Abstract
Abstract 2,3,4,5-Tetra(2-thienyl)cyclopentadienone and the related compounds, here first synthesized, show large bathochromic shift of visible absorptions and appreciably higher amphoteric redox properties than tetraphenylcyclopentadienone; 2-thienyl groups at 2,5-positions exert stronger substituent effects than those at 3,4-positions.
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.
