Cation complexation behavior of pyrene-and anthracene-appended new crown ether derivatives

Z Wang, SH Chang, TJ Kang - Spectrochimica Acta Part A: Molecular and …, 2008 - Elsevier
Pyrene-and anthracene-appended new crown ether derivatives have been synthesized by
Schiff's base reaction, and cation complexation behavior was investigated by fluorescence …

Synthesis of Novel Chiral C 2-symmetric Diaza-18-crown-6 Ether Derivatives and their Enantioselective Recognition of Amino Acid Derivatives

Y Turgut, N Demirel, H Hoşgören - Journal of inclusion phenomena and …, 2006 - Springer
Abstract New chiral diaza-18-crown-6 ether derivatives, 5 and 6 were synthesized from (R)-(-
)-2-amino-1-bütanol. These chiral artificial receptors exhibit pronounced chiral recognition …

Estimation of τ value in proton NMR relaxation times of dibenzo diaza 18-crown-6 ether derivative in solution

A Yılmaz, MZ Köylü, H Budak - Chemical physics letters, 2006 - Elsevier
Spin–lattice (T1) and spin–spin (T2) relaxation times of seven peaks in dibenzo diaza 18-
crown-6 ether derivative were measured at 300K with a Bruker 400MHz NMR spectrometer …

[PDF][PDF] Temperature dependence of NMR T1 relaxation of dibenzo diaza 18-crown-6 ether derivative in solution

MZ Koylu, H Budak - Asian Journal of Chemistry, 2007 - researchgate.net
Spin-lattice relaxation times in one of dibenzo diaza 18-crown-6 ether derivative were
measured vs. increasing temperature. The relaxation times (ln T1) were fitted vs. l/T over a …

[PDF][PDF] 1H NMR Study of Chiral Monoaza-15-crown-5 Ether Derivative by Relaxation Time T1

M Askin, MZ Koylu, M Tutsi - Asian Journal of Chemistry, 2008 - researchgate.net
Measurement of spin-lattice relaxation time T1 has been performed for the chiral monoaza-
15-crown-5 ether derivative as a function of temperature. Activation energies Ea and …