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Pentamethylcyclopentadiene

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Pentamethylcyclopentadiene
Skeletal formula of pentamethylcyclopentadiene
Ball-and-stick model of the pentamethylcyclopentadiene molecule
Names
Preferred IUPAC name
1,2,3,4,5-Pentamethylcyclopenta-1,3-diene
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.021.586 Edit this at Wikidata
UNII
  • InChI=1S/C10H16/c1-6-7(2)9(4)10(5)8(6)3/h6H,1-5H3 ☒N
    Key: WQIQNKQYEUMPBM-UHFFFAOYSA-N ☒N
  • InChI=1/C10H16/c1-6-7(2)9(4)10(5)8(6)3/h6H,1-5H3
    Key: WQIQNKQYEUMPBM-UHFFFAOYAI
  • CC1=C(C)C(C)C(C)=C1C
Properties
C10H16
Molar mass 136.238 g·mol−1
Appearance Colorless liquid[1]
Odor Mild[1]
Density 0.87 g/cm3[2]
Boiling point 55 to 60 °C (131 to 140 °F; 328 to 333 K) at 13 mmHg (1.7 kPa)
Sparingly soluble
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Flammable
GHS labelling:
GHS02: Flammable
Warning
H226
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).
☒N verify (what is checkY☒N ?)

1,2,3,4,5-Pentamethylcyclopentadiene is a cyclic diene with the formula C5(CH3)5H, often written C5Me5H, where Me is CH3.[3] It is a colorless liquid.[1]

1,2,3,4,5-Pentamethylcyclopentadiene is the precursor to the ligand 1,2,3,4,5-pentamethylcyclopentadienyl, which is often denoted Cp* (C5Me5) and read as "C P star", the "star" signifying the five methyl groups radiating from the core of the ligand. Thus, the 1,2,3,4,5-pentamethylcyclopentadiene's formula is also written Cp*H. In contrast to less-substituted cyclopentadiene derivatives, Cp*H is not prone to dimerization.

Synthesis

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Pentamethylcyclopentadiene is commercially available. It was first prepared from tiglaldehyde and 2-butenyllithium, via 2,3,4,5-tetramethylcyclopent-2-enone, with a Nazarov cyclization reaction as a key step.[4]

Synthesis of pentamethylcyclopentadiene from tiglaldehyde

Alternatively, 2-butenyllithium adds to ethyl acetate followed by acid-catalyzed dehydrocyclization:[5][6]

Synthesis of pentamethylcyclopentadiene from ethyl acetate
Sample of pentamethylcyclopentadiene in ampoule.

Organometallic derivatives

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Cp*–metal complexes
Cp*2Fe yellow
Cp*TiCl3 red
[Cp*Fe(CO)2]2 red-violet
[Cp*RhCl2]2 red
[Cp*IrCl2]2 orange
Cp*Re(CO)3 colorless
Cp*Mo(CO)2CH3 orange

Cp*H is a precursor to organometallic compounds containing the C
5Me−
5 ligand, commonly called Cp*−.[7]

Some representative reactions leading to such Cp*–metal complexes follow:[8] Deprotonation with n-butyllithium:

Cp*H + C4H9Li → Cp*Li + C4H10

Synthesis of (pentamethylcyclopentadienyl)titanium trichloride:

Cp*Li + TiCl4 → Cp*TiCl3 + LiCl

Synthesis of (pentamethylcyclopentadienyl)iron dicarbonyl dimer from iron pentacarbonyl:

2 Cp*H + 2 Fe(CO)5]] → [η5-Cp*Fe(CO)2]2 + H2 + 6 CO

This method is analogous to the route to the related Cp complex, see cyclopentadienyliron dicarbonyl dimer.

