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Synthesis of Tetrathia–Oligothiophene Macrocycles

[Image: see text] The synthesis of six tetrathia–oligothiophene macrocycles is described with modest ring-closing yields between 21 and 55%. Single-crystal X-ray studies of four of the macrocycles indicated that encapsulated solvent or guest molecules were possible. A variety of guest molecules were...

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Detalles Bibliográficos
Autores principales: Press, David J., Gendy, Chris, Pasalkar, Samruddhi, Schechtel, Shauna, Heyne, Belinda, Sutherland, Todd C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648883/
https://www.ncbi.nlm.nih.gov/pubmed/31459556
http://dx.doi.org/10.1021/acsomega.8b03444
Descripción
Sumario:[Image: see text] The synthesis of six tetrathia–oligothiophene macrocycles is described with modest ring-closing yields between 21 and 55%. Single-crystal X-ray studies of four of the macrocycles indicated that encapsulated solvent or guest molecules were possible. A variety of guest molecules were explored for inclusion complexes via NMR, absorption, emission, and X-ray techniques. The solution-phase inclusion complexes were uninformative; yet the solid-state experiments revealed that solvent exchangeable channels exist through the macrocyclic pores.