Ruthenium Nitrides: Redox Chemistry and Photolability of the Ru–Nitrido Group
✍ Scribed by Lucia Bonomo; Euro Solari; Rosario Scopelliti; Carlo Floriani
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 99 KB
- Volume
- 113
- Category
- Article
- ISSN
- 0044-8249
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## on the occasion of his 65th birthday In spite of the high interest in halide salts as promoters for a variety of carbon ± carbon bond-forming reactions, [1±4] little is known about the reactivity of simple carbonyl(halo)ruthenium(ii) complexes such as the interconvertible species 1 ± 3 (Scheme
## Abstract The reactions of V^V^O(O‐__i__Pr)~3~ with [PS3′]H~3~ and [PS3]H~3~ {[PS3′]H~3~ = P(C~6~H~3~‐5‐Me‐2‐SH)~3~, [PS3]H~3~ = P(C~6~H~4~‐2‐SH)~3~} led to the formation of [V^IV^(L)] [L = P2S4′ (1a), P2S4 (1b)], where L was formed by the oxidative coupling of two PS3′ or PS3 ligands by a disulf
Ahstraet-Wf-assembled monolayers of the alkanethiols having OH, COOH and NH, terminal group were formed on a gold electrode via a sulfur attachment. The effects of their terminal groups on the redox responses of Fe&N):-, Ru(NH&+ and l,l'-ferrocenedimethanol (FcDM') aqueous solutions were investigate