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Applications include their use as NMR "shift reagents" and as catalysts for organic synthesis, and precursors to industrial hydroformylation catalysts. C 5 H 7 O − 2 in some cases also binds to metals through the central carbon atom; this bonding mode is more common for the third-row transition metals such as platinum(II) and iridium(III).
Iridium acetylacetonate is the iridium coordination complex with the formula Ir(O 2 C 5 H 7) 3, which is sometimes known as Ir(acac) 3. The molecule has D 3 -symmetry. [ 2 ] It is a yellow-orange solid that is soluble in organic solvents.
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
Organoiridium compounds share many characteristics with those of rhodium, but less so with cobalt. Iridium can exist in oxidation states of -III to +V, but iridium(I) and iridium(III) are the more common. iridium(I) compounds (d 8 configuration) usually occur with square planar or trigonal bipyramidal geometries, whereas iridium(III) compounds (d 6 configuration) typically have an octahedral ...
Indium acetate is an acetate of indium, with the chemical formula In(CH 3 COO) 3. It is soluble in water, acetic acid and mineral acids. [ 1 ] It is the precursor of indium-containing compounds such as the solar cell materials CuInS 2 [ 2 ] and indium phosphide quantum dots .
3 in hydrochloric acid, is often used as a starting material for the synthesis of other Ir(III) compounds. [2] Another compound used as a starting material is ammonium hexachloroiridate(III), (NH 4) 3 IrCl 6. In the presence of air, iridium metal dissolves in molten alkali-metal cyanides to produce the Ir(CN) 3− 6 (hexacyanoiridate) ion.
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In aqueous solution, it has a pK a value of 4.76. [21] Its conjugate base is acetate (CH 3 COO −). A 1.0 M solution (about the concentration of domestic vinegar) has a pH of 2.4, indicating that merely 0.4% of the acetic acid molecules are dissociated. [a] Cyclic dimer of acetic acid; dashed green lines represent hydrogen bonds