Cargando…

Open-air green-light-driven ATRP enabled by dual photoredox/copper catalysis

Photoinduced atom transfer radical polymerization (photo-ATRP) has risen to the forefront of modern polymer chemistry as a powerful tool giving access to well-defined materials with complex architecture. However, most photo-ATRP systems can only generate radicals under biocidal UV light and are oxyg...

Descripción completa

Detalles Bibliográficos
Autores principales: Szczepaniak, Grzegorz, Jeong, Jaepil, Kapil, Kriti, Dadashi-Silab, Sajjad, Yerneni, Saigopalakrishna S., Ratajczyk, Paulina, Lathwal, Sushil, Schild, Dirk J., Das, Subha R., Matyjaszewski, Krzysztof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557244/
https://www.ncbi.nlm.nih.gov/pubmed/36320395
http://dx.doi.org/10.1039/d2sc04210j
_version_ 1784807262119788544
author Szczepaniak, Grzegorz
Jeong, Jaepil
Kapil, Kriti
Dadashi-Silab, Sajjad
Yerneni, Saigopalakrishna S.
Ratajczyk, Paulina
Lathwal, Sushil
Schild, Dirk J.
Das, Subha R.
Matyjaszewski, Krzysztof
author_facet Szczepaniak, Grzegorz
Jeong, Jaepil
Kapil, Kriti
Dadashi-Silab, Sajjad
Yerneni, Saigopalakrishna S.
Ratajczyk, Paulina
Lathwal, Sushil
Schild, Dirk J.
Das, Subha R.
Matyjaszewski, Krzysztof
author_sort Szczepaniak, Grzegorz
collection PubMed
description Photoinduced atom transfer radical polymerization (photo-ATRP) has risen to the forefront of modern polymer chemistry as a powerful tool giving access to well-defined materials with complex architecture. However, most photo-ATRP systems can only generate radicals under biocidal UV light and are oxygen-sensitive, hindering their practical use in the synthesis of polymer biohybrids. Herein, inspired by the photoinduced electron transfer-reversible addition–fragmentation chain transfer (PET-RAFT) polymerization, we demonstrate a dual photoredox/copper catalysis that allows open-air ATRP under green light irradiation. Eosin Y was used as an organic photoredox catalyst (PC) in combination with a copper complex (X–Cu(II)/L). The role of PC was to trigger and drive the polymerization, while X–Cu(II)/L acted as a deactivator, providing a well-controlled polymerization. The excited PC was oxidatively quenched by X–Cu(II)/L, generating Cu(I)/L activator and PC˙(+). The ATRP ligand (L) used in excess then reduced the PC˙(+), closing the photocatalytic cycle. The continuous reduction of X–Cu(II)/L back to Cu(I)/L by excited PC provided high oxygen tolerance. As a result, a well-controlled and rapid ATRP could proceed even in an open vessel despite continuous oxygen diffusion. This method allowed the synthesis of polymers with narrow molecular weight distributions and controlled molecular weights using Cu catalyst and PC at ppm levels in both aqueous and organic media. A detailed comparison of photo-ATRP with PET-RAFT polymerization revealed the superiority of dual photoredox/copper catalysis under biologically relevant conditions. The kinetic studies and fluorescence measurements indicated that in the absence of the X–Cu(II)/L complex, green light irradiation caused faster photobleaching of eosin Y, leading to inhibition of PET-RAFT polymerization. Importantly, PET-RAFT polymerizations showed significantly higher dispersity values (1.14 ≤ Đ ≤ 4.01) in contrast to photo-ATRP (1.15 ≤ Đ ≤ 1.22) under identical conditions.
format Online
Article
Text
id pubmed-9557244
