ReviewOrganic & biomolecular chemistry2016
Fluorinated porphyrinoids as efficient platforms for new photonic materials, sensors, and therapeutics.
Review in Organic & biomolecular chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
27 citing papers in PubMed.
- Synthesis and Functional Properties of Fluorinated Phosphonate-Substituted Porphyrins: Excellent Photosensitizers and Robust Precursors for Photoactive Langmuir-Schaefer Films.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026Article
- From Porphyrins to Versatile Photostable Bacteriochlorins: Triplet-State-Driven Design of Perfluorinated Photosensitizers.Journal of medicinal chemistry · 2026Article
- Understanding the Photodynamic Behavior of Red Emitting Re(I)dipyrrinates in Triple-Negative Breast Cancer Cells.ACS medicinal chemistry letters · 2026Article
- Geometrical and Electronic Structure of Fluorinated and Non-Fluorinated Platinum(II) Tetraphenylporphyrin Complexes.Chemphyschem : a European journal of chemical physics and physical chemistry · 2025Article
- An ambipolar PEDOT-perfluorinated porphyrin electropolymer: application as an active material in energy storage systems.RSC advances · 2024Article
- A new platform for the synthesis of diketopyrrolopyrrole derivatives via nucleophilic aromatic substitution reactions.Beilstein journal of organic chemistry · 2024Article
- 5,10,15,20-Tetrakis(pentafluorophenyl)porphyrin as a Functional Platform for Peptide Stapling and Multicyclisation.Chemistry (Weinheim an der Bergstrasse, Germany) · 2023Article
- Perfluorocarbon Nanoemulsions with Fluorous Chlorin-Type Photosensitizers for Antitumor Photodynamic Therapy in Hypoxia.International journal of molecular sciences · 2023Article
- Two birds one stone: β-fluoropyrrolyl-cysteine SChemical science · 2023Article
- Tuning the Molecular Structure of Corroles to Enhance the Antibacterial Photosensitizing Activity.Pharmaceutics · 2023Article
- Porphyrin Polymers BearingPolymers · 2022Article
- First Example of a Heptazine-Porphyrin Dyad; Synthesis and Spectroscopic Properties.Molecules (Basel, Switzerland) · 2022Article
- Maltotriose-Chlorin e6 Conjugate LinkedACS omega · 2021Article
- Leveraging synthetic chlorins for bio-imaging applications.Chemical communications (Cambridge, England) · 2020Article
- Crystal structure of 2,3-dimeth-oxy-Acta crystallographica. Section E, Crystallographic communications · 2020Article
- Distorted Phthalocyanines by Click Chemistry: Photoacoustic, Photothermal, and Surface-Enhanced Resonance Raman Studies.Chemistry (Weinheim an der Bergstrasse, Germany) · 2019Article
- Arylation Chemistry for Bioconjugation.Angewandte Chemie (International ed. in English) · 2019Review
- Article
- Photochemotherapeutic Properties of a Linear Tetrapyrrole Palladium(II) Complex displaying an Exceptionally High Phototoxicity Index.Inorganic chemistry · 2018Article
- Structural and Electronic Effects Due to Fluorine Atoms on Dibenzotetraaza-Annulenes Complexes.ACS omega · 2018Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
Porphyrinoids are robust heterocyclic dyes studied extensively for their applications in medicine and as photonic materials because of their tunable photophysical properties, diverse means of modifying the periphery, and the ability to chelate most transition metals. Commercial applications include their use as phthalocyanine dyes in optical discs, porphyrins in photodynamic therapy, and as oxygen sensors. Most applications of these dyes require exocyclic moieties to improve solubility, target diseases, modulate photophysical properties, or direct the self-organization into architectures with desired photonic properties. The synthesis of the porphyrinoid depends on the desired application, but the de novo synthesis often involves several steps, is time consuming, and results in low isolated yields. Thus, the application of core porphyrinoid platforms that can be rapidly and efficiently modified to evaluate new molecular architectures allows researchers to focus on the design concepts rather than the synthesis methods, and opens porphyrinoid chemistry to a broader scientific community. We have focused on several widely available, commercially viable porphyrinoids as platforms: meso-perfluorophenylporphyrin, perfluorophthalocyanine, and meso-perfluorophenylcorrole. The perfluorophenylporphyrin is readily converted to the chlorin, bacteriochlorin, and isobacteriochlorin. Derivatives of all six of these core platforms can be efficiently and controllably made via mild nucleophilic aromatic substitution reactions using primary S, N, and O nucleophiles bearing a wide variety of functional groups. The remaining fluoro groups enhance the photo and oxidative stability of the dyes and can serve as spectroscopic signatures to characterize the compounds or in imaging applications using (19)F NMR. This review provides an overview of the chemistry of fluorinated porphyrinoids that are being used as a platform to create libraries of photo-active compounds for applications in medicine and materials.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.