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GF35631200

Iridium

foil, light tested, 25x25mm, thickness 0.025mm, as rolled, 99.9%

Synonym(s):
Iridium, IR000205
Empirical Formula (Hill Notation):
Ir
CAS Number:
Molecular Weight:
192.22
MDL number:
PubChem Substance ID:
NACRES:
NA.23

Assay

99.9%

form

foil

manufacturer/tradename

Goodfellow 356-312-00

resistivity

4.71 μΩ-cm

size × thickness

25x25 mm × 0.025 mm

bp

4130 °C (lit.)

mp

2450 °C (lit.)

density

22.65 g/cm3 (lit.)

SMILES string

[Ir]

InChI

1S/Ir

InChI key

GKOZUEZYRPOHIO-UHFFFAOYSA-N

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1 of 4

This Item
GF07858974GF98486982GF96543209
Iridium foil, light tested, 25x25mm, thickness 0.025mm, as rolled, 99.9%

GF35631200

Iridium

Iridium foil, light tested, 25x25mm, thickness 0.05mm, as rolled, 99.9%

GF07858974

Iridium

Iridium foil, 25x25mm, thickness 0.15mm, as rolled, 99.9%

GF98486982

Iridium

Iridium foil, 25x25mm, thickness 0.125mm, as rolled, 99.9%

GF96543209

Iridium

form

foil

form

foil

form

foil

form

foil

manufacturer/tradename

Goodfellow 356-312-00

manufacturer/tradename

Goodfellow 078-589-74

manufacturer/tradename

Goodfellow 984-869-82

manufacturer/tradename

Goodfellow 965-432-09

resistivity

4.71 μΩ-cm

resistivity

4.71 μΩ-cm

resistivity

4.71 μΩ-cm

resistivity

4.71 μΩ-cm

bp

4130 °C (lit.)

bp

4130 °C (lit.)

bp

4130 °C (lit.)

bp

4130 °C (lit.)

mp

2450 °C (lit.)

mp

2450 °C (lit.)

mp

2450 °C (lit.)

mp

2450 °C (lit.)

General description

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

Legal Information

Product of Goodfellow

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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
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

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