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Merck

GF81468030

Iridium

foil, 0.05m coil, thickness 0.05mm, coil width .5mm, as rolled, 99.9%

Sinónimos:

Iridium, IR000201

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About This Item

Fórmula empírica (notación de Hill):
Ir
Número de CAS:
Peso molecular:
192.22
Número MDL:
Código UNSPSC:
12141720
ID de la sustancia en PubChem:
NACRES:
NA.23
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Ensayo

99.9%

Formulario

foil

fabricante / nombre comercial

Goodfellow 814-680-30

resistividad

4.71 μΩ-cm

L × An × grosor

0.05 m × 0.5 mm × 0.05 mm

bp

4130 °C (lit.)

mp

2450 °C (lit.)

densidad

22.65 g/cm3 (lit.)

cadena SMILES

[Ir]

InChI

1S/Ir

Clave InChI

GKOZUEZYRPOHIO-UHFFFAOYSA-N

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Descripción general

For updated SDS information please visit www.goodfellow.com.

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Veronica Marin et al.
Chemical Society reviews, 36(4), 618-635 (2007-03-28)
The need for novel materials with luminescent properties and advanced processing features requires reliable and reproducible synthetic routes for the design of suitable materials, such as e.g. polypyridyl ruthenium(II) and iridium(III)-containing polymers. The most popular ligand for those purposes is
Etienne Baranoff et al.
Chemical Society reviews, 33(3), 147-155 (2004-03-18)
In order to mimic the photosynthetic reaction centre and better understand photoinduced electron transfer processes, a family of compounds has been studied for the past 15 years. These are transition metal complexes, M(tpy)(2) where tpy is a 2,2':6',2" terpyridine based
S Murahashi et al.
Accounts of chemical research, 33(4), 225-233 (2000-04-25)
The discovery of a new chemical reaction often leads to new applications and new chemical principles. Low-valent ruthenium and iridium hydride complexes are highly useful redox Lewis acid and base catalysts. Nitriles are activated by these catalysts and undergo reactions
Paolo Tosatti et al.
Organic & biomolecular chemistry, 10(16), 3147-3163 (2012-03-13)
Since their discovery in 1997, iridium-catalysed asymmetric allylic substitutions have been developed into a broadly applicable tool for the synthesis of chiral building blocks via C-C and C-heteroatom bond formation. The remarkable generality of these reactions and the high levels
Stephen J Roseblade et al.
Accounts of chemical research, 40(12), 1402-1411 (2007-08-04)
Asymmetric hydrogenation is one of the most important catalytic methods for the preparation of optically active compounds. For a long time the range of olefins that could be hydrogenated with high enantiomeric excess was limited to substrates bearing a coordinating

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