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New Organic Dyes from Phthalonitrile via Interesting Nucleophilic Reactions
Synlett ( IF 1.7 ) Pub Date : 2020-06-03 , DOI: 10.1055/s-0040-1707858
Cheng-Hui Li , Wei Zheng

Phthalonitrile (PN) is regarded mostly as an important precursor for phthalocyanine (Pc). However, the presence of two ortho triple bonds also endow PN with significant potential to form novel conjugated systems. Based on several unexpected nucleophilic reactions, our group has discovered novel applications of PN for the synthesis of asymmetric benzo-fused aza-BOIDPYs and new fused-ring phthalorubines (Pr). This Synpacts highlights our recent advances in this field. 1 Introduction 2 Benzo-Fused Aza-BODIPYs 3 Phthalorubines 4 Conclusion

中文翻译:

通过有趣的亲核反应从邻苯二甲腈中制备新的有机染料

邻苯二甲腈 (PN) 主要被认为是酞菁 (Pc) 的重要前体。然而,两个邻位三键的存在也赋予了 PN 形成新型共轭系统的巨大潜力。基于几个意想不到的亲核反应,我们的团队发现了 PN 在合成不对称苯并稠合氮杂-BOIDPY 和新型稠环酞菁 (Pr) 方面的新应用。Synpact 突出了我们在该领域的最新进展。1 引言 2 苯并融合的 Aza-BODIPYs 3 酞红素 4 结论
更新日期:2020-06-03
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