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Enantiopure trinuclear lanthanide(III) complexes: cooperative formation of Ln3(μ3-OH)2 core within the macrocycle.
Autorzy
Rok wydania
2011
Czasopismo
Inorganic Chemistry Communications
Numer woluminu
14
Strony
92-95
DOI
10.1016/j.inoche.2010.09.039
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
The large trioxahexaaza chiral macrocyclic amine L binds three lanthanide(III) ions (Sm(III), Eu(III) and Tm(III)) in such a way that the Ln(III) ions are bridged by the phenolate oxygen atoms of the macrocycle and additional hydroxo bridges. The formation of symmetrical trinuclear complexes is confirmed by 1H NMR, ESI-MS and elemental analyses. X-ray crystal data for the Eu(III) complex reveal the presence of the Ln3(μ3-OH)2 cluster in the centre of the macrocycle. On the other hand, the larger La(III) or Pr(III) lanthanide ions form dinuclear complexes with the macrocycle L under similar conditions. The titration of the macrocycle L with europium(III) nitrate and sodium hydroxide solutions indicates formation of mononuclear and trinuclear species, while no substantial amount of dinuclear complexes are observed. The formation of the Ln3(μ3-OH)2 core in the trinuclear complexes is cooperative, i.e. the binding of the third Ln(III) ion by the macrocycle L is stronger than the binding of the second Ln(III) ion.
Słowa kluczowe
lanthanides, macrocycles, Trinuclear complexes, Chiral complexes, Cooperativity, X-ray crystal structures
Adres publiczny
https://doi.org/10.1016/j.inoche.2010.09.039
Strona internetowa wydawcy
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