Porphyrin–Nanodiamond Hybrid Materials—Active, Stable and Reusable Cyclohexene Oxidation Catalysts

Bibliographic Details
Main Author: Dias, Lucas Danilo
Publication Date: 2020
Other Authors: Rodrigues, Fábio M.S., Calvete, Mário J. F., Carabineiro, Sónia A. C., Scherer, Marisa D., Caires, Anderson R. L., Buijnsters, Josephus G., Figueiredo, José L., Bagnato, Vanderlei S., Pereira, Mariette M.
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://hdl.handle.net/10316/105855
https://doi.org/10.3390/catal10121402
Summary: The quest for active, yet “green” non-toxic catalysts is a continuous challenge. In this work, covalently linked hybrid porphyrin–nanodiamonds were prepared via ipso nitro substitution reaction and characterized by X-ray photoelectron spectroscopy (XPS), fluorescence spectroscopy, infrared spectroscopy (IR) and thermogravimetry-differential scanning calorimetry (TG-DSC). The amine-functionalized nanodiamonds (ND@NH2) and 2-nitro-5,10,15,20-tetra(4-trifluoromethylphenyl)porphyrin covalently linked to nanodiamonds (ND@ NH-TPPpCF3) were tested using Allium cepa as a plant model, and showed neither phytotoxicity nor cytotoxicity. The hybrid nanodiamond–copper(II)–porphyrin material ND@ NH-TPPpCF3-Cu(II) was also evaluated as a reusable catalyst in cyclohexene allylic oxidation, and displayed a remarkable turnover number (TON) value of 265,000, using O2 as green oxidant, in the total absence of sacrificial additives, which is the highest activity ever reported for said allylic oxidation. Additionally, ND@ NH-TPPpCF3-Cu(II) could be easily separated from the reaction mixture by centrifugation, and reused in three consecutive catalytic cycles without major loss of activity.
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spelling Porphyrin–Nanodiamond Hybrid Materials—Active, Stable and Reusable Cyclohexene Oxidation Catalystsnanodiamondscopper (II) porphyrinallylic oxidationThe quest for active, yet “green” non-toxic catalysts is a continuous challenge. In this work, covalently linked hybrid porphyrin–nanodiamonds were prepared via ipso nitro substitution reaction and characterized by X-ray photoelectron spectroscopy (XPS), fluorescence spectroscopy, infrared spectroscopy (IR) and thermogravimetry-differential scanning calorimetry (TG-DSC). The amine-functionalized nanodiamonds (ND@NH2) and 2-nitro-5,10,15,20-tetra(4-trifluoromethylphenyl)porphyrin covalently linked to nanodiamonds (ND@ NH-TPPpCF3) were tested using Allium cepa as a plant model, and showed neither phytotoxicity nor cytotoxicity. The hybrid nanodiamond–copper(II)–porphyrin material ND@ NH-TPPpCF3-Cu(II) was also evaluated as a reusable catalyst in cyclohexene allylic oxidation, and displayed a remarkable turnover number (TON) value of 265,000, using O2 as green oxidant, in the total absence of sacrificial additives, which is the highest activity ever reported for said allylic oxidation. Additionally, ND@ NH-TPPpCF3-Cu(II) could be easily separated from the reaction mixture by centrifugation, and reused in three consecutive catalytic cycles without major loss of activity.This research was funded by FCT—Foundation for Science and Technology, I.P., under projects UIDB/00313/2020; PTDC/QUI-OUT/27996/2017 (DUALPI); POCI-01-0145-FEDER-027996; POCI-01–0145-FEDER- 016387; UIDB/50006/2020 (Associate Laboratory for Green Chemistry—LAQV); MATIS (CENTRO-010145-FEDER-00014); Base Funding—UIDB/50020/2020 of the Associate Laboratory LSRE-LCM—funded by national funds through FCT/MCTES (PIDDAC); and 5625-DRI-DAAD-2020/21. SACC also acknowledges FCT Investigador FCT program (IF/01381/2013/CP1160/CT0007) and Scientific Employment Stimulus - Institutional Call (CEECINST/00102/2018). The authors also thank Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) for CEPOF 2013/07276-1, and INCT “Basic Optics and Applied to Life Sciences” (FAPESP 2014/50857-8, CNPq 465360/2014-9). A.R.L. Caires acknowledges CAPES-PrInt funding program (grant number 88887.353061/2019-00 and 88881.311921/2018-01). J.G.B. thanks the Dutch Research Council (NWO) for funding as a part of the Open Technology Programme (project number 16361). L.D. Dias thanks FAPESP for the Post-doc