Abstract
A series of di-, tri-, and tetraferrocenylarenes were synthesized by using the nickel- and palladium-catalyzed cross coupling reactions of ferrocenylzinc chloride with the corresponding di-, tri-, and tetrahalogenoarenes. Redox properties of these ferrocenylarenes were studied by cyclic voltammetry in order to examine the intramolecular interaction between the ferrocenyl substituents.
Original language | English |
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Pages (from-to) | 35-36 |
Number of pages | 2 |
Journal | Chemistry Letters |
Issue number | 1 |
DOIs | |
Publication status | Published - 1997 Jan 1 |
Externally published | Yes |
ASJC Scopus subject areas
- Chemistry(all)