Utilize este identificador para referenciar este registo: https://hdl.handle.net/10316/111857
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dc.contributor.authorMahmoud, Abdallah G.-
dc.contributor.authorLibrando, Ivy L.-
dc.contributor.authorPaul, Anup-
dc.contributor.authorCarabineiro, Sónia A. C.-
dc.contributor.authorFerraria, Ana Maria-
dc.contributor.authorBotelho do Rego, Ana Maria-
dc.contributor.authorGuedes da Silva, M. Fátima C.-
dc.contributor.authorGeraldes, Carlos F. G. C.-
dc.contributor.authorPombeiro, Armando J. L.-
dc.date.accessioned2024-01-12T11:41:06Z-
dc.date.available2024-01-12T11:41:06Z-
dc.date.issued2023-
dc.identifier.issn09205861pt
dc.identifier.urihttps://hdl.handle.net/10316/111857-
dc.description.abstractNew organotin compounds with general formula [(PTA-CH2-C6H4-p-COO)SnR3]Br (where R is Me for 3 and Ph for 4; PTA = 1,3,5-triaza-7-phosphaadamantane), bearing the methylene benzoate PTA derivative, were synthesized through a mild two-step process. The compounds were characterized by Fourier transform infrared spectroscopy, electrospray ionization mass spectrometry, elemental analysis and nuclear magnetic resonance spectroscopy (NMR). They were heterogenized on commercially available activated carbon (AC) and multiwalled carbon nanotubes (CNT), as well as on their chemically modified analogues. The obtained materials were characterized by scanning electron microscopy, transmission electron microscopy and X-ray photoelectron spectroscopy. Complex 3 supported on activated carbon (3-AC) was found to be an active and recyclable catalyst for the cyanosilylation of several aromatic and aliphatic aldehydes. Using 3-AC with a low loading of 0.1 mol% several substrates were quantitatively converted, within just 5 min at 50 ◦C and under microwave irradiation in solvent-free conditions. Multinuclear NMR analysis suggested a mechanism that potentially involves a double activation process, where the nucleophilic phosphorus at the PTA derivative acts as a Lewis base and the Sn(IV) metal centre as a Lewis acid.pt
dc.description.sponsorshipThe work was also funded by national funds through FCT, under the Scientific Employment Stimulus-Institutional Call (CEEC-INST/ 00102/2018). AGM is grateful to Associaçao do Instituto Superior Tecnico para a Investigaçao e Desenvolvimento (IST-ID) for his post-doctoral fellowship through grant no. BL133/2021-IST-ID. ILL acknowledges the CATSUS PhD Program from FCT for her grant PD/BD/135555/2018. AP and AMF are grateful to FCT and Instituto Superior T´ecnico (IST), Portugal through DL/57/2017 (Contract no. IST-ID/197/2019 and ISTID/ 131/2018). This publication is also supported by the RUDN University Strategic Academic Leadership Program (recipient AJLP, preparation).pt
dc.language.isoengpt
dc.publisherElsevierpt
dc.relationUIDB/00100/2020pt
dc.relationUIDP/00100/2020pt
dc.relationLA/P/0056/2020pt
dc.relationUIDB/04565/2020pt
dc.relationUIDP/04565/2020pt
dc.relationLA/P/0140/2020pt
dc.relationUIDB/50020/2020pt
dc.relationUIDP/50020/2020pt
dc.relationUIDB/50006/2020pt
dc.relationUIDP/50006/2020pt
dc.relationUIDB/00313/2020pt
dc.relationUIDP/00313/2020pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt
dc.subjectCyanosilylationpt
dc.subjectCarbon materialspt
dc.subjectHeterogeneous catalysispt
dc.subject1,3,5-triaza-7-phosphaadamantanept
dc.subjectMicrowavept
dc.subjectTetrel σ-hole bondpt
dc.titleNovel organotin-PTA complexes supported on mesoporous carbon materials as recyclable catalysts for solvent-free cyanosilylation of aldehydespt
dc.typearticle-
degois.publication.firstPage114270pt
degois.publication.titleCatalysis Todaypt
dc.peerreviewedyespt
dc.identifier.doi10.1016/j.cattod.2023.114270pt
degois.publication.volume423pt
dc.date.embargo2023-01-01*
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.grantnoCentro de Química Estrutural-
crisitem.project.grantnoCentro de Química Estrutural-
crisitem.project.grantnoInstitute of Molecular Sciences - IMS-
crisitem.project.grantnoInstitute for Bioengineering and Biosciences -iBB-
crisitem.project.grantnoInstitute for Bioengineering and Biosciences-
crisitem.project.grantnoLaboratory of Separation and Reaction Engineering - Laboratory of Catalysis and Materials-
crisitem.project.grantnoLaboratory of Separation and Reaction Engineering-
crisitem.project.grantnoAssociated Laboratory for Green Chemistry - Clean Technologies and Processes- REQUIMTE-
crisitem.project.grantnoAssociated Laboratory for Green Chemistry - Clean Technologies and Processes-
crisitem.project.grantnoCoimbra Chemistry Center-
crisitem.project.grantnoCoimbra Chemistry Center-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-0837-8329-
Aparece nas coleções:I&D CQC - Artigos em Revistas Internacionais
FCTUC Ciências da Vida - Artigos em Revistas Internacionais
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