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Merck

227722

Sigma-Aldrich

Silver hexafluorophosphate

98%

Synonym(s):

Silver(I) hexafluorophosphate

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About This Item

Linear Formula:
AgPF6
CAS Number:
Molecular Weight:
252.83
EC Number:
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22

Pricing and availability is not currently available.

Quality Level

Assay

98%

form

solid

reaction suitability

core: silver
reagent type: catalyst

mp

102 °C (dec.) (lit.)

SMILES string

[Ag+].F[P-](F)(F)(F)(F)F

InChI

1S/Ag.F6P/c;1-7(2,3,4,5)6/q+1;-1

InChI key

SCQBROMTFBBDHF-UHFFFAOYSA-N

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1 of 4

This Item
208361225673668001
reaction suitability

core: silver, reagent type: catalyst

reaction suitability

core: silver, reagent type: catalyst

reaction suitability

-

reaction suitability

core: silver, reagent type: catalyst

form

solid

form

-

form

lumps and powder

form

solid

mp

102 °C (dec.) (lit.)

mp

70-73 °C (lit.)

mp

652 °C (lit.)

mp

248.8 °C

General description

Silver hexafluorophosphate can be used as a catalyst for the sulfimidation, hydrogenation of aldehydes to alcohols, and hydroacyloxylation of alkynes with carboxylic acids[1][2][3].

Application

Used to prepare silver 3,3′-dicyanodiphenylacetylene coordination networks for study of the effect of ligands on network structure toward the goal of engineering novel materials.[4] Preparation of supramolecular networks of Ag(I) complexes.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Gold (I)-catalyzed addition of carboxylic acids to alkynes
Chary B, et al.
The Journal of Organic Chemistry, 75, 7928-7931 (2010)
Silver-Catalyzed Hydrogenation of Aldehydes in Water
Jia Z, et al.
Angewandte Chemie (International Edition in English), 52, 11871-11874 (2013)
Journal of Organometallic Chemistry, 692, 4093-4093 (2007)
Silver-Catalyzed Enantioselective Sulfimidation Mediated by Hydrogen Bonding Interactions
Annapureddy R, et al.
Angewandte Chemie (International Edition in English), 133, 7999-8005 (2021)
Keith A. Hirsch et al.
Inorganic chemistry, 36(14), 2960-2968 (1997-07-02)
Coordination networks of 3,3'-dicyanodiphenylacetylene (3,3'-DCPA, 1) with silver(I) salts characterized by single-crystal X-ray analysis are described. Network topology is found to depend on both the counterion and solvent employed during crystallization. The conformation adopted by the ligand varies between planar

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