Metal ammine complex
In coordination chemistry, metal ammine complexes are metal complexes containing at least one ammonia (NH3) ligand. "Ammine" is spelled this way due to historical reasons; in contrast, alkyl or aryl bearing ligands are spelt with a single "m". Almost all metal ions bind ammonia as a ligand, but the most prevalent examples of ammine complexes are for Cr(III), Co(III), Ni(II), Cu(II) as well as several platinum group metals.
Ammine complexes played a major role in the development of coordination chemistry, specifically determination of the stereochemistry and structure. They are easily prepared, and the metal-nitrogen ratio can be determined by elemental analysis. Through studies mainly on the ammine complexes, Alfred Werner developed his Nobel Prize-winning concept of the structure of coordination compounds (see Figure).
Homoleptic poly(ammine) complexes are known for many of the transition metals. Most often, they have the formula [M(NH3)6]n+ where n = 2, 3, and even 4 (M = Pt).
Platinum group metalsEdit
Platinum group metals form diverse ammine complexes. Pentaamine(dinitrogen)ruthenium(II) and the Creutz–Taube complex are well studied examples or historic significance. The complex cis-PtCl2(NH3)2, under the name Cisplatin, is an important anticancer drug. Pentamminerhodium chloride is the dichloride salt of the dicationic pentammine complex [RhCl(NH3)5]2+. This salt is an intermediate in the purification of rhodium from its ores.
Carboplatin, a widely used anticancer drug.
Pentamminerhodium chloride, the dichloride salt one a cationic pentammine halide complex.
Hexamminecobalt(III) chloride, the trichloride salt of the hexammine complex [Co(NH3)6]3+. It is famously stable in concentrated hydrochloric acid.
Cobalt(III) and chromium(III)Edit
The ammines of chromium(III) and cobalt(III) are of historic significance. Both families of amines are relatively inert kinetically, which allows the separation of isomers. For example, tetraamminedichlorochromium(III) chloride, [Cr(NH3)4Cl2]Cl, has two forms - the cis isomer is violet, while the trans isomer is green. The trichloride of the hexaammine (hexamminecobalt(III) chloride, [Co(NH3)6]Cl3)) exists as only a single isomer. "Reinecke's salt" with the formula NH4[Cr(NCS)4(NH3)2].H2O was first reported in 1863.
Nickel(II), zinc(II), copper(II)Edit
Zinc(II) forms a colorless tetraammine with the formula [Zn(NH3)4]2+. Like most zinc complexes, it has a tetrahedral structure. Hexaamminenickel is violet, and the copper(II) complex is deep blue. The latter is characteristic of the presence of copper(II) in qualitative inorganic analysis.
Copper(I), silver(I), and gold(I)Edit
Copper(I) forms only labile complexes with ammonia, including the trigonal planar [Cu(NH3)3]+. Silver gives the diammine complex [Ag(NH3)2]+ with linear coordination geometry. It is this complex that forms when otherwise rather insoluble silver chloride dissolves in aqueous ammonia. The same complex is the active ingredient in Tollen's reagent. Gold(I) chloride forms a compound with six ammonia, but X-ray crystallography reveals that only two ammonia molecules are ligands.
Ligand exchange and redox reactionsEdit
Since ammonia is a stronger ligand in the spectrochemical series than water, metal ammine complexes are stabilized relative to the corresponding aquo complexes. For similar reasons, metal ammine complexes are less strongly oxidizing than are the corresponding aquo complexes. The latter property is illustrated by the stability of [Co(NH3)6]3+ in aqueous solution and the nonexistence of [Co(H2O)6]3+ (which would oxidize water).
Once complexed to a metal ion, ammonia is not basic. This property is illustrated by the stability of some metal ammine complexes in strong acid solutions. When the M-NH3 bond is weak, the ammine ligand dissociates and protonation ensues. The behavior is illustrated by the non-reaction and reaction with [Co(NH3)6]3+ and [Ni(NH3)6]2+, respectively.
The ammine ligands are more acidic than is ammonia (pKa ~ 33). For highly cationic complexes such as [Pt(NH3)6]4+, the conjugate base can be obtained. The deprotonation of cobalt(III) ammine-halide complexes, e.g. [CoCl(NH3)5]2+ labilises the Co-Cl bond, according to the Sn1CB mechanism.
Metal ammine complexes find many uses. Cisplatin (PtCl2(NH3)2) is a coordination compound containing two chloro and two ammine ligands. This is a drug used in treating cancer. Many other amine complexes of the platinum group metals have been evaluated for this application.
In the separation of the individual platinum metals from their ore, several schemes rely on the precipitation of [RhCl(NH3)5]Cl2. In some separation schemes, palladium is purified by manipulating equilibria involving [Pd(NH3)4]Cl2, PdCl2(NH3)2, and Pt(NH3)4[PdCl4].
In the processing of cellulose, the copper ammine complex known as Schweizer's reagent ([Cu(NH3)4(H2O)2](OH)2) is sometimes used to solubilise the polymer. Schweizer's reagent is prepared by treating an aqueous solutions of copper(II) ions with ammonia. Initially, the light blue hydroxide precipitates only to redissolve upon addition of more ammonia:
- [Cu(H2O)6]2+ + 2 OH− → Cu(OH)2 + 6 H2O
- Cu(OH)2 + 4 NH3 + 2 H2O → [Cu(NH3)4(H2O)2]2+ + 2 OH−
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