RT info:eu-repo/semantics/article
T1 Templating conformations with cucurbiturils
A1 Thompson, Nathan A.
A1 Barbero San Juan, Héctor
A1 Masson, Eric
AB 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.
PB Royal Society of Chemistry
SN 1359-7345
YR 2019
FD 2019
LK https://uvadoc.uva.es/handle/10324/66291
UL https://uvadoc.uva.es/handle/10324/66291
LA eng
NO Chem. Commun., 2019,55, 12160-12163
NO Producción Científica
DS UVaDOC
RD 13-may-2024