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On Demand Switching of Polymerization Mechanism and Monomer Selectivity with Orthogonal Stimuli
[Image: see text] The development of next-generation materials is coupled with the ability to predictably and precisely synthesize polymers with well-defined structures and architectures. In this regard, the discovery of synthetic strategies that allow on demand control over monomer connectivity dur...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161045/ https://www.ncbi.nlm.nih.gov/pubmed/30276257 http://dx.doi.org/10.1021/acscentsci.8b00401 |
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author | Peterson, Brian M. Kottisch, Veronika Supej, Michael J. Fors, Brett P. |
author_facet | Peterson, Brian M. Kottisch, Veronika Supej, Michael J. Fors, Brett P. |
author_sort | Peterson, Brian M. |
collection | PubMed |
description | [Image: see text] The development of next-generation materials is coupled with the ability to predictably and precisely synthesize polymers with well-defined structures and architectures. In this regard, the discovery of synthetic strategies that allow on demand control over monomer connectivity during polymerization would provide access to complex structures in a modular fashion and remains a grand challenge in polymer chemistry. In this Article, we report a method where monomer selectivity is controlled during the polymerization by the application of two orthogonal stimuli. Specifically, we developed a cationic polymerization where polymer chain growth is controlled by a chemical stimulus and paired it with a compatible photocontrolled radical polymerization. By alternating the application of the chemical and photochemical stimuli the incorporation of vinyl ethers and acrylates could be dictated by switching between cationic and radical polymerization mechanisms, respectively. This enables the synthesis of multiblock copolymers where each block length is governed by the amount of time a stimulus is applied, and the quantity of blocks is determined by the number of times the two stimuli are toggled. This new method allows on demand control over polymer structure with external influences and highlights the potential for using stimuli-controlled polymerizations to access novel materials. |
format | Online Article Text |
id | pubmed-6161045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-61610452018-10-01 On Demand Switching of Polymerization Mechanism and Monomer Selectivity with Orthogonal Stimuli Peterson, Brian M. Kottisch, Veronika Supej, Michael J. Fors, Brett P. ACS Cent Sci [Image: see text] The development of next-generation materials is coupled with the ability to predictably and precisely synthesize polymers with well-defined structures and architectures. In this regard, the discovery of synthetic strategies that allow on demand control over monomer connectivity during polymerization would provide access to complex structures in a modular fashion and remains a grand challenge in polymer chemistry. In this Article, we report a method where monomer selectivity is controlled during the polymerization by the application of two orthogonal stimuli. Specifically, we developed a cationic polymerization where polymer chain growth is controlled by a chemical stimulus and paired it with a compatible photocontrolled radical polymerization. By alternating the application of the chemical and photochemical stimuli the incorporation of vinyl ethers and acrylates could be dictated by switching between cationic and radical polymerization mechanisms, respectively. This enables the synthesis of multiblock copolymers where each block length is governed by the amount of time a stimulus is applied, and the quantity of blocks is determined by the number of times the two stimuli are toggled. This new method allows on demand control over polymer structure with external influences and highlights the potential for using stimuli-controlled polymerizations to access novel materials. American Chemical Society 2018-08-08 2018-09-26 /pmc/articles/PMC6161045/ /pubmed/30276257 http://dx.doi.org/10.1021/acscentsci.8b00401 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Peterson, Brian M. Kottisch, Veronika Supej, Michael J. Fors, Brett P. On Demand Switching of Polymerization Mechanism and Monomer Selectivity with Orthogonal Stimuli |
title | On Demand Switching of Polymerization Mechanism and
Monomer Selectivity with Orthogonal Stimuli |
title_full | On Demand Switching of Polymerization Mechanism and
Monomer Selectivity with Orthogonal Stimuli |
title_fullStr | On Demand Switching of Polymerization Mechanism and
Monomer Selectivity with Orthogonal Stimuli |
title_full_unstemmed | On Demand Switching of Polymerization Mechanism and
Monomer Selectivity with Orthogonal Stimuli |
title_short | On Demand Switching of Polymerization Mechanism and
Monomer Selectivity with Orthogonal Stimuli |
title_sort | on demand switching of polymerization mechanism and
monomer selectivity with orthogonal stimuli |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161045/ https://www.ncbi.nlm.nih.gov/pubmed/30276257 http://dx.doi.org/10.1021/acscentsci.8b00401 |
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