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327638

Sigma-Aldrich

Bromopentacarbonylrhenium(I)

98%

Synonym(s):

Pentacarbonylbromorhenium, Pentacarbonylrhenium bromide, Rhenium(I) pentacarbonyl bromide

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About This Item

Linear Formula:
Re(CO)5Br
CAS Number:
14220-21-4
Molecular Weight:
406.16
EC Number:
238-084-8
MDL number:
MFCD00013295
UNSPSC Code:
12161600
PubChem Substance ID:
24859676
NACRES:
NA.22

Assay

98%

reaction suitability

core: rhenium
reagent type: catalyst

SMILES string

Br[Re].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+]

InChI

1S/5CO.BrH.Re/c5*1-2;;/h;;;;;1H;/q;;;;;;+1/p-1

InChI key

NWJBOTGGBYFKEJ-UHFFFAOYSA-M

Application

Used to study π-electron deficient complexes between tricarbonylhalorhenium and diimine ligands and also to prepare [3]-ferrocenophane complexes.
Starting material for rhenium-polypyridine complexes that have potential applications in catalysis and solar energy conversion.
Used to study π-electron deficient complexes between tricarbonylhalorhenium and diimine ligands.

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Ruimao Hua et al.
The Journal of organic chemistry, 69(17), 5782-5784 (2004-08-17)
The addition of carboxylic acids to terminal alkynes is efficiently catalyzed by the early transition-metal complex Re(CO)5Br in toluene or n-heptane at 110 degrees C in an air atmosphere, affording the anti-Markovnikov adducts in good yields with high selectivity. In
Jia-Li Jiang et al.
The Journal of organic chemistry, 70(1), 381-383 (2004-12-31)
In the presence of a catalytic amount of Re(CO)(5)Br, the coupling of epoxides with supercritical CO(2) without an organic solvent at 110 degrees C has afforded cyclic carbonates in good to excellent yields.
Nishiyama, Y.; Kakushou, F. et al.
Bulletin of the Chemical Society of Japan, 73, 2779-2779 (2000)
Tomás F Beltrán et al.
Dalton transactions (Cambridge, England : 2003), 46(28), 9036-9048 (2017-07-01)
The superbulky N-heterocyclic carbenes (NHCs) 2,6-bis(diphenylmethyl)-4-methylimidazol-2-ylidene (IDip*Me) and its 4-methoxy analogue (IDip*OMe) reacted instantaneously with carbon disulfide to afford the corresponding imidazolium-2-dithiocarboxylate zwitterions in high yields. These new dithiolate ligands were fully characterized and their coordination chemistry toward common Re(i)
Inorganic Chemistry, 29, 253-253 (1990)
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