Some Cp* complexes are prepared using silyl transfer:

Cp*Li + Me3SiCl → Cp*SiMe3 + LiCl
Cp*SiMe3 + TiCl4 → Cp*TiCl3 + Me3SiCl

A now-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, but has been discontinued with the increased commercial availability of Cp*H. Such syntheses rely on a hydrohalic acid induced rearrangement of hexamethyl Dewar benzene[9][10] to a substituted pentamethylcyclopentadiene prior to reaction with the hydrate of either iridium(III) chloride[11] or rhodium(III) chloride.[12]

Synthesis of the iridium(III) dimer [Cp*IrCl2]2 using hexamethyl Dewar benzene

Comparison to other Cp ligands

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Structure of tBu3C5H3, a prototypical bulky cyclopentadiene

Complexes of pentamethylcyclopentadienyl differ in several ways from the more common cyclopentadienyl (Cp) derivatives. Being more electron-rich, Cp*− is a stronger donor and dissociation, like ring-slippage, is more difficult with Cp* than with Cp.[13] The fluorinated ligand, (trifluoromethyl)tetramethylcyclopentadienyl, C5Me4CF3, combines the properties of Cp and Cp*: it possesses the steric bulk of Cp* but has electronic properties similar to Cp, the electron-donation from the methyl groups being "canceled out" by the electron-accepting nature of the trifluoromethyl substituent.[14] Its steric bulk stabilizes complexes with fragile ligands. Its bulk also attenuates intermolecular interactions, decreasing the tendency to form polymeric structures. Its complexes also tend to be more soluble in non-polar solvents. The methyl group in Cp* complexes can undergo C–H activation leading to "tuck-in complexes". Bulky cyclopentadienyl ligands are known that are far more sterically encumbered than Cp*.

See also

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References

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  1. ^ a b c https://pubchem.ncbi.nlm.nih.gov/compound/1_2_3_4_5-Pentamethylcyclopentadiene
  2. ^ https://www.sigmaaldrich.com/GB/en/sds/aldrich/214027
  3. ^ Elschenbroich, C.; Salzer, A. (1989). Organometallics: A Concise Introduction. VCH. p. 47. ISBN 9783527278183.
  4. ^ 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.
  5. ^ Threlkel, S.; Bercaw, J. E.; Seidler, P. F.; Stryker, J. M.; Bergman, R. G. (1993). "1,2,3,4,5-Pentamethylcyclopentadiene". Organic Syntheses; Collected Volumes, vol. 8, p. 505.
  6. ^ 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. Vol. 29. pp. 193–198. doi:10.1002/9780470132609.ch47. ISBN 978-0-470-13260-9.
  7. ^ Yamamoto, A. (1986). Organotransition Metal Chemistry: Fundamental Concepts and Applications. Wiley-Interscience. p. 105. ISBN 9780471891710.
  8. ^ 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.
  9. ^ 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.
  10. ^ 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.
  11. ^ 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.
  12. ^ Kang, J. W.; Maitlis, P. M. (1968). "Conversion of Dewar Hexamethylbenzene to Pentamethylcyclopentadienylrhodium(III) Chloride". J. Am. Chem. Soc. 90 (12): 3259–3261. doi:10.1021/ja01014a063.
  13. ^ Kuwabara, Takuya; Tezuka, Ryogen; Ishikawa, Mikiya; Yamazaki, Takuya; Kodama, Shintaro; Ishii, Youichi (2018-06-25). "Ring Slippage and Dissociation of Pentamethylcyclopentadienyl Ligand in an (η 5 -Cp*)Ir Complex with a κ 3 - O , C , O Tridentate Calix[4]arene Ligand under Mild Conditions". Organometallics. 37 (12): 1829–1832. doi:10.1021/acs.organomet.8b00257. ISSN 0276-7333.
  14. ^ Gassman, Paul G.; Mickelson, John W.; Sowa, John R. (1992-08-01). "1,2,3,4-Tetramethyl-5-(trifluoromethyl)cyclopentadienide: a unique ligand with the steric properties of pentamethylcyclopentadienide and the electronic properties of cyclopentadienide". Journal of the American Chemical Society. 114 (17): 6942–6944. doi:10.1021/ja00043a065. ISSN 0002-7863.
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