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Coordination Complexes of a Neutral 1,2,4-Benzotriazinyl Radical Ligand: Synthesis, Molecular and Electronic Structures, and Magnetic Properties

机译:中性1,2,4-苄基三嗪基自由基配体的配位化合物:合成,分子和电子结构,以及磁性能

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摘要

A series of d-block metal complexes of the recently reported coordinating neutral radical ligand 1-phenyl-3-(pyrid-2-yl)-1,4-dihydro-1,2,4-benzotriazin-4-yl (1) was synthesized. The investigated systems contain the benzotriazinyl radical 1 coordinated to a divalent metal cation, Mn-II, Fe-II, Co-II, or Ni-II, with 1,1,1,5,5,5-hexafluoroacetylacetonato (hfac) as the auxiliary ligand of choice. The synthesized complexes were fully characterized by single-crystal X-ray diffraction, magnetic susceptibility measurements, and electronic structure calculations. The complexes [Mn(1)(hfac)(2)] and [Fe(1)(hfac)(2)] displayed antiferromagnetic coupling between the unpaired electrons of the ligand and the metal cation, whereas the interaction was found to be ferromagnetic in the analogous Ni-II complex [Ni(1)(hfac)(2)]. The magnetic properties of the complex [Co(1)(hfac)(2)] were difficult to interpret owing to significant spin-orbit coupling inherent to octahedral high-spin Co-II metal ion. As a whole, the reported data clearly demonstrated the favorable coordinating properties of the radical 1, which, together with its stability and structural tunability, make it an excellent new building block for establishing more complex metal-radical architectures with interesting magnetic properties.
机译:最近报道的配位中性自由基配体1-苯基-3-(吡啶-2-基)-1,4-二氢-1,2,4-苯并三嗪-4-基的一系列d嵌段金属配合物(1)是合成的。所研究的系统包含与二价金属阳离子Mn-II,Fe-II,Co-II或Ni-II配位的苯并三嗪基自由基1,其中1,1,1,5,5,5,5-六氟乙酰丙酮(hfac)为选择的辅助配体。合成的配合物通过单晶X射线衍射,磁化率测量和电子结构计算得到充分表征。配合物[Mn(1)(hfac)(2)和[Fe(1)(hfac)(2)]在未配对的配体电子与金属阳离子之间显示出反铁磁耦合,但发现相互作用是铁磁性的在类似的Ni-II络合物[Ni(1)(hfac)(2)]中。复杂的[Co(1)(hfac)(2)]的磁性很难解释,因为八面体高自旋Co-II金属离子固有的自旋轨道耦合。总体而言,所报告的数据清楚地表明了基团1的良好配位性能,以及其稳定性和结构可调性,使其成为建立具有令人感兴趣的磁性能的更复杂的金属自由基结构的极佳新构件。

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