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Guest-Induced Reversible Transformation between an Azulene-Based Pd2L4 Lantern-Shaped Cage and a Pd4L8 Tetrahedron.
Walther, Alexandre; Regeni, Irene; Holstein, Julian J; Clever, Guido H.
Afiliação
  • Walther A; Department of Chemistry and Chemical Biology, TU Dortmund University, Otto Hahn Straße 6, 44227 Dortmund, Germany.
  • Regeni I; Department of Chemistry and Chemical Biology, TU Dortmund University, Otto Hahn Straße 6, 44227 Dortmund, Germany.
  • Holstein JJ; Leiden Institute of Chemistry, Leiden University, Einsteinweg 55, 2333CC Leiden, The Netherlands.
  • Clever GH; Department of Chemistry and Chemical Biology, TU Dortmund University, Otto Hahn Straße 6, 44227 Dortmund, Germany.
J Am Chem Soc ; 145(46): 25365-25371, 2023 Nov 22.
Article em En | MEDLINE | ID: mdl-37960849
ABSTRACT
Azulene, a blue structural isomer of naphthalene, is introduced as the backbone for a new family of Pd(II)-based self-assemblies. Three organic ligands, equipped with varying donor groups, produce three [Pd2L4] cages of different cavity dimensions. Unexpectedly, the addition of organic disulfonate guests to the smallest lantern-shaped cage (featuring pyridine donors) led to a rapid and quantitative transformation to a distorted-tetrahedral [Pd4L8] species. On the contrary, [Pd2L4] cages formed from ligands with isoquinoline donors either just encapsulated the guests or showed no interaction. The tetrahedral species could be fully reverted back to its original [Pd2L4] topology by capturing the guest by another, stronger binding [Pd2L'4] coordination cage, narcissistically self-sorting from the first cage. The azulenes, serving as colored hydrocarbon backbones of minimal atom count, allow one to follow cage assembly and guest-induced transformation by the naked eye. Furthermore, we propose that their peculiar electronic structure influences the system's assembly behavior.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article