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Tetraphenylcyclopentadienone

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Tetraphenylcyclopentadienone
Skeletal formula

Perspective view, showing the canted phenyl rings[1]
Names
Preferred IUPAC name
2,3,4,5-Tetraphenylcyclopenta-2,4-dien-1-one
Other names
Tetracyclone, TPCPD, Cyclone
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.006.847 Edit this at Wikidata
UNII
  • InChI=1S/C29H20O/c30-29-27(23-17-9-3-10-18-23)25(21-13-5-1-6-14-21)26(22-15-7-2-8-16-22)28(29)24-19-11-4-12-20-24/h1-20H checkY
    Key: PLGPSDNOLCVGSS-UHFFFAOYSA-N checkY
  • InChI=1/C29H20O/c30-29-27(23-17-9-3-10-18-23)25(21-13-5-1-6-14-21)26(22-15-7-2-8-16-22)28(29)24-19-11-4-12-20-24/h1-20H
    Key: PLGPSDNOLCVGSS-UHFFFAOYAO
  • O=C2C(=C(/C(=C2/c1ccccc1)c3ccccc3)c4ccccc4)\c5ccccc5
Properties
C29H20O
Molar mass 384.478 g·mol−1
Appearance black solid
Melting point 219 to 220 °C (426 to 428 °F; 492 to 493 K)[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tetraphenylcyclopentadienone is an organic compound with the formula (C6H5C)4C4C=O. It is classified as a cyclic dienone. It is a dark purple to black crystalline solid that is soluble in organic solvents. It is an easily made building block for many organic and organometallic compounds.

Structure

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The C5O core of the molecule is planar and conjugated, but the bonds have a definite alternating single- and double-bond nature. The C2–C3 and C4–C5 distances are 1.35 Å, while the C1–C2, C3–C4, C5–C1 are closer to single bonds with distances near 1.50 Å.[1] The phenyl groups of tetraphenylcyclopentadienone adopt a "propeller" shape in its 3D conformation. The four phenyl rings are rotated out of the plane of the central ring because of steric repulsion with each other.[3]

Unlike the parent compound cyclopentadienone, which rapidly dimerizes,[4] the tetraphenyl derivative is isolable at room temperature.

Synthesis

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Tetraphenylcyclopentadienone can be synthesized by a double aldol condensation involving benzil and dibenzyl ketone in the presence of a basic catalyst.[2][5]

Reactions

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The central ring can serve as a diene in Diels–Alder reactions with various dienophiles. For example, reaction with benzyne leads to 1,2,3,4-tetraphenylnaphthalene and reaction with diphenylacetylene leads to hexaphenylbenzene.[5] In this way, it is a precursor to graphene-like molecules,[6] such as coronene.

Similarly, pentaphenylpyridine derivatives may be prepared via a Diels–Alder reaction between tetraphenylcyclopentadienone and benzonitrile.[7]

Tetraphenylcyclopentadienone can provide an effective alternative to DDQ in aromatization of porphyrins:[8]

Ligand in organometallic chemistry

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The Shvo catalyst is a ruthenium complex of tetraphenylcyclopentadienone

Tetraarylcyclopentadienones are a well studied class of ligands in organometallic chemistry. The Shvo catalyst, useful for certain hydrogenations, is derived from tetraphenylcyclopentadienone.[9]

References

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  1. ^ a b J. C. Barnes; W. M. Horspool; F. I. Mackie (1991). "2,3,4,5-Tetraphenylcyclopenta-2,4-dien-1-one and 5,6,7,8-tetrachloro-3a,9a-dihydro-2,3,3a,9a-tetraphenylcyclopenta[2,3-b][1,4]benzodioxin-1-one–toluene (2/1): Compounds of photochemical interest". Acta Crystallogr. C. 47 (1): 164–168. Bibcode:1991AcCrC..47..164B. doi:10.1107/S0108270190005145.
  2. ^ a b John R. Johnson, J. R.; Grummitt, O. (1943). "Tetraphenylcyclopentadienone". Organic Syntheses. 23: 92{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 3, p. 805.
  3. ^ Sheley, C. F.; Shechter, H. (1970). "Cyclopentadienones from 1,2,4-cyclopentanetriones, 2-cyclopentene-1,4-diones, and 3-cyclopentene-1,2-diones". The Journal of Organic Chemistry. 35 (7): 2367–2374. doi:10.1021/jo00832a058.
  4. ^ Ogliaruso, Michael A.; Romanelli, Michael G.; Becker, Ernest I. (1965). "Chemistry of Cyclopentadienones". Chemical Reviews. 65 (3): 261–367. doi:10.1021/cr60235a001.
  5. ^ a b Fieser, L. F. (1966). "Hexaphenylbenzene". Organic Syntheses. 46: 44. doi:10.15227/orgsyn.046.0044.
  6. ^ Feng, Xinliang; Pisula, Wojciech; Müllen, Klaus (31 January 2009). "Large polycyclic aromatic hydrocarbons: Synthesis and discotic organization". Pure and Applied Chemistry. 81 (12): 2203–2224. doi:10.1351/PAC-CON-09-07-07. S2CID 98098882.
  7. ^ Hawkins, P. J.; Janz, J. G. (1949). "315. The reaction of cyanogen and related nitriles with 1 : 3-dienes. Part I. Thermodynamic considerations, and a study of the uncatalysed reaction of cyanogen and related nitriles with 1:3-butadiene". Journal of the Chemical Society: 1479–148. doi:10.1039/JR9490001479.
  8. ^ M.A. Filatov; A.Y. Lebedev; S.A. Vinogradov; A.V. Cheprakov (2008). "Synthesis of 5,15-Diaryltetrabenzoporphyrins". J. Org. Chem. 73 (11): 4175–4185. doi:10.1021/jo800509k. PMC 2491715. PMID 18452337.
  9. ^ Quintard, Adrien; Rodriguez, Jean (14 April 2014). "Iron Cyclopentadienone Complexes: Discovery, Properties, and Catalytic Reactivity". Angewandte Chemie International Edition. 53 (16): 4044–4055. doi:10.1002/anie.201310788. PMID 24644277.