Narayan Ch. Jana, Zvonko Jagličić, Radovan Herchel, Paula Brandão, Rakhi Nandy and Anangamohan Panja*,
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All three complexes were structurally characterized in which Cu<sup>II</sup> and Ln<sup>III</sup> ions occupy inner N<sub>2</sub>O<sub>2</sub> and outer O<sub>2</sub>O′<sub>2</sub> compartments of the doubly deprotonated Schiff base ligand, respectively. Moreover, another closely related complex [Cu(L)]<sub>2</sub>[CuDy(L)(OAc)(NO<sub>3</sub>)(H<sub>2</sub>O)](NO<sub>3</sub>)·5H<sub>2</sub>O (<b>4</b>) has been synthesized starting from the same Schiff base ligand H<sub>2</sub>L to examine the effect of the coordination environment around the Dy<sup>III</sup> ion on the dynamic magnetic behavior in these systems. Variable-temperature direct-current magnetic susceptibility measurements suggest a ferromagnetic exchange interaction between Cu<sup>II</sup> and Ln<sup>III</sup> ions, especially in <b>1</b>–<b>3</b>, which is further supported by DFT calculations. However, alternating-current magnetic susceptibility measurements resulted in the most interesting part of this report. Remarkably, despite the isotropic nature of the Gd<sup>III</sup> ion, compound <b>1</b> displayed slow relaxation of the magnetization in the presence of an applied field together with its anisotropic counterparts Tb<sup>III</sup> (<b>2</b>) and Dy<sup>III</sup> (<b>3</b>). Based on the literature study, this is a rare system in which Cu<sup>II</sup>–Gd<sup>III</sup> complexes showed single-molecule magnet behavior. Moreover, theoretical calculations were also performed by means of DFT and CASSCF levels of theory to obtain precise information on the magnetic exchange coupling between Cu<sup>II</sup> and Ln<sup>III</sup> ions together with the distinct magnetic dynamics in these systems.</p>","PeriodicalId":34,"journal":{"name":"Crystal Growth & Design","volume":"24 18","pages":"7537–7548 7537–7548"},"PeriodicalIF":3.2000,"publicationDate":"2024-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Insight into the Magnetic Exchange Interactions and Anisotropy in Heterobimetallic CuII–LnIII Complexes: A Rare Example of Cu–Gd Single-Molecule Magnets\",\"authors\":\"Narayan Ch. Jana, Zvonko Jagličić, Radovan Herchel, Paula Brandão, Rakhi Nandy and Anangamohan Panja*, \",\"doi\":\"10.1021/acs.cgd.4c0075210.1021/acs.cgd.4c00752\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The exploration of heterometallic complexes containing both 3d and 4f metal ions has been on the rise with advancements in the field of 3d–4f single-molecule magnets. The motivation stemmed from early investigations into the Cu<sup>II</sup>–Ln<sup>III</sup> systems, particularly the Cu<sup>II</sup>/Gd<sup>III</sup> one, that revealed a ferromagnetic interaction between these ions, irrespective of the complex’s topology or nuclearity. In this context, we have synthesized three new isostructural and isomorphous [CuLn(L)(NO<sub>3</sub>)<sub>3</sub>(H<sub>2</sub>O)] complexes (Ln = Gd (<b>1</b>), Tb (<b>2</b>), and Dy (<b>3</b>)) derived from a compartmental Schiff base ligand H<sub>2</sub>L. All three complexes were structurally characterized in which Cu<sup>II</sup> and Ln<sup>III</sup> ions occupy inner N<sub>2</sub>O<sub>2</sub> and outer O<sub>2</sub>O′<sub>2</sub> compartments of the doubly deprotonated Schiff base ligand, respectively. Moreover, another closely related complex [Cu(L)]<sub>2</sub>[CuDy(L)(OAc)(NO<sub>3</sub>)(H<sub>2</sub>O)](NO<sub>3</sub>)·5H<sub>2</sub>O (<b>4</b>) has been synthesized starting from the same Schiff base ligand H<sub>2</sub>L to examine the effect of the coordination environment around the Dy<sup>III</sup> ion on the dynamic magnetic behavior in these systems. Variable-temperature direct-current magnetic susceptibility measurements suggest a ferromagnetic exchange interaction between Cu<sup>II</sup> and Ln<sup>III</sup> ions, especially in <b>1</b>–<b>3</b>, which is further supported by DFT calculations. However, alternating-current magnetic susceptibility measurements resulted