posted on 2014-12-09, 00:00authored byJeannette M. García, Gavin
O. Jones, Julien DeWinter, Hans W. Horn, Olivier Coulembier, Philippe Dubois, Pascal Gerbaux, James L. Hedrick
Identifying
solvent- and catalyst-free conditions for polymerizations
of engineering thermoplastics is of increasing interest due to new
polymer processing technologies such as 3-D printing. We report the
selective formation of linear poly(aryl ether sulfone)s (PESs) from
the polycondensation of trimethylsilyl-protected bisphenol A (TMS-BPA)
with nitro-substituted diaryl fluorides without added solvent or catalyst.
DFT calculations show that nitro groups strategically placed in the ortho-position to the fluoride leaving group form a stable
Meisenheimer complex during polyether synthesis. This strategy represents
a route to linear PESs that employs anionic conditions, destabilizing
propagating phenoxide chain ends preventing backbiting while simultaneously
stabilizing the Meisenheimer complex intermediate. Thermodynamic over
kinetic control in the polycondensation minimizes cyclic PES formation
and promotes the formation of pure linear PESs.