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GF35631200

Iridium

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

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Synonym(s):

Iridium, IR000205

Empirical Formula (Hill Notation):

CAS Number:

7439-88-5

Molecular Weight:

192.22

MDL number:

MFCD00011062

PubChem Substance ID:

329805417

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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This Item	GF07858974	GF98486982	GF96543209
GF35631200 Iridium	GF07858974 Iridium	GF98486982 Iridium	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

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Recent advances and applications of iridium-catalysed asymmetric allylic substitution.

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

Iridium-catalyzed asymmetric hydrogenation of olefins.

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

Functional ruthenium(II)- and iridium(III)-containing polymers for potential electro-optical applications.

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

Low-valent ruthenium and iridium hydride complexes as alternatives to Lewis acid and base catalysts.

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

From ruthenium(II) to iridium(III): 15 years of triads based on bis-terpyridine complexes.

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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