to the [Cp*Be](+) cation. Cp*Be-F-Al(ORF)(3) nevertheless includes some potential to provide [Cp*Be](+) in polar solution. Its potential neutral or ionic fission was investigated by DFT calculations.

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