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Inne
Structural variations in Co(II), Co(III) and Zn(II) complexes of a chiral triphenolic macrocycle
Autorzy
Rok wydania
2025
Czasopismo
Numer woluminu
273
Strony
117472/1-117472/12
DOI
10.1016/j.poly.2025.117472
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
Five homonuclear cobalt(II) and zinc(II) complexes and two mixed-valence Co(II)/Co(III) coordination species derived from the enantiomers of the macrocycle H3L were synthesized, characterized by spectroscopic methods and their X-ray crystal structures were determined. The large macrocyclic amine L3− composed of three phenol moieties and three trans-1,2-diaminocyclohexane units can accommodate three Co(II), Co(III) or Zn(II) ions in three N2O2 compartments, forming [M3L]n+ type complexes. The geometry of these complexes is different for the Zn(II) and Co(II) ions and depends on the counteranion used. Additionally, this macrocycle binds only two metal ions in its partly deprotonated (H2L)− form to give complexes of the type [M2(H2L)]n+. Amine H2L− also forms a tetranuclear [M4(H2L)2]n+ complex, where two macrocyclic units are additionally connected by bridging anions. XRD structures of seven additional coordination species that were isolated as single crystals are also presented.
Słowa kluczowe
Macrocyclic complexes, Polynuclear complexes, Co(II), Zn(II), Chiral ligands, Coordination chemistry, Magnetic properties
Adres publiczny
http://dx.doi.org/10.1016/j.poly.2025.117472
Strona internetowa wydawcy
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