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GF75905680

Iridium

wire reel, 1m, diameter 0.1mm, as drawn, 99.9%

Synonym(e):

Iridium

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About This Item

Empirische Formel (Hill-System):
Ir
CAS-Nummer:
7439-88-5
Molekulargewicht:
192.22
MDL-Nummer:
MFCD00011062
UNSPSC-Code:
12141720
PubChem Substanz-ID:
329811371
NACRES:
NA.23

Assay

99.9%

Form

wire

Hersteller/Markenname

Goodfellow 759-056-80

Widerstandsfähigkeit

4.71 μΩ-cm

L × Durchm.

1 m × 0.1 mm

bp

4130 °C (lit.)

mp (Schmelzpunkt)

2450 °C (lit.)

Dichte

22.65 g/cm3 (lit.)

SMILES String

[Ir]

InChI

1S/Ir

InChIKey

GKOZUEZYRPOHIO-UHFFFAOYSA-N

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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
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
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
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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