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-95572442022-10-31 Open-air green-light-driven ATRP enabled by dual photoredox/copper catalysis Szczepaniak, Grzegorz Jeong, Jaepil Kapil, Kriti Dadashi-Silab, Sajjad Yerneni, Saigopalakrishna S. Ratajczyk, Paulina Lathwal, Sushil Schild, Dirk J. Das, Subha R. Matyjaszewski, Krzysztof Chem Sci Chemistry Photoinduced atom transfer radical polymerization (photo-ATRP) has risen to the forefront of modern polymer chemistry as a powerful tool giving access to well-defined materials with complex architecture. However, most photo-ATRP systems can only generate radicals under biocidal UV light and are oxygen-sensitive, hindering their practical use in the synthesis of polymer biohybrids. Herein, inspired by the photoinduced electron transfer-reversible addition–fragmentation chain transfer (PET-RAFT) polymerization, we demonstrate a dual photoredox/copper catalysis that allows open-air ATRP under green light irradiation. Eosin Y was used as an organic photoredox catalyst (PC) in combination with a copper complex (X–Cu(II)/L). The role of PC was to trigger and drive the polymerization, while X–Cu(II)/L acted as a deactivator, providing a well-controlled polymerization. The excited PC was oxidatively quenched by X–Cu(II)/L, generating Cu(I)/L activator and PC˙(+). The ATRP ligand (L) used in excess then reduced the PC˙(+), closing the photocatalytic cycle. The continuous reduction of X–Cu(II)/L back to Cu(I)/L by excited PC provided high oxygen tolerance. As a result, a well-controlled and rapid ATRP could proceed even in an open vessel despite continuous oxygen diffusion. This method allowed the synthesis of polymers with narrow molecular weight distributions and controlled molecular weights using Cu catalyst and PC at ppm levels in both aqueous and organic media. A detailed comparison of photo-ATRP with PET-RAFT polymerization revealed the superiority of dual photoredox/copper catalysis under biologically relevant conditions. The kinetic studies and fluorescence measurements indicated that in the absence of the X–Cu(II)/L complex, green light irradiation caused faster photobleaching of eosin Y, leading to inhibition of PET-RAFT polymerization. Importantly, PET-RAFT polymerizations showed significantly higher dispersity values (1.14 ≤ Đ ≤ 4.01) in contrast to photo-ATRP (1.15 ≤ Đ ≤ 1.22) under identical conditions. The Royal Society of Chemistry 2022-09-20 /pmc/articles/PMC9557244/ /pubmed/36320395 http://dx.doi.org/10.1039/d2sc04210j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Szczepaniak, Grzegorz
Jeong, Jaepil
Kapil, Kriti
Dadashi-Silab, Sajjad
Yerneni, Saigopalakrishna S.
Ratajczyk, Paulina
Lathwal, Sushil
Schild, Dirk J.
Das, Subha R.
Matyjaszewski, Krzysztof
Open-air green-light-driven ATRP enabled by dual photoredox/copper catalysis
title Open-air green-light-driven ATRP enabled by dual photoredox/copper catalysis
title_full Open-air green-light-driven ATRP enabled by dual photoredox/copper catalysis
title_fullStr Open-air green-light-driven ATRP enabled by dual photoredox/copper catalysis
title_full_unstemmed Open-air green-light-driven ATRP enabled by dual photoredox/copper catalysis
title_short Open-air green-light-driven ATRP enabled by dual photoredox/copper catalysis
title_sort open-air green-light-driven atrp enabled by dual photoredox/copper catalysis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557244/
https://www.ncbi.nlm.nih.gov/pubmed/36320395
http://dx.doi.org/10.1039/d2sc04210j
work_keys_str_mv AT szczepaniakgrzegorz openairgreenlightdrivenatrpenabledbydualphotoredoxcoppercatalysis
AT jeongjaepil openairgreenlightdrivenatrpenabledbydualphotoredoxcoppercatalysis
AT kapilkriti openairgreenlightdrivenatrpenabledbydualphotoredoxcoppercatalysis
AT dadashisilabsajjad openairgreenlightdrivenatrpenabledbydualphotoredoxcoppercatalysis
AT yernenisaigopalakrishnas openairgreenlightdrivenatrpenabledbydualphotoredoxcoppercatalysis
AT ratajczykpaulina openairgreenlightdrivenatrpenabledbydualphotoredoxcoppercatalysis
AT lathwalsushil openairgreenlightdrivenatrpenabledbydualphotoredoxcoppercatalysis
AT schilddirkj openairgreenlightdrivenatrpenabledbydualphotoredoxcoppercatalysis
AT dassubhar openairgreenlightdrivenatrpenabledbydualphotoredoxcoppercatalysis
AT matyjaszewskikrzysztof openairgreenlightdrivenatrpenabledbydualphotoredoxcoppercatalysis