Cobalt Nanoparticles Supported on TiO2 for Highly Selective Formation of N-Benzylideneanilines from Nitroarenes and Benzaldehyde via Reductive Imination Reaction

Author:

González-Vera Daniela1ORCID,Bustamante Tatiana M.2ORCID,Díaz de León J. Noé3ORCID,Torres Cecilia C.4ORCID,Campos Cristian H.1ORCID

Affiliation:

1. Departamento de Fisicoquímica, Facultad de Ciencias Químicas, Universidad de Concepción, Concepción 4070371, Chile

2. Departamento de Ingeniería Química, Facultad de Ingeniería, Universidad de Concepción, Concepción 4070409, Chile

3. Centro de Nanociencias y Nanotecnología, Universidad Nacional Autónoma de México, Ensenada 22860, BC, Mexico

4. Departamento de Ciencias Químicas, Facultad de Ciencias Exactas, Universidad Andres Bello, Autopista Concepción-Talcahuano 7100, Talcahuano 4300866, Chile

Abstract

The search for active, inexpensive, and stable heterogeneous catalysts to produce desired imines in fine chemistry presents an ongoing challenge for both academia and industry. This work reports the utilization of Co nanoparticles supported on TiO2 derived from the H2-assisted reduction of the perovskite-type mixed oxide CoTiO3. The entire preparation process is operationally simple and straightforward, enabling scalability for practical applications. The resulting catalyst comprises metallic cobalt nanoparticles responsible for the hydrogenation process, whereas the TiOx thin layer surrounding the cobalt promotes the adsorption of C=O, thereby enhancing the formation of desired products. Notably, at lower temperatures, the reaction yields the target imine product. Our study demonstrates a synergistic effect between nitrobenzene and benzaldehyde in the presence of a Co-TiOx interface, which reduces the apparent activation energy for the hydrogenation of the-NO2 group. Furthermore, under moderate reaction conditions, the catalytic system offers applicability to various nitrobenzene compounds substituted at the 4-position and benzaldehyde, resulting in high yields of the corresponding imines with electron-density-donating substituent groups. Finally, the catalyst exhibits facile separation for subsequent reuse, displaying moderate stability with minimal selectivity for the desired product.

Funder

Agencia Nacional de Investigación y Desarrollo

Publisher

MDPI AG

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