A [2]Rotaxane-Based Circularly Polarized Luminescence Switch
Author(s) -
Arthur H. G. David,
Raquel Casares,
Juan M. Cuerva,
Araceli G. Campaña,
Víctor Blanco
Publication year - 2019
Publication title -
journal of the american chemical society
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.9b07143
Subject(s) - chemistry , rotaxane , luminescence , stereocenter , fluorescence , crown ether , covalent bond , hydrogen bond , stereochemistry , enantiomer , photochemistry , supramolecular chemistry , crystallography , molecule , organic chemistry , crystal structure , enantioselective synthesis , optoelectronics , ion , physics , quantum mechanics , catalysis
A rotaxane-based molecular shuttle has been synthesized in which the switching of the position of a fluorescent macrocycle on the thread turns "on" or "off" the circularly polarized luminescence (CPL) of the system while maintaining similar fluorescence profiles and quantum yields in both states. The chiroptical activity relies on the chiral information transfer from an ammonium salt incorporating d- or l-phenylalanine residues as chiral stereogenic covalent units to an otherwise achiral crown ether macrocycle bearing a luminescent 2,2'-bipyrene unit when they interact through hydrogen bonding. Each enantiomeric thread induces CPL responses of opposite signs on the macrocycle. Upon addition of base, the switching of the position of the macrocycle to a triazolium group disables the chiral information transfer to the macrocycle, switching "off" the CPL response. The in situ switching upon several acid/base cycles is also demonstrated.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom