N-Oxoammonium salt
N-Oxoammonium salts are a class of organic compounds with the formula [R1R2=O]X−. The cation [R1R2=O] is of interest for the dehydrogenation of alcohols. Oxoammonium salts are diamagnetic, whereas the nitroxide has a doublet ground state. A prominent N-oxoammonium salt is prepared by oxidation of (2,2,6,6-tetramethylpiperidin-1-yl)oxyl, commonly referred to as [TEMPO]+. A less expensive analogue is Bobbitt's salt.
Structure and bonding[edit]
Oxoammonium cations are isoelectronic with carbonyls and structurally related to aldoximes (hydroxylamines), and aminoxyl (nitroxide) radicals, with which they can interconvert via a series of redox steps. According to X-ray crystallography, the N–O distance in [TEMPO]BF4 is 1.184 Å, 0.1 Å shorter than the N–O distance of 1.284 Å in the charge-neutral TEMPO. Similarly, the N in [TEMPO]+ is nearly planar, but the O moves 0.1765 Å out of the plane in the neutral TEMPO.[1]
The N-oxoammonium salts are used for oxidation of alcohols to carbonyl groups,[2] as well as other forms of oxoammonium-catalyzed oxidations. The nitroxyl TEMPO reacts via its N-oxoammonium salt.[3]
See also[edit]
- Nitrone – structurally related, the N-oxide of an imine
References[edit]
- ^ Yonekuta Yasunori; Oyaizu Kenichi; Nishide Hiroyuki (2007). "Structural Implication of Oxoammonium Cations for Reversible Organic One-electron Redox Reaction to Nitroxide Radicals". Chemistry Letters. 36 (7): 866–867. doi:10.1246/cl.2007.866.
- ^ Bobbitt, James M.; Brückner, Christian; Merbouh, Nabyl (2010). "Oxoammonium- and Nitroxide-Catalyzed Oxidations of Alcohols". Organic Reactions. pp. 103–424. doi:10.1002/0471264180.or074.02. ISBN 978-0471264187.
- ^ N. E. Leadbeater; J. M. Bobbitt (2014). "TEMPO-Derived Oxoammonium Salts as Versatile Oxidizing Agents" (PDF). Aldrichimica Acta. 47 (3): 65–74.
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