Biphenyl Explained

Biphenyl (also known as diphenyl, phenylbenzene, 1,1′-biphenyl, lemonene[1] or BP) is an organic compound that forms colorless crystals. Particularly in older literature, compounds containing the functional group consisting of biphenyl less one hydrogen (the site at which it is attached) may use the prefixes xenyl or diphenylyl.[2]

It has a distinctively pleasant smell. Biphenyl is an aromatic hydrocarbon with a molecular formula (C6H5)2. It is notable as a starting material for the production of polychlorinated biphenyls (PCBs), which were once widely used as dielectric fluids and heat transfer agents.

Biphenyl is also an intermediate for the production of a host of other organic compounds such as emulsifiers, optical brighteners, crop protection products, and plastics. Biphenyl is insoluble in water, but soluble in typical organic solvents. The biphenyl molecule consists of two connected phenyl rings.

Properties and occurrence

Biphenyl is a solid at room temperature, with a melting point of . In the gas phase the molecule exists in two enantiomorphic twisted forms with an angle between the planes of the two rings of 44.4°. In the room-temperature solid, biphenyl is crystalline with space group P2/c, which does not allow for chiral crystals. Rather than there being a double-well potential entailing the two twisted conformations, the potential energy is minimized at zero twist.[3] [4]

Biphenyl occurs naturally in coal tar, crude oil, and natural gas and can be isolated from these sources via distillation.[5] It is produced industrially as a byproduct of the dealkylation of toluene to produce methane:

The other principal route is by the oxidative dehydrogenation of benzene:

Annually 40,000,000 kg are produced by these routes.[6]

In the laboratory, biphenyl can also be synthesized by treating phenylmagnesium bromide with copper(II) salts.

It can also be prepared using diazonium salts. When aniline is treated with NaNO2+dilute HCl at 5°C, it yields benzene diazonium chloride. When this is further reacted with benzene, biphenyl is formed. This is known as the Gomberg–Bachmann reaction.

Ph-NH2->[\text{NaNO}_2\text{(aq), HCl}][T\text{=273-278K}] Ph-N2+ ->[\text{Ph-H, Δ}] Ph-Ph

Reactions and uses

Lacking functional groups, biphenyl is fairly non-reactive, which is the basis of its main application: in a eutectic mixture with diphenyl ether, as a heat transfer agent. This mixture is stable to 400 °C.[6]

Biphenyl does undergo sulfonation which, followed by base hydrolysis, produces p-hydroxybiphenyl and p,p′-dihydroxybiphenyl, which are useful fungicides. In other substitution reactions, it undergoes halogenation. Polychlorinated biphenyls were once popular pesticides.[6]

Li biphenyl radical

Lithium biphenyl contains the radical anion, which is highly reducing (-3.1 V vs Fc+/0). Several solvates of alkali metal salts of biphenyl anion have been characterized by X-ray crystallography.[7] These salts, usually prepared in situ, are versatile reducing agents.[8] Lithium biphenyl offers some advantages relative to the related lithium naphthene.[9] Related to Li/biphenyl is the derivative with tert-butyl groups on the biphenyl.[10]

Stereochemistry

Rotation about the single bond in biphenyl, and especially its ortho-substituted derivatives, is sterically hindered. For this reason, some substituted biphenyls show atropisomerism; that is, the individual C2-symmetric-isomers are optically stable. Some derivatives, as well as related molecules such as BINAP, find application as ligands in asymmetric synthesis. In the case of unsubstituted biphenyl, the equilibrium torsional angle is 44.4° and the torsional barriers are quite small, 6.0 kJ/mol at 0° and 6.5 kJ/mol at 90°.[11] Adding ortho substituents greatly increases the barrier: in the case of the 2,2'-dimethyl derivative, the barrier is 17.4 kcal/mol (72.8 kJ/mol).[12]

Biphenyl compounds

Substituted biphenyls have many uses. They are prepared by various coupling reactions including the Suzuki-Miyaura reaction and the Ullmann reaction. Polychlorinated biphenyls were once used as cooling and insulating fluids and polybrominated biphenyls are flame retardants. The biphenyl motif also appears in drugs such as diflunisal and telmisartan. The abbreviation E7 stands for a liquid crystal mixture consisting of several cyanobiphenyls with long aliphatic tails used commercially in liquid crystal displays (5CB, 7CB, 8OCB and 5CT[13]). A variety of benzidine derivatives are used in dyes and polymers. Research into biphenyl liquid crystal candidates mainly focuses on molecules with highly polar heads (for example cyano or halide groups) and aliphatic tails. It is part of the active group in the antibiotic oritavancin.

