| Literature DB >> 29251391 |
Tomoki Ogoshi1,2,3, Kazuki Saito1, Ryuta Sueto1, Ryosuke Kojima1, Yukie Hamada1, Shigehisa Akine1,3, Adhitya Mangala Putra Moeljadi4, Hajime Hirao2,4,5, Takahiro Kakuta1, Tada-Aki Yamagishi1.
Abstract
Activated crystals of pillar[6]arene produced by removing the solvent upon heating were able to take up branched and cyclic alkane vapors as a consequence of their gate-opening behavior. The uptake of branched and cyclic alkane vapors by the activated crystals of pillar[6]arene induced a crystal transformation to form one-dimensional channel structures. However, the activated crystals of pillar[6]arene hardly took up linear alkane vapors because the cavity size of pillar[6]arene is too large to form stable complexes with linear alkanes. This shape-selective uptake behavior of pillar[6]arene was further utilized for improving the research octane number of an alkane mixture of isooctane and n-heptane: interestingly, the research octane number was dramatically improved from a low research octane number (17 %) to a high research octane number (>99 %) using the activated crystals of pillar[6]arene.Entities:
Keywords: alkanes; host-guest chemistry; macrocyclic compounds; pillar[n]arenes; separation
Year: 2018 PMID: 29251391 DOI: 10.1002/anie.201711575
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336