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Chiral Open-[60]Fullerene Ligands with Giant Dissymmetry Factors.
Hashikawa, Yoshifumi; Okamoto, Shu; Sadai, Shumpei; Murata, Yasujiro.
Afiliação
  • Hashikawa Y; Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan.
  • Okamoto S; Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan.
  • Sadai S; Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan.
  • Murata Y; Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan.
J Am Chem Soc ; 144(41): 18829-18833, 2022 Oct 19.
Article em En | MEDLINE | ID: mdl-36169337
ABSTRACT
The optical resolution of open-[60]fullerenes has been limited to only one example since 1998, while the recent advances revealed the excellence of fullerenes as revisited chiral functional materials. Different from conventional chiral induction on [60]fullerene by a multiple-functionalization, a random disruption of the spherical π-conjugation is avoidable for open-[60]fullerenes. Moreover, the macrocyclic orifices enable a metal coordination which endows modulated electronic structures on chiral chromophores. Herein, we showcase Li+-coordination behavior and optical resolution of three chiral open-[60]fullerene ligands, showing a giant dissymmetry factor up to 0.20 owing to a congenital topology of the spherical π-conjugation.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article