American Chemical Society
jo070030l_si_008.cif (23.1 kB)

Isomeric 2,6-Pyridino-Cryptands Based on Dibenzo-24-crown-8

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posted on 2007-04-27, 00:00 authored by Harry W. Gibson, Hong Wang, Carla Slebodnick, Joseph Merola, W. Scott Kassel, Arnold L. Rheingold
Cryptands 4 and 5 were synthesized from cis- and trans-bis(hydroxymethylbenzo)-24-crown-8 by reaction with pyridine-2,6-dicarboxylic acid chloride in 42 and 48% yields, respectively. The new cryptands form pseudorotaxanes with the paraquat derivative N,N‘-bis(β-hydroxyethyl)-4,4‘-bipyridinium bis(hexafluorophosphate) (“paraquat diol”, 6):  Ka = 1.0 × 104 and 1.4 × 104 M-1, respectively. The cryptands also form complexes with ammonium hexafluorophosphate. Formation of the paraquat/cryptand-based pseudorotaxanes can be switched off and on in a controllable manner on the basis of the cryptands' abilities to complex KPF6 strongly, providing a new mechanism for control of molecular shuttles. K+ displaces paraquat diol from the cryptands, converting yellow-orange solutions to colorless; however, addition of 18-crown-6 binds the KPF6 and allows the colored cryptand−paraquat complex to reform. Crystal structures are reported for both cryptands, both paraquat diol-based pseudorotaxanes, both NH4PF6 complexes, and both KPF6 complexes.