Highly Effective N-TiO <sub>2</sub> Supported Pt Catalyst for Selective Hydrogenation of Nitroarenes under Mild Conditions

Heterogeneous catalysts are widely explored in the chemoselective hydrogenation of nitroarenes, but achieving a balance between high activity and selectivity remains a significant challenge. Construction of dual active sites is demonstrated as an efficient strategy to break the scaling relationship. Herein, an efficient N-TiO2 supported Pt catalyst was synthesized, which exhibits better catalytic performance than an undoped Pt/TiO2 catalyst in the hydrogenation of p-chloronitrobenzene, yielding 97.8% conversion and >99% selectivity of p-chloroaniline under the conditions of 30 °C and 0.5 MPa, as well as good stability and substrate universality. Various characterizations and theoretical calculations disclose that the formed Ti–N species can stabilize the metal Pt and enhance the adsorption of a nitro group, which further cooperates with metal Pt to endow the catalyst with good catalytic performance under mild conditions.

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Publication Details

Journal
Industrial & Engineering Chemistry Research
Published
2025-10-18
DOI
https://doi.org/10.1021/acs.iecr.5c02830
Citations
1
Primary Topic
Nanomaterials for catalytic reactions
Type
article
Field-Weighted Citation Impact
0.94
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article

Highly Effective N-TiO 2 Supported Pt Catalyst for Selective Hydrogenation of Nitroarenes under Mild Conditions

Xinwei Du, Yujing Ren, Haisheng Wei, Jing Li
1 citations
Industrial & Engineering Chemistry Research
Nanomaterials for catalytic reactions
0.94
article

Highly Effective N-TiO 2 Supported Pt Catalyst for Selective Hydrogenation of Nitroarenes under Mild Conditions

Xinwei Du, Yujing Ren, Haisheng Wei, Jing Li
article en
1 citations

Abstract

Heterogeneous catalysts are widely explored in the chemoselective hydrogenation of nitroarenes, but achieving a balance between high activity and selectivity remains a significant challenge. Construction of dual active sites is demonstrated as an efficient strategy to break the scaling relationship. Herein, an efficient N-TiO2 supported Pt catalyst was synthesized, which exhibits better catalytic performance than an undoped Pt/TiO2 catalyst in the hydrogenation of p-chloronitrobenzene, yielding 97.8% conversion and >99% selectivity of p-chloroaniline under the conditions of 30 °C and 0.5 MPa, as well as good stability and substrate universality. Various characterizations and theoretical calculations disclose that the formed Ti–N species can stabilize the metal Pt and enhance the adsorption of a nitro group, which further cooperates with metal Pt to endow the catalyst with good catalytic performance under mild conditions.

Industrial & Engineering Chemistry ResearchVol. 64(43)
Northwestern Polytechnical University (CN), Yantai University (CN), Institute of Catalysis and Petrochemistry (RU)
Openalex Percentile: Top 20%
Nanomaterials for catalytic reactions
0.94
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