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Prismarenes: A New Class of Macrocyclic Hosts Obtained by Templation in a Thermodynamically Controlled Synthesis

[Image: see text] The novel title macrocycles, based on methylene-bridged 1,5-naphthalene units, have been obtained by template effect in a thermodynamically controlled synthesis. In detail, the prism[5]arene 1 or the prism[6]arene 3 was selectively removed from the equilibrium mixture by using the...

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Detalles Bibliográficos
Autores principales: Della Sala, Paolo, Del Regno, Rocco, Talotta, Carmen, Capobianco, Amedeo, Hickey, Neal, Geremia, Silvano, De Rosa, Margherita, Spinella, Aldo, Soriente, Annunziata, Neri, Placido, Gaeta, Carmine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7993634/
https://www.ncbi.nlm.nih.gov/pubmed/31898458
http://dx.doi.org/10.1021/jacs.9b12216
Descripción
Sumario:[Image: see text] The novel title macrocycles, based on methylene-bridged 1,5-naphthalene units, have been obtained by template effect in a thermodynamically controlled synthesis. In detail, the prism[5]arene 1 or the prism[6]arene 3 was selectively removed from the equilibrium mixture by using the complementary ammonium-templating agent. When only the solvent 1,2-DCE was used, the 1,4-confused derivative 2 was obtained. The prism[5]arene here described shows a deep π-electron-rich aromatic cavity that exhibits a great affinity for the quaternary ammonium guests, originating from favorable cation···π and (+)NC–H···π interactions. This recognition motif is the basis of the templated synthesis of the prism[n]arenes here reported.