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665142

Sigma-Aldrich

Tris(triphenylphosphinegold)oxonium tetrafluoroborate

Synonym(s):

Oxotris((triphenylphosphine)gold) tetrafluoroborate, Oxotris(triphenylphosphine)trigold tetrafluoroborate, Tris[(triphenylphosphino)aurio(I)]oxonium tetrafluoroborate

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About This Item

Empirical Formula (Hill Notation):
C54H45P3OAu3BF4
CAS Number:
Molecular Weight:
1480.56
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22

form

solid

reaction suitability

core: gold
reagent type: catalyst

SMILES string

[Au][O+]([Au])[Au].F[B-](F)(F)F.c1ccc(cc1)P(c2ccccc2)c3ccccc3.c4ccc(cc4)P(c5ccccc5)c6ccccc6.c7ccc(cc7)P(c8ccccc8)c9ccccc9

InChI

1S/3C18H15P.3Au.BF4.O/c3*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;;2-1(3,4)5;/h3*1-15H;;;;;/q;;;;;;-1;+1

InChI key

HTZIGJMQHZNAQD-UHFFFAOYSA-N

Application

Used in a variety of gold catalyzed reactions including propargyl Claisen rearrangements.[1]

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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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Benjamin D Sherry et al.
Journal of the American Chemical Society, 126(49), 15978-15979 (2004-12-09)
Homoallenic alcohols are prepared from propargyl vinyl ethers using a trinuclear gold(I)-oxo complex, [(Ph3PAu)3O]BF4, as a catalyst for propargyl Claisen rearrangement at room temperature. The gold(I)-catalyzed reaction is effective for a diverse collection of propargyl vinyl ethers, including substrates containing

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