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Tetrafluoroborate

Base Information
  • Chemical Name:Tetrafluoroborate
  • CAS No.:14874-70-5
  • Molecular Formula:BF4
  • Molecular Weight:86.8
  • Hs Code.:
  • UNII:4YCF3545OY
  • Nikkaji Number:J209.513K
  • Wikidata:Q27118029
  • ChEMBL ID:CHEMBL1789400
  • Mol file:14874-70-5.mol
Tetrafluoroborate

Synonyms:fluoboric acid;fluoboric acid (HBF4);fluoroboric acid;tetrafluoroborate anion;tetrafluoroborate ion;tetrafluoroboric acid

Suppliers and Price of Tetrafluoroborate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 11 raw suppliers
Chemical Property of Tetrafluoroborate
Chemical Property:
  • PSA:0.00000 
  • LogP:1.30000 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:0
  • Exact Mass:87.0029178
  • Heavy Atom Count:5
  • Complexity:19.1
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:[B-](F)(F)(F)F
  • Recent ClinicalTrials:Positron Emission Tomography (PET) Imaging Studies With NIS Reporter
Refernces

A direct route to platinum NCN-pincer complexes derived from 1,3-bis(imino)benzenes and an investigation into their activity as catalysts for carbon-carbon bond formation

10.1021/om020566r

The research focuses on the synthesis and investigation of Platinum NCN-pincer complexes derived from 1,3-bis(imino)benzenes as catalysts for carbon-carbon bond formation. The purpose of this study was to develop a direct route to these complexes, which are of significant interest due to their potential applications in catalysis and organometallic materials. The researchers successfully synthesized a range of platinum NCN-pincer complexes by reacting 1,3-bis(imino)benzenes with K2PtCl4 in glacial acetic acid, yielding the desired complexes in moderate to good yields. The study also explored the activation of these complexes through chloride abstraction, resulting in water-coordinated adducts with either tetrafluoroborate or triflate counterions. The triflate salt of the complex was found to display moderate activity as a catalyst for the Michael and Diels-Alder reactions involving nitrile substrates.

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