in the most interesting part of this report. Remarkably, despite the isotropic nature of the Gd<sup>III</sup> ion, compound <b>1</b> displayed slow relaxation of the magnetization in the presence of an applied field together with its anisotropic counterparts Tb<sup>III</sup> (<b>2</b>) and Dy<sup>III</sup> (<b>3</b>). Based on the literature study, this is a rare system in which Cu<sup>II</sup>–Gd<sup>III</sup> complexes showed single-molecule magnet behavior. Moreover, theoretical calculations were also performed by means of DFT and CASSCF levels of theory to obtain precise information on the magnetic exchange coupling between Cu<sup>II</sup> and Ln<sup>III</sup> ions together with the distinct magnetic dynamics in these systems.</p>\",\"PeriodicalId\":34,\"journal\":{\"name\":\"Crystal Growth & Design\",\"volume\":\"24 18\",\"pages\":\"7537–7548 7537–7548\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-09-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Crystal Growth & Design\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.cgd.4c00752\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Crystal Growth & Design","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.cgd.4c00752","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Insight into the Magnetic Exchange Interactions and Anisotropy in Heterobimetallic CuII–LnIII Complexes: A Rare Example of Cu–Gd Single-Molecule Magnets
The exploration of heterometallic complexes containing both 3d and 4f metal ions has been on the rise with advancements in the field of 3d–4f single-molecule magnets. The motivation stemmed from early investigations into the CuII–LnIII systems, particularly the CuII/GdIII one, that revealed a ferromagnetic interaction between these ions, irrespective of the complex’s topology or nuclearity. In this context, we have synthesized three new isostructural and isomorphous [CuLn(L)(NO3)3(H2O)] complexes (Ln = Gd (1), Tb (2), and Dy (3)) derived from a compartmental Schiff base ligand H2L. All three complexes were structurally characterized in which CuII and LnIII ions occupy inner N2O2 and outer O2O′2 compartments of the doubly deprotonated Schiff base ligand, respectively. Moreover, another closely related complex [Cu(L)]2[CuDy(L)(OAc)(NO3)(H2O)](NO3)·5H2O (4) has been synthesized starting from the same Schiff base ligand H2L to examine the effect of the coordination environment around the DyIII ion on the dynamic magnetic behavior in these systems. Variable-temperature direct-current magnetic susceptibility measurements suggest a ferromagnetic exchange interaction between CuII and LnIII ions, especially in 1–3, which is further supported by DFT calculations. However, alternating-current magnetic susceptibility measurements resulted in the most interesting part of this report. Remarkably, despite the isotropic nature of the GdIII ion, compound 1 displayed slow relaxation of the magnetization in the presence of an applied field together with its anisotropic counterparts TbIII (2) and DyIII (3). Based on the literature study, this is a rare system in which CuII–GdIII complexes showed single-molecule magnet behavior. Moreover, theoretical calculations were also performed by means of DFT and CASSCF levels of theory to obtain precise information on the magnetic exchange coupling between CuII and LnIII ions together with the distinct magnetic dynamics in these systems.
期刊介绍:
The aim of Crystal Growth & Design is to stimulate crossfertilization of knowledge among scientists and engineers working in the fields of crystal growth, crystal engineering, and the industrial application of crystalline materials.
Crystal Growth & Design publishes theoretical and experimental studies of the physical, chemical, and biological phenomena and processes related to the design, growth, and application of crystalline materials. Synergistic approaches originating from different disciplines and technologies and integrating the fields of crystal growth, crystal engineering, intermolecular interactions, and industrial application are encouraged.