首页> 外文期刊>Open Journal of Inorganic Chemistry >Preparation of Single Substituted Phenyl Porphyrins Form Meso-Tetraphenyl Porphyrin-Synthetic Example from Symmetric Porphyrin into Asymmetric Porphyrins
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Preparation of Single Substituted Phenyl Porphyrins Form Meso-Tetraphenyl Porphyrin-Synthetic Example from Symmetric Porphyrin into Asymmetric Porphyrins

机译:介孔-四苯基卟啉单取代苯基卟啉的制备-对称卟啉合成不对称卟啉的合成实例

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摘要

Two asymmetric porphyrins, 5-(4-chloromethylphenyl)-10, 15, 20-triphenyl porphyrin and 5-(4-formylphenyl)-10, 15, 20-triphenyl porphyrin, were successfully prepared by the symmetric meso-tetraphenyl porphyrin and relative molecular configurations and properties were characterized by spectral determinations. This work presented an example for synthesis of asymmetric porphyrin derivatives from the symmetric porphyrin. Both asymmetric porphyrins are reactive in molecular assembly, the concerned reactions including alkylation with Grignard reagents, etherification with alcohols, aldol condensation and Mannich reaction for modification and enhancing their functionality. In this work, the reaction conditions were improved, synthetic strategy and route were confirmed.
机译:通过对称的 meso成功地制备了两种不对称的卟啉5-(4-氯甲基苯基)-10、15、20-三苯基卟啉和5-(4-甲酰基苯基)-10、15、20-三苯基卟啉。通过光谱测定表征了em>-四苯基卟啉及其相对分子构型和性质。这项工作为从对称卟啉合成不对称卟啉衍生物提供了一个实例。两种不对称卟啉在分子组装中均具有反应性,涉及的反应包括用格氏试剂烷基化,用醇醚化,醇醛缩合和曼尼希反应以修饰和增强它们的功能。改进了反应条件,确定了合成策略和路线。

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