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449229

Sigma-Aldrich

Iridium

evaporation slug, diam. × L 0.6 cm × 1.2 cm, 99.9% trace metals basis

Synonyme(s) :

Iridium black

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About This Item

Formule empirique (notation de Hill):
Ir
Numéro CAS:
7439-88-5
Poids moléculaire :
192.22
Numéro MDL:
MFCD00011062
Code UNSPSC :
12141720
ID de substance PubChem :
24868465
Nomenclature NACRES :
NA.23

Essai

99.9% trace metals basis

Forme

evaporation slug

Résistivité

4.71 μΩ-cm

Diam. × L

0.6 cm × 1.2 cm

Poids

~7.6 g (one slug)

pb

4130 °C (lit.)

Pf

2450 °C (lit.)

Densité

22.65 g/cm3 (lit.)

Chaîne SMILES 

[Ir]

InChI

1S/Ir

Clé InChI

GKOZUEZYRPOHIO-UHFFFAOYSA-N

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Catégories apparentées

Application

  • Single Atom Iridium Decorated Nickel Alloys Supported on Segregated MoO(2) for Alkaline Water Electrolysis.: The study presents an innovative approach to enhance alkaline water electrolysis using single-atom iridium catalysts, resulting in improved efficiency and stability of the process (Wang et al., 2024).
  • An Aqueous Redox Flow Battery Using CO(2) as an Active Material with a Homogeneous Ir Catalyst.: This paper explores the use of iridium catalysts in an aqueous redox flow battery, utilizing CO2 as an active material to improve energy storage capabilities (Kanega et al., 2023).
  • Kinetic Acceleration of Lithium Polysulfide Conversion via a Copper-Iridium Alloying Catalytic Strategy in Li-S Batteries.: This research highlights the use of copper-iridium alloys to accelerate the conversion of lithium polysulfides, significantly enhancing the performance of lithium-sulfur batteries (Zhai et al., 2022).
  • Introducing High-Valence Iridium Single Atoms into Bimetal Phosphides toward High-Efficiency Oxygen Evolution and Overall Water Splitting.: The study demonstrates the integration of high-valence iridium single atoms into bimetal phosphides, leading to highly efficient oxygen evolution and water splitting processes (Yang et al., 2023).

Code de la classe de stockage

13 - Non Combustible Solids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number
S80742V
S88245
S80742
S74773
07714AJ

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Chun-I Lee et al.
Journal of the American Chemical Society, 135(9), 3560-3566 (2013-02-05)
Compounds with carbon-boron bonds are versatile intermediates for building more complex molecules via the elaboration of the carbon-boron bonds into other carbon-element bonds. The synthesis of carbon-boron bonds by catalytic dehydrogenative borylation of carbon-hydrogen bonds with dialkoxyboranes (RO)2BH is particularly
Enantioselective iridium-catalyzed hydrogenation of 1- and 3-substituted isoquinolinium salts.
Zhi-Shi Ye et al.
Angewandte Chemie (International ed. in English), 52(13), 3685-3689 (2013-02-21)
Daniel Shiu-Hin Chan et al.
PloS one, 8(3), e60114-e60114 (2013-03-28)
We report herein a novel luminescent iridium(III) complex with two hydrophobic carbon chains as a non-reaction based chemosensor for the detection of Hg(2+) ions in aqueous solution (<0.002% of organic solvent attributed to the probe solution). Upon the addition of
Carl W Liskey et al.
Journal of the American Chemical Society, 135(9), 3375-3378 (2013-02-21)
The borylation of cyclopropanes catalyzed by the combination of (η(6)-mes)IrBpin3 or [Ir(COD)OMe]2 and a phenanthroline derivative is reported. The borylation occurs selectively at the methylene C-H bonds of the cyclopropane ring over methine or methyl C-H bonds. High diasteroselectivities were
Yuyang Zhou et al.
Chemical communications (Cambridge, England), 49(31), 3230-3232 (2013-03-14)
Five iridium(III) complexes with two N-heterocyclic carbene (NHC) ligands and an ancillary ligand have been designed and successfully synthesized. With multicolor photoluminescence and low toxicity, these carbene complexes were tested, for the first time, as living cell imaging reagents and
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