Optimization of synthetic parameters of high-purity trifunctional mercaptoesters and their curing behavior for the thiol–epoxy click reaction
Author:
Affiliation:
1. Materials Chemistry & Engineering Laboratory, School of Polymer System Engineering, Dankook University, Yongin, Gyeonggi-do 16890, Republic of Korea
Abstract
Funder
Gyeonggi-do Regional Research Center
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/RA/D1RA05981E
Reference21 articles.
1. Multifunctional thiols from the highly selective reaction of mercaptoalcohols with chlorosilanes
2. Proton Transfer Hydrogels: Versatility and Applications
3. Recent Advances and Challenges in the Design of Organic Photoacid and Photobase Generators for Polymerizations
4. Functionalized Molecular Bottlebrushes
5. Thiol-Epoxy “Click” Chemistry to Engineer Cytocompatible PEG-Based Hydrogel for siRNA-Mediated Osteogenesis of hMSCs
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1. Analysis of the non-ideal crosslinking process in thiol-X “click” thermosets;European Polymer Journal;2024-05
2. Synthesis and Characterization of Multifunctional Secondary Thiol Hardeners Using 3-Mercaptobutanoic Acid and Their Thiol–Epoxy Curing Behavior;ACS Omega;2022-06-10
3. Synthesis and characteristics of novel 2-hydroxy-3-mercaptopropyl terminated polyoxypropylene glyceryl ether as an epoxy hardener of epoxy-based adhesives;Polymer Testing;2022-06
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