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首页> 外文期刊>Acta crystallographica. Section C, Structural chemistry. >Structural explanation of the spectral features of the nonsymmetrical complex {2,3,7,8,12,13,17,18-octaethyl-5-[(methylimino)methyl]porphyrinato-κ~4N~21,N~22,N~23,N~24}palladium(II)
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Structural explanation of the spectral features of the nonsymmetrical complex {2,3,7,8,12,13,17,18-octaethyl-5-[(methylimino)methyl]porphyrinato-κ~4N~21,N~22,N~23,N~24}palladium(II)

机译:非对称复合物的光谱特征的结构解释{2,3,7,8,12,13,17,18-十八乙基-5 - [(甲基咪唑酯甲基]卟啉-κ〜4N〜21,n〜22,n 〜23,n〜24}钯(II)

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摘要

The features of porphyrins defining their functionality are related to their conformational flexibility. The degree of nonplanarity of metalloporphyrins depends directly on the number of substituents, their size and their location. The introduction of substituents in the meso positions of β-substituted porphyrins increases the steric interaction and leads to distortions of the porphyrin core. Increasing the distortion of the porphyrin core would augment the bathochromic (red) shift of the electronic absorption spectra. A new nonsymmetrical 2,3,7,8,12,13,17,18-octaethyl-5-[(methylimino)methyl]porphyrin complex of palla-dium(II), [Pd(C_38H_47N_5)], was synthesized and characterized by NMR, mass spectrometry and X-ray analysis. The features of the electronic absorption spectrum of the synthesized complex are explained by the planarity of the porphyrin core and the π-system of the imino group orthogonal to it.
机译:定义其功能的卟啉的特征与其构象的灵活性有关。 金属卟啉的非平移程度直接取决于取代基的数量,其尺寸及其位置。 在β-取代的卟啉的中间位置中的取代基引入取代基增加了空间相互作用并导致卟啉核的扭曲。 增加卟啉核心的变形将增加电子吸收光谱的碱基致铬(红色)偏移。 合成钯(II),[Pd(C_38H_47N_5)]的新的非对称2,3,7,7,8,12,13,18,18-十四烷基-5 - [(甲基咪脊基)甲基]卟啉络合物,进行了合成,其特征 通过NMR,质谱和X射线分析。 合成复合物的电子吸收光谱的特征是通过卟啉核的平坦性和与其正交的亚氨基组的π-系统来解释。

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