Poly(hydridocarbyne)

Poly(hydridocarbyne)
Formula [HC]n
Molecular mass 200,000 to 100 million Daltons
Melting point decomposes @ 100°C
Boiling point N/A
Density ??.?? g/cm³
CAS number ???-??-?
SMILES ???????

Poly(hydridocarbyne) (PHC) is one of a class of carbon-based random network polymers primarily composed of tetrahedrally hybridized carbon atoms, each having one hydride substituent, exhibiting the generic formula [HC]n. PHC is made from bromoform, a liquid halocarbon that is commercially manufactured from methane. At room temperature, poly(hydridocarbyne) is a dark brown powder. It can be easily dissolved in a number of solvents (tetrahydrofuran, ether, toluene etc.), forming a colloidal suspension that is clear and non-viscous, which may then be deposited as a film or coating on various substrates. Upon thermolysis in argon at atmospheric pressure and temperatures of 110°C to 1000°C, decomposition of poly(hydridocarbyne) results in hexagonal diamond (Lonsdaleite).

More recently poly(hydridocarbyne) has been synthesized by a much simpler method using electrolysis of chloroform (May 2008) [1] and hexachloroethane (June 2009).[2]

The novelty of PHC (and its related polymer poly(methylsilyne)) is that the polymer may be readily fabricated into various forms (e.g. films, fibers, plates) and then thermolized into a final hexagonal diamond ceramic.

References

Notes

  1. ^ Toppare L et al. (2008) Facile Synthesis of Poly(hydridocarbyne): A Precursor to Diamond and Diamond-like Ceramics, Journal of Macromolecular Science, Part A 45 (5), May, 358–363, doi=10.1080/10601320801946108.
  2. ^ Toppare L et al. (2009) Electrochemical polymerizatıon of hexachloroethane to form poly(hydridocarbyne): a pre-ceramic polymer for diamond production, Journal of Materials Science 44 2774–2779, doi=10.1007/s10853-009-3364-4.

External links