Abstract
Novel sulfonamide [2]catenanes were successfully prepared through a self-templation approach. The catenated skeletons were confirmed by traveling-wave ion-mobility spectrometry (TWIMS) combined with gradient tandem mass spectroscopy (gMS2). Moreover, two pyrene units were further introduced into the [2]catenane through the alkylation reaction of the sulfonamide moieties, resulting in the successful synthesis of a novel pyrene-functionalized [2]catenane which displayed a switchable optical output controlled by cation-induced conformation transformation.
| Original language | English |
|---|---|
| Pages (from-to) | 4994-5001 |
| Number of pages | 8 |
| Journal | Organic Chemistry Frontiers |
| Volume | 8 |
| Issue number | 18 |
| DOIs | |
| State | Published - 21 Sep 2021 |