An easily recoverable and highly reproducible agar-supported palladium catalyst for Suzuki-Miyaura coupling reactions and reduction of o-nitroaniline
dc.contributor.author | Baran, Talat | |
dc.contributor.author | Yılmaz Baran, Nuray | |
dc.contributor.author | Menteş, Ayfer | |
dc.date.accessioned | 13.07.201910:50:10 | |
dc.date.accessioned | 2019-07-29T19:27:06Z | |
dc.date.available | 13.07.201910:50:10 | |
dc.date.available | 2019-07-29T19:27:06Z | |
dc.date.issued | 2018 | |
dc.department | Sabire Yazıcı Fen Edebiyat Fakültesi | |
dc.description.abstract | Polysaccharides are excellent support materials for catalytic systems due to their superior metal binding capacity, high mechanical strength, and green nature. Among the polysaccharides, agar can be considered a good support material for catalytic reactions from the point of its low cost, easy availability, high thermal durability, and biodegradability. In this study, agar-supported palladium catalyst (AG-Pd) was designed for the first time, and then its catalytic performance was tested towards (i) Suzuki-Miyaura coupling reactions and (ii) catalytic reduction of o-nitroaniline to o-phenylenediamine under mild reaction conditions. Additionally, the reproducibility of the designed AG-Pd catalyst was investigated in both catalytic reactions, and the tests showed that the catalyst could be reused many times. AG-Pd catalyst displayed excellent selectivity and efficiency in Suzuki-Miyaura coupling reactions in only 6 min under solvent-free media. In addition, AG-Pd catalyst provided good catalytic reduction by completely reducing o-nitroaniline in 90 s at room temperature. These findings reveal that agar is a good support material, and it can be used for different catalytic systems as a support. (C) 2018 Elsevier B.V. All rights reserved. | |
dc.description.sponsorship | Aksaray University Scientific Research Projects Coordination [2017-047] | |
dc.description.sponsorship | The authors would like to thank Aksaray University Scientific Research Projects Coordination for their financial support (Project number: 2017-047). | |
dc.identifier.doi | 10.1016/j.ijbiomac.2018.04.057 | |
dc.identifier.endpage | 256 | en_US |
dc.identifier.issn | 0141-8130 | |
dc.identifier.issn | 1879-0003 | |
dc.identifier.pmid | 29660458 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 249 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.ijbiomac.2018.04.057 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12451/5788 | |
dc.identifier.volume | 115 | en_US |
dc.identifier.wos | WOS:000438662500029 | |
dc.identifier.wosquality | N/A | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | |
dc.publisher | Elsevier Science Bv | |
dc.relation.ispartof | International Journal of Biological Macromolecules | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | Agar | |
dc.subject | Catalytic Reduction | |
dc.subject | Suzuki-Miyaura Reaction | |
dc.subject | Reproducibility | |
dc.title | An easily recoverable and highly reproducible agar-supported palladium catalyst for Suzuki-Miyaura coupling reactions and reduction of o-nitroaniline | |
dc.type | Article |
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