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Thompson, Nathan A. Barbero San Juan, Héctor Masson, Eric 2024-02-16T12:16:58Z 2024-02-16T12:16:58Z 2019 Chem. Commun., 2019,55, 12160-12163 1359-7345 https://uvadoc.uva.es/handle/10324/66291 10.1039/C9CC06766C 12160 81 12163 Chemical Communications 55 1364-548X The trans- and cis conformations of 5,5′-substituted 2,2′-dithiophenes can be stabilized when those are secured with two Cucurbit[8]uril macrocycles (CB[8]) on top of rigid 2,6- and 2,7-substituted naphthalenes, which respectively mimic the trans and cis conformations of the dithiophene. The substituents are Pt(II) terpyridyl groups bearing CB[8]-binding sites at their 4′-position, as those form dimers in the presence of the macrocycle through Pt–Pt and dispersive interactions between the terpyridyl ligands. eng info:eu-repo/semantics/restrictedAccess http://creativecommons.org/licenses/by-nc-nd/4.0/ Royal Society of Chemistry Attribution-NonCommercial-NoDerivatives 4.0 Internacional Templating conformations with cucurbiturils info:eu-repo/semantics/article