Safety and bioactivity

Biphenyl prevents the growth of molds and fungus, and is therefore used as a preservative (E230, in combination with E231, E232 and E233), particularly in the preservation of citrus fruits during transportation. It is no longer approved as a food additive in the European Union.

Biphenyl is mildly toxic, but can be degraded biologically by conversion into nontoxic compounds. Some bacteria are able to hydroxylate biphenyl and its polychlorinated biphenyls (PCBs).[14]

See also

References

External links

Notes and References

  1. Web site: Biphenyl . NIST Chemistry WebBook . US National Institute of Standards and Technology. An obscure name, according to Web site: Limonene . Molecule of the Week Archive . . Nov 1, 2021.
  2. Web site: Beilsteins Handbuch der organischen Chemie, Volume 5.
  3. Dr. Bruno Landeros-Rivera, Jesús Hernández-Trujillo . Control of Molecular Conformation and Crystal Packing of Biphenyl Derivatives . . Dec 15, 2021 . 10.1002/cplu.202100492 .
  4. Landeros‐Rivera . Bruno . Jancik . Vojtech . Moreno‐Esparza . Rafael . Martínez Otero . Diego . Hernández‐Trujillo . Jesús . May 27, 2021 . Non‐Covalent Interactions in the Biphenyl Crystal: Is the Planar Conformer a Transition State? . . en . 27 . 46 . 11912–11918 . 10.1002/chem.202101490 . 0947-6539.
  5. Adams, N. G., and D. M. Richardson, 1953. Isolation and Identification of Biphenyls from West Edmond Crude Oil. Analytical Chemistry 25 (7): 1073-1074
  6. Karl Griesbaum, Arno Behr, Dieter Biedenkapp, Heinz-Werner Voges, Dorothea Garbe, Christian Paetz, Gerd Collin, Dieter Mayer, Hartmut Höke "Hydrocarbons" in Ullmann's Encyclopedia of Industrial Chemistry 2002 Wiley-VCH, Weinheim.
  7. 10.1039/C5NJ02841H. Isolation of gravimetrically quantifiable alkali metal arenides using 18-crown-6. 2016. Castillo. Maximiliano. Metta-Magaña. Alejandro J.. Fortier. Skye. New Journal of Chemistry. 40. 3. 1923–1926.
  8. Regio- and Stereoselective Carboxylation of Allylic Barium Reagents: (E)-4,8-dimethyl-3,7-nonadienoic Acid. Akira . Yanagisawa . Katsutaka . Yasue . Hisashi . Yamamoto. Org. Synth.. 1997. 74. 178. 10.15227/orgsyn.074.0178.
  9. Highly Reactive Calcium for the Preparation of Organocalcium Reagents: 1-Adamantyl Calcium Halides and Their Addition to Ketones: 1-(1-Adamantyl)cyclohexanol. Reuben D. . Rieke. Tse-Chong . Wu. Loretta I.. Rieke. Org. Synth.. 1995. 72. 147. 10.15227/orgsyn.072.0147.
  10. 1,3-Diols from Lithium β-Lithioalkoxides Generated by The Reductive Lithiation of Epoxides: 2,5-Dimethyl-2,4-hexanediol. Boguslaw . Mudryk. Theodore . Cohen. Org. Synth.. 1995. 72. 173. 10.15227/orgsyn.072.0173.
  11. J. Chem. Theory Comput. . 10.1021/ct800182e . Torsional Barriers and Equilibrium Angle of Biphenyl: Reconciling Theory with Experiment . 2008 . Mikael P. Johansson and Jeppe Olsen . 4 . 1460–1471 . 9. 26621432 .
  12. Book: Stereochemistry . Christoph Tamm . B. Testa . 18 . Elsevier . 1982 . The geometry of molecules: basic principles and nomenclatures.
  13. Mouquinho . Ana . Saavedra . Mara . Maiau . Alexandre . Petrova . Krasimira . Barros . M. Teresa . Figueirinhas . J. L. . Sotomayor . João . Films Based on New Methacrylate Monomers: Synthesis, Characterisation and Electro-Optical Properties . Molecular Crystals and Liquid Crystals . 30 June 2011 . 542 . 1 . 132/[654]–140/[662] . 10.1080/15421406.2011.570154. 97514765 .
  14. Web site: Biphenyl degradation - Streptomyces coelicolor, at GenomeNet Database. genome.jp.