209686
Iridium
powder, 99.9% trace metals basis
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About This Item
Formule empirique (notation de Hill):
Ir
Numéro CAS:
Poids moléculaire :
192.22
Numéro CE :
Numéro MDL:
Code UNSPSC :
12141720
ID de substance PubChem :
Nomenclature NACRES :
NA.23
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Niveau de qualité
Pureté
99.9% trace metals basis
Forme
powder
Résistivité
4.71 μΩ-cm
Point d'ébullition
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
Description générale
Iridium is a rare and dense transition metal that belongs to the platinum group of metals and is known for its remarkable physical and chemical properties. Iridium is used in high-temperature applications such as crucibles for crystal growth and in devices that operate under extreme conditions due to its high melting point and stability at elevated temperatures. It is also used in electrical contacts and electrodes because of its excellent corrosion resistance and electrical conductivity. In addition, iridium is used as a catalyst in various organic reactions including hydrogenation, water splitting, C-C coupling, and olefin metathesis.
Application
- Iridium-based double perovskites for efficient water oxidation in acid media: This study highlights the development of iridium-based double perovskites that reduce iridium content while maintaining high activity and stability for water oxidation, significant for energy-related applications in material science (Diaz-Morales et al., 2016).
- Recent advances in understanding oxygen evolution reaction mechanisms over iridium oxide: This paper provides insights into the oxygen evolution reaction (OER) mechanisms on iridium oxide, crucial for improving catalytic processes in industrial applications (Naito et al., 2021).
- Iridium oxide fabrication and application: A review: A comprehensive review that discusses various methods for the fabrication of iridium oxides and their applications, particularly in sensors and catalysts, relevant to both drug discovery and material science (Chen et al., 2020).
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Flam. Sol. 1
Code de la classe de stockage
4.1B - Flammable solid hazardous materials
Classe de danger pour l'eau (WGK)
nwg
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Les clients ont également consulté
Dik-Lung Ma et al.
PloS one, 8(2), e55751-e55751 (2013-03-05)
A cell permeable cyclometalated iridium(III) complex has been developed as a phosphorescent probe for cell imaging. The iridium(III) solvato complex [Ir(phq)2(H2O]2)] preferentially stains the cytoplasm of both live and dead cells with a bright luminescence.
Le Guo et al.
Organic letters, 15(5), 1144-1147 (2013-02-16)
The first α-alkylation of unactivated amides with primary alcohols is described. An effective and robust iridium pincer complex has been developed for selective α-alkylation of tertiary and secondary acetamides involving a "borrowing hydrogen" methodology. The method is compatible with alcohols
Matthew R Kelley et al.
Inorganic chemistry, 52(5), 2564-2580 (2013-02-21)
A series of seven [Ir{ArNC(NR2)NAr}(cod)] complexes (1a-1g; where R = Me or Et; Ar = Ph, 4-MeC6H4, 4-MeOC6H4, 2,6-Me2C6H3, or 2,6-(i)Pr2C6H3; and cod = 1,5-cyclooctadiene) were synthesized by two different methods from the neutral guanidines, ArN═C(NR2)NHAr, using either MeLi and
Shiguang Pan et al.
Organic letters, 15(8), 1902-1905 (2013-04-02)
A cationic Ir(I) complex-catalyzed O-to-N-alkyl migration in 2-alkoxypyridines bearing a secondary alkyl group on the oxygen atom by C-O bond cleavage is described. The present transformation gave various N-alkylpyridones in moderate to good yields. The addition of sodium acetate played
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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