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  2. Indium acetate - Wikipedia

    en.wikipedia.org/wiki/Indium_acetate

    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. Organoiridium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoiridium_chemistry

    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 ...

  4. Iridium compounds - Wikipedia

    en.wikipedia.org/wiki/Iridium_compounds

    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 ...

  5. Indole-3-acetic acid - Wikipedia

    en.wikipedia.org/wiki/Indole-3-acetic_acid

    Indole-3-acetic acid (IAA, 3-IAA) is the most common naturally occurring plant hormone of the auxin class. It is the best known of the auxins, and has been the subject of extensive studies by plant physiologists. [1]

  6. Organorhodium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organorhodium_chemistry

    A typical example of this category viz. novel hexacoordinated orthometalated rhodium(III) thiolato complex trans-[Rh(C ∧ N ∧ S)Cl(PPh 3) 2] was synthesized from benzyl 2-(phenylazo)phenyl thioether and RhCl 3 ·3H 2 O in the presence of excess PPh 3 via in situ C(sp 2)−H and C(sp 3)−S bond scissions. This is the first example for a ...

  7. Metal acetylacetonates - Wikipedia

    en.wikipedia.org/wiki/Metal_acetylacetonates

    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).

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  9. International Numbering System for Food Additives - Wikipedia

    en.wikipedia.org/wiki/International_Numbering...

    The International Numbering System for Food Additives (INS) is an international naming system for food additives, aimed at providing a short designation of what may be a lengthy actual name. [1] It is defined by Codex Alimentarius , the international food standards organisation of the World Health Organization (WHO) and Food and Agriculture ...