TY - JOUR A1 - Klose, Jennifer A1 - Severin, Tobias A1 - Hahn, Peter A1 - Jeremies, Alexander A1 - Bergmann, Jens A1 - Fuhrmann, Daniel A1 - Griebel, Jan A1 - Abel, Bernd A1 - Kersting, Berthold T1 - Coordination chemistry and photoswitching of dinuclear macrocyclic cadmium-, nickel-, and zinc complexes containing azobenzene carboxylato co-ligands JF - Beilstein Journal of Organic Chemistry PY - 2019/// VL - 15 SP - 840 EP - 851 SN - 1860-5397 DO - 10.3762/bjoc.15.81 PB - Beilstein-Institut JA - Beilstein J. Org. Chem. UR - https://doi.org/10.3762/bjoc.15.81 KW - azobenzene carboxylates KW - cadmium KW - complexes KW - macrocyclic ligands KW - nickel KW - zinc N2 - The synthesis of mixed-ligand complexes of the type [M2L(μ-L')]+, where L represents a 24-membered macrocyclic hexaaza-dithiophenolate ligand, L' is an azobenzene carboxylate co-ligand, and M = Cd(II), Ni(II) or Zn(II), is reported. A series of new complexes were synthesized, namely [M2L(μ-L')]+ (L' = azo-H, M = Cd (1), Ni (2); L' = azo-OH, M = Zn (3), Ni (4); L' = azo-NMe2, M = Zn (5), Cd (6), Ni (7); L' = azo-CO2Me, M = Cd (8), Ni (9)), and characterized by elemental analysis, electrospray ionization mass spectrometry (ESIMS), IR, UV–vis and NMR spectroscopy (for diamagnetic Zn and Cd complexes) and X-ray single crystal structure analysis. The crystal structures of 3' and 5–8 display an isostructural series of compounds with bridging azobenzene carboxylates in the trans form. The paramagnetic Ni complexes 2, 4 and 7 reveal a weak ferromagnetic exchange interaction with magnetic exchange coupling constant values between 21 and 23 cm−1 (H = −2JS1S2). Irradiation of 1 with λ = 365 nm reveals a photoisomerization of the co-ligand from the trans to the cis form. ER -