Biswas Soumava, Havlicek Lubomir, Nemec Ivan, Salitros Ivan, Mandal Leena, Neugebauer Petr, Kuppusamy Senthil Kumar, Ruben Mario
Dr. Vishwanath Karad MIT World Peace University Survey No, 124, Paud Rd, Kothrud, Pune, 411038, Maharashtra, India.
Central European Institute of Technology, Brno University of Technology, Purkynova 656/123, 61200, Brno, Czech Republic.
Chem Asian J. 2024 Sep 2;19(17):e202400574. doi: 10.1002/asia.202400574. Epub 2024 Jul 30.
A new Co(II) complex, [Co(NCS)(L)] (1) has been synthesized based on levamisole (L) as a new ligand. Single-crystal X-ray diffraction analyses confirm that the Co(II) ion is having a distorted tetrahedral coordination geometry in the complex. Notably strong intramolecular S⋅⋅⋅S and S⋅⋅⋅N interactions has been confirmed by employing Quantum Theory of Atoms in Molecules (QTAIM). These intramolecular interactions occur among the sulfur and nitrogen atoms of the levamisole ligands and also the nitrogen atoms of the thiocyanate. Direct current (dc) magnetic analyses reveal presence of zero field splitting (ZFS) and large magnetic anisotropy on Co(II). Detailed ab initio ligand field theory calculations quantitatively predicted the magnitude of ZFS. Prominent field-induced single-ion magnet (SIM) behavior was observed for 1 from dynamic magnetization measurements. Slow magnetic relaxation follows an Orbach mechanism with the effective energy barrier U=29.6 (7) K and relaxation time τ=1.4 (4)×10 s.
基于左旋咪唑(L)作为新配体合成了一种新型钴(II)配合物[Co(NCS)(L)](1)。单晶X射线衍射分析证实,配合物中的Co(II)离子具有扭曲的四面体配位几何结构。值得注意的是,通过分子中的原子量子理论(QTAIM)证实了强烈的分子内S⋅⋅⋅S和S⋅⋅⋅N相互作用。这些分子内相互作用发生在左旋咪唑配体的硫和氮原子之间以及硫氰酸盐的氮原子之间。直流(dc)磁性分析表明Co(II)存在零场分裂(ZFS)和大的磁各向异性。详细的从头算配体场理论计算定量预测了ZFS的大小。通过动态磁化测量观察到1具有显著的场诱导单离子磁体(SIM)行为。慢磁弛豫遵循Orbach机制,有效能垒U = 29.6(7)K,弛豫时间τ = 1.4(4)×10 s。