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Chasing the Mond Cation: Synthesis and Characterization of the Homoleptic Nickel Tetracarbonyl Cation and its Tricarbonyl-Nitrosyl Analogue.
Schmitt, Manuel; Mayländer, Maximilian; Goost, Julian; Richert, Sabine; Krossing, Ingo.
Afiliação
  • Schmitt M; Institut für Anorganische und Analytische Chemie and Freiburger Materialforschungszentrum (FMF), Albert-Ludwigs-Universität Freiburg, Albertstr. 21, 79104, Freiburg, Germany.
  • Mayländer M; Institut für Physikalische Chemie, Albert-Ludwigs-Universität Freiburg, Albertstr. 21, 79104, Freiburg, Germany.
  • Goost J; Institut für Anorganische und Analytische Chemie and Freiburger Materialforschungszentrum (FMF), Albert-Ludwigs-Universität Freiburg, Albertstr. 21, 79104, Freiburg, Germany.
  • Richert S; Institut für Physikalische Chemie, Albert-Ludwigs-Universität Freiburg, Albertstr. 21, 79104, Freiburg, Germany.
  • Krossing I; Institut für Anorganische und Analytische Chemie and Freiburger Materialforschungszentrum (FMF), Albert-Ludwigs-Universität Freiburg, Albertstr. 21, 79104, Freiburg, Germany.
Angew Chem Int Ed Engl ; 60(27): 14800-14805, 2021 Jun 25.
Article em En | MEDLINE | ID: mdl-33734545
130 years after Mond discovered the first homoleptic carbonyl complex Ni(CO)4 , we report on a [Ni(CO)4 ].+ salt as the first synthesis of any homoleptic nickel carbonyl cation in the condensed phase. It was prepared by oxidation of nickel metal with the synergistic oxidant Ag[F{Al(ORF )3 }2 ]/0.5 I2 (RF =C(CF3 )3 ) in CO atmosphere. This D2d -symmetric metalloradical represents the last missing entry among the structurally characterized homoleptic carbonyl cations of Groups 6 to 11. Additionally, the nickel tricarbonyl-nitrosyl cation [Ni(CO)3 (NO)]+ was obtained by usage of NO[F{Al(ORF )3 }2 ] and all products were fully characterized by means of IR, Raman, NMR/EPR, single crystal and powder XRD.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article