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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 .
structure of the cation called basic iron acetate as determined from X-ray crystallography [4] Basic iron acetate forms on treating aqueous solutions of iron(III) sources with acetate salts. It is slowly soluble in water and poorly soluble in acetic acid. [5] A typical precursor is freshly precipitated iron oxide/hydroxide, which is halide-free ...
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 ...
Hydrated iridium trichloride, a common salt of iridium. The coordination complexes of iridium are extensive. Iridium in its complexes is always low-spin. Ir(III) and Ir(IV) generally form octahedral complexes. [2] Polyhydride complexes are known for the +5 and +3 oxidation states. [11] One example is IrH 5 (P i Pr 3) 2. [12] The ternary hydride ...
[1]: 293–307 The process is based on an iridium-containing catalyst, such as the complex [Ir(CO) 2 I 2] − (1). The Cativa and Monsanto processes are sufficiently similar that they can use the same chemical plant. Initial studies by Monsanto had shown iridium to be less active than rhodium for the carbonylation of methanol. [2]
Acetate is the ion resulting from loss of H + from acetic acid. The name "acetate" can also refer to a salt containing this anion, or an ester of acetic acid. [11] (The symbol Ac for the acetyl functional group is not to be confused with the symbol Ac for the element actinium; context prevents confusion among organic chemists).
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Methyl acetate is used in place of methanol as a source of methyl iodide. [5] CH 3 CO 2 CH 3 + CO → (CH 3 CO) 2 O. In this process lithium iodide converts methyl acetate to lithium acetate and methyl iodide, which in turn affords, through carbonylation, acetyl iodide. Acetyl iodide reacts with acetate salts or acetic acid to give the anhydride.