Wydział Chemii

Jan Janczak

Tomasz Paćkowski

Janusz Gregoliński

Jerzy Lisowski

2023

Polyhedron

244

116628/1-116628/7

10.1016/j.poly.2023.116628

Naukowa

Angielski

Artykuł

An extended macrocyclic amine L derived from the [6+6] condensation of trans-1,2-diaminocyclohexane and 2,6-diformylpyridine contains 18 nitrogen atoms in its main cycle. All of these atoms can be engaged in the formation of polynuclear complexes with transition metal ions and the macrocycle L is able to bind six Cu(II), Ni(II) or Zn(II) ions within its interior. X-ray crystal structures of these complexes indicate variable coordination numbers of metal ions as well as various conformations adopted by the macrocyclic ligand. In the hexanuclear Cu(II) complex with coordinated nitrate anions Cu(II) ions are hexacoordinate and exhibit highly distorted octahedral geometry, while in analogous complexes with coordinated sulphate anions Cu(II) ions are pentacoordinate of distorted square pyramid geometry. Both complexes are relatively symmetric having (approximate) S₆ axis and adopt a circular doughnut shape with a central void not occupied by metal ions. The NMR spectrum of the zinc(II) derivative also reflects the symmetrical coordination. In contrast, the macrocycle L is squeezed and less symmetric in the octanuclear chloride derivative where two additional Cu(II) ions are linked to a hexanuclear macrocyclic unit via chloride bridges. The macrocycle is also squeezed in the hexanuclear Ni(II) complex containing metal ions of approximate octahedral geometry. In all three Cu(II) complexes the macrocycle provides N₃ donor set for each metal ion, while in the Ni(II) complex alternating N₃ and N₄ environments of the metal ions are observed.

Macrocyclic complexes, Polynuclear complexes, Nickel(II), Copper(II), Crystal structure

http://dx.doi.org/10.1016/j.poly.2023.116628

http://www.elsevier.com