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Iminopyrrole‐Based Self‐Assembly: A Route to Intrinsically Flexible Molecular Links and Knots.
- Source :
-
Angewandte Chemie International Edition . Jan2024, Vol. 63 Issue 4, p1-12. 12p. - Publication Year :
- 2024
-
Abstract
- The use of 2,5‐diformylpyrrole in self‐assembly reactions with diamines and Zn(II)/Cd(II) salts allowed the preparation of [2]catenane, trefoil knot, and Borromean rings. The intrinsically dynamic nature of the diiminopyrrole motif rendered all of the formed assemblies intramolecularly flexible. The presence of diiminopyrrole revealed new coordination motifs and influenced the host–guest chemistry of the systems, as illustrated by hexafluorophosphate encapsulation by Borromean rings. [ABSTRACT FROM AUTHOR]
- Subjects :
- *HOST-guest chemistry
*SUPRAMOLECULAR chemistry
*DIAMINES
*CATENANES
Subjects
Details
- Language :
- English
- ISSN :
- 14337851
- Volume :
- 63
- Issue :
- 4
- Database :
- Academic Search Index
- Journal :
- Angewandte Chemie International Edition
- Publication Type :
- Academic Journal
- Accession number :
- 174782102
- Full Text :
- https://doi.org/10.1002/anie.202316489