64028-06-4Relevant articles and documents
Synthesis and chemistry of perfluoro macrocycles
Lin,Lin,Clark,Lagow,Larson,Simonsen,Lynch,Brodbelt,Maleknia,Liou
, p. 5172 - 5179 (2007/10/02)
The perfluoro macrocycles perfluoro-18-crown-6, perfluoro-12-crown-4, perfluoro-15-crown-5, perfluoro-cyclohexano-15-crown-5, perfluorodicyclohexano-18-crown-6, perfluorodicyclohexano-24-crown-8, and perfluoro-4,7,13,16,21,24-hexaoxa-1, 10-diazabicyclo[8,8,8] hexacosane (perflorocyptand [222] have been prepared by carefully controlled elemental fluorination. Although they are much weaker bases than their hydrocarbon analogues, these perfluoromacrocycles are very stable materials which should have a number of applications. The crystal structures of perfluoro-18-crown-6 and of a perfluorodicyclohexano-18-crown-6 isomer are reported. Gas-phase studies with several perfluoro crown ethers and with the perfluorocryptand [222] have shown that such macrocycles tenaciously bind O2- and F-. Perfluoro crown ethers and cryptands coordinate anions preferentially over cations. The collisionally activated mass spectra of several perfluoro macrocylic ions are described.
The First Perfluoro Crown Ethers
Lin, Wen-Huey,Bailey, Webb I.,Lagow, Richard J.
, p. 1350 - 1352 (2007/10/02)
The first perfluoro crown ethers, perfluoro 18-crown-6, perfluoro 15-crown-5, and perfluoro 12-crown-4, have been prepared by carefully controlled elemental fluorination; although they are weaker bases than their parent compounds, perfluoro crown ethers are materials which will have a number of applications.
