Year-end Sale % OFF 
Abstract
Two novel chiral fluorescence calix[4]arenes functionalized at the lower rim with diphenylethylenediamine and thiourea units were synthesized and examined for their enantioselective recognition abilities by the fluorescence and 1H NMR spectra in DMSO. The results indicate that 1 and 2 both formed a 1:1 complex with amino alcohol and exhibit good enantioselective fluorescent responses for phenylglycinol (receptor 1 K L/K D = 4.85, ΔΔG0 = − 3.90 kJ mol− 1).
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
