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245011

Sigma-Aldrich

Triruthenium dodecacarbonyl

99%

Synonym(s):

Ruthenium carbonyl, tri-Ruthenium dodecacarbonyl

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About This Item

Linear Formula:
Ru3(CO)12
CAS Number:
Molecular Weight:
639.33
EC Number:
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

crystals

reaction suitability

core: ruthenium
reaction type: C-H Activation
reagent type: catalyst

SMILES string

[Ru].[Ru].[Ru].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+]

InChI

1S/12CO.3Ru/c12*1-2;;;

InChI key

NQZFAUXPNWSLBI-UHFFFAOYSA-N

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General description

Atomic number of base material: 44 Ruthenium

Application

Carbonyl cluster precursor and H-transfer catalyst. Used in the reductive carbonylation of aromatic nitro compounds to carbamates. The phosphine-stabilized carbonyl cluster has been tethered to oxide supports. Applied in improved catalysis of the allylic amination of unactivated olefins by nitroarenes.
Catalyst used in a [3+2+1] carbonylative cycloaddition of silylacteylenes and α,ß-unsaturated ketones providing good yields of α-pyrones.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Inhalation

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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Journal of the American Chemical Society, 106, 4647-4647 (1984)
Ajeet Singh et al.
Dalton transactions (Cambridge, England : 2003), 47(39), 14033-14040 (2018-09-21)
The synthesis of pyridine alcohol based ruthenium carbonyl clusters Ru3(hep)2(CO)8 (1), Ru3(hpp)2(CO)8 (2), and Ru3(bhmp-H)2(CO)8 (3) {hep-H = 2-(2-hydroxyethyl)pyridine, hpp-H = 2-(3-hydroxypropyl)pyridine and bhmp-H2 = 2,6-bis(hydroxymethyl)pyridine} has been carried out by the reaction of the corresponding pyridine-alcohol ligands with Ru3(CO)12.
Ragaini, F. et al.
Organometallics, 18, 929-929 (1999)
Takahide Fukuyama et al.
Organic letters, 9(4), 587-589 (2007-01-25)
Ruthenium catalyzes a carbonylative [3+2+1] cycloaddition, using silylacetylenes, alpha,beta-unsaturated ketones, and CO as the starting materials, providing the new method for the synthesis of tetrasubstituted alpha-pyrones. In this reaction, the carbonyl group and alpha-carbon of vinyl ketones are incorporated as
J. Chem. Soc., Dalton Trans., 2649-2649 (1988)

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