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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Synthesis and molecular structures of nitrosoarene metalloporphyrin complexes of ruthenium
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Synthesis and molecular structures of nitrosoarene metalloporphyrin complexes of ruthenium

机译:钌亚硝基芳烃金属卟啉配合物的合成及分子结构

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Several new ruthenium porphyrins containing nitrosoarene ligands have been synthesized and characterized by IR and 1H NMR spectroscopy, and by single-crystal X-ray crystallography. Bis-nitrosoarene complexes of the form (por)Ru(ArNO)_2(Ar = aryl group; por = TPP, TTP; TPP = tetraphenylporphyrinato dianion, TTP = tetratolylporphyrinato dianion) were prepared in good yields from the reaction of the nitrosoarenes with (por)Ru(CO). The IR spectra of the complexes (as KBr pellets) display new bands in the 1346-1350 cm~(-1) region due to V_(NO). Reactions of the (por)Ru(ArNO)2 complexes with excess pyridine and 1-methylimidazole produce the mono-nitrosoarene complexes (por)Ru(ArNO)(py) and (por)Ru(ArNO)(1-MeIm), respectively. The IR spectra of these mono-nitrosoarene complexes reveal a lowering of NO by 14-44 cm~(-1), a feature consistent with the replacement of one of the π-acid ArNO ligands with the more basic pyridine and 1-MeIm ligands. The solid-state molecular structures of two members of each of the three classes of compounds, namely (por)Ru(ArNO)_2, (por)Ru(ArNO)(py) and (por)Ru(ArNO)(1-MeIm) were determined by single-crystal X-ray diffraction, and reveal the N-binding mode of the ArNO ligands.
机译:合成了几种含有亚硝基芳烃配体的钌卟啉,并通过IR和1H NMR光谱以及单晶X射线晶体学对其进行了表征。由亚硝基芳烃与(( por)Ru(CO)。由于V_(NO),配合物(作为KBr颗粒)的红外光谱在1346-1350 cm〜(-1)区域显示出新的谱带。 (por)Ru(ArNO)2配合物与过量吡啶和1-甲基咪唑的反应分别生成单亚硝基芳烃配合物(por)Ru(ArNO)(py)和(por)Ru(ArNO)(1-MeIm) 。这些单亚硝基芳烃配合物的红外光谱显示NO降低了14-44 cm〜(-1),此特征与用更碱性的吡啶和1-MeIm配体取代π-酸ArNO配体之一一致。三类化合物中的每一种的两个成员的固态分子结构,即(por)Ru(ArNO)_2,(por)Ru(ArNO)(py)和(por)Ru(ArNO)(1-MeIm通过单晶X射线衍射确定),并揭示了ArNO配体的N-结合模式。

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