Reactions of dibenzotetraaza [14]annulene Ni(II) complexes 1 and 2 with oxalyl chloride and chiral terpene alcohols (( -)menthol, (-)borneol), and the Cinchona alkaloid (quinine) afforded new mono and disubstituted derivatives bearing corresponding ester groups at the meso positions. The demetallati
β¦ LIBER β¦
Chemically-modified electrodes based on new metal-dibenzotetraaza [14] annulenes
β Scribed by B. Keita; Y.W. Lu; L. Nadjo
- Publisher
- Elsevier
- Year
- 1994
- Tongue
- English
- Weight
- 616 KB
- Volume
- 367
- Category
- Article
- ISSN
- 1572-6657
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The electrochemical treatment of an electropolymerized (Ni"L), thin film (where L represents 5,7,12,14-tetramethyl-dibenzo[b, i]-I ,4,8,1 Itetraaza [I41 annulene) gives rise to a nickel-based catalytic deposit on conducting substrates [glassy carbon (GC), platinum, or gold electrodes], which shows s