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Rapid one-pot synthesis of magnetically separable Fe3O4-Pd nanocatalysts: a highly reusable catalyst for the Suzuki-Miyaura coupling reaction.
Xiao, Xiangyun; Lee, Sunhee; Ma, Hyeonjong; Yang, Jiwoong; Han, Won-Sik; Yu, Taekyung.
Afiliação
  • Xiao X; Department of Chemical Engineering, College of Engineering, Integrated Engineering Major, Kyung Hee University, Yongin 17104, Korea. tkyu@khu.ac.kr.
  • Lee S; Department of Chemistry, Seoul Women's University, 01797, Korea. wshan@swu.ac.kr.
  • Ma H; Department of Energy Science and Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Republic of Korea.
  • Yang J; Energy Science and Engineering Research Center, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Republic of Korea.
  • Han WS; Department of Energy Science and Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Republic of Korea.
  • Yu T; Energy Science and Engineering Research Center, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Republic of Korea.
Dalton Trans ; 51(30): 11485-11490, 2022 Aug 02.
Article em En | MEDLINE | ID: mdl-35833526
Heterogeneous catalysts comprising noble metals and magnetic materials allow a straightforward separation from a reaction using an external magnet and are recovered easily. In this study, we synthesized magnetic Fe3O4-Pdn hybrid heterogeneous catalysts via a rapid one-pot aqueous-phase method. The synthesized Fe3O4-Pd NPs dispersed well with small size (∼50 nm), maintaining high magnetic responsiveness, and showed high reactivity and reusability for the Suzuki-Miyaura coupling reaction between aryl halides and phenylboronic acid. The synthesized Fe3O4-Pd50 catalyst could be recycled at least ten times with no significant loss of catalytic activity by external magnet separation.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article