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Alumanyl-Samarium(II): Synthesis, Characterization, and Reactivity Studies.
Feng, Genfeng; Chan, Ka Lok; Lin, Zhenyang; Yamashita, Makoto.
Afiliación
  • Feng G; Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Aichi, Japan.
  • Chan KL; Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon 999077, Hong Kong.
  • Lin Z; Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon 999077, Hong Kong.
  • Yamashita M; Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Aichi, Japan.
J Am Chem Soc ; 146(11): 7204-7209, 2024 Mar 20.
Article en En | MEDLINE | ID: mdl-38505938
ABSTRACT
Metal-metal bonded species involving lanthanides are intriguing but rare. The recently reported salt metathesis reaction of an Al anion and SmI2(thf)2 yields novel heterometallic compound possessing two distinctive Al-Sm bonds. Although the Al-Sm bonds were considerably long [3.518(1) and 3.543(1) Å], DFT calculations indicated polar character of the Alδ--Smδ+ bonds. This is the first example of lanthanide species containing X-type Al ligands. Reactivity studies have demonstrated that the introduction of Sm(II) produces unique reactivity. The reaction with carbodiimide led to an insertion of carbodiimide into the Al-Sm bonds and reductive coupling of carbodiimide to create an oxalamidinate moiety, facilitated by Sm(II). Exposure of the Al-Sm-Al complex toward ethylene furnished a Sm(II) salt of anionic aluminacyclopropane that was spontaneously isomerized to a 1,4-dialuminacyclohexane derivative. The important role of Sm(II) to facilitate the ring expansion through an alkyl-relay mechanism was elucidated by DFT calculations.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2024 Tipo del documento: Article País de afiliación: Japón