Amidosulfite
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Amidosulfites are chemical compounds containing the group =NS(O)O-. Substituents can attach two bonds to the nitrogen and one to the oxygen. These have the form RR'NS(O)OR" compounds can be a zwitterion with a positive charge on the nitrogen, and a negative charge on the oxygen, which then has no group attached. These can be called inner salts. This allows three groups to bond to the nitrogen: RR'R"N S(O)O−.[1]
The simplest amidosulfite is amidosulfurous acid H2NS(O)OH. It has ammonium salt H2NS(O)O−NH4 . These are purportedly produced when sulfur dioxide mixes with ammonia in ratios 1:1 or 1:2.[1]
Known compounds include N-(2-dimethylammonio-ethyl)amidosulfite, N-(2-diethylammonio-ethyl)amidosulfite, N-[2-(1-Piperidinium-1-yl)-ethyl]amidosulfite, N-[2-(4-Morpholinium-4-yl)-ethyl]amidosulfite, sodium N-ethylamidosulfite (C2H5NHS(O)ONa), Ethyl N-ethylamidosulfite (C2H5NHS(O)OC2H5), diethyl-phosphanyl N-methylamidosulfite, diphenyl-phosphanyl N-methylamidosulfite, N,N-dimethylamidosulfurous acid, N,N-diethylamidosulfurous acid, N,N-bis(2-hydroxyethyl)diethylamidosulfurous acid, sodium N,N-dimethylamidosulfite, sodium N,N-diethylamidosulfite, lithium N,N-diethylamidosulfite, lithium N-hexafluoroisopropylideneamidosulfite (with double bond to nitrogen), sodium 1-piperidinesulfinate Na(CH2)5NHS(O)O. [1]
Organometallic substituents can produce for example trimethylsilyl N,N-diethylamidosulfite, trimethyltin N,N-dimethylamidosulfite, or dimethylthallium N,N-dimethylamidosulfite.[1]
References
[edit]- ^ a b c d Baumann, Norbert; Fachmann, Hans-Jürgen; Heibel, Brigitte; Jotter, Reimund; Ledüc, Birgit (2013). S Sulfur-Nitrogen Compounds: Compounds with Sulfur of Oxidation Number IV. Springer Science & Business Media. ISBN 9783662063637.
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