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Design, Synthesis and Characterization of a Visible‐Light‐Sensitive Molecular Switch and Its PEGylation Towards a Self‐Assembling Molecule
HBDI‐like chromophores represent a novel set of biomimetic switches mimicking the fluorophore of the green fluorescent protein that are currently studied with the hope to expand the molecular switch/motor toolbox. However, until now members capable of absorbing visible light in their neutral (i. e....
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541190/ https://www.ncbi.nlm.nih.gov/pubmed/35695822 http://dx.doi.org/10.1002/chem.202201477 |
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author | Paolino, Marco Saletti, Mario Reale, Annalisa Licciardi, Mariano Varvarà, Paola Marquette, Arnaud Léonard, Jérémie Bonechi, Claudia Donati, Alessandro Giorgi, Gianluca Giuliani, Germano Carlotti, Benedetta Ortica, Fausto Latterini, Loredana Gentile, Mariangela Paccagnini, Eugenio Olivucci, Massimo Cappelli, Andrea |
author_facet | Paolino, Marco Saletti, Mario Reale, Annalisa Licciardi, Mariano Varvarà, Paola Marquette, Arnaud Léonard, Jérémie Bonechi, Claudia Donati, Alessandro Giorgi, Gianluca Giuliani, Germano Carlotti, Benedetta Ortica, Fausto Latterini, Loredana Gentile, Mariangela Paccagnini, Eugenio Olivucci, Massimo Cappelli, Andrea |
author_sort | Paolino, Marco |
collection | PubMed |
description | HBDI‐like chromophores represent a novel set of biomimetic switches mimicking the fluorophore of the green fluorescent protein that are currently studied with the hope to expand the molecular switch/motor toolbox. However, until now members capable of absorbing visible light in their neutral (i. e. non‐anionic) form have not been reported. In this contribution we report the preparation of an HBDI‐like chromophore based on a 3‐phenylbenzofulvene scaffold capable of absorbing blue light and photoisomerizing on the picosecond timescale. More specifically, we show that double‐bond photoisomerization occurs in both the E‐to‐Z and Z‐to‐E directions and that these can be controlled by irradiating with blue and UV light, respectively. Finally, as a preliminary applicative result, we report the incorporation of the chromophore in an amphiphilic molecule and demonstrate the formation of a visible‐light‐sensitive nanoaggregated state in water. |
format | Online Article Text |
id | pubmed-9541190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95411902022-10-14 Design, Synthesis and Characterization of a Visible‐Light‐Sensitive Molecular Switch and Its PEGylation Towards a Self‐Assembling Molecule Paolino, Marco Saletti, Mario Reale, Annalisa Licciardi, Mariano Varvarà, Paola Marquette, Arnaud Léonard, Jérémie Bonechi, Claudia Donati, Alessandro Giorgi, Gianluca Giuliani, Germano Carlotti, Benedetta Ortica, Fausto Latterini, Loredana Gentile, Mariangela Paccagnini, Eugenio Olivucci, Massimo Cappelli, Andrea Chemistry Research Articles HBDI‐like chromophores represent a novel set of biomimetic switches mimicking the fluorophore of the green fluorescent protein that are currently studied with the hope to expand the molecular switch/motor toolbox. However, until now members capable of absorbing visible light in their neutral (i. e. non‐anionic) form have not been reported. In this contribution we report the preparation of an HBDI‐like chromophore based on a 3‐phenylbenzofulvene scaffold capable of absorbing blue light and photoisomerizing on the picosecond timescale. More specifically, we show that double‐bond photoisomerization occurs in both the E‐to‐Z and Z‐to‐E directions and that these can be controlled by irradiating with blue and UV light, respectively. Finally, as a preliminary applicative result, we report the incorporation of the chromophore in an amphiphilic molecule and demonstrate the formation of a visible‐light‐sensitive nanoaggregated state in water. John Wiley and Sons Inc. 2022-07-13 2022-09-06 /pmc/articles/PMC9541190/ /pubmed/35695822 http://dx.doi.org/10.1002/chem.202201477 Text en © 2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Paolino, Marco Saletti, Mario Reale, Annalisa Licciardi, Mariano Varvarà, Paola Marquette, Arnaud Léonard, Jérémie Bonechi, Claudia Donati, Alessandro Giorgi, Gianluca Giuliani, Germano Carlotti, Benedetta Ortica, Fausto Latterini, Loredana Gentile, Mariangela Paccagnini, Eugenio Olivucci, Massimo Cappelli, Andrea Design, Synthesis and Characterization of a Visible‐Light‐Sensitive Molecular Switch and Its PEGylation Towards a Self‐Assembling Molecule |
title | Design, Synthesis and Characterization of a Visible‐Light‐Sensitive Molecular Switch and Its PEGylation Towards a Self‐Assembling Molecule |
title_full | Design, Synthesis and Characterization of a Visible‐Light‐Sensitive Molecular Switch and Its PEGylation Towards a Self‐Assembling Molecule |
title_fullStr | Design, Synthesis and Characterization of a Visible‐Light‐Sensitive Molecular Switch and Its PEGylation Towards a Self‐Assembling Molecule |
title_full_unstemmed | Design, Synthesis and Characterization of a Visible‐Light‐Sensitive Molecular Switch and Its PEGylation Towards a Self‐Assembling Molecule |
title_short | Design, Synthesis and Characterization of a Visible‐Light‐Sensitive Molecular Switch and Its PEGylation Towards a Self‐Assembling Molecule |
title_sort | design, synthesis and characterization of a visible‐light‐sensitive molecular switch and its pegylation towards a self‐assembling molecule |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541190/ https://www.ncbi.nlm.nih.gov/pubmed/35695822 http://dx.doi.org/10.1002/chem.202201477 |
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