mercure, on constate que cc sont les raies du groupe 1850 A, et les raies 1941,1971 et 2000 A qui sont surtout responsables de la production ci'ozone. Bien des arguments exposes ci-dessus ont pu 6tre d6duits des mesures effectu6es dans le laboratoire de spectroscopic L I'Universiti. de B&le, du Pro
Synthèse électrochimique de complexes Ni(O)-diazabutadiène
✍ Scribed by José Coulombeix; Franz-Peter Emmenegger
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- German
- Weight
- 342 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Electrochemical Synthesis of the Ni(O)‐Diazabutadiene Complexes
The electrochemical reduction of Ni salts in the presence of diazabutadiene ligands (DAB = RNCHCHNR, R = t‐Bu, o‐xylyl, p‐anisoyl, p‐tolyl) has been studied in DMF by cyclic voltammetry and rotating disc polarography. In solutions containing DAB and halide X^−^, Ni(II) can be reduced to Ni(DAB)~2~, and the features of this reduction agree with a mechanism where the second DAB replaces X^−^ in the coordination sphere of Ni only after its reduction to Ni(O). Rather concentrated (≃ 0.1M) solutions of NiBr~2~ · DME and DAB in DMF have been electrolyzed without a supporting electrolyte, making the isolation of the product Ni(DAB)~2~ particularly easy. Thus, gram quantities of Ni(DAB)~2~ can be conveniently prepared within a few hours.
📜 SIMILAR VOLUMES
Several synthetic methods of bifunctional germylenes GeYz (Y = RO, PhO, RS, CH3CO0, Acac; YZ = OCHZCHZO, SCHZCHZS) or GeXY (Y = RO, X = C1; Y = RS, X = CI; Y = Acac, X = Cl) such as exchange reactions, dechlorhydratation reactions and nucleophilic substitutions from GeClz . dioxane are described.
Synthises dans le clomairie des hydrocarbures canc6rigines VI (\*) Nouvellc syntlibse du 1 :2,3:4-Dibenzofluor&ne (\*\*) par R.H. MARTIN et S. VASSART (Rruxelles) S u i u M A n y . -A new synthesis of 1:2,5:4-ctibenzfluorene (X) is This synthesis involves the following steps : a) condensation of 2-