388297
Ferrocenium hexafluorophosphate
97%, powder
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About This Item
Empirical Formula (Hill Notation):
C10H10F6FeP
CAS Number:
Molecular Weight:
331.00
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Product Name
Ferrocenium hexafluorophosphate, 97%
SMILES string
[Fe+].[CH]1[CH][CH][CH][CH]1.[CH]2[CH][CH][CH][CH]2.F[P-](F)(F)(F)(F)F
InChI
1S/2C5H5.F6P.Fe/c2*1-2-4-5-3-1;1-7(2,3,4,5)6;/h2*1-5H;;/q;;-1;+1
InChI key
JTRCXNUQIANBAN-UHFFFAOYSA-N
assay
97%
form
powder
reaction suitability
core: iron, reagent type: catalyst
Quality Level
Application
The ferrocenium cation has been used to prepare catalysts for the asymmetric epoxidation of olefins, carbonylations of nitroaromatics, and the isomerization of a strained diene.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Giorgia Zampardi et al.
Physical chemistry chemical physics : PCCP, 19(41), 28381-28387 (2017-10-17)
High voltage operating active materials are among the most promising components for positive electrodes of future high energy lithium-ion batteries. However, the operating potential range of such materials often exceeds anodically the thermodynamic stability window of the electrolyte. A surface
Johanna Karppi et al.
Frontiers in chemistry, 8, 11-11 (2020-02-13)
Pyranose dehydrogenases (PDHs; EC 1.1.99.29; AA3_2) demonstrate ability to oxidize diverse carbohydrates. Previous studies of these enzymes have also uncovered substrate-dependent regioselectivity, along with potential to introduce more than one carbonyl into carbohydrate substrates. Enzymatic oxidation of carbohydrates facilitates their
Krishnan Venkatasubbaiah et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(2), 444-458 (2007-12-12)
A series of mixed-valent (MV) complexes [(FeCp)2(mu-C10H6(BPh)2)]+X ([1+]X; X=I 5, PF6, SbF6, B(C6F5)4) were prepared by oxidation of diboradiferrocene [(FeCp)2(mu-C10H6(BPh)2)] (1) with I 2, AgPF6, and AgSbF6, respectively, and through anion exchange of the I 5(-) salt with [Li(Et2O)x][B(C6F5)4] in
Aifang Wang et al.
Journal of the American Chemical Society, 131(19), 6652-6653 (2009-05-01)
Redox-active ferrocenyl-terminated dendrimers have been used to build robust and active interfaces in which the inherent properties of the dendrimers are preserved. The procedure is based on the preparation of a polyarylcarboxylate layer through the controlled reduction of aryldiazonium salts
Tetrahedron Asymmetry, 2, 481-481 (1991)
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