Porphyrin-Based Compounds: Synthesis and Application

Porphyrins, metalloporphyrins, and their analogs are a family of macrocycles that are ubiquitous in nature, playing key roles in a myriad of biological functions, such as in plant light-harvesting (e.g., chlorophyll, a magnesium-chlorin complex), oxygen binding and transport (e.g., heme group, an ir...

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Other Authors: Monteiro, Carlos J. P. (Editor), Faustino, M. Amparo F. (Editor), Serpa, Carlos (Editor)
Format: Electronic Book Chapter
Language:English
Published: Basel MDPI - Multidisciplinary Digital Publishing Institute 2023
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520 |a Porphyrins, metalloporphyrins, and their analogs are a family of macrocycles that are ubiquitous in nature, playing key roles in a myriad of biological functions, such as in plant light-harvesting (e.g., chlorophyll, a magnesium-chlorin complex), oxygen binding and transport (e.g., heme group, an iron-porphyrin complex, responsible for animal cellular respiration), and bacteria photosynthesis. The pivotal functions fulfilled by these naturally occurring porphyrinoids have motivated and inspired organic chemists to produce synthetic porphyrins and analogs in the laboratory. In recent years, a multitude of applications for porphyrins has shifted the focus from purely academic interest to industrial processes. There is a growing recognition of the need to develop new, more selective, and environmentally friendly synthetic methods. Within this Special Issue, readers will find a collection of 16 original research papers and a comprehensive review, all dedicated to exploring the synthesis and functionalization of tetrapyrrolic macrocycles. These papers shed light on the vast potential applications of these compounds across various fields. 
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650 7 |a Chemistry  |2 bicssc 
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653 |a porphyrin 
653 |a human serum albumin 
653 |a spectroscopy 
653 |a molecular docking 
653 |a chemical-biological interactions 
653 |a Spirulina maxima 
653 |a chlorophyll a derivatives 
653 |a photosensitizers 
653 |a semisynthesis 
653 |a photodynamic inactivation 
653 |a array 
653 |a artificial photosynthesis 
653 |a building block 
653 |a copper-free Sonogashira coupling 
653 |a ethyne 
653 |a perylene 
653 |a solar 
653 |a carboxylated pyrrolidine-fused chlorin 
653 |a fluorescence 
653 |a glutathione detection 
653 |a porphyrin macrocycles 
653 |a photodynamic therapy 
653 |a theranostic agents 
653 |a corroles 
653 |a trans-A2B-corroles 
653 |a photophysics 
653 |a photobiology 
653 |a asymmetrical porphyrins 
653 |a human U937 monocytic cells 
653 |a transmembrane potential 
653 |a membrane anisotropy 
653 |a sarco/endoplasmic reticulum Ca2+-ATPase (SERCA2b) 
653 |a Slo1 
653 |a SUR2 
653 |a asymmetric catalysis 
653 |a Diels-Alder reaction 
653 |a imidazolidin-4-ones 
653 |a organocatalysis 
653 |a photocatalysis 
653 |a porphyrins 
653 |a reductive amination 
653 |a sulfonamides 
653 |a MRSA 
653 |a antimicrobial resistance 
653 |a photosensitizer 
653 |a singlet oxygen 
653 |a potassium iodide 
653 |a gram-positive bacteria 
653 |a Staphylococcus aureus 
653 |a copper-64 
653 |a positron emission tomography 
653 |a circular dichroism 
653 |a chirality 
653 |a chiral layers 
653 |a supramolecular chirality 
653 |a reflectance anisotropy spectroscopy 
653 |a DFT 
653 |a organometallic 
653 |a density functionals 
653 |a transition metals 
653 |a green chemistry 
653 |a C-H functionalization 
653 |a epoxidation 
653 |a iron porphyrin 
653 |a oxidation catalysis 
653 |a renewable aromatics 
653 |a phthalocyanines 
653 |a solubility 
653 |a gas sensors 
653 |a quartz microbalances 
653 |a porphyrinoids 
653 |a phenothiazine 
653 |a radical cation 
653 |a EPR spectroscopy 
653 |a ENDOR 
653 |a HYSCORE 
653 |a spectroelectrochemistry 
653 |a BODIPY 
653 |a pyridyl 
653 |a nitro 
653 |a chloro 
653 |a methyl ester 
653 |a n/a 
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