Highly efficient and reusable Pd nanoparticles decorated on a novel Schiff base polymer for reduction of nitroarenes and Suzuki coupling reactions

dc.contributor.authorYılmaz Baran, Nuray
dc.date.accessioned2024-07-25T08:39:43Z
dc.date.available2024-07-25T08:39:43Z
dc.date.issued2024
dc.departmentSabire Yazıcı Fen Edebiyat Fakültesi
dc.description.abstractEnvironmental pollutants such as nitroarenes which released from several factories threaten flora, fauna and human life. Therefore, removal of these toxic substances from waste waters is of significance. Catalytic systems involving metal nanoparticles are effective to reduce hazardous nitroarenes and to fabricate biaryls, which are significant for pharmaceutical and natural product industries, via cross coupling reactions. The current research was conducted to produce a quick, highly efficient, simply recoverable and reusable nanocatalyst (Pd NPs@P(2- FAN)) involving Pd nanoparticles (Pd NPs) immobilized on a novel Schiff base polymer, Poly(2-((furan-2- ylmethylene)amino)-5-nitrophenol) (P(2-FAN)) for reduction of several toxic nitroarenes to harmless and useful organic molecules in water and fabrication of useful biaryls via Suzuki coupling (SC) reactions. UV–Vis, FTIR, TGA, XRD, FE-SEM and EDS techniques were used for characterizations of the synthesized materials. Then, catalytic performance of the produced Pd NPs@P(2-FAN) was examined in reduction of 2-nitroaniline, 4- nitroaniline, 4-nitrophenol, 4-nitro-o-phenylenediamine. Pd NPs@P(2-FAN) was reduced all these hazardous nitroarenes in water in very short time (between 30 and 85 s) with only 3 mg nanocatalyst using NaBH4. Moreover, Pd NPs@P(2-FAN) accomplished the fabrication of several biaryls via SC reactions using the microwave irradiation method in a solventless medium. This resulted in excellent reaction yields (99 %) with a very low catalyst amount (0.006 mol%) and a rapid reaction time (6 min). Additionally, performed reusability test results displayed that the nanocatalyst was simply recoverable and repeatedly reusable for successive six and eight cycles for reduction of nitroarenes and production of biaryls, respectively.
dc.identifier.doi10.1016/j.jorganchem.2024.123047
dc.identifier.issn0022-328X
dc.identifier.issn1872-8561
dc.identifier.issue-en_US
dc.identifier.scopusqualityQ2
dc.identifier.urihttps:/dx.doi.org/10.1016/j.jorganchem.2024.123047
dc.identifier.urihttps://hdl.handle.net/20.500.12451/12220
dc.identifier.volume1008en_US
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofJournal of Organometallic Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBiaryls
dc.subjectNitroarene Reduction
dc.subjectPalladium Nanoparticles
dc.subjectPolyazomethines
dc.subjectSchiff Base Polymers
dc.subjectSuzuki Coupling Reactions
dc.titleHighly efficient and reusable Pd nanoparticles decorated on a novel Schiff base polymer for reduction of nitroarenes and Suzuki coupling reactions
dc.typeArticle

Dosyalar

Orijinal paket
Listeleniyor 1 - 1 / 1
[ X ]
İsim:
yilmaz baran-nuray-2024.pdf
Boyut:
8.37 MB
Biçim:
Adobe Portable Document Format
Açıklama:
Tam Metin / Full Text
Lisans paketi
Listeleniyor 1 - 1 / 1
[ X ]
İsim:
license.txt
Boyut:
1.44 KB
Biçim:
Item-specific license agreed upon to submission
Açıklama: