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Porphyrinoid rotaxanes: building a mechanical picket fence

Building on recent progress in the synthesis of functional porphyrins for a range of applications using the Cu-mediated azide–alkyne cycloaddition (CuAAC) reaction, we describe the active template CuAAC synthesis of interlocked triazole functionalised porphyrinoids in excellent yield. By synthesisin...

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Autores principales: Ngo, T. H., Labuta, J., Lim, G. N., Webre, W. A., D'Souza, F., Karr, P. A., Lewis, J. E. M., Hill, J. P., Ariga, K., Goldup, S. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103255/
https://www.ncbi.nlm.nih.gov/pubmed/30155230
http://dx.doi.org/10.1039/c7sc03165c
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author Ngo, T. H.
Labuta, J.
Lim, G. N.
Webre, W. A.
D'Souza, F.
Karr, P. A.
Lewis, J. E. M.
Hill, J. P.
Ariga, K.
Goldup, S. M.
author_facet Ngo, T. H.
Labuta, J.
Lim, G. N.
Webre, W. A.
D'Souza, F.
Karr, P. A.
Lewis, J. E. M.
Hill, J. P.
Ariga, K.
Goldup, S. M.
author_sort Ngo, T. H.
collection PubMed
description Building on recent progress in the synthesis of functional porphyrins for a range of applications using the Cu-mediated azide–alkyne cycloaddition (CuAAC) reaction, we describe the active template CuAAC synthesis of interlocked triazole functionalised porphyrinoids in excellent yield. By synthesising interlocked analogues of previously studied porphyrin–corrole conjugates, we demonstrate that this approach gives access to rotaxanes in which the detailed electronic properties of the axle component are unchanged but whose steric properties are transformed by the mechanical “picket fence” provided by the threaded rings. Our results suggest that interlocked functionalised porphyrins, readily available using the AT-CuAAC approach, are sterically hindered scaffolds for the development of new catalysts and materials.
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spelling pubmed-61032552018-08-28 Porphyrinoid rotaxanes: building a mechanical picket fence Ngo, T. H. Labuta, J. Lim, G. N. Webre, W. A. D'Souza, F. Karr, P. A. Lewis, J. E. M. Hill, J. P. Ariga, K. Goldup, S. M. Chem Sci Chemistry Building on recent progress in the synthesis of functional porphyrins for a range of applications using the Cu-mediated azide–alkyne cycloaddition (CuAAC) reaction, we describe the active template CuAAC synthesis of interlocked triazole functionalised porphyrinoids in excellent yield. By synthesising interlocked analogues of previously studied porphyrin–corrole conjugates, we demonstrate that this approach gives access to rotaxanes in which the detailed electronic properties of the axle component are unchanged but whose steric properties are transformed by the mechanical “picket fence” provided by the threaded rings. Our results suggest that interlocked functionalised porphyrins, readily available using the AT-CuAAC approach, are sterically hindered scaffolds for the development of new catalysts and materials. Royal Society of Chemistry 2017-09-01 2017-08-04 /pmc/articles/PMC6103255/ /pubmed/30155230 http://dx.doi.org/10.1039/c7sc03165c Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Ngo, T. H.
Labuta, J.
Lim, G. N.
Webre, W. A.
D'Souza, F.
Karr, P. A.
Lewis, J. E. M.
Hill, J. P.
Ariga, K.
Goldup, S. M.
Porphyrinoid rotaxanes: building a mechanical picket fence
title Porphyrinoid rotaxanes: building a mechanical picket fence
title_full Porphyrinoid rotaxanes: building a mechanical picket fence
title_fullStr Porphyrinoid rotaxanes: building a mechanical picket fence
title_full_unstemmed Porphyrinoid rotaxanes: building a mechanical picket fence
title_short Porphyrinoid rotaxanes: building a mechanical picket fence
title_sort porphyrinoid rotaxanes: building a mechanical picket fence
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103255/
https://www.ncbi.nlm.nih.gov/pubmed/30155230
http://dx.doi.org/10.1039/c7sc03165c
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