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Double Chalcogen Bonding Recognition Arrays in Solution.
Romito, Deborah; Kählig, Hanspeter; Tecilla, Paolo; Sosso, Gabriele C; Bonifazi, Davide.
Afiliación
  • Romito D; Department of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.
  • Kählig H; Department of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.
  • Tecilla P; Dipertimento di Scienze Chimiche e Farmaceutiche, Università degli Studi di Trieste, Via Giorgieri 1, 34127, Trieste, Italy.
  • Sosso GC; Department of Chemistry, University of Warwick, CV4 7AL, Coventry, UK.
  • Bonifazi D; Department of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.
Chemistry ; 30(60): e202401346, 2024 Oct 28.
Article en En | MEDLINE | ID: mdl-39058415
ABSTRACT
N-substituted pyridino-based congeners of Ebselen, named here as Pyrselen, incorporating proximal Se and N atoms, undergo dimerization in solution and the solid state through a dual donor-acceptor arrangement of chalcogen bonding sites. Dimerization constants were measured within the 5-50 M-1 range. Computational studies on the dimers depict a notable charge-transfer contribution to the association, validating Pyrselen as an effective scaffold for designing chalcogen-bonding-based recognition motifs.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Austria