Ismayilova, Sabina Z.Sabina Z.IsmayilovaGuliyeva, Lala Sh.Lala Sh.GuliyevaIsmayilov, Rayyat H.Rayyat H.IsmayilovTagiyev, Dilgam B.Dilgam B.TagiyevValiyev, Fuad F.Fuad F.ValiyevYalcin, BahattinBahattinYalcinMedjidov, Ajdar A.Ajdar A.MedjidovHuseynova, Mansura T.Mansura T.HuseynovaChien, Su-YingSu-YingChienLee, Gene-HsiangGene-HsiangLeePeng, Shie-MingShie-MingPeng2026-02-102026-02-102025-12-12https://scholars.lib.ntu.edu.tw/handle/123456789/735905Through the pyrimidine-modulated hexapyridylpentaamine ligand N2-(pyridin-2-yl)-N6-(6-((6-((6-(pyrimidin-2-ylamino)pyridin-2-yl)amino)pyridin-2-yl)amino)pyridin-2-yl)pyridine-2,6-diamine (H5N11-tpm), a new mononuclear copper(II) complex [Cu(H5N11-tpm)](ClO4)2 (1) were synthesized and structurally characterized. The single crystal X-ray analysis showed distorted trigonal bypyramidal geometry (Addison parameter value τ = 0.69) of the complex (1), which is well consistent with the “inverted type” of ESR spectra (g∥ < g⊥), measured magnetic susceptibility, and electronic spectroscopy studies. The equatorial copper-nitrogen distances (Cu–N(1) = 2.094(9) Å; Cu–N(5) = 2.045(9) Å; Cu–N(9) = 2.214(9) Å), along with the axial Cu–N distances (Cu–N(3) = 1.999(9) Å and Cu–N(7) = 2.001(9) Å), fall well within the range typically reported for Cu(II) complexes that incorporate this type of ligand. All Cu–N distances are short, ranging from 1.999(9) to 2.094(9) Å, which suggests a strong binding affinity of the chelating ligand. The monohelical H5N11-tpm ligand coordinates with the metal atom, exhibiting an all-anti conformation. The extensive hydrogen bonds were observed between the amino groups and uncoordinated perchlorate anions, resulting in the formation of a three-dimensional network (3D) of the complex. The synthesized complex has high potential for the creation of novel cholinesterase inhibitors since it contains a number of pyridine and pyrimidine rings.enaddison parametercopper complexcrystal structurehydrogen bondslong-chain ligandmagnetic measurementmodulated oligo-α-aminopyridine ligandspectroscopyjournal article10.31489/2959-0663/4-25-6