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Transition metal dithiocarbamate complexes

Transition metal dithiocarbamate complexes are coordination complexes containing one or more dithiocarbamate ligand, which are typically abbreviated R<sub>2</sub>dtc<sup>−</sup>. Many complexes are known. Several homoleptic derivatives have the formula M(R<sub>2</sub>dtc)<sub>n</sub> where n = 2 and 3.

Ligand characteristics

Dithiocarbamate anions are classified as L-X ligand in the Covalent bond classification method. In the usual electron counting method, they are three-electron ligands. With respect to HSAB theory, they are classified as soft.

Because of the pi-donor properties of the amino substituent, the two sulfur centers show enhanced basicity relative to dithiocarboxylates. This situation is represented by the zwitterionic resonance structure that depicts a positive charge on N and negative charges on both sulfurs. This N to C pi-bonding results in partial double bond character for the C-N bond. Consequently, barriers to rotational about this bond are elevated. Another consequence of their high basicity, dithiocarbamates often stabilize complexes in some uncharacteristically high oxidation state (e.g., Fe(IV), Co(IV), Ni(III), Cu(III)).

Dithiocarbamate salts are easily synthesized by treating secondary amines with carbon disulfide in the presence of sodium hydroxide:

R<sub>2</sub>NH + CS<sub>2</sub> + NaOH → R<sub>2</sub>NCS<sub>2</sub><sup>−</sup>Na<sup>+</sup> + H<sub>2</sub>O

A wide variety of secondary amines give the corresponding dtc ligands. Popular amines include dimethylamine (Me<sub>2</sub>NH), diethylamine (Et<sub>2</sub>NH), and pyrrolidine ((CH<sub>2</sub>)<sub>4</sub>NH). Complexes of , derived from the parent dithiocarbamic acid have been reported.

Related ligands

Dithiocarbamates are classified as derivatives of dithiocarbamic acid. Their properties as ligands resemble the conjugate bases of many related "1,1-dithioacids":

Synthetic methods

Commonly, metal dithiocarbamates are prepared by salt metathesis reactions using alkali metal dithiocarbamates:

NiCl<sub>2</sub> + 2NaS<sub>2</sub>CNMe<sub>2</sub> → Ni(S<sub>2</sub>CNMe<sub>2</sub>)<sub>2</sub> + 2NaCl

In some cases, the dithiocarbamate serves as a reductant, followed by its complexation.

A complementary method entails oxidative addition of thiuram disulfides to low-valent metal complexes:

Mo(CO)<sub>6</sub> + 2[S<sub>2</sub>CNMe<sub>2</sub>]<sub>2</sub> → Mo(S<sub>2</sub>CNMe<sub>2</sub>)<sub>4</sub> + 6CO

Metal amido complexes, such as tetrakis(dimethylamido)titanium, react with carbon disulfide:

Ti(NMe<sub>2</sub>)<sub>4</sub> + 4CS<sub>2</sub> → Ti(S<sub>2</sub>CNMe<sub>2</sub>)<sub>4</sub>

Homoleptic complexes

Bis complexes
  • nickel bis(dimethyldithiocarbamate), palladium bis(dimethyldithiocarbamate), platinum bis(dimethyldithiocarbamate), all square-planar complexes
  • copper bis(diethyldithiocarbamate), a square-planar complex
Tris complexes
  • vanadium tris(diethyldithiocarbamate), an octahedral complex
  • chromium tris(diethylditiocarbamate), an octahedral complex
  • manganese tris(dimthylthtiocarbamate), an octahedral complex
  • iron tris(diethyldithiocarbamate), ruthenium tris(diethyldithiocarbamate), osmium tris(diethyldithiocarbamate), all octahedral complexes
  • cobalt tris(diethyldithiocarbamate), rhodium tris(diethyldithiocarbamate), iridium tris(diethyldithiocarbamate), all octahedral complexes
Tetrakis complexes
  • titanium tetrakis(dimethyldithiocarbamate)
  • molybdenum tetrakis(diethyldithiocarbamate)
Dimetallic complexes

Reactions

Dithiocarbamate complexes do not undergo characteristic reactions. They can be removed from complexes by oxidation, as illustrated by the iodination of the iron tris(diethyldithiocarbamate):

They degrade to metal sulfides upon heating.

Applications

Dtc complexes find several applications:

References