Pentacyanocyclopentadiene
Pentacyanocyclopentadiene is an anionic ligand with 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
- ^ Webster, O. W. (1966). J. Am. Chem. Soc. 88: 4055.
{{cite journal}}: Missing or empty|title=(help) - ^ Reed, C. (2004). Chem. Commun.: 706.
{{cite journal}}: Missing or empty|title=(help) - ^ a b Wright, D. S. (2011). Chem. Commun. 47: 10007.
{{cite journal}}: Missing or empty|title=(help) - ^ a b Wright, D. S. (2012). Dalton Trans. 41: 5919.
{{cite journal}}: Missing or empty|title=(help) - ^ Bacsa, J. (2011). Angew. Chem. Int. Ed. 50: 8279.
{{cite journal}}: Missing or empty|title=(help) - ^ Less, R. J. (2013). Eur. J. Inorg. Chem. 7: 1161.
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