Ring‐Opening Terpolymerisation of Elemental Sulfur Waste with Propylene Oxide and Carbon Disulfide via Lithium Catalysis

Author:

Gallizioli Cesare1,Battke David2,Schlaad Helmut3,Deglmann Peter4,Plajer Alex J.1ORCID

Affiliation:

1. Makromolekulare Chemie I Universität Bayreuth Universitätsstraße 30 95447 Bayreuth

2. Institut für Chemie und Biochemie Freie Universität Berlin Fabeckstraße 34–36 14195 Berlin

3. Institute für Chemie Universität Potsdam Karl-Liebknecht-Straße 24–25 14476 Potsdam

4. BASF SE Carl-Bosch-Straße 38 67056 Ludwigshafen am Rhein

Abstract

AbstractElemental 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.

Funder

Verband der Chemischen Industrie

Publisher

Wiley

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