The reaction of (diaqua)(N,NЈ-ethylene-bis(salicylidiniminato)manganese(III) with aqueous sulphite buffer results in the formation of the corresponding mono sulphito complex, [Mn(Salen)(SO 3 )] Ϫ (S-bonded isomer) via three distinct paths: (i) Mn(Salen)(OH 2 ) 2 ϩ ϩ HSO 3 Ϫ : (k 1 ); (ii) Mn(Salen)(
✦ LIBER ✦
Binuclear Homoleptic Manganese(III,III) and Manganese(IV,III) Complexes with Deprotonated D-Mannose from Aqueous Solution
✍ Scribed by Andreas Geisselmann; Peter Klüfers; Bernd Pilawa
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 113 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0044-8249
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✦ Synopsis
Just a "reducing" sugar-namely, D-mannose-is a starting material in the synthesis of a mixed-valence complex of manganese in the oxidation states +III and +IV. Ba [Mn Mn (β-D-ManfH ) ]Cl⋅14 H O (Manf=mannofuranose; the structure of the anion is shown on the right) is prepared in aqueous solution by oxidation of an analogous Mn complex with oxygen. In neutral solutions the Mn Mn binuclear complex is formed by disproportionation of the Mn precursor.
📜 SIMILAR VOLUMES
Kinetics and mechanism of the reaction o
✍
A. C. Dash; A. Das
📂
Article
📅
1999
🏛
John Wiley and Sons
🌐
English
⚖ 173 KB
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