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The salt's anion consists of two carbon atoms linked by a triple bond.
This triple bond consists of a sigma bond and two pi bonds.
Each double bond has two additional localized electrons, while each triple bond has four additional electrons (two pairs) between the bonded atoms.
If there are both double bonds and triple bonds, en (double bond) is written before yne (triple bond).
Therefore, the molecule falls into the cyanide group as well due to the presence of the carbon nitrogen triple bond.
This radical can in turn attack the triple bond in acetylene and react efficiently even at low temperatures.
There is one triple bond between carbon atoms 19 and 20.
In these compounds the boron and oxygen form a triple bond prone to cyclotrimerization to boroxines.
The molecule resembles carbon monoxide with a triple bond between carbon and sulfur.
The most common triple bond, that between two carbon atoms, can be found in alkynes.
It is the synthetic and reactive equivalent of an acyl carbocation, but the actual structure has the oxygen and carbon linked by a triple bond.
Besides the single bond, a covalent bond can be either a double bond or a triple bond.
Nevertheless, strained alkyne is a better description of the triple bond nature of ortho-benzyne than biradical (larger singlet-triplet gap and alkyne-like reactivity).
Other functional groups containing a triple bond are cyanides and isocyanides.
Sometimes a number between hyphens is inserted before it to state which atoms the triple bond is between.
