Literature DB >> 26514229

Fluorinated porphyrinoids as efficient platforms for new photonic materials, sensors, and therapeutics.

N V S Dinesh K Bhupathiraju1, Waqar Rizvi, James D Batteas, Charles Michael Drain.   

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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Year:  2016        PMID: 26514229      PMCID: PMC6180335          DOI: 10.1039/c5ob01839k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  101 in total

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5.  1,3-dipolar cycloaddition reactions of porphyrins with azomethine ylides.

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Journal:  Tetrahedron Lett       Date:  2011-10-19       Impact factor: 2.415

7.  Synthesis and photophysical properties of thioglycosylated chlorins, isobacteriochlorins, and bacteriochlorins for bioimaging and diagnostics.

Authors:  Sunaina Singh; Amit Aggarwal; Sebastian Thompson; João P C Tomé; Xianchun Zhu; Diana Samaroo; Mikki Vinodu; Ruomei Gao; Charles Michael Drain
Journal:  Bioconjug Chem       Date:  2010-10-21       Impact factor: 4.774

Review 8.  Selective functionalisation of saturated C-H bonds with metalloporphyrin catalysts.

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10.  Porphyrin Tessellation by Design: Metal-Mediated Self-Assembly of Large Arrays and Tapes.

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  13 in total

1.  Carbon-1 versus Carbon-3 Linkage of d-Galactose to Porphyrins: Synthesis, Uptake, and Photodynamic Efficiency.

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Review 2.  Arylation Chemistry for Bioconjugation.

Authors:  Chi Zhang; Ekaterina V Vinogradova; Alexander M Spokoyny; Stephen L Buchwald; Bradley L Pentelute
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3.  Photochemotherapeutic Properties of a Linear Tetrapyrrole Palladium(II) Complex displaying an Exceptionally High Phototoxicity Index.

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4.  Leveraging synthetic chlorins for bio-imaging applications.

Authors:  Javier Hernández-Gil; Jason S Lewis; Thomas Reiner; Charles Michael Drain; Junior Gonzales
Journal:  Chem Commun (Camb)       Date:  2020-10-20       Impact factor: 6.222

5.  Tuning the Structure and Photophysics of a Fluorous Phthalocyanine Platform.

Authors:  Christopher Farley; N V S Dinesh K Bhupathiraju; Bianca K John; Charles Michael Drain
Journal:  J Phys Chem A       Date:  2016-09-14       Impact factor: 2.781

6.  Distorted Phthalocyanines by Click Chemistry: Photoacoustic, Photothermal, and Surface-Enhanced Resonance Raman Studies.

Authors:  Waqar Rizvi; Naxhije Berisha; Christopher Farley; N V S Dinesh K Bhupathiraju; Chrysafis Andreou; Emaad Khwaja; German V Fuentes; Moritz F Kircher; Ruomei Gao; Charles Michael Drain
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7.  Facile synthesis of chlorin bioconjugates by a series of click reactions.

Authors:  Junior Gonzales; N V S Dinesh K Bhupathiraju; William Perea; Huong Chu; Naxhije Berisha; Veronica Bueno; Naser Dodic; Julia Rozenberg; Nancy L Greenbaum; Charles Michael Drain
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8.  Tetrafluorobenzo-Fused BODIPY: A Platform for Regioselective Synthesis of BODIPY Dye Derivatives.

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9.  One-Pot Synthesis of Four Chlorin Derivatives by a Divergent Ylide.

Authors:  Junior Gonzales; N V S Dinesh K Bhupathiraju; Daniel Hart; Man Yuen; Maria Pia Sifuentes; Bleron Samarxhiu; Mark Maranan; Naxhije Berisha; James Batteas; Charles Michael Drain
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10.  Cancer cell spheroids are a better screen for the photodynamic efficiency of glycosylated photosensitizers.

Authors:  Patrícia M R Pereira; Naxhije Berisha; N V S Dinesh K Bhupathiraju; Rosa Fernandes; João P C Tomé; Charles Michael Drain
Journal:  PLoS One       Date:  2017-05-17       Impact factor: 3.240

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