This article is about chemical reactions in which ammonia is a reactant. For chemical reactions involving amines, see aminolysis.
In chemistry, ammonolysis (/am·mo·nol·y·sis/) is the process of splitting ammonia into .[1] Ammonolysis reactions can be conducted with organic compounds to produce amines (molecules containing a nitrogen atom with a lone pair, :N),[2] or with inorganic compounds to produce nitrides.[3][4] This reaction is analogous to hydrolysis in which water molecules are split. Similar to water, liquid ammonia also undergoes auto-ionization, ,[5] where the rate constant is k = 1.9 × 10-38.[6]
Organic compounds such as alkyl halides, hydroxyls (hydroxyl nitriles and carbohydrates), carbonyl (aldehydes/ketones/esters/alcohols), and sulfur (sulfonyl derivatives) can all undergo ammonolysis in liquid ammonia.[5]
^Speight, James G. (2017-01-01), Speight, James G. (ed.), "Chapter 3 - Industrial Organic Chemistry", Environmental Organic Chemistry for Engineers, Butterworth-Heinemann, pp. 87–151, doi:10.1016/b978-0-12-804492-6.00003-4, ISBN 978-0-12-804492-6, retrieved 2022-12-07
^Stevenson, Arthur C. (September 1948). "Ammonolysis". Industrial & Engineering Chemistry. 40 (9): 1584–1589. doi:10.1021/ie50465a006. ISSN 0019-7866.
^Reichert, Malinda D.; White, Miles A.; Thompson, Michelle J.; Miller, Gordon J.; Vela, Javier (2015). "Preparation and Instability of Nanocrystalline Cuprous Nitride". Inorganic Chemistry. 54 (13): 6356−6362. doi:10.1021/acs.inorgchem.5b00679. PMID 26091284.
^ abFernelius, W. Conard.; Bowman, Glade B. (1940-02-01). "Ammonolysis in Liquid Ammonia". Chemical Reviews. 26 (1): 3–48. doi:10.1021/cr60083a002. ISSN 0009-2665.
^Pleskov, V.A (1935). Acta Physiochim. {{cite journal}}: Missing or empty |title= (help)
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original on 23 February 2013. Retrieved 25 June 2012. "13.1.3.5. Oxidative ammonolysis of hydrocarbons". ChemAnalitica.com. 1 April 2009. Retrieved 22 October...
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