Issue 1, 2020, Issue in Progress

Synthesis and properties of porous polymers synthesized by Michael addition reactions of multi-functional acrylate, diamine, and dithiol compounds

Abstract

Porous polymers have been synthesized by Michael addition reactions of multi-functional acrylate and diamine or dithiol compounds. Aza-Michael addition reaction of multi-functional acrylate, trimethylolpropane propoxylate triacrylate (TPT) and hexamethylene diamine (HDA) in dimethyl sulfoxide (DMSO) successfully yielded the porous polymer. The porous structure was characterized by connected globules or co-continuous structure, and could be controlled by the reaction conditions. Mechanical properties of the porous polymers were investigated by compression test. The porous polymers with co-continuous structure showed higher Young's modulus than those with connected globules. The porous polymer absorbed some organic solvents, especially CHCl3. The porous polymer as prepared in DMSO state showed coloring induced by Christiansen filter effect depending on the reaction time and observation temperature. The thio-Michael addition reaction of TPT and 1,6-hexanedithiol (HDT) in DMSO using different base catalysts also yielded the porous polymer. The porous structure could be controlled by the catalysts amount when the reaction was initiated by a photo-base generator as the base catalyst. The present reaction systems make it possible to synthesize the porous polymers with simple process without phase separator.

Graphical abstract: Synthesis and properties of porous polymers synthesized by Michael addition reactions of multi-functional acrylate, diamine, and dithiol compounds

Supplementary files

Article information

Article type
Paper
Submitted
19 Nov 2019
Accepted
16 Dec 2019
First published
23 Dec 2019
This article is Open Access
Creative Commons BY license

RSC Adv., 2020,10, 60-69

Synthesis and properties of porous polymers synthesized by Michael addition reactions of multi-functional acrylate, diamine, and dithiol compounds

N. Naga, S. Fujioka, D. Inose, K. Ahmed, H. Nageh and T. Nakano, RSC Adv., 2020, 10, 60 DOI: 10.1039/C9RA09684A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements