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First Generation and Trapping of a Dehydrometallophthalocyanine Starting from Triazole-Functionalized Zinc Phthalocyanine

机译:从三唑官能化酞菁锌开始的第一代脱氢金属酞菁捕获

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摘要

Direct 1N-amination of the triazole-fused zinc phthalocyanine 2 and oxidation of the formed amino derivative 3 resulted in the generation of the very reactive intermediate,the de-hydrometallophthalocyanine 4,which was not known previously.The latter was trapped in situ with different dienes,for example,furan,tetraphenyl-cyclopentadienone,and anthracene to form the corresponding Diels-Alder adducts.The products were characterized by ~1H and ~(13)C-deptl35 NMR,and UV/Vis spectroscopy,MALDI-TOF mass spectrometry,and elemental analysis,which are fully in agreement with their structure.The developed synthetic procedure opens a simple and versatile pathway towards unsymmetrical peripheral modification of phthalocya-nines,which is readily applicable to the micromol scale and is important for the design of new interesting Pc-based systems.
机译:三唑稠合的酞菁锌2的直接1N胺化反应以及所形成的氨基衍生物3的氧化反应导致生成了非常活泼的中间体,即氢加氢酞菁4,该中间体以前是未知的。二呋喃,呋喃,四苯基-环戊二烯酮和蒽形成相应的Diels-Alder加合物。产物的特征在于〜1H和〜(13)C-deptl35 NMR,UV / Vis光谱,MALDI-TOF质谱,以及元素分析,这与它们的结构完全吻合。发达的合成方法为邻苯二甲腈的不对称外围修饰开辟了一条简单而通用的途径,该途径易于应用于小分子规模,对于设计新的有趣分子很重要。基于PC的系统。

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