Anion and pH dependent molecular motion by a halogen bonding [2]rotaxane
Author(s) -
Harry A. Klein,
Heike Kuhn,
Paul D. Beer
Publication year - 2019
Publication title -
chemical communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.837
H-Index - 333
eISSN - 1364-548X
pISSN - 1359-7345
DOI - 10.1039/c9cc04752b
Subject(s) - rotaxane , chemistry , protonation , halogen bond , ion , chloride , hydrogen bond , halogen , conjugated system , photochemistry , bistability , molecule , stereochemistry , crystallography , supramolecular chemistry , materials science , organic chemistry , polymer , alkyl , optoelectronics
A bistable [2]rotaxane containing a halogen bonding benzimidazole-iodotriazole station directly conjugated to a naphthalimide station axle component is demonstrated to undergo macrocycle shuttling translocation only upon both protonation and chloride anion recognition. A naked-eye detectable colour response results from the co-conformational change of the host structure.
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