Cargando…
Mechanically Interlocked Chiral Self‐Templated [2]Catenanes from 2,6‐Bis(1,2,3‐triazol‐4‐yl)pyridine (btp) Ligands
We report the efficient self‐templated formation of optically active 2,6‐bis(1,2,3‐triazol‐4‐yl)pyridine (btp) derived homocircuit [2]catenane enantiomers. This represents the first example of the enantiopure formation of chiral btp homocircuit [2]catenanes from starting materials consisting of a cl...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457180/ https://www.ncbi.nlm.nih.gov/pubmed/34106499 http://dx.doi.org/10.1002/chem.202101773 |
Sumario: | We report the efficient self‐templated formation of optically active 2,6‐bis(1,2,3‐triazol‐4‐yl)pyridine (btp) derived homocircuit [2]catenane enantiomers. This represents the first example of the enantiopure formation of chiral btp homocircuit [2]catenanes from starting materials consisting of a classical chiral element; X‐ray diffraction crystallography enabled the structural characterization of the [2]catenane. The self‐assembly reaction was monitored closely in solution facilitating the characterization of the pseudo‐rotaxane reaction intermediate prior to mechanically interlocking the pre‐organised system via ring‐closing metathesis. |
---|