Abstract
A series of tetrathiafulvalene (TTF) derivatives functionalized by one or two β-diketonatoboron difluoride groups were synthesized through the addition of borontrifluoride to TTF substituted by one or two acetylacetone functions. The influence of the β-diketonatoboron difluoride moiety on the redox properties of the TTF has been investigated by cyclic voltammetry.
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 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.
