Vinylidene group

In chemistry, vinylidenes are compounds with the functional group C=CH2. An example is 1,1-dichloroethene (CCl2=CH2) commonly called vinylidene chloride. It and vinylidene fluoride are precursors to commercially useful polymers.

Monomers and polymers

Vinylidene chloride and fluoride can be converted to linear polymers polyvinylidene chloride (PVDC) and polyvinylidene fluoride (PVDF). The polymerization reaction is shown:

n CH2=CX2 → (CH2−CX2)n

These vinylidene polymers are isomeric with those produced from vinylene monomers. Thus polyvinylene fluoride from vinylene fluoride (HFC=CHF).

Vinylidene complexes

Although vinylidenes are only transient species, they are found as ligands in organometallic chemistry. They typically arise by the protonation of metal acetylides or by the reaction of metal electrophiles with terminal alkynes. The complex chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium readily forms such complexes:[1]

CpRu(PPh3)2Cl + RC2H + KPF6 → [CpRu(PPh3)2(=C=C(H)Ph]PF6 + KCl

Gas phase existence of vinylidenes

Featuring divalent carbon, vinylidenes are unusual species in organic chemistry. They are unstable as solids or liquids but can be generated as stable dilute gases. The parent member of this series is methylidenecarbene. With the formula :C=CH2), it is a carbene.

IUPAC nomenclature

In IUPAC nomenclature, 1,1-ethenediyl describes the connectivity >C=CH2 The related species ethenylidenes have the connectivity =C=CH2.[2]

See also

References

  1. ↑ Barry M. Trost; Andrew McClory "Metal Vinylidenes as Catalytic Species in Organic Reactions" Chem Asian J. 2008, volume 3, 164–194.doi:10.1002/asia.200
  2. ↑ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "vinylidenes".