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Chlorobis(cyclooctene)iridium dimer

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Chlorobis(cyclooctene)iridium dimer
Names
IUPAC name
Chlorobis(cyclooctene)iridium(I) dimer
Other names
Di-μ-chlorotetrakis(cyclooctene)diiridium(I), [Ir(coe)2Cl]2
Identifiers
3D model (JSmol)
ECHA InfoCard 100.159.657 Edit this at Wikidata
  • InChI=1S/4C8H14.2ClH.2Ir/c4*1-2-4-6-8-7-5-3-1;;;;/h4*1-2H,3-8H2;2*1H;;/p-2/b4*2-1-;;;;
    Key: CJJIQMGSHWWMCK-XFCUKONHSA-L
  • C1CCCC=CCC1.C1CCCC=CCC1.C1CCCC=CCC1.C1CCCC=CCC1.[Cl-].[Cl-].[Ir].[Ir]
Properties
C32H56Cl2Ir2
Molar mass 896.13
Appearance yellow solid
Melting point 160-165 °C
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H315, H319, H335[1]

[1]

P261, P280, P304+P340, P305+P351+P338, P321, P332+P313, P362, P403+P233, P405, P501[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Chlorobis(cyclooctene)iridium dimer is an organoiridium compound with the formula Ir2Cl2(C8H14)4, where C8H14 is cis-cyclooctene. Sometimes abbreviated Ir2Cl2(coe)4, it is a yellow, air-sensitive solid that is used as a precursor to many other organoiridium compounds and catalysts.

The compound is prepared by heating an alcohol solution of sodium hexachloroiridate with cyclooctene in ethanol.[2] The coe ligands are easily displaced by other more basic ligands, more so than the diene ligands in the related complex cyclooctadiene iridium chloride dimer.

References

  1. ^ a b c "Chlorobis(cyclooctene)iridium Dimer SDS". American Elements. Retrieved 2018-08-24.
  2. ^ Van der Ent, A.; Onderdelinden, A. L. "Chlorobis(cyclooctene)rhodium(I) and di-μ-chlorobis[bis(cryclooctene)iridium] (I) complexes" Inorganic Syntheses 1973, volume 14, pp. 92-5. doi:10.1002/9780470132456.ch18