| Literature DB >> 26136350 |
Tomoki Ogoshi1,2, Ryuta Sueto3, Kumiko Yoshikoshi3, Yoko Sakata3, Shigehisa Akine4, Tada-aki Yamagishi3.
Abstract
Activated perethylated pillar[5]arene crystals show an unexpected alkane-shape- and -length-selective gate-opening behavior. Activated crystals were obtained upon removing solvents from perethylated pillar[5]arene crystals by heating. The activated crystals could quantitatively take up n-alkanes with carbon chains containing more than five carbon atoms as a consequence of their gate-opening pressure. As the chain length of the n-alkanes increased, the gate pressure decreased. A transformation into a herringbone structure was induced when n-hexane was used as a guest. By contrast, cyclic and branched alkanes were not taken up and could not induce a crystal transformation because they were too large to fit in the cavities of the pillar[5]arene. Alkane-shape-selective molecular recognition of pillar[5]arenes in the solution state was translated into the vapor/crystal state.Entities:
Keywords: alkanes; crystals; host-guest chemistry; macrocyclic compound; pillar[n]arenes
Year: 2015 PMID: 26136350 DOI: 10.1002/anie.201503489
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336