Biomass-Derived Catalysts for Selective Hydrogenation of Nitroarenes.

ChemSusChem

Leibniz-Institut für Katalyse e.V. an der, Universität Rostock, Albert-Einstein-Straße 29a, 18059, Rostock, Germany.

Published: August 2017

Development of catalytically active materials from biowaste represents an important aspect of sustainable chemical research. Three heterogeneous materials were synthesized from inexpensive biomass-based chitosan and abundant Co(OAc) using complexation followed by pyrolysis at various temperatures. These materials were applied in the catalytic hydrogenation of nitroarenes using molecular hydrogen. A variety of diversely functionalized nitroarenes including some pharmaceutically active compounds were converted into aromatic amines in high yields, with high selectivity, and with excellent functional group tolerance. This green protocol has also been implemented for the synthesis of a biologically important TRPC3 inhibitor.

Download full-text PDF

Source
http://dx.doi.org/10.1002/cssc.201700796DOI Listing

Publication Analysis

Top Keywords

hydrogenation nitroarenes
8
biomass-derived catalysts
4
catalysts selective
4
selective hydrogenation
4
nitroarenes development
4
development catalytically
4
catalytically active
4
active materials
4
materials biowaste
4
biowaste represents
4

Similar Publications

Sintering Ag Nanoclusters on TiO Nanoparticles as an Efficient Catalyst for Nitroarene Reduction.

Materials (Basel)

December 2024

Key Laboratory of Green Chemical Process of Ministry of Education, School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, China.

Polydispersed Ag species-modified TiO samples with abundant oxygen vacancies were successfully prepared through the calcination of atomically precise Ag nanocluster-loaded TiO at an optimal temperature under a nitrogen atmosphere. The ligands of the Ag nanoclusters are removed by extracting lattice oxygen from TiO during the calcination, leading to the formation of CO, SO, and HO vapor. This process simultaneously induces Ag species sintering on the surface of TiO.

View Article and Find Full Text PDF

Herein, we have established the formation of diaryl amide by aminocarbonylation of nitrobenzene with boronic acids. The method works in the catalytic presence of economical and commercially available CuI salt, which was significantly promoted by the FeSe(CO) cluster. Mo(CO) serves as a source of CO, and it also acts as a reductant with a combination of iron cluster.

View Article and Find Full Text PDF

Nanoporous High Entropy Alloy Al-Pt-Pd-Ru as an Efficient Catalyst for One-Pot Reductive Amination of Nitroarenes.

Small

December 2024

State Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, Dalian University of Technology, Dalian, 116024, China.

High entropy alloys (HEAs) are promising heterocatalysts because of their unique physicochemical properties, but research on HEA-catalyzed tandem reactions is lacking. Moreover, limited research on HEAs for molecular transformation has hindered their development. Herein, an unsupported nanoporous HEA Al-Pt-Pd-Ru (HEANPore) prepared using a top-down dealloying method is reported.

View Article and Find Full Text PDF

Precisely Tailoring the Second Coordination Sphere of a Cobalt Single-Atom Catalyst for Selective Hydrogenation of Halogenated Nitroarenes.

Angew Chem Int Ed Engl

November 2024

School of Nuclear Science and Technology, Key Laboratory of Precision and Intelligent Chemistry, National Synchrotron Radiation Laboratory, School of Chemistry and Materials Science, Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, 230026, China.

The development of highly efficient and cost-effective nonprecious metal catalysts for the selective hydrogenation of halogenated nitroarenes is very appealing yet challenging. Here, we demonstrate that the hydrogenation activity and selectivity of Co single-atom catalyst (SAC) can be tuned by tailoring the structure of second coordination sphere via P doping. As revealed by synchrotron radiation-based X-ray absorption spectroscopy characterizations, such a P doping on N-coordinated Co SAC results in the unsymmetric Co-NP coordination structure.

View Article and Find Full Text PDF

This study developed a novel and highly active heterogeneous catalyst of nickel nanoparticles supported on β-cyclodextrin-grafted magnetic FeO nanoparticles (Ni@β-CD@FeO). β-CD, a biodegradable, biocompatible, green, and non-toxic cyclic oligosaccharide, was modified with FeO nanoparticles to create β-CD@FeO. The nickel was then immobilized onto this support.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!