grant 2019/13569-8. F.M.S.R. thanks FCT for the PhD grant (PD/BD/114340/2016).MDPI2020info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://hdl.handle.net/10316/105855https://hdl.handle.net/10316/105855https://doi.org/10.3390/catal10121402eng2073-4344Dias, Lucas DaniloRodrigues, Fábio M.S.Calvete, Mário J. F.Carabineiro, Sónia A. C.Scherer, Marisa D.Caires, Anderson R. L.Buijnsters, Josephus G.Figueiredo, José L.Bagnato, Vanderlei S.Pereira, Mariette M.info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2023-04-06T10:19:51Zoai:estudogeral.uc.pt:10316/105855Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T05:56:16.990996Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Porphyrin–Nanodiamond Hybrid Materials—Active, Stable and Reusable Cyclohexene Oxidation Catalysts
title Porphyrin–Nanodiamond Hybrid Materials—Active, Stable and Reusable Cyclohexene Oxidation Catalysts
spellingShingle Porphyrin–Nanodiamond Hybrid Materials—Active, Stable and Reusable Cyclohexene Oxidation Catalysts
Dias, Lucas Danilo
nanodiamonds
copper (II) porphyrin
allylic oxidation
title_short Porphyrin–Nanodiamond Hybrid Materials—Active, Stable and Reusable Cyclohexene Oxidation Catalysts
title_full Porphyrin–Nanodiamond Hybrid Materials—Active, Stable and Reusable Cyclohexene Oxidation Catalysts
title_fullStr Porphyrin–Nanodiamond Hybrid Materials—Active, Stable and Reusable Cyclohexene Oxidation Catalysts
title_full_unstemmed Porphyrin–Nanodiamond Hybrid Materials—Active, Stable and Reusable Cyclohexene Oxidation Catalysts
title_sort Porphyrin–Nanodiamond Hybrid Materials—Active, Stable and Reusable Cyclohexene Oxidation Catalysts
author Dias, Lucas Danilo
author_facet Dias, Lucas Danilo
Rodrigues, Fábio M.S.
Calvete, Mário J. F.
Carabineiro, Sónia A. C.
Scherer, Marisa D.
Caires, Anderson R. L.
Buijnsters, Josephus G.
Figueiredo, José L.
Bagnato, Vanderlei S.
Pereira, Mariette M.
author_role author
author2 Rodrigues, Fábio M.S.
Calvete, Mário J. F.
Carabineiro, Sónia A. C.
Scherer, Marisa D.
Caires, Anderson R. L.
Buijnsters, Josephus G.
Figueiredo, José L.
Bagnato, Vanderlei S.
Pereira, Mariette M.
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Dias, Lucas Danilo
Rodrigues, Fábio M.S.
Calvete, Mário J. F.
Carabineiro, Sónia A. C.
Scherer, Marisa D.
Caires, Anderson R. L.
Buijnsters, Josephus G.
Figueiredo, José L.
Bagnato, Vanderlei S.
Pereira, Mariette M.
dc.subject.por.fl_str_mv nanodiamonds
copper (II) porphyrin
allylic oxidation
topic nanodiamonds
copper (II) porphyrin
allylic oxidation
description The quest for active, yet “green” non-toxic catalysts is a continuous challenge. In this work, covalently linked hybrid porphyrin–nanodiamonds were prepared via ipso nitro substitution reaction and characterized by X-ray photoelectron spectroscopy (XPS), fluorescence spectroscopy, infrared spectroscopy (IR) and thermogravimetry-differential scanning calorimetry (TG-DSC). The amine-functionalized nanodiamonds (ND@NH2) and 2-nitro-5,10,15,20-tetra(4-trifluoromethylphenyl)porphyrin covalently linked to nanodiamonds (ND@ NH-TPPpCF3) were tested using Allium cepa as a plant model, and showed neither phytotoxicity nor cytotoxicity. The hybrid nanodiamond–copper(II)–porphyrin material ND@ NH-TPPpCF3-Cu(II) was also evaluated as a reusable catalyst in cyclohexene allylic oxidation, and displayed a remarkable turnover number (TON) value of 265,000, using O2 as green oxidant, in the total absence of sacrificial additives, which is the highest activity ever reported for said allylic oxidation. Additionally, ND@ NH-TPPpCF3-Cu(II) could be easily separated from the reaction mixture by centrifugation, and reused in three consecutive catalytic cycles without major loss of activity.
publishDate 2020
dc.date.none.fl_str_mv 2020
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv https://hdl.handle.net/10316/105855
https://hdl.handle.net/10316/105855
https://doi.org/10.3390/catal10121402
url https://hdl.handle.net/10316/105855
https://doi.org/10.3390/catal10121402
dc.language.iso.fl_str_mv eng
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dc.publisher.none.fl_str_mv MDPI
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