GF81040463
Iridium
foil, 0.18m coil, thickness 0.05mm, coil width .5mm, as rolled, 99.9%
Sinonimo/i:
Iridium, IR000201
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About This Item
Formula empirica (notazione di Hill):
Ir
Numero CAS:
Peso molecolare:
192.22
Numero MDL:
Codice UNSPSC:
12352300
ID PubChem:
NACRES:
NA.23
Saggio
99.9%
Forma fisica
foil
Produttore/marchio commerciale
Goodfellow 810-404-63
Resistività
4.71 μΩ-cm
Lungh. × largh. × spess.
0.18 m × 0.5 mm × 0.05 mm
P. eboll.
4130 °C (lit.)
Punto di fusione
2450 °C (lit.)
Densità
22.65 g/cm3 (lit.)
Stringa SMILE
[Ir]
InChI
1S/Ir
GKOZUEZYRPOHIO-UHFFFAOYSA-N
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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
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
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