**Macrocyclic Complexes of Lanthanides: Stability and Electrochemical Behaviour in Methanol and Propylene Carbonate** The stabilities of the 1:1 complexes of the trivalent lanthanides with the diazapolyoxamacrocycles (2.1.) and (2.2.1.) in anhydrous methanol and propylene carbonate have been determ
Stabilité dans le méthanol et propriétés thermodynamiques de transfert des cryptates de certains cations de transition et de métaux lourds
✍ Scribed by Par Bernard Spiess; Françoise Arnaud-Neu; Marie-José Schwing-Weill
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- German
- Weight
- 448 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Stability in Methanol and Thermodynamic Transfer Properties of the Cryptates of some Transition Cations and Heavy Metals
The nature and stability of the macrocyclic and macrobicyclic complexes of Ag^+^, Cd^2+^, and Pb^2+^ (M^n+^) with 21, 22, 211, 221 and 222 in anhydrous methanol 0.05M in Et~4~N^+^ClO^−^~4~, at 25° (see Scheme) have been determined by potentiometry and spectrophotometry. Binuclear complexes M~2~L^2n+^ have been observed in all cases, besides the mononuclear ML^n+^ complexes. The macrobicyclic 1:1 complexes ML^n+^ exhibit an important ‘cryptate effect’ with M^n+^=Ag^+^, Pb^2+^ and Cd^2+^, but not with Cu^2+^ and Zn^2+^; their stability is in all cases maximum with 221.
The applicability to our results of the recent extrathermodynamic hypothesis involving ML^n+^ cryptates is examined.
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