Repozytorium

Enantiopure trinuclear lanthanide(III) complexes: cooperative formation of Ln33-OH)2 core within the macrocycle.

Autorzy

Marta Paluch

Katarzyna Ślepokura

Tadeusz Lis

Jerzy Lisowski

Rok wydania

2011

Czasopismo

Inorganic Chemistry Communications

Numer woluminu

14

Strony

92-95

DOI

10.1016/j.inoche.2010.09.039

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

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 Ln33-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 Ln33-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

http://www.elsevier.com

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