2020
DOI: 10.1016/j.poly.2020.114375
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Acidic polymer containing sulfunic acid and carboxylic acid groups heterogenized with natural clay: A novel metal free and heterogeneous catalyst for acid-catalyzed reactions

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Cited by 25 publications
(18 citation statements)
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“…The latter, was then vinyl functionalized with 3-(trimethoxysilane) propyl methacrylate (3-TMSPMA) to furnish BC@GCN-V and subsequently tolerated polymerization reaction with 1-vinylimidazole, 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) and acrylic acid (AA), Figure 1 . The polymeric moiety (P-IL) that has been grown on BC@GCN contained both acidic (–COOH and –SO 3 H) [ 66 ] and IL moieties on its backbone. Hence, it was assumed that it could promote various classic, acid-catalyzed chemical transformations efficiently under mild reaction condition.…”
Section: Resultsmentioning
confidence: 99%
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“…The latter, was then vinyl functionalized with 3-(trimethoxysilane) propyl methacrylate (3-TMSPMA) to furnish BC@GCN-V and subsequently tolerated polymerization reaction with 1-vinylimidazole, 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) and acrylic acid (AA), Figure 1 . The polymeric moiety (P-IL) that has been grown on BC@GCN contained both acidic (–COOH and –SO 3 H) [ 66 ] and IL moieties on its backbone. Hence, it was assumed that it could promote various classic, acid-catalyzed chemical transformations efficiently under mild reaction condition.…”
Section: Resultsmentioning
confidence: 99%
“…In this research, we targeted preparation of a metal-free catalyst that could catalyze conventional chemical transformations in aqueous media under a mild reaction condition. In this regard, BC@GCN was prepared and then, a polymeric moiety that contained both IL and acid functionalities (–SO 3 H and –COOH) [ 66 , 68 ] was incorporated to the structure of the catalyst. It was assumed that both IL and acidic functionalities could effectively promote the acid-catalyzed reactions.…”
Section: Resultsmentioning
confidence: 99%
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“…The solvent of the ltrate was evaporated under vacuum and products were puri ed by column chromatography (ethyl acetate / hexane 1:5). All of the products were synthetic 41 and their characterization was conducted by comparing their melting points and spectral data ( 1 HNMR and 13 CNMR) with authentic samples, Figure S1-8. To estimate the yields of the reactions GC was used.…”
Section: Knoevenagel Condensation Reactionmentioning
confidence: 99%