GF25136490
Iridium
wire reel, 0.5m, diameter 0.38mm, as drawn, 99.9%
Sinônimo(s):
Iridium, IR005125
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About This Item
Fórmula empírica (Notação de Hill):
Ir
Número CAS:
Peso molecular:
192.22
Número MDL:
Código UNSPSC:
12141720
ID de substância PubChem:
NACRES:
NA.23
Produtos recomendados
Ensaio
99.90%
forma
wire
fabricante/nome comercial
Goodfellow 251-364-90
resistividade
4.71 μΩ-cm
C × diâmetro
0.5 m × 0.38 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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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
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
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
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
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