Heterogeneous iron-based
catalysts governing selectivity for the
reduction of nitroarenes and aldehydes have received tremendous attention
in the arena of catalysis, but relatively less success has been achieved.
Herein, we report a green strategy for the facile synthesis of a lignin
residue-derived carbon-supported magnetic iron (γ-Fe
2
O
3
/LRC-700) nanocatalyst. This active nanocatalyst exhibits
excellent activity and selectivity for the hydrogenation of nitroarenes
to anilines, including pharmaceuticals (e.g., flutamide and nimesulide).
Challenging and reducible functionalities such as halogens (e.g.,
chloro, iodo, and fluoro) and ketone, ester, and amide groups were
tolerated. Moreover, biomass-derived aldehyde (e.g., furfural) and
other aromatic aldehydes were also effective for the hydrogenation
process, often useful in biomedical sciences and other important areas.
Before and after the reaction, the γ-Fe
2
O
3
/LRC-700 nanocatalyst was thoroughly characterized by X-ray diffraction
(XRD), N
2
adsorption–desorption, X-ray photoelectron
spectroscopy (XPS), high-resolution transmission electron microscopy
(HR-TEM), Raman spectroscopy, and thermogravimetric analysis (TGA).
Additionally, the γ-Fe
2
O
3
/LRC-700 nanocatalyst
is stable and easily separated using an external magnet and recycled
up to five cycles with no substantial drop in the activity. Eventually,
sustainable and green credentials for the hydrogenation reactions
of 4-nitrobenzamide to 4-aminobenzamide and benzaldehyde to benzyl
alcohol were assessed with the help of the CHEM21 green metrics toolkit.