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The Synthesis and Characterization of Hydroxy-8-Quinoline and Naphthol-1 Substituted Phthalocyanines

机译:羟基-8-喹啉和萘酚-1取代的酞菁的合成与表征

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Several hydroxy-8-quinoline and hydroxy-1-naphthol substituted zinc phthalocyanines were synthesized with phthalonitriles as starting materials. A two- step procedure was used. For the first step, the phenoxy phthalonitrile intermediates were synthesized, and the second step involves the reaction of the intermediates with zinc acetate in the presence of DBU (1, 8-diazabicyclo (5. 4. 0) undec-7-ene) as catalyst to produce the substituted zinc phthalocyanine. The compounds were analyzed according to UV/vis, IR and fluorescence spectra. The results showed that there exists intense absorption in the visible region and typical IR bands at 3030 cm-1, 1090 cm-1 and 1500 cm-1. For α substituted phthalocyanines, a new red-shifted band beyond normal Q band was observed, also noted is the red shift of α substituted Pc (phthalocyanine) relative to β substituted Pcs (phthalocyanines). However, for β substituted Pcs, both Q band and the new bands appeared.
机译:几种羟基-8-喹啉和羟基-1-萘酚取代的锌酞菁用酞氯腈作为原料合成。使用两步程序。对于第一步,合成苯氧基酞硫硝基中间体,第二步涉及中间体与乙酸锌的反应在DBU(1,8-二氮杂双环(5.4.4.4.4)的情况下作为产生取代的锌酞菁的催化剂。根据UV / VI,IR和荧光光谱分析化合物。结果表明,在可见区域和3030cm-1,1090cm-1和1500cm-1的可见区域中存在强烈吸收和典型的IR条带。对于α取代的酞菁,观察到超过正常Q带的新的红色偏移带,还注意到α取代的PC(酞菁)相对于β取代的PC(酞菁)的红色移位。但是,对于β代替的PC,Q频段和新频段出现。

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