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Development of iron-based single atom materials for general and efficient synthesis of amines.
Ma, Zhuang; Kuloor, Chakreshwara; Kreyenschulte, Carsten; Bartling, Stephan; Malina, Ondrej; Haumann, Michael; Menezes, Prashanth W; Zboril, Radek; Beller, Matthias; Jagadeesh, Rajenahally V.
Affiliation
  • Ma Z; Leibniz Institute for Catalysis, Catalysis, GERMANY.
  • Kuloor C; Leibniz Institute for Catalysis, Catalysis, GERMANY.
  • Kreyenschulte C; Leibniz Institute for Catalysis, Analytics, GERMANY.
  • Bartling S; Leibniz Institute for Catalysis, Analytics, GERMANY.
  • Malina O; Palacky University Olomouc, Chemistry, CZECH REPUBLIC.
  • Haumann M; FU Berlin, Chemistry, GERMANY.
  • Menezes PW; Helmholtz Zentrum Berlin, Chemistry, GERMANY.
  • Zboril R; Palacky University Olomouc, Chemistry, CZECH REPUBLIC.
  • Beller M; Leibniz-Institut für Katalyse, Homogeneous Catalysis, Albert-Einstein-Straße 29a, 18059, Rostock, GERMANY.
  • Jagadeesh RV; Leibniz Institute for Catalysis, Catalysis, GERMANY.
Angew Chem Int Ed Engl ; : e202407859, 2024 Jun 24.
Article in En | MEDLINE | ID: mdl-38923207
ABSTRACT
Heterogeneous catalysts with highly active and at the same time stable isolated metal sites constitute a key factor for the advancement of sustainable and cost-effective chemical synthesis. In particular, the development of more practical, and durable iron-based materials is of central interest for organic synthesis, especially for the preparation of chemical products related to life science applications. Here, we report the preparation of Fe-single atom catalysts (Fe-SACs) entrapped in N-doped mesoporous carbon support with unprecedented potential in the preparation of different kinds of amines. The synthetic protocol of Fe-SACs is based on primary pyrolysis of Fe-nitrogen complexes on SiO2 and subsequent removal of silica resulting in the formation of unique mesoporous N-doped carbon support with the pore size controlled by the size of the original silica nanoparticles. The resulting stable and reusable Fe-SACs allow for the reductive amination of a broad range of aldehydes and ketones with ammonia and amines to produce diverse primary, secondary, and tertiary amines including N-methylated products as well as drugs, agrochemicals, and other biomolecules (amino acid esters and amides) utilizing green hydrogen.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2024 Document type: Article Affiliation country: