Abstract
A series of medium ring-sized macrocycles 4a–4e bearing catechol-type moiety were synthesized readily by direct cyclization of di(acid chloride) 1 with diamine derivatives without high-dilution conditions followed by tandem Claisen rearrangement. Complexation of macrocycles 4 with 1-pyrene-boronic acid yielded their corresponding neutral macrocyclic boron complexes 5 with pyrene unit as fluorophore in high yields. Anion sensing properties of these neutral boron complexes were also investigated.
Sign-in/Register to access full text options 
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 callMore From: Journal of Inclusion Phenomena and Macrocyclic Chemistry
Disclaimer: 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.
