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Ring Opening Copolymerization of Boron-Containing Anhydride with Epoxides as a Controlled Platform to Functional Polyesters
[Image: see text] Boron-functionalized polymers are used in opto-electronics, biology, and medicine. Methods to produce boron-functionalized and degradable polyesters remain exceedingly rare but relevant where (bio)dissipation is required, for example, in self-assembled nanostructures, dynamic polym...
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/PMC10311538/ https://www.ncbi.nlm.nih.gov/pubmed/37311063 http://dx.doi.org/10.1021/jacs.3c03261 |
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author | Vidal, Fernando Smith, Sevven Williams, Charlotte K. |
author_facet | Vidal, Fernando Smith, Sevven Williams, Charlotte K. |
author_sort | Vidal, Fernando |
collection | PubMed |
description | [Image: see text] Boron-functionalized polymers are used in opto-electronics, biology, and medicine. Methods to produce boron-functionalized and degradable polyesters remain exceedingly rare but relevant where (bio)dissipation is required, for example, in self-assembled nanostructures, dynamic polymer networks, and bio-imaging. Here, a boronic ester-phthalic anhydride and various epoxides (cyclohexene oxide, vinyl-cyclohexene oxide, propene oxide, allyl glycidyl ether) undergo controlled ring-opening copolymerization (ROCOP), catalyzed by organometallic complexes [Zn(II)Mg(II) or Al(III)K(I)] or a phosphazene organobase. The polymerizations are well controlled allowing for the modulation of the polyester structures (e.g., by epoxide selection, AB, or ABA blocks), molar masses (9.4 < M(n) < 40 kg/mol), and uptake of boron functionalities (esters, acids, “ates”, boroxines, and fluorescent groups) in the polymer. The boronic ester-functionalized polymers are amorphous, with high glass transition temperatures (81 < T(g) < 224 °C) and good thermal stability (285 < T(d) < 322 °C). The boronic ester-polyesters are deprotected to yield boronic acid- and borate-polyesters; the ionic polymers are water soluble and degradable under alkaline conditions. Using a hydrophilic macro-initiator in alternating epoxide/anhydride ROCOP, and lactone ring opening polymerization, produces amphiphilic AB and ABC copolyesters. Alternatively, the boron-functionalities are subjected to Pd(II)-catalyzed cross-couplings to install fluorescent groups (BODIPY). The utility of this new monomer as a platform to construct specialized polyesters materials is exemplified here in the synthesis of fluorescent spherical nanoparticles that self-assemble in water (D(h) = 40 nm). The selective copolymerization, variable structural composition, and adjustable boron loading represent a versatile technology for future explorations of degradable, well-defined, and functional polymers. |
format | Online Article Text |
id | pubmed-10311538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-103115382023-07-01 Ring Opening Copolymerization of Boron-Containing Anhydride with Epoxides as a Controlled Platform to Functional Polyesters Vidal, Fernando Smith, Sevven Williams, Charlotte K. J Am Chem Soc [Image: see text] Boron-functionalized polymers are used in opto-electronics, biology, and medicine. Methods to produce boron-functionalized and degradable polyesters remain exceedingly rare but relevant where (bio)dissipation is required, for example, in self-assembled nanostructures, dynamic polymer networks, and bio-imaging. Here, a boronic ester-phthalic anhydride and various epoxides (cyclohexene oxide, vinyl-cyclohexene oxide, propene oxide, allyl glycidyl ether) undergo controlled ring-opening copolymerization (ROCOP), catalyzed by organometallic complexes [Zn(II)Mg(II) or Al(III)K(I)] or a phosphazene organobase. The polymerizations are well controlled allowing for the modulation of the polyester structures (e.g., by epoxide selection, AB, or ABA blocks), molar masses (9.4 < M(n) < 40 kg/mol), and uptake of boron functionalities (esters, acids, “ates”, boroxines, and fluorescent groups) in the polymer. The boronic ester-functionalized polymers are amorphous, with high glass transition temperatures (81 < T(g) < 224 °C) and good thermal stability (285 < T(d) < 322 °C). The boronic ester-polyesters are deprotected to yield boronic acid- and borate-polyesters; the ionic polymers are water soluble and degradable under alkaline conditions. Using a hydrophilic macro-initiator in alternating epoxide/anhydride ROCOP, and lactone ring opening polymerization, produces amphiphilic AB and ABC copolyesters. Alternatively, the boron-functionalities are subjected to Pd(II)-catalyzed cross-couplings to install fluorescent groups (BODIPY). The utility of this new monomer as a platform to construct specialized polyesters materials is exemplified here in the synthesis of fluorescent spherical nanoparticles that self-assemble in water (D(h) = 40 nm). The selective copolymerization, variable structural composition, and adjustable boron loading represent a versatile technology for future explorations of degradable, well-defined, and functional polymers. American Chemical Society 2023-06-13 /pmc/articles/PMC10311538/ /pubmed/37311063 http://dx.doi.org/10.1021/jacs.3c03261 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 | Vidal, Fernando Smith, Sevven Williams, Charlotte K. Ring Opening Copolymerization of Boron-Containing Anhydride with Epoxides as a Controlled Platform to Functional Polyesters |
title | Ring Opening Copolymerization
of Boron-Containing
Anhydride with Epoxides as a Controlled Platform to Functional Polyesters |
title_full | Ring Opening Copolymerization
of Boron-Containing
Anhydride with Epoxides as a Controlled Platform to Functional Polyesters |
title_fullStr | Ring Opening Copolymerization
of Boron-Containing
Anhydride with Epoxides as a Controlled Platform to Functional Polyesters |
title_full_unstemmed | Ring Opening Copolymerization
of Boron-Containing
Anhydride with Epoxides as a Controlled Platform to Functional Polyesters |
title_short | Ring Opening Copolymerization
of Boron-Containing
Anhydride with Epoxides as a Controlled Platform to Functional Polyesters |
title_sort | ring opening copolymerization
of boron-containing
anhydride with epoxides as a controlled platform to functional polyesters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311538/ https://www.ncbi.nlm.nih.gov/pubmed/37311063 http://dx.doi.org/10.1021/jacs.3c03261 |
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