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Merck
CN

245011

Triruthenium dodecacarbonyl

99%, crystals

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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
EC Number:
239-287-4
MDL number:
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Product Name

Triruthenium dodecacarbonyl, 99%

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

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,β-unsaturated ketones providing good yields of α-pyrones.


pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Inhalation

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves, type P3 (EN 143) respirator cartridges



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Articles

High Purity Metalorganic Precursors for CPV Device Fabrication

Related Content

The Krische group has developed a broad class of “C-C bond forming transfer hydrogenations” wherein the exchange of hydrogen between alcohols and unsaturated reactants serves to generate aldehyde-organometal pairs that combine to give products of carbonyl addition.


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
Ragaini, F. et al.
Organometallics, 18, 929-929 (1999)
Ragaini, F. et al.
Organometallics, 18, 928-928 (1999)



Global Trade Item Number

SKUGTIN
245011-1G04061825772424
245011-50G04061833410615
245011-5G04061825772431