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Synthesis and Characterization of Charge-Stabilized Poly(4-hydroxybutyl acrylate) Latex by RAFT Aqueous Dispersion Polymerization: A New Precursor for Reverse Sequence Polymerization-Induced Self-Assembly
[Image: see text] The reversible addition–fragmentation chain transfer (RAFT) aqueous dispersion polymerization of 4-hydroxybutyl acrylate (HBA) is conducted using a water-soluble RAFT agent bearing a carboxylic acid group. This confers charge stabilization when such syntheses are conducted at pH 8,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273316/ https://www.ncbi.nlm.nih.gov/pubmed/37333840 http://dx.doi.org/10.1021/acs.macromol.3c00534 |
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author | Buksa, Hubert Neal, Thomas J. Varlas, Spyridon Hunter, Saul J. Musa, Osama M. Armes, Steven P. |
author_facet | Buksa, Hubert Neal, Thomas J. Varlas, Spyridon Hunter, Saul J. Musa, Osama M. Armes, Steven P. |
author_sort | Buksa, Hubert |
collection | PubMed |
description | [Image: see text] The reversible addition–fragmentation chain transfer (RAFT) aqueous dispersion polymerization of 4-hydroxybutyl acrylate (HBA) is conducted using a water-soluble RAFT agent bearing a carboxylic acid group. This confers charge stabilization when such syntheses are conducted at pH 8, which leads to the formation of polydisperse anionic PHBA latex particles of approximately 200 nm diameter. The weakly hydrophobic nature of the PHBA chains confers stimulus-responsive behavior on such latexes, which are characterized by transmission electron microscopy, dynamic light scattering, aqueous electrophoresis, and (1)H NMR spectroscopy. Addition of a suitable water-miscible hydrophilic monomer such as 2-(N-(acryloyloxy)ethyl pyrrolidone) (NAEP) leads to in situ molecular dissolution of the PHBA latex, with subsequent RAFT polymerization leading to the formation of sterically stabilized PHBA–PNAEP diblock copolymer nanoparticles of approximately 57 nm diameter. Such formulations constitute a new approach to reverse sequence polymerization-induced self-assembly, whereby the hydrophobic block is prepared first in aqueous media. |
format | Online Article Text |
id | pubmed-10273316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102733162023-06-17 Synthesis and Characterization of Charge-Stabilized Poly(4-hydroxybutyl acrylate) Latex by RAFT Aqueous Dispersion Polymerization: A New Precursor for Reverse Sequence Polymerization-Induced Self-Assembly Buksa, Hubert Neal, Thomas J. Varlas, Spyridon Hunter, Saul J. Musa, Osama M. Armes, Steven P. Macromolecules [Image: see text] The reversible addition–fragmentation chain transfer (RAFT) aqueous dispersion polymerization of 4-hydroxybutyl acrylate (HBA) is conducted using a water-soluble RAFT agent bearing a carboxylic acid group. This confers charge stabilization when such syntheses are conducted at pH 8, which leads to the formation of polydisperse anionic PHBA latex particles of approximately 200 nm diameter. The weakly hydrophobic nature of the PHBA chains confers stimulus-responsive behavior on such latexes, which are characterized by transmission electron microscopy, dynamic light scattering, aqueous electrophoresis, and (1)H NMR spectroscopy. Addition of a suitable water-miscible hydrophilic monomer such as 2-(N-(acryloyloxy)ethyl pyrrolidone) (NAEP) leads to in situ molecular dissolution of the PHBA latex, with subsequent RAFT polymerization leading to the formation of sterically stabilized PHBA–PNAEP diblock copolymer nanoparticles of approximately 57 nm diameter. Such formulations constitute a new approach to reverse sequence polymerization-induced self-assembly, whereby the hydrophobic block is prepared first in aqueous media. American Chemical Society 2023-06-02 /pmc/articles/PMC10273316/ /pubmed/37333840 http://dx.doi.org/10.1021/acs.macromol.3c00534 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Buksa, Hubert Neal, Thomas J. Varlas, Spyridon Hunter, Saul J. Musa, Osama M. Armes, Steven P. Synthesis and Characterization of Charge-Stabilized Poly(4-hydroxybutyl acrylate) Latex by RAFT Aqueous Dispersion Polymerization: A New Precursor for Reverse Sequence Polymerization-Induced Self-Assembly |
title | Synthesis and
Characterization of Charge-Stabilized
Poly(4-hydroxybutyl acrylate) Latex by RAFT Aqueous Dispersion Polymerization:
A New Precursor for Reverse Sequence Polymerization-Induced Self-Assembly |
title_full | Synthesis and
Characterization of Charge-Stabilized
Poly(4-hydroxybutyl acrylate) Latex by RAFT Aqueous Dispersion Polymerization:
A New Precursor for Reverse Sequence Polymerization-Induced Self-Assembly |
title_fullStr | Synthesis and
Characterization of Charge-Stabilized
Poly(4-hydroxybutyl acrylate) Latex by RAFT Aqueous Dispersion Polymerization:
A New Precursor for Reverse Sequence Polymerization-Induced Self-Assembly |
title_full_unstemmed | Synthesis and
Characterization of Charge-Stabilized
Poly(4-hydroxybutyl acrylate) Latex by RAFT Aqueous Dispersion Polymerization:
A New Precursor for Reverse Sequence Polymerization-Induced Self-Assembly |
title_short | Synthesis and
Characterization of Charge-Stabilized
Poly(4-hydroxybutyl acrylate) Latex by RAFT Aqueous Dispersion Polymerization:
A New Precursor for Reverse Sequence Polymerization-Induced Self-Assembly |
title_sort | synthesis and
characterization of charge-stabilized
poly(4-hydroxybutyl acrylate) latex by raft aqueous dispersion polymerization:
a new precursor for reverse sequence polymerization-induced self-assembly |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273316/ https://www.ncbi.nlm.nih.gov/pubmed/37333840 http://dx.doi.org/10.1021/acs.macromol.3c00534 |
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