Pentamethylcyclopentadiene

Pentamethylcyclopentadiene
Skeletal formula of pentamethylcyclopentadiene
Ball-and-stick model of the pentamethylcyclopentadiene molecule
Identifiers
4045-44-7 YesY
3D model (Jmol) Interactive image
ChemSpider 70069 N
ECHA InfoCard 100.021.586
PubChem 77667
Properties
C10H16
Molar mass 136.24 g/mol
Boiling point 55 to 60 °C (131 to 140 °F; 328 to 333 K) at 13 mmHg (1.7 kPa)
Sparingly soluble
Hazards
Flash point 114 °C (237 °F; 387 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

1,2,3,4,5-Pentamethylcyclopentadiene is a cyclic dialkene with the formula C5Me5H (Me = CH3).[1] 1,2,3,4,5-Pentamethylcyclopentadiene is the precursor to the ligand 1,2,3,4,5-pentamethylcyclopentadienyl, which is often denoted as Cp* (to signify the five methyl groups radiating from the periphery of this ligand as in a five-pointed star). In contrast to less substituted cyclopentadiene derivatives, Cp*H is not prone to dimerization.

Synthesis

Pentamethylcyclopentadiene is commercially available. It was first prepared from tiglaldehyde via 2,3,4,5-tetramethylcyclopent-2-enone.[2] Alternatively 2-butenyllithium adds to ethylacetate followed by acid-catalyzed dehydrocyclization:[3][4]

2 MeCH=C(Li)Me + MeC(O)OEt → (MeCH=C(Me))2C(OLi)Me + LiOEt
(MeCH=C(Me))2C(OLi)Me + H+ → Cp*H + H2O + Li+

Organometallic derivatives

Cp*H is a precursor to organometallic compounds containing the C
5Me−
5 (Cp*−) ligand.[5]

Cp*–metal complexes
Cp*2Fe yellow
Cp*TiCl3 red
[Cp*Fe(CO)2]2 red-violet
[Cp*RhCl2]2 red
Cp*IrCl22 orange
Cp*Re(CO)3 colorless
Cp*Mo(CO)2CH3 orange

Some representative reactions leading to such Cp*-metal complexes follow:[6]

Cp*H + C4H9Li → Cp*Li + C4H10
Cp*Li + TiCl4 → Cp*TiCl3 + LiCl
2 Cp*H + 2 Fe(CO)5 → [Cp*Fe(CO)2]2 + H2 + CO

For the related Cp complex, see cyclopentadienyliron dicarbonyl dimer.

An instructive but obsolete route to Cp* complexes involves the use of hexamethyl Dewar benzene. This method was traditionally used for preparation of the chloro-bridged dimers [Cp*IrCl2]2 and [Cp*RhCl2]2. Such syntheses rely on a hydrohalic acid induced rearrangement of hexamethyl Dewar benzene[7][8] to a substituted pentamethylcyclopentadiene prior to reaction with the hydrate of either iridium(III) chloride[9] or rhodium(III) chloride.[10]

Comparison of Cp* with Cp

Complexes of pentamethylcyclopentadienyl differ in several ways from the more common cyclopentadienyl (Cp) derivatives. Being more electron-rich, Cp* is a stronger donor and is less easily removed from the metal. Consequently, its complexes exhibit increased thermal stability. Its steric bulk allows the isolation of complexes with fragile ligands. Its bulk also attenuates intermolecular interactions, decreasing the tendency to form polymeric structures. Its complexes also tend to be highly soluble in non-polar solvents. The methyl group in Cp* complexes can undergo C–H activation leading to "tuck-in complexes".

See also

References

  1. ↑ Elschenbroich, C.; Salzer, A. (1989). Organometallics: A Concise Introduction. VCH. p. 47. ISBN 9783527278183.
  2. ↑ De Vries, L. (1960). "Preparation of 1,2,3,4,5-Pentamethyl-cyclopentadiene, 1,2,3,4,5,5-Hexamethyl-cyclopentadiene, and 1,2,3,4,5-Pentamethyl-cyclopentadienylcarbinol". J. Org. Chem. 25 (10): 1838. doi:10.1021/jo01080a623.
  3. ↑ Threlkel, S.; Bercaw, J. E.; Seidler, P. F.; Stryker, J. M.; Bergman, R. G. (1993). "1,2,3,4,5-Pentamethylcyclopentadiene". Org. Synth.; Coll. Vol., 8, p. 505
  4. ↑ Fendrick, C. M.; Schertz, L. D.; Mintz, E. A.; Marks, T. J. (1992). "Large-Scale Synthesis of 1,2,3,4,5-Pentamethylcyclopentadiene". Inorganic Syntheses. Inorganic Syntheses. 29: 193–198. doi:10.1002/9780470132609.ch47. ISBN 978-0-470-13260-9.
  5. ↑ Yamamoto, A. (1986). Organotransition Metal Chemistry: Fundamental Concepts and Applications. Wiley-Interscience. p. 105. ISBN 9780471891710.
  6. ↑ King, R. B.; Bisnette, M. B. (1967). "Organometallic chemistry of the transition metals XXI. Some π-pentamethylcyclopentadienyl derivatives of various transition metals". J. Organomet. Chem. 8 (2): 287–297. doi:10.1016/S0022-328X(00)91042-8.
  7. ↑ Paquette, L. A.; Krow, G. R. (1968). "Electrophilic Additions to Hexamethyldewarbenzene". Tetrahedron Lett. 9 (17): 2139–2142. doi:10.1016/S0040-4039(00)89761-0.
  8. ↑ Criegee, R.; Gruner, H. (1968). "Acid-catalyzed Rearrangements of Hexamethyl-prismane and Hexamethyl-Dewar-benzene". Angew. Chem. Int. Ed. Engl. 7 (6): 467–468. doi:10.1002/anie.196804672.
  9. ↑ Kang, J. W.; Mosley, K.; Maitlis, P. M. (1968). "Mechanisms of Reactions of Dewar Hexamethylbenzene with Rhodium and Iridium Chlorides". Chem. Commun. (21): 1304–1305. doi:10.1039/C19680001304.
  10. ↑ Kang, J. W.; Maitlis, P. M. (1968). "Conversion of Dewar Hexamethylbenzene to Pentamethylcyclopentadienylrhodium(III) Chloride". J. Amer. Chem. Soc. 90 (12): 3259–3261. doi:10.1021/ja01014a063.
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