Phenyl group

The structure of the phenyl group attached to an "R" group.

In organic chemistry, the phenyl group or phenyl ring is a cyclic group of atoms with the formula C₆H₅. Phenyl groups are closely related to benzene and can be viewed as a benzene ring, minus a hydrogen, serving as a functional group. Phenyl groups have six carbon atoms bonded together in a hexagonal planar ring, five of which are bonded to individual hydrogen atoms, with the remaining carbon bonded to a substituent. Phenyl groups are commonplace in organic chemistry.^[1] Although often depicted with alternating double and single bonds, phenyl groups are chemically aromatic and show nearly equal bond lengths between carbon atoms in the ring.^[1][2]

Nomenclature

Usually, a "phenyl group" is synonymous to C₆H₅– and is represented by the symbol Ph or, archaically, Φ. Benzene is sometimes denoted as PhH. Phenyl groups are generally attached to other atoms or groups. For example, triphenylmethane (Ph₃CH) has three phenyl groups attached to the same carbon center. Many or even most phenyl compounds are not described with the term "phenyl". For example the chloro derivative C₆H₅Cl is normally called chlorobenzene, although it could be called phenyl chloride. In special (and rare) cases, isolated phenyl groups are detected: the phenyl anion (C₆H₅⁻), the phenyl cation (C₆H₅⁺), and the phenyl radical (C₆H₅^·).π

Although Ph and phenyl uniquely denote C₆H₅, substituted derivatives also are described using the phenyl terminology. For example, O₂NC₆H₄ is nitrophenyl and F₅C₆ is pentafluorophenyl. Monosubstituted phenyl groups (that is, disubstituted benzenes) are associated with electrophilic aromatic substitution reactions and the products follow the arene substitution pattern. So, a given substituted phenyl compound has three isomers, ortho (1,2-disubstitution), meta (1,3-disubstitution) and para (1,4-disubstitution). A disubstituted phenyl compound (trisubstituted benzene) may be, for example, 1,3,5-trisubstituted, or 1,2,3-trisubstituted. Higher degrees of substitution, of which the pentafluorophenyl group is an example, exist, and are named according to IUPAC nomenclature.

Etymology

Phenyl is derived from the French word phényle, which in turn derived from Greek phaino – "shining", as the first phenyl compounds named were byproducts of making and refining various gases used for lighting.^[3]

Structure, bonding, characterization

Phenyl compounds are derived from benzene (C₆H₆), at least conceptually and often in terms of their production. In terms of its electronic properties, the phenyl group is related to a vinyl group. It is generally considered an inductively withdrawing group (-I), because of the higher electronegativity of sp² carbon atoms, and a resonance donating group (+M), due to the ability of its π system to donate electron density when conjugation is possible.^[4] The phenyl group is hydrophobic. Phenyl groups tend to resist oxidation and reduction. Phenyl groups (like all aromatic compounds) have enhanced stability in comparison to equivalent bonding in aliphatic (non-aromatic) groups. This increased stability is due to the unique properties of aromatic molecular orbitals.^[2]

The bond lengths between carbon atoms in a phenyl group are approximately 1.4 Å.^[5]

In ¹H-NMR spectroscopy, protons of a phenyl group typically have chemical shifts around 7.27 ppm. These chemical shifts are influenced by aromatic ring current and may change depending on substituents.

Preparation, occurrence, and applications

Phenyl groups are usually introduced using reagents that behave as sources of the phenyl anion or the phenyl cation. Representative reagents include phenyllithium (C₆H₅Li) and phenylmagnesium bromide (C₆H₅MgBr). Electrophiles attack benzene to give phenyl derivatives:

C₆H₆ + E⁺ → C₆H₅E + H⁺

where E⁺ (the "electrophile") = Cl⁺, NO₂⁺, SO₃. These reactions are called electrophilic aromatic substitutions.

• Representative compounds containing phenyl groups
• 
  Atorvastatin (Lipitor), a blockbuster drug featuring two phenyl and one p-fluorophenyl groups. It is used to lower cholesterol in people with hypercholesterolaemia.
• 
  Fexofenadine (Allegra, Telfast), another blockbuster drug, which features a diphenylmethyl group as well as a p-phenylene (C₆H₄) group. It is an antihistamine used to treat allergies.
• 
  Phenylalanine, a common amino acid.
• 
  Biphenyl, consisting of two phenyl groups. The two rings tend not to be coplanar.
• 
  Chlorobenzene (or phenyl chloride), a solvent.

Phenyl groups are found in many organic compounds, both natural and synthetic (see figure). Most common among natural products is the amino acid phenylalanine, which contains a phenyl group. A major product of the petrochemical industry is "BTX" consisting of benzene, toluene, and xylene - all of which are building blocks for phenyl compounds. The polymer polystyrene is derived from a phenyl-containing monomer and owes its properties to the rigidity and hydrophobicity of the phenyl groups. Many drugs as well as many pollutants contain phenyl rings. biphe One of the simplest phenyl-containing compounds is phenol, C₆H₅OH. It is often said the resonance stability of phenol makes it a stronger acid than that of aliphatic alcohols such as ethanol (pK_a = 10 vs. 16–18). However, a significant contribution is the greater electronegativity of the sp² alpha carbon in phenol compared to the sp³ alpha carbon in aliphatic alcohols.^[6]

References

1. March, Jerry (1992). Advanced organic chemistry : reactions, mechanisms, and structure (4th ed.). New York: Wiley. ISBN 0-471-60180-2.
2. "Virtual Textbook of Organic Chemistry: Aromaticity". Michigan State University. http://www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/react3.htm
3. "phenyl: definition of phenyl in Oxford dictionary (American English) (US)". Retrieved 3 March 2016.
4. Hansch, Corwin.; Leo, A.; Taft, R. W. (1991-03-01). "A survey of Hammett substituent constants and resonance and field parameters". Chemical Reviews. 91 (2): 165–195. doi:10.1021/cr00002a004. ISSN 0009-2665.
5. Hameka, Hendrik F. (1987). "Computation of the structures of the phenyl and benzyl radicals with the UHF method". The Journal of Organic Chemistry. 52 (22): 5025–5026. doi:10.1021/jo00231a035. ISSN 0022-3263.
6. Silva, Pedro Jorge (2009). "Inductive and Resonance Effects on the Acidities of Phenol, Enols, and Carbonyl α-Hydrogens". The Journal of Organic Chemistry. 74 (2): 914–916. doi:10.1021/jo8018736. ISSN 0022-3263.