Ontology highlight
ABSTRACT:
SUBMITTER: Han Y
PROVIDER: S-EPMC4923850 | biostudies-other | 2016
REPOSITORIES: biostudies-other
Scientific reports 20160628
A series of mono-amide-functionalized pillar[5]arenes with different lengths of N-ω-aminoalkyl groups as the side chain on the rim were designed and synthesized, which all formed pseudo[1]rotaxanes in the crystal state. And these pseudo[1]rotaxanes could be transformed into [1]rotaxanes or open forms in the crystal state. In addition, they were also studied in solution by (1)H NMR spectroscopy. ...[more]