Abstract
A facile synthesis of peri-naphthoindigo (PNI) was reported for the first time from simple precursor. Installation of a chromophore at the peri-position of naphthalene is very unique in terms of synthetic challenges and properties. PNI exists in monoenol form, undergoes halochromism in acidic medium, and displays a wide and strong absorption band (ε = 33390 M-1cm-1) with maxima at 632 nm (chloroform). The dye undergoes oxidation and reduction at +0.30 and -0.58 V (vs Fc/Fc+), respectively, in chloroform.
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.
