首页> 外文期刊>Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry >MIXED-LIGAND LANTHANIDE COMPLEXES .8. PARAMAGNETIC SHIFT INDUCED BY PR(FOD)3PZ AND PR(FOD)3PYZ IN THE NMR SPECTRUM OF DI-N-BUTYL ETHER
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MIXED-LIGAND LANTHANIDE COMPLEXES .8. PARAMAGNETIC SHIFT INDUCED BY PR(FOD)3PZ AND PR(FOD)3PYZ IN THE NMR SPECTRUM OF DI-N-BUTYL ETHER

机译:混合配体镧系元素化合物.8。二正丁基醚的核磁共振谱中PR(FOD)3PZ和PR(FOD)3PYZ引起的顺磁位移

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Two adducts of Pr(fod)(3), Pr(fod)(3)pz and Pr(fod)(3)pyz, where pz stands for pyrazole and pyz for pyrazine, have been scanned as potential NMR shift reagents using di-n-butyl ether. Although di-n-butyl is a very weak donor, complexes associate with the base and induce large hyperfine isotropic shifts in the resonance frequencies of the magnetic substrate nuclei. The t-butyl resonances of the complexes are strongly shifted upfield in the presence of the substrate. This observation, together with the fact that the spectrum of the substrate is unaffected by the addition of any amount of the complexes, are taken as evidence that the specific coordination of the complexes to the substrate occurs through the agency of the oxygen lone-pair electrons. [References: 14]
机译:已对使用Pr-fod(3)的Pr(fod)(3)pz和Pr(fod)(3)pyz(其中pz代表吡唑和pyz代表吡嗪)的两个加合物作为潜在的NMR位移试剂进行了扫描正丁基醚。尽管二正丁基是非常弱的供体,但络合物与碱结合并在磁性底物核的共振频率中引起大的超细各向同性位移。在底物的存在下,配合物的叔丁基共振强烈地向高场偏移。该观察结果以及底物的光谱不受添加任何量的配合物影响的事实,被视为证明配合物与底物的特定配位是通过氧孤对电子的作用而发生的。 。 [参考:14]

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