Carboxylate, nitrate, sulfonate, and phosphate catalysts for living radical polymerization : via oxygen-iodine halogen bonding catalysis

Four families of oxyanions, i.e., carboxylate, nitrate, phosphate, and sulfonate, were studied as novel catalysts in living (or reversible deactivation) radical polymerization via oxygen-iodine halogen bonding catalysis. Oxyanions with sodium and tetraalkylammonium counter-cations exhibited good cat...

Full description

Saved in:
Bibliographic Details
Main Authors: Mao, Weijia, Wang, Chen Gang, Lu, Yunpeng, Faustinelie, Winnie, Goto, Atsushi
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2020
Subjects:
Online Access:https://hdl.handle.net/10356/137718
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-137718
record_format dspace
spelling sg-ntu-dr.10356-1377182023-02-28T19:21:10Z Carboxylate, nitrate, sulfonate, and phosphate catalysts for living radical polymerization : via oxygen-iodine halogen bonding catalysis Mao, Weijia Wang, Chen Gang Lu, Yunpeng Faustinelie, Winnie Goto, Atsushi School of Physical and Mathematical Sciences Science::Chemistry Radical Polymerization BNOAc Four families of oxyanions, i.e., carboxylate, nitrate, phosphate, and sulfonate, were studied as novel catalysts in living (or reversible deactivation) radical polymerization via oxygen-iodine halogen bonding catalysis. Oxyanions with sodium and tetraalkylammonium counter-cations exhibited good catalytic activities and high solubilities in hydrophilic and hydrophobic monomers. These oxyanion catalysts were amenable for methyl methacrylate, functional methacrylates, styrene, and acrylonitrile, and also afforded block copolymers with low dispersities. The catalytic activities of the oxyanions were also theoretically studied using density functional theory (DFT) calculation. The studied four families of oxyanions are abundant in natural and synthetic compounds. Non-Toxic natural carboxylates were successfully used to synthesize well-defined biocompatible polymers. The low cost, low toxicity, and accessibility for a range of polymer designs are attractive features for practical use. NRF (Natl Research Foundation, S’pore) MOE (Min. of Education, S’pore) Accepted version 2020-04-09T08:27:10Z 2020-04-09T08:27:10Z 2019 Journal Article Mao, W., Wang, C.-G., Lu, Y., Faustinelie, & Goto, A. (2020). Carboxylate, nitrate, sulfonate, and phosphate catalysts for living radical polymerization : via oxygen-iodine halogen bonding catalysis. Polymer Chemistry, 11(1), 53-60. doi:10.1039/c9py01533g 1759-9954 https://hdl.handle.net/10356/137718 10.1039/c9py01533g 2-s2.0-85077075497 1 11 53 60 en Polymer Chemistry © 2020 The Royal Society of Chemistry. All rights reserved. This paper was published in Polymer Chemistry and is made available with permission of The Royal Society of Chemistry. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry
Radical Polymerization
BNOAc
spellingShingle Science::Chemistry
Radical Polymerization
BNOAc
Mao, Weijia
Wang, Chen Gang
Lu, Yunpeng
Faustinelie, Winnie
Goto, Atsushi
Carboxylate, nitrate, sulfonate, and phosphate catalysts for living radical polymerization : via oxygen-iodine halogen bonding catalysis
description Four families of oxyanions, i.e., carboxylate, nitrate, phosphate, and sulfonate, were studied as novel catalysts in living (or reversible deactivation) radical polymerization via oxygen-iodine halogen bonding catalysis. Oxyanions with sodium and tetraalkylammonium counter-cations exhibited good catalytic activities and high solubilities in hydrophilic and hydrophobic monomers. These oxyanion catalysts were amenable for methyl methacrylate, functional methacrylates, styrene, and acrylonitrile, and also afforded block copolymers with low dispersities. The catalytic activities of the oxyanions were also theoretically studied using density functional theory (DFT) calculation. The studied four families of oxyanions are abundant in natural and synthetic compounds. Non-Toxic natural carboxylates were successfully used to synthesize well-defined biocompatible polymers. The low cost, low toxicity, and accessibility for a range of polymer designs are attractive features for practical use.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Mao, Weijia
Wang, Chen Gang
Lu, Yunpeng
Faustinelie, Winnie
Goto, Atsushi
format Article
author Mao, Weijia
Wang, Chen Gang
Lu, Yunpeng
Faustinelie, Winnie
Goto, Atsushi
author_sort Mao, Weijia
title Carboxylate, nitrate, sulfonate, and phosphate catalysts for living radical polymerization : via oxygen-iodine halogen bonding catalysis
title_short Carboxylate, nitrate, sulfonate, and phosphate catalysts for living radical polymerization : via oxygen-iodine halogen bonding catalysis
title_full Carboxylate, nitrate, sulfonate, and phosphate catalysts for living radical polymerization : via oxygen-iodine halogen bonding catalysis
title_fullStr Carboxylate, nitrate, sulfonate, and phosphate catalysts for living radical polymerization : via oxygen-iodine halogen bonding catalysis
title_full_unstemmed Carboxylate, nitrate, sulfonate, and phosphate catalysts for living radical polymerization : via oxygen-iodine halogen bonding catalysis
title_sort carboxylate, nitrate, sulfonate, and phosphate catalysts for living radical polymerization : via oxygen-iodine halogen bonding catalysis
publishDate 2020
url https://hdl.handle.net/10356/137718
_version_ 1759854346093199360