β-未取代的5-单氮杂卟啉及其衍生物

IF 0.9 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Journal of Porphyrins and Phthalocyanines Pub Date : 2023-07-06 DOI:10.1142/s1088424623501079
Rong Yuan, Le Liu, Bangshao Yin, Ling Xu, Mingbo Zhou, Yutao Rao, Jianxin Song
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引用次数: 0

摘要

[公式:见文]以1,19-二溴四吡喃与NaN3-CuI反应,合成了未取代的5-单氮卟啉(MAP)铜配合物10,15,20-三硝基-5-单氮卟啉铜(II) (Cu-MAP) 3,收率较高。经过脱金属、金属化和溴化反应,顺利制备了重要前驱体3,7-二溴-10,15,20-三硝基-5-单氮卟啉镍(II)([公式:见文],[公式:见文]-二溴Ni-MAP) 6。6与三种有机硼化物的Suzuki-Miyaura偶联反应,分别生成了“耳形”Ni-MAP 7、吡咯桥接Ni-MAP低聚物8和9、苯桥接Ni-MAP低聚物10和11。通过x射线衍射分析证实了map3、6、7、8、10和11的结构。进行了光学和电化学研究以了解其电子性质。
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β-Unsubstituted 5-monoazaporphyrin and its derivatives
[Formula: see text]-Unsubstituted 5-monoazaporphyrin (MAP) copper complex 10,15,20-tritolyl-5-monoazaporphyrinato copper(II) (Cu-MAP) 3 was synthesized by reaction of 1,19-dibromotetrapyrrane with NaN3-CuI in good yield. Following successive reactions of demetallation, metallation and bromination, the important precursor 3,7-dibromo-10,15,20-tritolyl-5-monoazaporphyrinato nickel(II) ([Formula: see text],[Formula: see text]′-dibromo Ni-MAP) 6was prepared smoothly. Suzuki-Miyaura coupling reactions of 6 with three organic borides resulted in the “earring” Ni-MAP 7, pyrrole bridged Ni-MAP oligomers 8 and 9, and benzene bridged Ni-MAP oligomers 10 and 11, respectively. The structures of MAPs 3, 6, 7, 8, 10 and 11 were confirmed by X-ray diffraction analysis. Optical and electrochemical studies were performed to understand their electronic properties.
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来源期刊
CiteScore
2.10
自引率
20.00%
发文量
62
审稿时长
1 months
期刊介绍: The Journal of Porphyrins and Phthalocyanines (JPP) covers research in the chemistry, physics, biology and technology of porphyrins, phthalocyanines and related macrocycles. Research papers, review articles and short communications deal with the synthesis, spectroscopy, processing and applications of these compounds.
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