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Synthesis, Properties of Gadolinium Double-Decker Sandwich-Type Complex Containing Tetrabenzoporphyrin Ligand

机译:合成,钆双层夹层型络合物的性质含四苯卟啉配体

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A novel gadolinium double-decker sandwich-type complex with tetrabenzoporphyrin (TBP) ligands-Gd(TBP)2 was synthesized by the reaction of porphyrin 1 with Gd(acac)3. nH2O in boiling 1, 2, 4-Tcb for 15~17 h under Ar. Its structure is characterized byUv-Vis-NIR and HR-MS. The spectroscopic properties show that the longest-wavelength visible band (600-800 nm) and the strong near-IR absorption band centered near 1340 nm of Gd (TBP)2 complex are obviously red-shifted due to the extension of the π conjugated systems derived from the linear benzoannulation in the TBP ring. The magnetic studies also indicate that the observed value of χMT of Gd(TBP)2 complex is close to the combined value of Gd(III) and porphyrin radical anion at room temperature, and antiferromagnetic interaction that possibly results from the intramolecular spin exchange between the porphyrin π-radical electron, and the gadolinium f unpaired electrons dominates its magnetic properties over the whole temperature range.
机译:通过卟啉1与Gd(ACAC)3的反应合成了具有四苯基卟啉(TBP)配体-GD(TBP)2的新型钆双层夹层型复合物。 NH2O在沸腾1,2,4-TCB的AR下15〜17小时。 其结构特征在于uv-vis-nir和hr-ms。 光谱性质表明,由于π共轭系统的延伸,最长波长可见带(600-800nm)和中心近1340nm的近1340nm近的近1340nm近的近红外吸收带显然是红移的 从TBP环中的线性苯并渗透。 磁性研究还表明,观察到的Gd(TBP)2络合物的χmt值接近室温下的Gd(III)和卟啉基团阴离子的组合值,以及可能由分子内旋转交换之间产生的反铁磁性相互作用 卟啉π-自由基电子和钆不配对电子在整个温度范围内占据其磁性。

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