| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5222585 | Tetrahedron | 2009 | 5 Pages |
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.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
