Phenylcopper

Phenylcopper

Phenylcopper

Chemical compound


Phenylcopper is an organometallic chemical compound of copper.[1] Its chemical formula is C
6
H
5
Cu
.[2]

Quick Facts Names, Identifiers ...

Synthesis

Phenylcopper was the first known organocopper compound and was first prepared in 1923 from phenylmagnesium iodide and copper(I) iodide and in 1936 by Henry Gilman by transmetallation of phenylmagnesium iodide with copper(I) chloride.

Phenylcopper can be obtained by reacting phenyl lithium with copper(I) bromide in diethyl ether.[3]

C6H5Li + CuBr → C6H5Cu + LiBr

Properties

Phenylcopper is a colorless solid substance that is soluble in pyridine. It can be stored for a few days without decomposition under nitrogen or in vacuum. Rapid decomposition takes place in air. Water decomposes phenylcopper to form red copper (I) oxide and varying amounts of benzene and biphenyl. It forms stable complexes with tributylphosphine and triphenylphosphine.[4]

When dissolved in dimethyl sulfide, phenylcopper forms dimers and trimers (aggregates of two or three molecules).[5]

A diphenylcuprate(I) ion exists that can form a salt with lithium. (Li+[Cu(C6H5)2]).[5]

See also


References

  1. Costa, G.; Camus, A.; Gatti, L.; Marsich, N. (1966-06-01). "On phenylcopper". Journal of Organometallic Chemistry. 5 (6): 568–572. doi:10.1016/S0022-328X(00)85161-X. ISSN 0022-328X. Retrieved 2 June 2021.
  2. Frański, Rafał; Kozik, Tomasz; Staniszewski, Bartosz; Urbaniak, Włodzimierz (2010-06-01). "Phenylcopper(I) clusters in the gas phase obtained by laser desorption/ionization from bis(dibenzoylmethane)copper(II)". Open Chemistry. 8 (3): 508–512. doi:10.2478/s11532-010-0017-z. S2CID 94008194.
  3. Rappoport, Zvi; Marek, Ilan (2010). The Chemistry of Organocopper Compounds. John Wiley & Sons. p. 152. ISBN 9780470772966.
  4. Bertz, Steven H.; Dabbagh, Gary; He, Xiaoming; Power, Philip P. (December 1993). "New copper chemistry. 21. Phenylcopper(I) and diphenylcuprate(I): characterization of aggregation states by carbon-13 NMR spectroscopy". Journal of the American Chemical Society. 115 (24): 11640–11641. doi:10.1021/ja00077a090.

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