Onium ion
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In chemistry, an onium ion is a cation formally obtained by the protonation of mononuclear parent hydride of a pnictogen (group 15 of the periodic table), chalcogen (group 16), or halogen (group 17). The oldest-known onium ion, and the namesake for the class, is ammonium, Template:Chem2, the protonated derivative of ammonia, Template:Chem2.[1][2]
The name onium is also used for cations that would result from the substitution of hydrogen atoms in those ions by other groups, such as organic groups, or halogens; such as tetraphenylphosphonium, Template:Chem2. The substituent groups may be divalent or trivalent, yielding ions such as iminium and nitrilium.[1][2]
A simple onium ion has a charge of +1. A larger ion that has two onium ion subgroups is called a double onium ion, and has a charge of +2. A triple onium ion has a charge of +3, and so on.
Compounds of an onium cation and some other anion are known as onium compounds or onium salts.
Onium ions and onium compounds are inversely analogous to -ate ions and ate complexes:
- Lewis bases form onium ions when the central atom gains one more bond and becomes a positive cation.
- Lewis acids form -ate ions when the central atom gains one more bond and becomes a negative anion.[3]
Simple onium cations (hydrides with no substitutions)
Group 13 (boron group) onium cations
- boronium cation, Template:Chem2 (protonated borane)
- further boronium cations, Template:Chem/link (protonated boranes)
Group 14 (carbon group) onium cations
- carbonium ions (protonated hydrocarbons) have a pentacoordinated carbon atom with a +1 charge.
- alkanium cations, Template:Chem/link (protonated alkanes)
- methanium, Template:Chem2 (protonated methane) (Sometimes called carbonium, because it is the simplest member of that class, but that use is deprecated because of multiple definitions.[4] Sometimes called methonium, but methonium also has multiple definitions. Abundant in outer space.)
- ethanium, Template:Chem2 (protonated ethane)
- propanium, Template:Chem2 (propane protonated on an unspecified carbon)
- propylium, or propan-1-ylium (propane protonated on an end carbon)
- propan-2-ylium (propane protonated on the middle carbon)
- butanium, Template:Chem2 (butane protonated on an unspecified carbon)
- n-butanium (n-butane protonated on an unspecified carbon)
- n-butylium, or n-butan-1-ylium (n-butane protonated on an end carbon)
- n-butan-2-ylium (n-butane protonated on a middle carbon)
- isobutanium (isobutane protonated on an unspecified carbon)
- isobutylium, or isobutan-1-ylium (isobutane protonated on an end carbon)
- isobutan-2-ylium (isobutane protonated on the middle carbon)
- n-butanium (n-butane protonated on an unspecified carbon)
- octonium or octanium, Template:Chem2 (protonated octane)
- alkanium cations, Template:Chem/link (protonated alkanes)
- silanium (sometimes silonium), Template:Chem2 (protonated silane) (should not be called siliconium[5]
- disilanium, Template:Chem2 (protonated disilane)
- further silanium cations, Template:Chem/link (protonated silanes)
- germonium, Template:Chem2 (protonated germane)
- stannonium, Template:Chem2 (protonated Template:Chem2) (not protonated stannane Template:Chem2)
- plumbonium, Template:Chem2 (protonated Template:Chem2) (not protonated plumbane Template:Chem2)
- flerovonium, Template:Chem2 (protonated Template:Chem2) (not protonated flerovane Template:Chem2)
Group 15 (pnictogen) onium cations
- ammonium (IUPAC name azanium), Template:Chem2 (protonated ammonia (IUPAC name azane))
- phosphonium, Template:Chem2 (protonated phosphine)
- arsonium, Template:Chem2 (protonated arsine)
- stibonium, Template:Chem2 (protonated stibine)
- bismuthonium, Template:Chem2 (protonated bismuthine)
- moscovonium, Template:Chem2 (protonated moscovine)
Group 16 (chalcogen) onium cations
- oxonium, Template:Chem2 (protonated water (IUPAC name oxidane). Oxonium is better known as hydronium, though hydronium implies a solvated or hydrated proton. It may also be called hydroxonium.)
