Synthesis of block copolymers by mechanistic transformation from reversible complexation mediated living radical polymerization to the photoinduced radical oxidation/addition/deactivation process

A versatile strategy for the fabrication of block copolymers by the combination of two discrete living polymerization techniques-reversible complexation mediated living radical polymerization (RCMP) and photoinduced radical oxidation addition deactivation (PROAD) processes-is reported. First, RCMP i...

Full description

Saved in:
Bibliographic Details
Main Authors: Aydogan, Canus, Aykac, F. Simal, Yilmaz, Gorkem, Chew, Ye Qiu, Goto, Atsushi, Yagci, Yusuf
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2022
Subjects:
Online Access:https://hdl.handle.net/10356/156747
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-156747
record_format dspace
spelling sg-ntu-dr.10356-1567472023-02-28T20:02:39Z Synthesis of block copolymers by mechanistic transformation from reversible complexation mediated living radical polymerization to the photoinduced radical oxidation/addition/deactivation process Aydogan, Canus Aykac, F. Simal Yilmaz, Gorkem Chew, Ye Qiu Goto, Atsushi Yagci, Yusuf School of Physical and Mathematical Sciences Science::Chemistry::Organic chemistry::Polymers Copolymerization Polymers A versatile strategy for the fabrication of block copolymers by the combination of two discrete living polymerization techniques-reversible complexation mediated living radical polymerization (RCMP) and photoinduced radical oxidation addition deactivation (PROAD) processes-is reported. First, RCMP is conducted to yield poly(methyl methacrylate) with iodide end groups (PMMA-I). In the following step, PMMA-I is used as macroinitiator for living PROAD cationic polymerization of isobutyl vinyl ether. Successful formation of the block copolymers is confirmed by 1H NMR, FT-IR, GPC, and DSC investigations. National Research Foundation (NRF) Submitted/Accepted version The authors acknowledge the financial support from The Scientific and Technological Research Council of Turkey (Project 120C121) and the Istanbul Technical University Research Fund and National Research Foundation (NRF) Investigatorship in Singapore (NRF-NRFI05-2019-0001). 2022-04-21T04:31:05Z 2022-04-21T04:31:05Z 2022 Journal Article Aydogan, C., Aykac, F. S., Yilmaz, G., Chew, Y. Q., Goto, A. & Yagci, Y. (2022). Synthesis of block copolymers by mechanistic transformation from reversible complexation mediated living radical polymerization to the photoinduced radical oxidation/addition/deactivation process. ACS Macro Letters, 11(3), 342-346. https://dx.doi.org/10.1021/acsmacrolett.2c00004 2161-1653 https://hdl.handle.net/10356/156747 10.1021/acsmacrolett.2c00004 2-s2.0-85125922391 3 11 342 346 en NRF-NRFI05-2019-0001 ACS Macro Letters This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Macro Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsmacrolett.2c00004. 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::Organic chemistry::Polymers
Copolymerization
Polymers
spellingShingle Science::Chemistry::Organic chemistry::Polymers
Copolymerization
Polymers
Aydogan, Canus
Aykac, F. Simal
Yilmaz, Gorkem
Chew, Ye Qiu
Goto, Atsushi
Yagci, Yusuf
Synthesis of block copolymers by mechanistic transformation from reversible complexation mediated living radical polymerization to the photoinduced radical oxidation/addition/deactivation process
description A versatile strategy for the fabrication of block copolymers by the combination of two discrete living polymerization techniques-reversible complexation mediated living radical polymerization (RCMP) and photoinduced radical oxidation addition deactivation (PROAD) processes-is reported. First, RCMP is conducted to yield poly(methyl methacrylate) with iodide end groups (PMMA-I). In the following step, PMMA-I is used as macroinitiator for living PROAD cationic polymerization of isobutyl vinyl ether. Successful formation of the block copolymers is confirmed by 1H NMR, FT-IR, GPC, and DSC investigations.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Aydogan, Canus
Aykac, F. Simal
Yilmaz, Gorkem
Chew, Ye Qiu
Goto, Atsushi
Yagci, Yusuf
format Article
author Aydogan, Canus
Aykac, F. Simal
Yilmaz, Gorkem
Chew, Ye Qiu
Goto, Atsushi
Yagci, Yusuf
author_sort Aydogan, Canus
title Synthesis of block copolymers by mechanistic transformation from reversible complexation mediated living radical polymerization to the photoinduced radical oxidation/addition/deactivation process
title_short Synthesis of block copolymers by mechanistic transformation from reversible complexation mediated living radical polymerization to the photoinduced radical oxidation/addition/deactivation process
title_full Synthesis of block copolymers by mechanistic transformation from reversible complexation mediated living radical polymerization to the photoinduced radical oxidation/addition/deactivation process
title_fullStr Synthesis of block copolymers by mechanistic transformation from reversible complexation mediated living radical polymerization to the photoinduced radical oxidation/addition/deactivation process
title_full_unstemmed Synthesis of block copolymers by mechanistic transformation from reversible complexation mediated living radical polymerization to the photoinduced radical oxidation/addition/deactivation process
title_sort synthesis of block copolymers by mechanistic transformation from reversible complexation mediated living radical polymerization to the photoinduced radical oxidation/addition/deactivation process
publishDate 2022
url https://hdl.handle.net/10356/156747
_version_ 1759856649240051712