Journal
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
Volume 641, Issue 3-4, Pages 655-659Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/zaac.201400476
Keywords
Cyclopentadienyl; Beryllium; Weakly coordinating anion; Lewis acids; Density functional calculations
Categories
Funding
- University of Freiburg
- FRIAS
- ERC in the project UniChem.
- DFG in the Normalverfahren
- Fonds der Chemischen Industrie
Ask authors/readers for more resources
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.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available