Issue 30, 2021

Oxa-Michael polyaddition of vinylsulfonylethanol for aliphatic polyethersulfones

Abstract

Polyethersulfones are an interesting class of polymers for industrial applications due to their unusual properties such as a high refractive index, flame-retardant properties, and high temperature and chemical resistance. The common aromatic polymers however require high temperatures for processing, while alternative aliphatic polyethersulfones remain overall scarce in the literature with only oligomeric materials being reported so far. Nevertheless, these materials have similar promising properties to those observed for their aromatic equivalents. Here, we describe the reactivity of a novel AB-type monomer vinylsulfonylethanol, which enables a successful and straightforward synthesis of aliphatic polyethersulfones. Various organic and inorganic catalysts were tested, and the kinetics of the resulting polymerizations were examined. Rapid conversions were observed resulting in polymers with molar masses in the range of 2000 to 4000 g mol−1 within a few minutes. A closer characterization of the resulting polymers revealed that all organic catalysts initiate the polymerization process by a nucleophilic addition to the vinyl group, even if strong but sterically hindered bases are used. Inorganic bases in turn seem to deprotonate the hydroxy groups to initiate the polymerization, as the vinyl end groups are preserved. The resulting polymers are characterized by excellent heat resistance with degradation temperatures >300 °C in air, which is significantly higher than previous observations for other aliphatic polyolefinsulfones. Further analysis reveals a semi-crystalline nature of the polymer if processed from solvents although recrystallization appears to be kinetically hindered. With the possibility to prepare the starting material vinylsulfonylethanol by a straightforward method and on a large scale, such polymers become easily accessible using the described preparation routes, while the beneficial thermal properties of the polymer may open up interesting opportunities for their application.

Graphical abstract: Oxa-Michael polyaddition of vinylsulfonylethanol for aliphatic polyethersulfones

Supplementary files

Article information

Article type
Paper
Submitted
24 Feb 2021
Accepted
30 Apr 2021
First published
03 May 2021

Polym. Chem., 2021,12, 4337-4346

Oxa-Michael polyaddition of vinylsulfonylethanol for aliphatic polyethersulfones

N. Ziegenbalg, R. Lohwasser, G. D'Andola, T. Adermann and J. C. Brendel, Polym. Chem., 2021, 12, 4337 DOI: 10.1039/D1PY00256B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements