Repository logo
 
Publication

On the development of selective chelators for Cadmium: Synthesis, structure and chelating properties of 3-((5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl)amino)benzo[d]isothiazole 1,1-dioxide, a novel Thiadiazolyl Saccharinate

dc.contributor.authorLeal, Joana F.
dc.contributor.authorGuerreiro, Bruno
dc.contributor.authorAmado, Patrícia
dc.contributor.authorFernandes, André L.
dc.contributor.authorBarreira, Luísa
dc.contributor.authorPaixão, José A.
dc.contributor.authorLurdes S. Cristiano, M.
dc.date.accessioned2021-04-20T12:20:39Z
dc.date.available2021-04-20T12:20:39Z
dc.date.issued2021-03-10
dc.date.updated2021-03-26T14:06:35Z
dc.description.abstractAquatic contamination by heavy metals is a major concern for the serious negative consequences it has for plants, animals, and humans. Among the most toxic metals, Cd(II) stands out since selective and truly efficient methodologies for its removal are not known. We report a novel multidentate chelating agent comprising the heterocycles thiadiazole and benzisothiazole. 3-((5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl)amino)benzo[<i>d</i>]isothiazole 1,1-dioxide (AL14) was synthesized from cheap saccharin and characterized by different techniques, including single crystal X-ray crystallography. Our studies revealed the efficiency and selectivity of AL14 for the chelation of dissolved Cd(II) (as compared to Cu(II) and Fe(II)). Different spectral changes were observed upon the addition of Cd(II) and Cu(II) during UV-Vis titrations, suggesting different complexation interactions with both metals.pt_PT
dc.description.sponsorshipUIDB/04326/2020, UIDB/04564/2020, ALG-01-0145-FEDER-022121, SFRH/BD/130407/2017pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationMolecules 26 (6): 1501 (2021)pt_PT
dc.identifier.doi10.3390/molecules26061501pt_PT
dc.identifier.eissn1420-3049
dc.identifier.urihttp://hdl.handle.net/10400.1/15422
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectCadmium chelationpt_PT
dc.subjectAquatic remediationpt_PT
dc.subjectSaccharin-based ligandspt_PT
dc.subjectBenzisothiazolespt_PT
dc.subjectThiadiazolespt_PT
dc.subjectSelectivitypt_PT
dc.subjectMolecular structurept_PT
dc.subjectπ-π stackingpt_PT
dc.titleOn the development of selective chelators for Cadmium: Synthesis, structure and chelating properties of 3-((5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl)amino)benzo[d]isothiazole 1,1-dioxide, a novel Thiadiazolyl Saccharinatept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.startPage1051pt_PT
oaire.citation.titleMoleculespt_PT
oaire.citation.volume26pt_PT
person.familyNameLeal
person.familyNameGuerreiro
person.familyNameMenalha Amado
person.familyNameLourenço Fernandes
person.familyNameBarreira
person.familyNameCristiano
person.givenNameJoana F.
person.givenNameBruno
person.givenNamePatrícia Sofia
person.givenNameAndré
person.givenNameLuísa
person.givenNameMaria de Lurdes
person.identifier.ciencia-id7816-76B3-F5F5
person.identifier.ciencia-id1116-64F6-3D01
person.identifier.ciencia-id8617-A360-B70A
person.identifier.ciencia-idD512-BA1B-65C5
person.identifier.ciencia-id6D1A-17E5-1400
person.identifier.ciencia-idE411-6006-5A01
person.identifier.orcid0000-0002-0336-346X
person.identifier.orcid0000-0001-7219-7939
person.identifier.orcid0000-0002-7307-9210
person.identifier.orcid0000-0002-0355-7651
person.identifier.orcid0000-0002-4077-855X
person.identifier.orcid0000-0002-9447-2855
person.identifier.ridAAD-1990-2019
person.identifier.ridG-2345-2012
person.identifier.scopus-author-id35096256100
person.identifier.scopus-author-id9238724800
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublication0d6cc8b6-2421-401f-8ac0-bcf5aa9f396f
relation.isAuthorOfPublicationb29af8f2-6553-4fd0-a50f-4a51489f3d83
relation.isAuthorOfPublication5b28f1eb-1d56-4094-8242-2d1163618e5f
relation.isAuthorOfPublication47044937-8512-42f6-9652-24de1572c7ac
relation.isAuthorOfPublicationce3d77be-25df-4257-b5b3-aca8cff24116
relation.isAuthorOfPublicationb16751a6-748e-44b0-9c59-058cbd5b2cc3
relation.isAuthorOfPublication.latestForDiscoveryb16751a6-748e-44b0-9c59-058cbd5b2cc3

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
molecules-26-01501-v2.pdf
Size:
2.43 MB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
3.46 KB
Format:
Item-specific license agreed upon to submission
Description: