GF65585021
Iridium
wire reel, 0.1m, diameter 0.125mm, as drawn, 99.5%
Sinônimo(s):
Iridium, IR005106
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About This Item
Produtos recomendados
Ensaio
99.5%
forma
wire
fabricante/nome comercial
Goodfellow 655-850-21
resistividade
4.71 μΩ-cm
C × diâmetro
0.1 m × 0.125 mm
pb
4130 °C (lit.)
pf
2450 °C (lit.)
densidade
22.65 g/cm3 (lit.)
cadeia de caracteres SMILES
[Ir]
InChI
1S/Ir
chave InChI
GKOZUEZYRPOHIO-UHFFFAOYSA-N
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Descrição geral
For updated SDS information please visit www.goodfellow.com.
Informações legais
Product of Goodfellow
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Low-valent ruthenium and iridium hydride complexes as alternatives to Lewis acid and base catalysts.
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
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
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
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
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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