Utilize este identificador para referenciar este registo: https://hdl.handle.net/10316/106486
Campo DCValorIdioma
dc.contributor.authorVinagreiro, Carolina dos Santos-
dc.contributor.authorLopes, Rita-
dc.contributor.authorRoyo, Beatriz-
dc.contributor.authorSilva, Gabriela Jorge da-
dc.contributor.authorPereira, Mariette M.-
dc.date.accessioned2023-04-05T08:33:52Z-
dc.date.available2023-04-05T08:33:52Z-
dc.date.issued2020-06-24-
dc.identifier.issn1420-3049pt
dc.identifier.urihttps://hdl.handle.net/10316/106486-
dc.description.abstractThe synthesis and structural modulation of five pro-ligand salts was achieved using alternative sustainable synthetic strategies, the use of microwaves being the method of choice, with an 81% yield and an E factor of 43 for 3d. After complexation with Fe3(CO)12 by direct reaction with the appropriate pro-ligands at 130 °C, a set of iron(II) N-heterocyclic carbene (NHC) complexes were isolated and fully characterized (via 1H and 13C NMR and IR spectroscopy and elemental analysis). The antibacterial activities of the iron(II)-NHC complexes were tested against standard World Health Organization priority bacterial strains: Staphylococcus aureus ATCC 29213 and Escherichia coli ATCC 25922. The results showed a significant effect of the Fe(II)-NHC side-chain on the antibacterial activity against both Gram-negative and Gram-positive bacteria. Among all compounds, the most lipophilic iron complex, 3b, was found to be the most active one, with a minimum inhibitory concentration of 8 µg/mL. Pioneering mechanistic studies suggested an alternative mechanism of action (OH· formation), which opens the way for the development of a new class of antibiotics.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationUIDB/00313/2020pt
dc.relationPTDC/QUI-OUT/27996/2017pt
dc.relationLISBOA-01-0145-FEDER-007660pt
dc.relationUID/Multi/04551/2013pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectN-heterocyclic carbenept
dc.subjectiron(II)-NHC complexespt
dc.subjectantibacterial activitypt
dc.subject.meshAnti-Bacterial Agentspt
dc.subject.meshElectron Spin Resonance Spectroscopypt
dc.subject.meshEscherichia colipt
dc.subject.meshHeterocyclic Compoundspt
dc.subject.meshHydroxyl Radicalpt
dc.subject.meshImidazolespt
dc.subject.meshIronpt
dc.subject.meshMethanept
dc.subject.meshMicrobial Sensitivity Testspt
dc.subject.meshSpectrophotometry, Ultravioletpt
dc.subject.meshStaphylococcus aureuspt
dc.subject.meshStructure-Activity Relationshippt
dc.titleSynthesis of Iron(II)-N-Heterocyclic Carbene Complexes: Paving the Way for a New Class of Antibioticspt
dc.typearticle-
degois.publication.firstPage2917pt
degois.publication.issue12pt
degois.publication.titleMoleculespt
dc.peerreviewedyespt
dc.identifier.doi10.3390/molecules25122917pt
degois.publication.volume25pt
dc.date.embargo2020-06-24*
uc.date.periodoEmbargo0pt
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.project.grantnoCoimbra Chemistry Center-
crisitem.project.grantnoBioresources 4 Sustainability-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-7479-8540-
crisitem.author.orcid0000-0003-4958-7677-
Aparece nas coleções:I&D CQC - Artigos em Revistas Internacionais
FFUC- Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais
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