The bis-linking of tetrathiafulvalene (TTF) to C60: Towards the control of electron transfer between π-donors and C60
✍ Scribed by C. Boulle; J.M. Rabreau; P. Hudhomme; M. Cariou; M. Jubault; A. Gorgues; J. Orduna; J. Garín
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 134 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The bis-linking of a tetrathiafulvalene (ITF) to C60 is carried out by [4+2] Diels-Alder cycloaddition of C60 to the 2,3-dimethylene-TTF 2, this transient diene being generated by crown-6 mediated dibromine reductive elimination of the 2,3-bis(bromomethyl)'FYF 3. The C60-TTF target cycloadduct la is characterized by spectroscopy and electrochemical study.
📜 SIMILAR VOLUMES
The title reaction carried out from S-propargyl xanthate 3 or 2-(thi)oxo-4,5bis(bromomethyl)-l,3-dithioles 4a and 4b with C60 is presented and some conversions of the synthesized cycloadducts 2a and 2b in several 1,3-dithiole derivatives are described.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
We have measured the third-order susceptibility v h3i ijkl of a C 60 -TTF compounds in tetrahydrofuran (THF) solutions using the degenerate four wave mixing technique at k ¼ 532 nm in the picosecond regime. To know the physical nature of the optical non-linearities, we separate the electronic and nu