- sulfonium, Template:Chem2 (protonated hydrogen sulfide)
- selenonium, Template:Chem2 (protonated hydrogen selenide)
- telluronium, Template:Chem2 (protonated hydrogen telluride)
- polononium, Template:Chem2 (protonated hydrogen polonide)
- livermoronium, Template:Chem2 (protonated hydrogen livermoride)
Hydrogen onium cation
- hydrogenonium, better known as trihydrogen cation, Template:Chem2 (protonated molecular or diatomic hydrogen), found in ionized hydrogen and interstellar space
Group 17 (halogen) onium cations, halonium ions, Template:Chem2 (protonated hydrogen halides)
- fluoronium, Template:Chem2 (protonated hydrogen fluoride)
- chloronium, Template:Chem2 (protonated hydrogen chloride)
- bromonium, Template:Chem2 (protonated hydrogen bromide)
- iodonium, Template:Chem2 (protonated hydrogen iodide)
- astatonium, Template:Chem2 (protonated hydrogen astatide)
- tennessonium, Template:Chem2 (protonated hydrogen tennesside)
Pseudohalogen onium cations
- aminodiazonium, Template:Chem2 (protonated hydrogen azide)
- methylidyneammonium and hydrocyanonium, Template:Chem2, isomers Template:Chem2 (protonated hydrogen cyanide)
Group 18 (noble gas) onium cations
- hydrohelium or helonium, better known as helium hydride ion, Template:Chem2 (protonated helium)
- neonium, Template:Chem2 (protonated neon)
- argonium, Template:Chem2 (protonated argon)
- kryptonium, Template:Chem2 (protonated krypton)
- xenonium, Template:Chem2 (protonated xenon)
- radonium, Template:Chem2 (protonated radon)
- oganessonium Template:Chem2 (protonated oganesson)
Onium cations with monovalent substitutions
- primary ammonium cations, Template:Chem2 or Template:Chem2 (protonated primary amines)
- hydroxylammonium, Template:Chem2 (protonated hydroxylamine)
- methylammonium, Template:Chem2 (protonated methylamine)
- ethylammonium, Template:Chem2 (protonated ethylamine)
- hydrazinium, or diazanium, Template:Chem2 (protonated hydrazine, a.k.a. diazane)
- anilinium (a.k.a. phenylammonium), Template:Chem2 (protonated aniline, a.k.a. phenylamine, aminobenzene)
- secondary ammonium cations, Template:Chem2 (protonated secondary amines)
- dimethylammonium (sometimes dimethylaminium), Template:Chem2 (protonated dimethylamine)
- diethylammonium (sometimes diethylaminium), Template:Chem2 (protonated diethylamine)
- ethylmethylammonium, Template:Chem2 (protonated ethylmethylamine)
- diethanolammonium (sometimes diethanolaminium), Template:Chem2 (protonated diethanolamine)
- tertiary ammonium cations, Template:Chem2 (protonated tertiary amines)
- trimethylammonium Template:Chem2 (protonated trimethylamine)
- triethylammonium Template:Chem2 (protonated triethylamine)
- quaternary ammonium cations, Template:Chem2 or Template:Chem2
- tetrafluoroammonium, Template:Chem2
- tetramethylammonium, Template:Chem2
- tetraethylammonium, Template:Chem2
- tetrapropylammonium, Template:Chem2
- tetrabutylammonium, Template:Chem2 or abbreviated Template:Chem2
- trimethyl ammonium compounds, Template:Chem2
- didecyldimethylammonium, Template:Chem2
- pentamethylhydrazinium, Template:Chem2
- quaternary phosphonium cations, Template:Chem2 or Template:Chem2
- quaternary arsonium cations, Template:Chem2 or Template:Chem2
- quaternary stibonium cations, Template:Chem2 or Template:Chem2
- primary oxonium cations, Template:Chem2 (protonated alcohols Template:Chem2)
- alkyloxonium cations Template:Chem2 (protonated alcohols)
- methyloxonium, Template:Chem2 (protonated methanol)
- ethyloxonium, Template:Chem2 (protonated ethanol)
- dioxidanonium (hydroxylhydronium), Template:Chem2 (protonated hydrogen peroxide)
- alkyloxonium cations Template:Chem2 (protonated alcohols)
- secondary oxonium cations, Template:Chem2 (protonated ethers Template:Chem2)
- dialkyloxonium cations (protonated ethers)
- dimethyloxonium, Template:Chem2 (protonated dimethyl ether)
- dialkyloxonium cations (protonated ethers)
- tertiary oxonium cations, Template:Chem2
- trifluorooxonium, Template:Chem2 (hypothetical)
- trimethyloxonium, Template:Chem2
- triethyloxonium, Template:Chem2
- oxatriquinacene, Template:Chem2 (cyclic oxonium ion)
- oxatriquinane, Template:Chem2 (cyclic oxonium ion)
- primary sulfonium cations, Template:Chem2 (protonated thiols Template:Chem2)
- secondary sulfonium cations, Template:Chem2 (protonated thioethers Template:Chem2)
- dimethylsulfonium, Template:Chem2 (protonated dimethyl sulfide)
- tertiary sulfonium cations, Template:Chem2
- tertiary selenonium cations, Template:Chem2
- tertiary telluronium cations, Template:Chem2
