Ni nanoparticles on polyaromatic hyperbranched polymer support as a mild, tunable, and sustainable catalyst for catalytic transfer hydrogenation

Hyperbranched polyaromatic polymer (HBP) based on pyridylphenylene dendrimer as a multifunctional monomer was employed as a nanoreactor and a stabilizing matrix for synthesis of catalytic Ni nanoparticles (NPs). The HBP was found to have an effective control over NP size. The Ni NPs synthesized in H...

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Veröffentlicht in:Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology 2019-05, Vol.21 (5), p.1-14, Article 91
Hauptverfasser: Basaveni, S., Kuchkina, N. V., Shifrina, Z. B., Pal, M., Rajadurai, M.
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container_title Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology
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creator Basaveni, S.
Kuchkina, N. V.
Shifrina, Z. B.
Pal, M.
Rajadurai, M.
description Hyperbranched polyaromatic polymer (HBP) based on pyridylphenylene dendrimer as a multifunctional monomer was employed as a nanoreactor and a stabilizing matrix for synthesis of catalytic Ni nanoparticles (NPs). The HBP was found to have an effective control over NP size. The Ni NPs synthesized in HBP matrix had diameter between 3 and 4.5 nm with narrow size distribution and were reproducible in several batches. The HBP-encapsulated Ni NPs (Ni-HBP) had a good air stability, high activity, and controlled reactivity in catalytic transfer hydrogenation (CTH) of nitroarenes and alkenes. The catalytic reactions were performed under base-free, heterogeneously-catalyzed conditions without use of high pressure, strong acidic media, or highly flammable hydrogen source. This reduction system showed good tolerance towards hydroxyl, alkyne, or halogen substituents. Moreover, due to mild nature of the catalyst, the reaction may be controlled to selectively reduce only one functional group, leaving another one intact (e.g., nitro-group vs internal alkyne). Graphical abstract
doi_str_mv 10.1007/s11051-019-4533-2
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The HBP-encapsulated Ni NPs (Ni-HBP) had a good air stability, high activity, and controlled reactivity in catalytic transfer hydrogenation (CTH) of nitroarenes and alkenes. The catalytic reactions were performed under base-free, heterogeneously-catalyzed conditions without use of high pressure, strong acidic media, or highly flammable hydrogen source. This reduction system showed good tolerance towards hydroxyl, alkyne, or halogen substituents. Moreover, due to mild nature of the catalyst, the reaction may be controlled to selectively reduce only one functional group, leaving another one intact (e.g., nitro-group vs internal alkyne). 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identifier ISSN: 1388-0764
ispartof Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology, 2019-05, Vol.21 (5), p.1-14, Article 91
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1572-896X
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source SpringerNature Complete Journals
subjects Alkenes
Alkynes
Catalysis
Catalysts
Characterization and Evaluation of Materials
Chemical reactions
Chemical synthesis
Chemistry and Materials Science
Control stability
Flammability
Functional groups
High pressure
Hydrogen storage
Hydrogenation
Inorganic Chemistry
Lasers
Materials Science
Nanoparticles
Nanotechnology
Optical Devices
Optics
Photonics
Physical Chemistry
Polymers
Research Paper
Size distribution
title Ni nanoparticles on polyaromatic hyperbranched polymer support as a mild, tunable, and sustainable catalyst for catalytic transfer hydrogenation
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