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Rhenium Nanostructures Loaded into Amino-Functionalized Resin as a Nanocomposite Catalyst for Hydrogenation of 4-Nitrophenol and 4-Nitroaniline

The present work presents a new nanocomposite catalyst with rhenium nanostructures (ReNSs) for the catalytic hydrogenation of 4-nitrophenol and 4-nitroaniline. The catalyst, based on an anion exchange resin with functionality derived from 1,1′-carboimidazole, was obtained in the process involving an...

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Detalles Bibliográficos
Autores principales: Cyganowski, Piotr, Dzimitrowicz, Anna, Jamroz, Piotr, Jermakowicz-Bartkowiak, Dorota, Pohl, Pawel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8588495/
https://www.ncbi.nlm.nih.gov/pubmed/34771354
http://dx.doi.org/10.3390/polym13213796
Descripción
Sumario:The present work presents a new nanocomposite catalyst with rhenium nanostructures (ReNSs) for the catalytic hydrogenation of 4-nitrophenol and 4-nitroaniline. The catalyst, based on an anion exchange resin with functionality derived from 1,1′-carboimidazole, was obtained in the process involving anion exchange of ReO(4)(–) ions followed by their reduction with NaBH(4). The amino functionality present in the resin played a primary role in the stabilization of the resultant ReNSs, consisting of ≈1% (w/w) Re in the polymer mass. The synthesized and capped ReNSs were amorphous and had the average size of 3.45 ± 1.85 nm. Then, the obtained catalyst was used in a catalytic reduction of 4-nitrophenol (4-NP) and 4-nitroaniline (4-NA). Following the pseudo-first-order kinetics, 5 mg of the catalyst led to a 90% conversion of 4-NP with the mass-normalized rate constant (k(m1)) of 6.94 × 10(−3) min(−1) mg(−1), while the corresponding value acquired for 4-NA was 7.2 × 10(−3) min(−1) mg(−1), despite the trace amount of Re in the heterogenous catalyst. The obtained material was also conveniently reused.