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Stepwise Adsorption of Alkoxy‐Pyrene Derivatives onto a Lamellar, Non‐Porous Naphthalenediimide‐Template on HOPG
The development of new strategies for the preparation of multicomponent supramolecular assemblies is a major challenge on the road to complex functional molecular systems. Here we present the use of a non‐porous self‐assembled monolayer from uC(33)‐NDI‐uC(33), a naphthalenediimide symmetrically func...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821129/ https://www.ncbi.nlm.nih.gov/pubmed/32893412 http://dx.doi.org/10.1002/chem.202004008 |
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author | Heideman, G. Henrieke Berrocal, José Augusto Stöhr, Meike Meijer, E. W. Feringa, Ben L. |
author_facet | Heideman, G. Henrieke Berrocal, José Augusto Stöhr, Meike Meijer, E. W. Feringa, Ben L. |
author_sort | Heideman, G. Henrieke |
collection | PubMed |
description | The development of new strategies for the preparation of multicomponent supramolecular assemblies is a major challenge on the road to complex functional molecular systems. Here we present the use of a non‐porous self‐assembled monolayer from uC(33)‐NDI‐uC(33), a naphthalenediimide symmetrically functionalized with unsaturated 33 carbon‐atom‐chains, to prepare bicomponent supramolecular surface systems with a series of alkoxy‐pyrene (PyrOR) derivatives at the liquid/HOPG interface. While previous attempts at directly depositing many of these PyrOR units at the liquid/HOPG interface failed, the multicomponent approach through the uC(33)‐NDI‐uC(33) template enabled control over molecular interactions and facilitated adsorption. The PyrOR deposition restructured the initial uC(33)‐NDI‐uC(33) monolayer, causing an expansion in two dimensions to accommodate the guests. As far as we know, this represents the first example of a non‐porous or non‐metal complex‐bearing monolayer that allows the stepwise formation of multicomponent supramolecular architectures on surfaces. |
format | Online Article Text |
id | pubmed-7821129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78211292021-01-26 Stepwise Adsorption of Alkoxy‐Pyrene Derivatives onto a Lamellar, Non‐Porous Naphthalenediimide‐Template on HOPG Heideman, G. Henrieke Berrocal, José Augusto Stöhr, Meike Meijer, E. W. Feringa, Ben L. Chemistry Communications The development of new strategies for the preparation of multicomponent supramolecular assemblies is a major challenge on the road to complex functional molecular systems. Here we present the use of a non‐porous self‐assembled monolayer from uC(33)‐NDI‐uC(33), a naphthalenediimide symmetrically functionalized with unsaturated 33 carbon‐atom‐chains, to prepare bicomponent supramolecular surface systems with a series of alkoxy‐pyrene (PyrOR) derivatives at the liquid/HOPG interface. While previous attempts at directly depositing many of these PyrOR units at the liquid/HOPG interface failed, the multicomponent approach through the uC(33)‐NDI‐uC(33) template enabled control over molecular interactions and facilitated adsorption. The PyrOR deposition restructured the initial uC(33)‐NDI‐uC(33) monolayer, causing an expansion in two dimensions to accommodate the guests. As far as we know, this represents the first example of a non‐porous or non‐metal complex‐bearing monolayer that allows the stepwise formation of multicomponent supramolecular architectures on surfaces. John Wiley and Sons Inc. 2020-10-14 2021-01-04 /pmc/articles/PMC7821129/ /pubmed/32893412 http://dx.doi.org/10.1002/chem.202004008 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Heideman, G. Henrieke Berrocal, José Augusto Stöhr, Meike Meijer, E. W. Feringa, Ben L. Stepwise Adsorption of Alkoxy‐Pyrene Derivatives onto a Lamellar, Non‐Porous Naphthalenediimide‐Template on HOPG |
title | Stepwise Adsorption of Alkoxy‐Pyrene Derivatives onto a Lamellar, Non‐Porous Naphthalenediimide‐Template on HOPG |
title_full | Stepwise Adsorption of Alkoxy‐Pyrene Derivatives onto a Lamellar, Non‐Porous Naphthalenediimide‐Template on HOPG |
title_fullStr | Stepwise Adsorption of Alkoxy‐Pyrene Derivatives onto a Lamellar, Non‐Porous Naphthalenediimide‐Template on HOPG |
title_full_unstemmed | Stepwise Adsorption of Alkoxy‐Pyrene Derivatives onto a Lamellar, Non‐Porous Naphthalenediimide‐Template on HOPG |
title_short | Stepwise Adsorption of Alkoxy‐Pyrene Derivatives onto a Lamellar, Non‐Porous Naphthalenediimide‐Template on HOPG |
title_sort | stepwise adsorption of alkoxy‐pyrene derivatives onto a lamellar, non‐porous naphthalenediimide‐template on hopg |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821129/ https://www.ncbi.nlm.nih.gov/pubmed/32893412 http://dx.doi.org/10.1002/chem.202004008 |
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