Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/10731
DC FieldValueLanguage
dc.contributor.authorMonteiro, Carlos J. P.-
dc.contributor.authorPereira, Mariette M.-
dc.contributor.authorAzenha, M. Emilia-
dc.contributor.authorBurrows, Hugh D.-
dc.contributor.authorSerpa, Carlos-
dc.contributor.authorArnaut, Luís G.-
dc.contributor.authorTapia, M. J.-
dc.contributor.authorSarakha, Mohamed-
dc.contributor.authorWong-Wah-Chung, Pascal-
dc.contributor.authorNavaratnam, Suppiah-
dc.date.accessioned2009-07-17T15:28:17Z-
dc.date.available2009-07-17T15:28:17Z-
dc.date.issued2005-06-28-
dc.identifier.citationPhotochemical & Photobiological Sciences. 4 (2005) 617-624en_US
dc.identifier.issn1474-905X-
dc.identifier.urihttps://hdl.handle.net/10316/10731-
dc.description.abstract5,10,15,20-Tetrakis(2,6-dichloro-3-chlorosulfophenyl)porphyrin and its tin and zinc complexes were synthesized with high yields and fully characterized. The corresponding water-soluble 5,10,15,20-tetrakis(2,6-dichloro-3-sulfophenyl)porphyrins were obtained by hydrolysis with water. An extensive photophysical study of the new water soluble porphyrinic compounds was carried out including absorption and fluorescence spectra, fluorescence quantum yields, triplet absorption spectra, triplet lifetimes, triplet and singlet oxygen quantum yields. These sensitizers were successfully used in the photodegradation of 4-chlorophenol and 2,6-dimethylphenol. A comparison is made of their efficiencies, and some mechanistic considerations are highlighted.en_US
dc.description.sponsorshipFCT; FEDER; POCTI; Universidad de Burgos; GRICES–CNRS; European Commission (HPRI-CT-2002-00183).en_US
dc.language.isoengen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsopenAccesseng
dc.titleA comparative study of water soluble 5,10,15,20-tetrakis(2,6-dichloro-3-sulfophenyl)porphyrin and its metal complexes as efficient sensitizers for photodegradation of phenolsen_US
dc.typearticleen_US
dc.identifier.doi10.1039/b507597a-
uc.controloAutoridadeSim-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.languageiso639-1en-
crisitem.author.deptFaculty of Sciences and Technology-
crisitem.author.parentdeptUniversity of Coimbra-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0003-4958-7677-
crisitem.author.orcid0000-0002-9495-2592-
crisitem.author.orcid0000-0003-3127-2298-
crisitem.author.orcid0000-0001-7004-0110-
crisitem.author.orcid0000-0002-3223-4819-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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