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GF10466760

Iridium

wire reel, 0.3m, diameter 0.5mm, as drawn, 99.9%

Synonym(e):

Iridium

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1 EA
2.880,00 €

2.880,00 €


Voraussichtliches Versanddatum16. April 2025


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1 EA
2.880,00 €

About This Item

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

2.880,00 €


Voraussichtliches Versanddatum16. April 2025


Bulk-Bestellung anfordern

Assay

99.90%

Form

wire

Hersteller/Markenname

Goodfellow 104-667-60

Widerstandsfähigkeit

4.71 μΩ-cm

L × Durchm.

0.3 m × 0.5 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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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
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
Soo Bong Han et al.
Chemical communications (Cambridge, England), (47)(47), 7278-7287 (2009-12-22)
Existing methods for enantioselective carbonyl allylation, crotylation and tert-prenylation require stoichiometric generation of pre-metallated nucleophiles, and often employ stoichiometric chiral modifiers. Under the conditions of transfer hydrogenation employing an ortho-cyclometallated iridium C,O-benzoate catalyst, enantioselective carbonyl allylations, crotylations and tert-prenylations are
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

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