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Tytuł:
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Novel magnetic lignosulfonate-supported Pd complex as an efficient nanocatalyst for N-arylation of 4-methylbenzenesulfonamide.
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Autorzy:
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Orooji Y; College of Materials Science and Engineering, Nanjing Forestry University, Nanjing 210037, China. Electronic address: .
Pakzad K; Faculty of Chemistry, University of Mazandaran, Babolsar 47416-13534, Iran.
Nasrollahzadeh M; Department of Chemistry, Faculty of Science, University of Qom, Qom 3716146611, Iran. Electronic address: .
Tajbakhsh M; Faculty of Chemistry, University of Mazandaran, Babolsar 47416-13534, Iran.
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Źródło:
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International journal of biological macromolecules [Int J Biol Macromol] 2021 Jul 01; Vol. 182, pp. 564-573. Date of Electronic Publication: 2021 Mar 30.
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Typ publikacji:
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Journal Article
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Język:
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English
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Imprint Name(s):
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Publication: Amsterdam : Elsevier
Original Publication: Guildford, Eng., IPC Science and Technology Press.
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MeSH Terms:
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Ferric Compounds/*chemistry
Lignin/*analogs & derivatives
Nanoconjugates/*chemistry
Palladium/*chemistry
Sulfonamides/*chemistry
Toluene/*analogs & derivatives
Catalysis ; Metal-Organic Frameworks/chemistry ; Toluene/chemistry ; Trientine/chemistry
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Contributed Indexing:
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Keywords: Heterogeneous nanocatalyst; Lignosulfonate; N-arylation; Palladium complex; Sulfonamide
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Substance Nomenclature:
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0 (Ferric Compounds)
0 (Metal-Organic Frameworks)
0 (Nanoconjugates)
0 (Sulfonamides)
1K09F3G675 (ferric oxide)
3FPU23BG52 (Toluene)
5TWQ1V240M (Palladium)
9005-53-2 (Lignin)
I8266RI90M (4-toluenesulfonamide)
SJ76Y07H5F (Trientine)
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Entry Date(s):
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Date Created: 20210402 Date Completed: 20210720 Latest Revision: 20210720
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Update Code:
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20240104
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DOI:
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10.1016/j.ijbiomac.2021.03.165
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PMID:
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33798580
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This study presents a novel, economical, and environmentally technique for synthesizing magnetic palladium complex conjugated to activated calcium lignosulfonate with triethylenetetramine (Fe 3 O 4 @lignosulfonate@triethylenetetramine@Pd complex (FLT-Pd complex)) as a practical and air-stable catalyst. FLT-Pd complex is used as a catalyst for the fabrication of 4-methyl-N-phenyl-benzenesulfonamide derivatives via N-arylation of 4-methylbenzenesulfonamide in good yields. Furthermore, because of the complex magnetic reparability and high stability, it could be removed easily from the reaction media using a magnet and reused 5 cycles without a remarkable loss of catalytic prowess.
(Copyright © 2021 Elsevier B.V. All rights reserved.)