Pentacyanocyclopentadiene

Pentacyanocyclopentadiene
Skeletal formula of pentacyanocyclopentadiene
Space-filling model of the pentacyanocyclopentadiene molecule
Names
IUPAC name
1,3-Cyclopentadiene-1,2,3,4,5-pentacarbonitrile
Identifiers
69239-40-3
3D model (Jmol) Interactive image
ChemSpider 11484097
Properties
C10HN5
Molar mass 191.15 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Pentacyanocyclopentadiene is a derivative of cyclopentadiene with five cyano groups with the molecular formula C5H(CN)5. The corresponding anion, pentacyanocyclopentadienide, is a ligand with the molecular formula C5(CN)5. In contrast to other anions based on a C5 ring unit it binds to metals through the pendant cyano groups rather than the C5 ring. The anion was first synthesised by Webster in the 1960s[1] and its conjugate acid much later on.[2] More recently Wright has discovered its extensive coordination chemistry.[3][4]

Synthesis

Pentacyanocyclopentadiene is synthesised by coupling carbon disulfide and sodium cyanide in dimethylformamide before oxidation using ammonium persulfate and final purification generates the ammonium pentacyanocyclopentadiene salt. Further reaction with sodium hydride generates NaC5(CN)5 which is a starting point for its coordination chemistry with transition metals.

Reactions & Coordination Chemistry

Coupling of sodium pentacyanocyclopentadiene (NaC5(CN)5) with transition metal halide salts generates metal complexes containing the C5(CN)5 anion.[3][4] Because the anion binds to metals through the cyanide group it can act as a pentagonal node. Thus it can form fullerene-like structures with large voids containing solvent.[5][6] This has important implications for gas storage and separation.

References

  1. Webster, O. W. (1966). "Diazotetracyanocyclopentadiene". Journal of the American Chemical Society. 88 (17): 4055–4060. doi:10.1021/ja00969a029.
  2. Reed, C. (2004). "Exploration of the pentacyano-cyclo-pentadienide ion, C5(CN)5?, as a weakly coordinating anion and potential superacid conjugate base". Chem. Commun.: 706. doi:10.1039/b316122f.
  3. 1 2 Wright, D. S. (2011). "Transition metal complexes of the pentacyanocyclopentadienide anion". Chem. Commun. 47: 10007. doi:10.1039/c1cc13021h.
  4. 1 2 Wright, D. S. (2012). "Group 11 complexes containing the [C5(CN)5]− ligand; 'coordination-analogues' of molecular organometallic systems". Dalton Trans. 41: 5919. doi:10.1039/c2dt30274h.
  5. Bacsa, J. (2011). "Assembly of the First Fullerene-Type Metal-Organic Frameworks Using a Planar Five-Fold Coordination Node". Angew. Chem. Int. Ed. 50: 8279–8282. doi:10.1002/anie.201102783.
  6. Less, R. J. (2013). "Solvent Direction of Molecular Architectures in Group 1 Metal Pentacyanocyclopentadienides". Eur. J. Inorg. Chem. 7: 1161–1169. doi:10.1002/ejic.201201342.
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