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GF01838101

Iridium

wire reel, 0.5m, diameter 0.125mm, as drawn, 99.5%

Synonym(e):

Iridium

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About This Item

Empirische Formel (Hill-System):
Ir
CAS-Nummer:
7439-88-5
Molekulargewicht:
192.22
MDL-Nummer:
MFCD00011062
UNSPSC-Code:
12141720
PubChem Substanz-ID:
329800273
NACRES:
NA.23

Assay

99.50%

Form

wire

Hersteller/Markenname

Goodfellow 018-381-01

Widerstandsfähigkeit

4.71 μΩ-cm

L × Durchm.

0.5 m × 0.125 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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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
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
Henrik Tækker Madsen et al.
Chemosphere, 109, 84-91 (2014-05-31)
Electrochemical oxidation is a promising technique for degradation of otherwise recalcitrant organic micropollutants in waters. In this study, the applicability of electrochemical oxidation was investigated concerning the degradation of the groundwater pollutant 2,6-dichlorobenzamide (BAM) through the electrochemical oxygen transfer process
I Haiduc et al.
In vivo (Athens, Greece), 3(4), 285-293 (1989-07-01)
Recent results on the antitumor activity of organometallic compounds of rhodium, iridium, copper and gold are reviewed. Coordination compounds of some organic ligands are also briefly mentioned. The most promising seem to be copper and gold complexes which exhibited remarkable
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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