|
| |||
| Names | |||
|---|---|---|---|
| Preferred IUPAC name
Methylium | |||
| Other names
Methyl cation; Carbanylium | |||
| Identifiers | |||
3D model (JSmol) |
|||
| 1839325 | |||
| ChEBI | |||
| ChemSpider | |||
| 48893 | |||
PubChem CID |
|||
| UNII | |||
CompTox Dashboard (EPA) |
|||
| |||
| |||
| Properties | |||
| CH3+ | |||
| Molar mass | 15.034 g·mol−1 | ||
| Related compounds | |||
Related isoelectronic |
borane | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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In organic chemistry, methenium (also called methylium, carbenium, methyl cation, or protonated methylene) is a cation with the formula CH+
3. It can be viewed as a methylene radical (:CH
2) with an added proton (H+
), or as a methyl radical (•CH
3) with one electron removed. It is a carbocation and an enium ion, making it the simplest of the carbenium ions.
Experiments and calculations generally agree that the methenium ion is planar, with threefold symmetry. The carbon atom is a prototypical (and exact) example of sp2 hybridization.
For mass spectrometry studies at low pressure, methenium can be obtained by ultraviolet photoionization of methyl radical, or by collisions of monatomic cations such as C+
and Kr+
with neutral methane. In such conditions, it will react with acetonitrile CH
3CN to form the ion (CH
3)
2CN+
.
Upon capture of a low-energy electron (less than 1 eV), it will spontaneously dissociate.
It is seldom encountered as an intermediate in the condensed phase. It is proposed as a reactive intermediate that forms upon protonation or hydride abstraction of methane with FSO3H-SbF5. The methenium ion is very reactive, even towards alkanes.
In June 2023, astronomers detected, for the first time outside the Solar System, methyl cation, CH3+ (and/or carbon cation, C+), the known basic ingredients of life, in interstellar space.