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dc.contributor.editorMonteiro, Carlos J. P.
dc.contributor.editorFaustino, M. Amparo F.
dc.contributor.editorSerpa, Carlos
dc.date.accessioned2023-11-30T20:55:56Z
dc.date.available2023-11-30T20:55:56Z
dc.date.issued2023
dc.identifierONIX_20231130_9783036594002_272
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/128820
dc.description.abstractPorphyrins, 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.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: generalen_US
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PN Chemistryen_US
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PN Chemistry::PNN Organic chemistryen_US
dc.subject.otherporphyrin
dc.subject.otherhuman serum albumin
dc.subject.otherspectroscopy
dc.subject.othermolecular docking
dc.subject.otherchemical-biological interactions
dc.subject.otherSpirulina maxima
dc.subject.otherchlorophyll a derivatives
dc.subject.otherphotosensitizers
dc.subject.othersemisynthesis
dc.subject.otherphotodynamic inactivation
dc.subject.otherarray
dc.subject.otherartificial photosynthesis
dc.subject.otherbuilding block
dc.subject.othercopper-free Sonogashira coupling
dc.subject.otherethyne
dc.subject.otherperylene
dc.subject.othersolar
dc.subject.othercarboxylated pyrrolidine-fused chlorin
dc.subject.otherfluorescence
dc.subject.otherglutathione detection
dc.subject.otherporphyrin macrocycles
dc.subject.otherphotodynamic therapy
dc.subject.othertheranostic agents
dc.subject.othercorroles
dc.subject.othertrans-A2B-corroles
dc.subject.otherphotophysics
dc.subject.otherphotobiology
dc.subject.otherasymmetrical porphyrins
dc.subject.otherhuman U937 monocytic cells
dc.subject.othertransmembrane potential
dc.subject.othermembrane anisotropy
dc.subject.othersarco/endoplasmic reticulum Ca2+-ATPase (SERCA2b)
dc.subject.otherSlo1
dc.subject.otherSUR2
dc.subject.otherasymmetric catalysis
dc.subject.otherDiels–Alder reaction
dc.subject.otherimidazolidin-4-ones
dc.subject.otherorganocatalysis
dc.subject.otherphotocatalysis
dc.subject.otherporphyrins
dc.subject.otherreductive amination
dc.subject.othersulfonamides
dc.subject.otherMRSA
dc.subject.otherantimicrobial resistance
dc.subject.otherphotosensitizer
dc.subject.othersinglet oxygen
dc.subject.otherpotassium iodide
dc.subject.othergram-positive bacteria
dc.subject.otherStaphylococcus aureus
dc.subject.othercopper-64
dc.subject.otherpositron emission tomography
dc.subject.othercircular dichroism
dc.subject.otherchirality
dc.subject.otherchiral layers
dc.subject.othersupramolecular chirality
dc.subject.otherreflectance anisotropy spectroscopy
dc.subject.otherDFT
dc.subject.otherorganometallic
dc.subject.otherdensity functionals
dc.subject.othertransition metals
dc.subject.othergreen chemistry
dc.subject.otherC-H functionalization
dc.subject.otherepoxidation
dc.subject.otheriron porphyrin
dc.subject.otheroxidation catalysis
dc.subject.otherrenewable aromatics
dc.subject.otherphthalocyanines
dc.subject.othersolubility
dc.subject.othergas sensors
dc.subject.otherquartz microbalances
dc.subject.otherporphyrinoids
dc.subject.otherphenothiazine
dc.subject.otherradical cation
dc.subject.otherEPR spectroscopy
dc.subject.otherENDOR
dc.subject.otherHYSCORE
dc.subject.otherspectroelectrochemistry
dc.subject.otherBODIPY
dc.subject.otherpyridyl
dc.subject.othernitro
dc.subject.otherchloro
dc.subject.othermethyl ester
dc.subject.othern/a
dc.titlePorphyrin-Based Compounds: Synthesis and Application
dc.typebook
oapen.identifier.doi10.3390/books978-3-0365-9401-9
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0
oapen.relation.isbn9783036594002
oapen.relation.isbn9783036594019
oapen.pages298
oapen.place.publicationBasel


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