Issue 34, 2018

Synthesis and characterization of poly(ethene–ketone–arylene–ketone)s containing pendant methylthio groups via metal-free catalyzed copolymerization of aryldiynes with DMSO

Abstract

A series of methylthio-substituted poly(ethene–ketone–arylene–ketone)s were synthesized by metal-free catalyzed copolymerization between aromatic diynes and dimethyl sulfoxide (DMSO). The copolymerization can be easily carried out under catalysis by I2 and BF3·Et2O in N,N-dimethyl formamide at 100 °C, resulting in good yields (up to 90.9%) and high molecular weights (Mw up to 13 100). Moreover, the effect of different substituents on the diyne monomers on the Mw, yield and solubility of the resultant polymers was investigated. All these polymers were well characterized by GPC, NMR, and FTIR, and their structures were confirmed. The obtained polymers showed high thermal stability and had high char yields at 800 °C. Moreover, most of the polymers had a high refractive indices of visible light (400 to 800 nm) due to their high sulfur contents. Given the high efficiency, monomer versatility, and excellent performance of the resultant products, this metal-free catalyzed copolymerization between diynes and DMSO opens up new opportunities to prepare advanced functional polymers.

Graphical abstract: Synthesis and characterization of poly(ethene–ketone–arylene–ketone)s containing pendant methylthio groups via metal-free catalyzed copolymerization of aryldiynes with DMSO

Supplementary files

Article information

Article type
Paper
Submitted
03 Jun 2018
Accepted
30 Jul 2018
First published
31 Jul 2018

Polym. Chem., 2018,9, 4404-4412

Synthesis and characterization of poly(ethene–ketone–arylene–ketone)s containing pendant methylthio groups via metal-free catalyzed copolymerization of aryldiynes with DMSO

W. Fu, L. Dong, J. Shi, B. Tong, Z. Cai, J. Zhi and Y. Dong, Polym. Chem., 2018, 9, 4404 DOI: 10.1039/C8PY00819A

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