Panja Anangamohan, Paul Sagar, Moreno-Pineda Eufemio, Herchel Radovan, Jana Narayan Ch, Brandão Paula, Novitchi Ghenadie, Wernsdorfer Wolfgang
Department of Chemistry, Gokhale Memorial Girls' College, 1/1 Harish Mukherjee Road, Kolkata-700020, India.
Department of Chemistry, Panskura Banamali College, Panskura RS, WB 721152, India.
Dalton Trans. 2024 Feb 6;53(6):2501-2511. doi: 10.1039/d3dt03557c.
In the last two decades, efforts have been devoted to obtaining insight into the magnetic interactions between Cu and Ln utilizing experimental and theoretical means. Experimentally, it has been observed that the exchange coupling () in Cu-Ln systems is often found to be ferromagnetic for ≥4f metal ions. However, exchange interactions at sub-Kelvin temperatures between Cu and the anisotropic/isotropic Ln ions are not often explored. In this report, we have synthesized a series of heterobimetallic [CuLn(HL)(μ-piv)(piv)] complexes (Ln = Gd (1), Tb (2), Dy (3) and Er (4)) from a new compartmental Schiff base ligand, ,-bis(3-methoxy-5-methylsalicylidene)-1,3-diamino-2-propanol (HL). X-ray crystallographic analysis reveals that all four complexes are isostructural and isomorphous. Magnetic susceptibility measurements reveal a ferromagnetic coupling between the Cu ion and its respective Ln ion for all the complexes, as often observed. Moreover, μ-SQUID studies, at sub-Kelvin temperatures, show S-shaped hysteresis loops indicating the presence of antiferromagnetic coupling in complexes 1-3. The antiferromagnetic interaction is explained by considering the shortest Cu⋯Cu distance in the crystal structure. The nearly closed loops for 1-3 highlight their fast relaxation characteristics, while the opened loops for 4 might arise from intermolecular ordering. CASSCF calculations allow the quantitative assessment of the interactions, which are further supported by BS-DFT calculations.
在过去二十年中,人们致力于通过实验和理论手段深入了解铜(Cu)与镧系元素(Ln)之间的磁相互作用。实验上,已观察到在Cu-Ln体系中,对于≥4f金属离子,交换耦合()通常呈铁磁性。然而,在低于开尔文温度下,Cu与各向异性/各向同性Ln离子之间的交换相互作用却鲜有研究。在本报告中,我们利用一种新型的间隔席夫碱配体,即,-双(3-甲氧基-5-甲基水杨醛)-1,3-二氨基-2-丙醇(HL),合成了一系列异双金属[CuLn(HL)(μ-特戊酸根)(特戊酸根)]配合物(Ln = Gd (1)、Tb (2)、Dy (3) 和 Er (4))。X射线晶体学分析表明,所有这四种配合物均为同构且结构相同。磁化率测量结果显示,与常见情况一样,所有配合物中Cu离子与其相应的Ln离子之间均存在铁磁耦合。此外,在低于开尔文温度下的μ-SQUID研究表明,配合物1-3呈现S形磁滞回线,这表明其中存在反铁磁耦合。通过考虑晶体结构中最短的Cu⋯Cu距离来解释这种反铁磁相互作用。配合物1-3近乎闭合的磁滞回线突出了它们的快速弛豫特性,而配合物4的开放磁滞回线可能源于分子间有序排列。完全活性空间自洽场(CASSCF)计算能够对相互作用进行定量评估,密度泛函理论(BS-DFT)计算进一步支持了这一评估结果。