Oxidative coupling

Oxidative coupling in chemistry is a coupling reaction of two molecular entities through an oxidative process. Usually oxidative couplings are catalysed by a transition metal complex like in classical cross-coupling reactions, although the underlying mechanism is different due to the oxidation process that requires an external (or internal) oxidant.[1][2] Many such couplings utilize dioxygen as the stoichiometric oxidant but proceed by electron transfer.[3]

C-C Couplings

Many oxidative couplings generate new C-C bonds. Early examples involve coupling of terminal alkynes:[4]

2 RC≡CH + 2 Cu(I) → RC≡C-C≡CR + 2 Cu + 2 H+

Coupling of methane

Coupling reactions involving methane are highly sought, related to C1 chemistry because C2 derivatives are far more valuable than methane. The oxidative coupling of methane gives ethylene:[5][6]

2CH
4 + O
2 → C
2H
4 + 2H
2O

Aromatic coupling
Idealized structure of lignin, showing several aryl-aryl linkages that arise from oxidative couplings.[7]

In oxidative aromatic coupling the reactants are electron-rich aromatic compounds. Typical substrates are phenols and typical catalysts are copper and iron compounds and enzymes.[8] The first reported synthetic application dates back to 1868 with Julius Löwe and the synthesis of ellagic acid by heating gallic acid with arsenic acid or silver oxide.[9] Another reaction is the synthesis of 1,1'-Bi-2-naphthol from 2-naphthol by iron chloride, discovered in 1873 by Alexander Dianin [10] (S)-BINOL can be prepared directly from an asymmetric oxidative coupling of 2-naphthol with copper(II) chloride.[11]

Other oxidative couplings

The oxygen evolution reaction entails, in effect, the oxidative coupling of water molecules to give O2.

Diagram showing the coupling reactions associated with water electrolysis.

References
  1. Oxidative Cross‐Coupling Reactions. Aiwen Lei, Wei Shi, Chao Liu, Wei Liu, Hua Zhang, Chuan He, Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim, Germany(1997). doi:10.1002/9783527680986
  2. Ignacio Funes-Ardoiz, Feliu Maseras (2018). "Oxidative Coupling Mechanisms: Current State of Understanding". ACS Catalysis. 8: 1161–1172. doi:10.1021/acscatal.7b02974.CS1 maint: uses authors parameter (link)
  3. IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). doi:10.1351/goldbook
  4. Alison E. Wendlandt, Alison M. Suess, Shannon S. Stahl (2011). "Copper‐Catalyzed Aerobic Oxidative C-H Functionalizations: Trends and Mechanistic Insights". Angew. Chem. Int. Ed. 50: 11062–11087. doi:10.1002/anie.201103945.CS1 maint: uses authors parameter (link)
  5. Zhang, Q. (2003). "Recent Progress in Direct Partial Oxidation of Methane to Methanol". J. Natural Gas Chem. 12: 81–89.
  6. Olah, G., Molnar, A. “Hydrocarbon Chemistry” John Wiley & Sons, New York, 2003. ISBN 978-0-471-41782-8.
  7. Lebo, Stuart E. Jr.; Gargulak, Jerry D.; McNally, Timothy J. (2001). "Lignin". Kirk-Othmer Encyclopedia of Chemical Technology. Kirk‑Othmer Encyclopedia of Chemical Technology. John Wiley & Sons, Inc. doi:10.1002/0471238961.12090714120914.a01.pub2. ISBN 0-471-23896-1. Retrieved 2007-10-14.
  8. Grzybowski, M., Skonieczny, K., Butenschön, H. and Gryko, D. T. (2013), Comparison of Oxidative Aromatic Coupling and the Scholl Reaction Angew. Chem. Int. Ed., 52: 9900–9930. doi:10.1002/anie.201210238
  9. Löwe, Zeitschrift für Chemie, 1868, 4, 603
  10. A. P. Dianin, Zh. Russ. Fiz.-Khim. O-va. 1874 , 183
  11. Brussee, J.; Jansen, A. C. A. (1983). "A highly stereoselective synthesis of S-(−)-[1,1′-binaphthalene]-2,2′-diol". Tetrahedron Letters. 24 (31): 3261–3262. doi:10.1016/S0040-4039(00)88151-4.
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