g-C3N4/γ-Fe2O3/TiO2/Pd: a new magnetically separable photocatalyst for visible-light-driven fluoride-free Hiyama and Suzuki–Miyaura cross-coupling reactions at room temperature

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Título: g-C3N4/γ-Fe2O3/TiO2/Pd: a new magnetically separable photocatalyst for visible-light-driven fluoride-free Hiyama and Suzuki–Miyaura cross-coupling reactions at room temperature
Autor/es: Jahanshahi, Roya | Khazaee, Asma | Sobhani, Sara | Sansano, Jose M.
Grupo/s de investigación o GITE: Síntesis Asimétrica (SINTAS)
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Química Orgánica | Universidad de Alicante. Instituto Universitario de Síntesis Orgánica
Palabras clave: g-C3N4/γ-Fe2O3/TiO2/Pd | Magnetically separable photocatalyst | Visible-light-driven | Fluoride-free | Hiyama and Suzuki–Miyaura | Cross-coupling reactions
Área/s de conocimiento: Química Orgánica
Fecha de publicación: 10-jun-2020
Editor: Royal Society of Chemistry
Cita bibliográfica: New Journal of Chemistry. 2020, 44: 11513-11526. doi:10.1039/D0NJ01599G
Resumen: In this paper, a new visible-light harvesting photocatalyst denoted as g-C3N4/γ-Fe2O3/TiO2/Pd was successfully fabricated and fully characterized by different techniques including FT-IR, XPS, XRD, TEM, SEM, elemental mapping, VSM, DRS, and ICP analysis. The as-prepared catalyst was utilized as an efficient magnetically separable photocatalyst in the fluoride-free Hiyama and Suzuki–Miyaura cross-coupling reactions at room temperature under visible light irradiation. By using this approach good to excellent yields of biaryls were achieved from the reaction of various aryl iodides/bromides and even chlorides as highly challenging substrates, which are more available and cheaper than aryl iodides and bromides, with triethoxyphenylsilane or phenylboronic acid. The superior photocatalytic activity of g-C3N4/γ-Fe2O3/TiO2/Pd could be attributed to the synergistic catalytic effects of Pd nanoparticles and g-C3N4/γ-Fe2O3/TiO2. Utilizing a sustainable and safe light source, no need to use any additive or heat, using an eco-friendly solvent and long-term stability and magnetic recyclability of the catalyst for at least seven successive runs are the advantages that support the current protocol towards green chemistry.
Patrocinador/es: Financial support of this project by the University of Birjand Research Council and the XPS facilities of the University of Alicante is appreciated.
URI: http://hdl.handle.net/10045/108062
ISSN: 1144-0546 (Print) | 1369-9261 (Online)
DOI: 10.1039/D0NJ01599G
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2020
Revisión científica: si
Versión del editor: https://doi.org/10.1039/D0NJ01599G
Aparece en las colecciones:INV - SINTAS - Artículos de Revistas

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