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Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization

Maleimide-containing fluorinated porphyrins and chlorins were prepared based on the reaction of Zn(II) or Ni(II) complexes of 5,10,15,20-tetrakis(4-amino-2,3,5,6-tetrafluorophenyl)porphyrin and chlorin with maleic anhydride. Porphyrin maleimide derivatives were also prepared by the reaction of 5,10,...

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Autores principales: Ol’shevskaya, Valentina A, Kononova, Elena G, Zaitsev, Andrei V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880841/
https://www.ncbi.nlm.nih.gov/pubmed/31807205
http://dx.doi.org/10.3762/bjoc.15.263
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author Ol’shevskaya, Valentina A
Kononova, Elena G
Zaitsev, Andrei V
author_facet Ol’shevskaya, Valentina A
Kononova, Elena G
Zaitsev, Andrei V
author_sort Ol’shevskaya, Valentina A
collection PubMed
description Maleimide-containing fluorinated porphyrins and chlorins were prepared based on the reaction of Zn(II) or Ni(II) complexes of 5,10,15,20-tetrakis(4-amino-2,3,5,6-tetrafluorophenyl)porphyrin and chlorin with maleic anhydride. Porphyrin maleimide derivatives were also prepared by the reaction of 5,10,15,20-tetrakis(4-azido-2,3,5,6-tetrafluorophenyl)porphyrinato Zn(II) or Ni(II) with N-propargylmaleimide via the CuAAC click reaction to afford fluorinated porphyrin–triazole–maleimide conjugates. New maleimide derivatives were isolated in reasonable yields and identified by UV–vis, (1)H NMR, (19)F NMR spectroscopy and mass-spectrometry.
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spelling pubmed-68808412019-12-05 Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization Ol’shevskaya, Valentina A Kononova, Elena G Zaitsev, Andrei V Beilstein J Org Chem Letter Maleimide-containing fluorinated porphyrins and chlorins were prepared based on the reaction of Zn(II) or Ni(II) complexes of 5,10,15,20-tetrakis(4-amino-2,3,5,6-tetrafluorophenyl)porphyrin and chlorin with maleic anhydride. Porphyrin maleimide derivatives were also prepared by the reaction of 5,10,15,20-tetrakis(4-azido-2,3,5,6-tetrafluorophenyl)porphyrinato Zn(II) or Ni(II) with N-propargylmaleimide via the CuAAC click reaction to afford fluorinated porphyrin–triazole–maleimide conjugates. New maleimide derivatives were isolated in reasonable yields and identified by UV–vis, (1)H NMR, (19)F NMR spectroscopy and mass-spectrometry. Beilstein-Institut 2019-11-13 /pmc/articles/PMC6880841/ /pubmed/31807205 http://dx.doi.org/10.3762/bjoc.15.263 Text en Copyright © 2019, Ol’shevskaya et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
Ol’shevskaya, Valentina A
Kononova, Elena G
Zaitsev, Andrei V
Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization
title Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization
title_full Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization
title_fullStr Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization
title_full_unstemmed Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization
title_short Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization
title_sort fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880841/
https://www.ncbi.nlm.nih.gov/pubmed/31807205
http://dx.doi.org/10.3762/bjoc.15.263
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