- primary fluoronium cations, Template:Chem2 (protonated fluorides RF)
- secondary fluoronium cations, Template:Chem2
- secondary iodonium cations, Template:Chem2
Onium cations with polyvalent substitutions
- secondary ammonium cations having one double-bonded substitution, Template:Chem2
- diazenium, Template:Chem2 (protonated diazene)
- guanidinium, Template:Chem2 (protonated guanidine) (has a resonance structure and a planar molecular geometry)
- tertiary ammonium cations having one triple-bonded substitution, R≡NH+
- nitrilium, Template:Chem2 (protonated nitrile)
- diazonium or diazynium, Template:Chem2 (protonated nitrogen, in other words, protonated diazyne)
- cyclic tertiary ammonium cations where nitrogen is a member of a ring, Template:Chem2 (the ring may be aromatic)
- pyridinium, Template:Chem2 (protonated pyridine)
- quaternary ammonium cations having one double-bonded substitution and two single-bonded substitutions, Template:Chem2
- iminium, Template:Chem2 (substituted protonated imine)
- diazenium, Template:Chem2 (substituted protonated diazene)
- thiazolium, Template:Chem2(substituted protonated thiazole)
- quaternary ammonium cations having two double-bonded substitutions, Template:Chem2
- quaternary ammonium cations having one triple-bonded substitution and one single-bonded substitution, Template:Chem2
- diazonium, Template:Chem2 (substituted protonated nitrogen, in other words, substituted protonated diazyne)
- nitrilium, Template:Chem2 (substituted protonated nitrile)
- tertiary oxonium cations having one triple-bonded substitution, Template:Chem2
- cyclic tertiary oxonium cations where oxygen is a member of a ring, Template:Chem2 (the ring may be aromatic)
- tertiary sulfonium cations having one triple-bonded substitution, Template:Chem2
- dihydroxyoxoammonium, Template:Chem2 (protonated nitric acid)
- trihydroxyoxosulfonium, Template:Chem2 (protonated sulfuric acid)
Double onium dications
- hydrazinediium or hydrazinium(2+) dication, Template:Chem2 (doubly protonated hydrazine, in other words, doubly protonated diazane)
- diazenediium cation, Template:Chem2 (doubly protonated diazene)
- diazynediium cation, Template:Chem2 (doubly protonated dinitrogen, in other words, doubly protonated diazyne)
Enium cations
The extra bond is added to a less-common parent hydride, a carbene analog, typically named -ene or -ylene, which is neutral with 2 fewer bonds than the more-common hydride, typically named -ane or -ine.
- borenium cations, Template:Chem2 (protonated borylenes a.k.a. boranylidenes)
- carbenium cations, Template:Chem2 (protonated carbenes) have a tricoordinated carbon atom with a +1 charge.
- alkenium cations, Template:Chem/link (n ≥ 2) (protonated alkenes)
- methenium cation, Template:Chem2 (protonated methylene)
- ethenium, Template:Chem2 (protonated ethene)
- benzenium, Template:Chem2 (protonated benzene)
- tropylium, Template:Chem2 (protonated tropylidene)
- alkenium cations, Template:Chem/link (n ≥ 2) (protonated alkenes)
- silylium cations, Template:Chem2 (protonated silylenes)
- nitrenium cations, Template:Chem2 (protonated nitrenes)
- phosphinidenium cations, Template:Chem2 (protonated phosphinidene)
- mercurinium cations, Template:Chem2 (protonated organomercury compounds; formed as intermediates in oxymercuration reactions)
Substituted eniums
- diphenylcarbenium, Template:Chem2 (di-substituted methenium)
- triphenylcarbenium, Template:Chem2 (tri-substituted methenium)
Ynium cations
- carbynium ions (protonated carbynes) have a carbon atom with a +1 charge.
- alkynium cations, Template:Chem/link (n ≥ 2) (protonated alkynes)
- methynium cation, Template:Chem2 (protonated methylidyne radical)
- ethynium, Template:Chem2 (protonated ethyne)
- alkynium cations, Template:Chem/link (n ≥ 2) (protonated alkynes)
See also
- Carbonium ion
- Lyonium ion, a protonated solvent molecule
- Lyate ion, a deprotonated solvent molecule
References
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- ↑ a b Onium compounds, IUPAC Gold Book
- ↑ a b Script error: No such module "citation/CS1".
- ↑ Advanced Organic Chemistry: Reactions and mechanisms, Maya Shankar Singh, 2007, Dorling Kindersley, Template:ISBN
- ↑ Carbonium ion, IUPAC Gold Book
- ↑ RC-82. Cations, Queen Mary University of London)
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External links
- Ions and Radicals, Queen Mary University of London
- Template:Replace at the U.S. National Library of Medicine Medical Subject Headings (MeSH)