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首页> 外文期刊>ACS Omega >Synthesis and Characterization of N,N′-Bismesityl Phenanthrene-9,10-diimine and Imine–Nitrone
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Synthesis and Characterization of N,N′-Bismesityl Phenanthrene-9,10-diimine and Imine–Nitrone

机译:N,N'-双联苯并菲-9,10-二亚胺和亚胺-硝酮的合成与表征

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The sterically bulky compounds N,N′-bismesityl phenanthrene-9,10-diimine [1] and imine–nitrone [2] were synthesized. To the best of our knowledge, this is the first report of the synthesis of a bulky steric imine–nitrone accessed from the secondary ketimine using urea hydrogen peroxide over methyltrioxorhenium catalyst. Purified compounds were characterized using 1H and 13C NMR, high-resolution mass spectrometry, and infrared spectrometry. We report the first crystal structure of compound 1. Detailed IR bands of compounds 1 and 2 were assigned by comparing experimentally measured spectra to individually animated modes of quantum mechanically computed spectra. We believe these compounds may be of use as bidentate ligands in the synthesis of novel organometallic compounds. The asymmetric N and O coordination sites of compound 2 might impart interesting electronic effects to organometallic compounds compared to the symmetric N,N′-coordination sites of compound 1.
机译:合成了空间体积较大的化合物N,N'-双甲氧基菲-9,10-二亚胺[1]和亚胺-硝酮[2]。据我们所知,这是有关使用甲基三氧or鎓催化剂上的过氧化氢尿素从仲酮亚胺中合成的庞大的空间亚胺-硝酮的首次报道。使用1 H和13 C NMR,高分辨率质谱和红外光谱对纯化的化合物进行表征。我们报告了化合物1的第一个晶体结构。通过将实验测量的光谱与量子力学计算的光谱的各个动画模式进行比较,确定了化合物1和2的详细红外波段。我们相信这些化合物可以用作新型有机金属化合物合成中的双齿配体。与化合物1的对称N,N'配位点相比,化合物2的不对称N和O配位点可能会给有机金属化合物带来有趣的电子效应。

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