molecules-logo

Journal Browser

Journal Browser

Porphyrin-Based Compounds: Synthesis and Application, 2nd Edition

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Organic Chemistry".

Deadline for manuscript submissions: 30 June 2024 | Viewed by 491

Special Issue Editors


E-Mail Website
Guest Editor
LAQV-REQUIMTE, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal
Interests: organic synthesis; fine chemistry; medicinal chemistry; pharmaceutical chemistry; drug development; porphyrin; photochemistry; photodynamic therapy; antimicrobial; ceramic materials; decarbonization; synthetic fuels
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Coimbra Chemistry Centre, Chemistry Department, University of Coimbra, Coimbra, Portugal
Interests: materials chemistry for energy and health applications; supramolecular nanocomposites; photo-responsive materials
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Porphyrins, metalloporphyrins, and their analogs constitute a family of macrocycles that are abundant in the natural world, playing crucial roles in a wide array of biological functions. These functions encompass vital processes in plants, as exemplified by chlorophyll, a magnesium-chlorin complex essential for light absorption. Similarly, heme groups, which are iron–porphyrin complexes, play a pivotal role in facilitating dioxygen binding and transport during cellular respiration in animals. Bacteriochlorophylls found in phototropic bacteria serve as an illustration of their role in bacterial photosynthesis. Moreover, they contribute to enzyme-mediated catalysis, as seen in Cytochromes P450 enzymes, which metabolize a diverse range of substances. Porphyrins also play a role in red blood cell formation, exemplified by cyanocobalamin, a cobalt–corrin complex.

Naturally occurring porphyrins are often referred to as "the Pigments of Life" due to their critical biological functions. Recognizing the significance of these natural porphyrinoids has inspired organic chemists to synthesize analogous compounds in the laboratory. Effective synthetic methodologies have been developed to create porphyrinoids with various functionalities, electronic properties, and photophysical attributes. This progress strongly encourages their application in diverse fields, including medicine (such as cancer photodynamic therapy, antimicrobial photodynamic inactivation, medical imaging, and theragnostics), as well as in catalysis, sensor receptors, solar cell dyes, nonlinear optics, molecular and supramolecular structures, materials, and devices.

In recent years, the versatile applications of porphyrins have shifted interest from purely academic interests to industrial applications, leading to an increasing demand for sustainable chemistry principles. This includes the development of new, selective, and environmentally friendly synthetic methods that minimize the use of hazardous solvents, reactants, and excessive energy consumption.

Building on the success of the first edition of the “Porphyrin-Based Compounds: Synthesis and Application” Special Issue, we are pleased to announce the launch of the current edition. This edition serves as a platform for the presentation of the latest and most exciting results and perspectives on the synthesis and functionalization of tetrapyrrolic macrocycles and their applications. We welcome original research papers and comprehensive reviews that cover any aspect related to the topics mentioned above.

Dr. Carlos J. P. Monteiro
Dr. M. Amparo F. Faustino
Dr. Carlos Serpa
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Molecules is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • synthesis of porphyrins and derivatives
  • functionalization/structural modification of porphyrinoids
  • structural and photophysical characterization
  • porphyrinic functional materials
  • biomedical applications optoelectronic applications
  • porphyrin–protein interactions

Related Special Issue

Published Papers (1 paper)

Order results
Result details
Select all
Export citation of selected articles as:

Research

17 pages, 2690 KiB  
Article
Synthesis, Spectroscopic Properties, and Metalation of 3-Alkoxybenziporphyrins
by Rachel A. Tomlovich and Timothy D. Lash
Molecules 2024, 29(8), 1903; https://0-doi-org.brum.beds.ac.uk/10.3390/molecules29081903 - 22 Apr 2024
Viewed by 272
Abstract
A series of 5-alkoxy-1,3-benzenedicarbaldehydes and related dimers were prepared in three steps from dimethyl 5-hydroxyisophthalate. Acid catalyzed condensation of the dialdehydes with a tripyrrane dicarboxylic acid, followed by oxidation with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone, afforded good yields of 3-alkoxybenziporphyrins, although dimeric tetraaldehydes failed to give isolatable [...] Read more.
A series of 5-alkoxy-1,3-benzenedicarbaldehydes and related dimers were prepared in three steps from dimethyl 5-hydroxyisophthalate. Acid catalyzed condensation of the dialdehydes with a tripyrrane dicarboxylic acid, followed by oxidation with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone, afforded good yields of 3-alkoxybenziporphyrins, although dimeric tetraaldehydes failed to give isolatable porphyrinoid products. Proton NMR spectroscopy gave no indication of an aromatic ring current, but addition of trifluoroacetic acid resulted in the formation of dications that exhibited weakly diatropic characteristics. Spectroscopic titration with TFA demonstrated that stepwise protonation took place, generating monocationic and dicationic species. 3-Alkoxybenziporphyrins reacted with nickel(II) or palladium(II) acetate to give the related nickel(II) or palladium(II) complexes. These stable organometallic derivatives showed increased diatropic properties that were most pronounced for the palladium(II) complexes. These unique porphyrinoids provide further insights into the properties of benziporphyrins. Full article
(This article belongs to the Special Issue Porphyrin-Based Compounds: Synthesis and Application, 2nd Edition)
Show Figures

Graphical abstract

Back to TopTop