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首页> 外文期刊>Journal of Porphyrins and Phthalocyanines >The structures of free-base carbahemiporphyrazines
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The structures of free-base carbahemiporphyrazines

机译:游离碱碳杂卟啉的结构

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In this report we present an X-ray crystallographic study of two N-deficient hemiporphyrazines: dicarbahemiporphyrazine (1) and benziphthalocyanine (2). Both compounds can be isolated in multiple crystal forms, and five different solvated forms of macrocycle 1 are presented. Four of the five are non-planar, showing the high degree of flexibility and capacity for hydrogen bonding from solvent to N-H groups in the macrocycle. The remaining structure of 1 is a planar dicationic species that represents a tautomeric form of the macrocycle often seen in metal binding. Four structures of macrocycle 2 are also presented in this report. The structure of 2 is also planar due to the tautomerism of the internal protons, and structural elucidation of this macrocycle reveals the presence of three ionizable protons rather than the expected single proton postulated by Elvidge and Golden.
机译:在本报告中,我们介绍了两种N缺陷的半卟啉:双碳杂卟啉(1)和苯并酞菁(2)的X射线晶体学研究。两种化合物都可以多种晶体形式分离,并提供了五种不同的大环化合物1溶剂化形式。五个中的四个是非平面的,显示出高度的灵活性和大环中从溶剂到N-H基团的氢键结合能力。 1的其余结构是平面的双键物质,代表金属环中常见的大环的互变异构形式。本报告还介绍了大周期2的四个结构。由于内部质子的互变异构,2的结构也是平面的,对该大环的结构解析表明存在三个可电离的质子,而不是Elvidge和Golden假定的单个质子。

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