Abstract
Elemental sulfur, a waste product of the oil
refinement process, represents a promising raw material for
the synthesis of degradable polymers. We show that simple
lithium alkoxides facilitate the polymerisation of elemental
sulfur S8 with industrially relevant propylene oxide (PO) and
CS2 (a base chemical sourced from waste S8 itself) to give
poly(monothiocarbonate-alt-Sx) in which x can be controlled
by the amount of supplied sulfur. The in-situ generation of
thiolate intermediates obtained by a rearrangement, which
follows CS2 and PO incorporation, allows to combine S8 and
epoxides into one polymer sequence that would otherwise
not be possible. Mechanistic investigations reveal that alkyl
oligosulfide intermediates from S8 ring opening and sulfur
chain length equilibration represent the better nucleophiles
for inserting the next PO if compared to the trithiocarbonates
obtained from the competing CS2 addition, which causes
the sequence selectivity. The polymers can be crosslinked
in-situ with multifunctional thiols to yield reprocessable and
degradable networks. Our report demonstrates how
mechanistic understanding allows to combine intrinsically
incompatible building blocks for sulfur waste utilisation.
Supplementary materials
Title
Supporting Information
Description
Supporting Information
Actions