Methenium


In organic chemistry, methenium is a cation with the formula. It can be viewed as a methylene radical with an added proton, or as a methyl radical with one electron removed. It is a carbocation and an enium ion, making it the simplest of the carbenium ions.

Structure

Experiments and calculations generally agree that the methenium ion is planar, with threefold symmetry. The carbon atom is a prototypical example of sp2 hybridization.

Preparation and reactions

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 and with neutral methane. In such conditions, it will react with acetonitrile to form the ion.
Upon capture of a low-energy electron, 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.