Please use this identifier to cite or link to this item:
https://hdl.handle.net/10316/106486
DC Field | Value | Language |
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dc.contributor.author | Vinagreiro, Carolina dos Santos | - |
dc.contributor.author | Lopes, Rita | - |
dc.contributor.author | Royo, Beatriz | - |
dc.contributor.author | Silva, Gabriela Jorge da | - |
dc.contributor.author | Pereira, Mariette M. | - |
dc.date.accessioned | 2023-04-05T08:33:52Z | - |
dc.date.available | 2023-04-05T08:33:52Z | - |
dc.date.issued | 2020-06-24 | - |
dc.identifier.issn | 1420-3049 | pt |
dc.identifier.uri | https://hdl.handle.net/10316/106486 | - |
dc.description.abstract | The 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.iso | eng | pt |
dc.publisher | MDPI | pt |
dc.relation | UIDB/00313/2020 | pt |
dc.relation | PTDC/QUI-OUT/27996/2017 | pt |
dc.relation | LISBOA-01-0145-FEDER-007660 | pt |
dc.relation | UID/Multi/04551/2013 | pt |
dc.rights | openAccess | pt |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | pt |
dc.subject | N-heterocyclic carbene | pt |
dc.subject | iron(II)-NHC complexes | pt |
dc.subject | antibacterial activity | pt |
dc.subject.mesh | Anti-Bacterial Agents | pt |
dc.subject.mesh | Electron Spin Resonance Spectroscopy | pt |
dc.subject.mesh | Escherichia coli | pt |
dc.subject.mesh | Heterocyclic Compounds | pt |
dc.subject.mesh | Hydroxyl Radical | pt |
dc.subject.mesh | Imidazoles | pt |
dc.subject.mesh | Iron | pt |
dc.subject.mesh | Methane | pt |
dc.subject.mesh | Microbial Sensitivity Tests | pt |
dc.subject.mesh | Spectrophotometry, Ultraviolet | pt |
dc.subject.mesh | Staphylococcus aureus | pt |
dc.subject.mesh | Structure-Activity Relationship | pt |
dc.title | Synthesis of Iron(II)-N-Heterocyclic Carbene Complexes: Paving the Way for a New Class of Antibiotics | pt |
dc.type | article | - |
degois.publication.firstPage | 2917 | pt |
degois.publication.issue | 12 | pt |
degois.publication.title | Molecules | pt |
dc.peerreviewed | yes | pt |
dc.identifier.doi | 10.3390/molecules25122917 | pt |
degois.publication.volume | 25 | pt |
dc.date.embargo | 2020-06-24 | * |
uc.date.periodoEmbargo | 0 | pt |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | open | - |
item.fulltext | Com Texto completo | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | article | - |
crisitem.author.researchunit | CNC - Center for Neuroscience and Cell Biology | - |
crisitem.author.researchunit | CQC - Coimbra Chemistry Centre | - |
crisitem.author.parentresearchunit | Faculty of Sciences and Technology | - |
crisitem.author.orcid | 0000-0002-7479-8540 | - |
crisitem.author.orcid | 0000-0003-4958-7677 | - |
Appears in Collections: | I&D CQC - Artigos em Revistas Internacionais FFUC- Artigos em Revistas Internacionais I&D CNC - Artigos em Revistas Internacionais |
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File | Description | Size | Format | |
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Synthesis-of-ironIINheterocyclic-carbene-complexes-Paving-the-way-for-a-new-class-of-antibioticsMolecules.pdf | 2.46 MB | Adobe PDF | View/Open |
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This item is licensed under a Creative Commons License