266841
Iridium
wire, diam. 0.15 mm, 99.9% trace metals basis
Sinonimo/i:
Iridium black
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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
Prodotti consigliati
Saggio
99.9% trace metals basis
Stato
wire
Resistività
4.71 μΩ-cm
Diametro
0.15 mm
P. ebollizione
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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Quantità
40mg=10cm, 400mg=100cm
Codice della classe di stoccaggio
13 - Non Combustible Solids
Classe di pericolosità dell'acqua (WGK)
nwg
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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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
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
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