2011
DOI: 10.1016/j.jorganchem.2011.08.045
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Synthesis and electrochemical properties of crown ether functionalized coumarin substituted cobalt and copper phthalocyanines

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Cited by 38 publications
(3 citation statements)
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References 51 publications
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“…[1,2,4] triazoles, a five membered ring having two carbon and three nitrogen atoms, have been reported as pharmacologically active compounds [16] and some used as anti-inflammatory [17], antiviral/anti-HIV and anti-tuberculosis [18], antibacterial agents [19] in medicine. On the other hand, Pcs having substituents including bulky groups and donor atoms may increase the solubility them [20,21]. To the best of our knowledge, there are many Pcs that have triazole moiety on the periphery, however aggregation and electrical properties investigation have been made for only a few of them [22e24], so we have preferred triazole moiety as substituent on Pc ring.…”
Section: Introductionmentioning
confidence: 99%
“…[1,2,4] triazoles, a five membered ring having two carbon and three nitrogen atoms, have been reported as pharmacologically active compounds [16] and some used as anti-inflammatory [17], antiviral/anti-HIV and anti-tuberculosis [18], antibacterial agents [19] in medicine. On the other hand, Pcs having substituents including bulky groups and donor atoms may increase the solubility them [20,21]. To the best of our knowledge, there are many Pcs that have triazole moiety on the periphery, however aggregation and electrical properties investigation have been made for only a few of them [22e24], so we have preferred triazole moiety as substituent on Pc ring.…”
Section: Introductionmentioning
confidence: 99%
“…The group of Bulut reported the synthesis of several phthalonitriles 60 and their conversion into phthalocyanines 61 carrying four or eight 4-(coumarin-3-yl)phenoxy substituents ( Scheme 16 and Table 2 ) [ 92 , 93 , 94 , 95 , 96 , 97 , 98 , 99 , 100 , 101 , 102 , 103 , 104 ].…”
Section: Coumarin–tetrapyrrolic Macrocycle Conjugatesmentioning
confidence: 99%
“…only one cathodic peak, attributed to the reduction of the phthalocyanine ring[102,103], which, nevertheless, were displaced from each other, appearing at -0.47 and -0.38, respectively.…”
mentioning
confidence: 93%