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Preparation and Properties of Gadolinium Homoleptic Double- and Triple-Decker Complexes Containing Tetrabenzoporphyrin Ligand

机译:含有四苯并卟啉配体的钆分选双和三甲板配合物的制备与性质

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Two novel gadolinium sandwich-type complexes containing tetrabenzoporphyrin (TBP) ligands- Gd(TBP)_2 and Gd(TBP)_3were prepared from porphyrin 1 and Gd(acac)_3. nH_2O under Ar by boiling 1, 2, 4-Tcb for 15~17h and 45-48 h respectively. Their structures are characterized by Uv-Vis, HR-MS and IR. The spectroscopic studies show that their longest-wavelength visible and near-IR absorption bands are obviously red-shifted due to the extension of the π conjugated systems in the TBP ring. The magnetic studies indicate that the observed value of Xm T for Gd(TBP)_2 is close to the combined value of Gd(III) and porphyrin radical anion at room temperature and that antiferromagnetic interaction possibly results from the intramolecular spin exchange between the porphyrin π-radical electron and that the gadolinium f unpaired electrons dominates its magnetic properties over the whole temperature range while there is no magnetic interactions between two Gd(III) ions in Gd(TBP)3 in the range from room temperature down to 20K and very weak antiferromagnetic coupling exsits between two Gd(III) ions below 20K. Since Buchler and co-workers first reported bis (porphyrinato) metal complexes M(Por)_2 such as a cerium~Ⅳ bisporphyrinate, Ce(TPP)_2 in 1983~[1], sandwich-type rare earth complexes containing porphyrin ligands have been the subject of intensive studies because of the unusual physical, spectroscopic, redox, electron transfer, and/or conductivity properties resulting from their strong π-π interactions~[2-3]. Whereas the chemistry and properties of homoleptic sandwich complexes with the same pophyrinato ligands of various lanthanide, actinides and group 4 transition metals have been extensively studied~[4], and the heteroleptic analogus containing mixed macrocyclic ligands have also been described~[5-6] for an intensive investigation of the π-π interactions, actually all of them are confined to the sandwich-type complexes containing meso-substituted porphyrin ligands except for octaethylporphyrin (OEP) or octamethylporphyrin (OMP). Little is known about sandwich-like complexes with aromatic ring-fused porphyrin ligands that contain a more delocalized % system. In this paper, we will describe the preparation, spectroscopic characterization and magnetic properties of two novel gadolinium homoleptic double- and triple-decker sandwich-type complexes with tetrabenzoporphyrin (TBP) ligand (Fig.1) .
机译:_3were从卟啉1和Gd(ACAC)_3制备含有四苯并卟啉(TBP)ligands-钆(TBP)_2和Gd(TBP)两种新的钆夹心型络合物。在Ar下nH_2O通过煮沸1,2,4-TCB为分别为15〜17小时和45-48小时。它们的结构通过UV-Vis,HR-MS和IR表征。该光谱研究表明,它们的最长波长的可见光和近红外吸收带明显红移由于TBP环π共轭系统的扩展。磁性的研究表明,XM T中的Gd(TBP)_2的观测值是接近的Gd(III)的组合值和卟啉在室温下自由基阴离子和反铁磁相互作用可能从卟啉π之间的分子内自旋交换结果 - 基团电子并且该钆˚F不成对电子在整个温度范围内占主导地位其磁特性,同时有下降到20K和非常弱二钆(III)离子之间在钆(TBP)3中的范围内没有磁相互作用从室温下面20K 2的Gd(III)离子之间的反铁磁耦合exsits。由于Buchler及其同事首次报道了双(卟啉)的金属配合物M(POR)_2如在1983年铈〜Ⅳbisporphyrinate,铈(TPP)_2〜[1],含卟啉的配体夹心型稀土配合物已经由于不寻常的物理,光谱,氧化还原,电子转移的深入细致的研究,和/或导电性能的主题从它们的强π-π相互作用造成〜[2-3]。而化学和各种镧系元素,锕系元素和4族过渡金属的相同配体pophyrinato均配型夹心复合物的性质进行了广泛的研究〜[4],和包含混合大环配体的杂analogus也已经被描述〜[5-6 ]为π-π相互作用的深入研究,实际上所有的人只限于含有除了八乙基卟啉(OEP)或octamethylporphyrin(OMP)的内消旋 - 取代的卟啉配位体的夹心型络合物。知之甚少夹层状的与其它具有更多个离域%系统的芳族环稠合的卟啉配体的络合物。在本文中,我们将描述的制备,光谱表征,并用四苯并卟啉(TBP)的配体(图1)的两个新的钆均配型双链和三重双层夹心型复合物的磁特性。

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