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Croconamides: a new dual hydrogen bond donating motif for anion recognition and organocatalysis.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Jeppesen, Anne S. Nielsen, Bjarne E. Larsen, Dennis Akselsen, Olivia M. Sølling, Theis I. Brock-Nannestad, Theis Pittelkow, Michael |
| Copyright Year | 2017 |
| Abstract | We introduce bis-aryl croconamides as a new member in the family of dual hydrogen bonding anion receptors. In this study a series of croconamides are synthesised, and the selectivity for anion binding is investigated (Cl- > Br- > I- in CH2Cl2). The croconamides exhibit different structures in the crystal phase depending on the substituents on the aromatic rings, and furthermore, the crystal structure revealed the presence of tautomers. DFT calculations elucidated the complex structures formed upon addition of anion to the croconamides, confirming the order of association constants towards the halogen anions. The use of croconamides as organocatalysts in a proof-of-concept study is demonstrated in the formation of THP ethers. In addition to this, construction of a Hammet plot further elucidates the mechanism in action on formation of THP ethers. |
| Starting Page | 2784 |
| Ending Page | 2790 |
| Page Count | 7 |
| File Format | PDF HTM / HTML |
| DOI | 10.1039/c7ob00441a |
| PubMed reference number | 28272644 |
| Journal | Medline |
| Volume Number | 15 |
| Issue Number | 13 |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/c7/ob/c7ob00441a/c7ob00441a1.pdf |
| Alternate Webpage(s) | http://www.pittelkow.kiku.dk/publications/59_croconamiced%20obc/c7ob00441a.pdf |
| Alternate Webpage(s) | https://doi.org/10.1039/c7ob00441a |
| Journal | Organic & biomolecular chemistry |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |
