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Organopolymer with dual chromophores and fast charge-transfer properties for sustainable photocatalysis
Photocatalytic polymers offer an alternative to prevailing organometallics and nanomaterials, and they may benefit from polymer-mediated catalytic and material enhancements. MPC-1, a polymer photoredox catalyst reported herein, exhibits enhanced catalytic activity arising from charge transfer states...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478678/ https://www.ncbi.nlm.nih.gov/pubmed/31015478 http://dx.doi.org/10.1038/s41467-019-09316-5 |
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author | Smith, Justin D. Jamhawi, Abdelqader M. Jasinski, Jacek B. Gallou, Fabrice Ge, Jin Advincula, Rigoberto Liu, Jinjun Handa, Sachin |
author_facet | Smith, Justin D. Jamhawi, Abdelqader M. Jasinski, Jacek B. Gallou, Fabrice Ge, Jin Advincula, Rigoberto Liu, Jinjun Handa, Sachin |
author_sort | Smith, Justin D. |
collection | PubMed |
description | Photocatalytic polymers offer an alternative to prevailing organometallics and nanomaterials, and they may benefit from polymer-mediated catalytic and material enhancements. MPC-1, a polymer photoredox catalyst reported herein, exhibits enhanced catalytic activity arising from charge transfer states (CTSs) between its two chromophores. Oligomeric and polymeric MPC-1 preparations both promote efficient hydrodehalogenation of α-halocarbonyl compounds while exhibiting different solubility properties. The polymer is readily recovered by filtration. MPC-1-coated vessels enable batch and flow photocatalysis, even with opaque reaction mixtures, via “backside irradiation.” Ultrafast transient absorption spectroscopy indicates a fast charge-transfer process within 20 ps of photoexcitation. Time-resolved photoluminescence measurements reveal an approximate 10 ns lifetime for bright valence states. Ultrafast measurements suggest a long CTS lifetime. Empirical catalytic activities of small-molecule models of MPC-1 subunits support the CTS hypothesis. Density functional theory (DFT) and time-dependent DFT calculations are in good agreement with experimental spectra, spectral peak assignment, and proposed underlying energetics. |
format | Online Article Text |
id | pubmed-6478678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64786782019-04-25 Organopolymer with dual chromophores and fast charge-transfer properties for sustainable photocatalysis Smith, Justin D. Jamhawi, Abdelqader M. Jasinski, Jacek B. Gallou, Fabrice Ge, Jin Advincula, Rigoberto Liu, Jinjun Handa, Sachin Nat Commun Article Photocatalytic polymers offer an alternative to prevailing organometallics and nanomaterials, and they may benefit from polymer-mediated catalytic and material enhancements. MPC-1, a polymer photoredox catalyst reported herein, exhibits enhanced catalytic activity arising from charge transfer states (CTSs) between its two chromophores. Oligomeric and polymeric MPC-1 preparations both promote efficient hydrodehalogenation of α-halocarbonyl compounds while exhibiting different solubility properties. The polymer is readily recovered by filtration. MPC-1-coated vessels enable batch and flow photocatalysis, even with opaque reaction mixtures, via “backside irradiation.” Ultrafast transient absorption spectroscopy indicates a fast charge-transfer process within 20 ps of photoexcitation. Time-resolved photoluminescence measurements reveal an approximate 10 ns lifetime for bright valence states. Ultrafast measurements suggest a long CTS lifetime. Empirical catalytic activities of small-molecule models of MPC-1 subunits support the CTS hypothesis. Density functional theory (DFT) and time-dependent DFT calculations are in good agreement with experimental spectra, spectral peak assignment, and proposed underlying energetics. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6478678/ /pubmed/31015478 http://dx.doi.org/10.1038/s41467-019-09316-5 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Smith, Justin D. Jamhawi, Abdelqader M. Jasinski, Jacek B. Gallou, Fabrice Ge, Jin Advincula, Rigoberto Liu, Jinjun Handa, Sachin Organopolymer with dual chromophores and fast charge-transfer properties for sustainable photocatalysis |
title | Organopolymer with dual chromophores and fast charge-transfer properties for sustainable photocatalysis |
title_full | Organopolymer with dual chromophores and fast charge-transfer properties for sustainable photocatalysis |
title_fullStr | Organopolymer with dual chromophores and fast charge-transfer properties for sustainable photocatalysis |
title_full_unstemmed | Organopolymer with dual chromophores and fast charge-transfer properties for sustainable photocatalysis |
title_short | Organopolymer with dual chromophores and fast charge-transfer properties for sustainable photocatalysis |
title_sort | organopolymer with dual chromophores and fast charge-transfer properties for sustainable photocatalysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478678/ https://www.ncbi.nlm.nih.gov/pubmed/31015478 http://dx.doi.org/10.1038/s41467-019-09316-5 |
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