2008
DOI: 10.1016/j.jfluchem.2008.05.014
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Functional fluoro substituted tetrakis-metallophthalocyanines: Synthesis, spectroscopy, electrochemistry and spectroelectrochemistry

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Cited by 25 publications
(2 citation statements)
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“…The solvent plays, however, a significant role in stabilizing these species, and a given phthalocyanine can be monomeric in a given solvent. [63][64][65][66][67][68][69][70][71][72] The aggregation studies of pyridine/quinoline substituted cobalt phthalocyanines (P-CoPc and Q-CoPc) were searched in diverse solvents such as THF, DMSO, and DMF to select a convenient solvent for investigation of their photocatalytic properties. These phthalocyanines did not show any aggregation in the given solvents (Figure 2).…”
Section: Aggregation Studies Of Phthalocyaninesmentioning
confidence: 99%
“…The solvent plays, however, a significant role in stabilizing these species, and a given phthalocyanine can be monomeric in a given solvent. [63][64][65][66][67][68][69][70][71][72] The aggregation studies of pyridine/quinoline substituted cobalt phthalocyanines (P-CoPc and Q-CoPc) were searched in diverse solvents such as THF, DMSO, and DMF to select a convenient solvent for investigation of their photocatalytic properties. These phthalocyanines did not show any aggregation in the given solvents (Figure 2).…”
Section: Aggregation Studies Of Phthalocyaninesmentioning
confidence: 99%
“…In spite of the fact that phthalocyanines bearing electron‐donating substituents have frequently been described, phthalocyanines with electron‐withdrawing groups, especially those containing fluorine atoms, have not been extensively studied . Also, fluorine‐atom‐containing phthalocyanines attract a great deal of attention owing to their thermal and chemical stability; they also possess electron‐transporting characteristics . In particular, SiPc complexes substituted with polyfluoro, perfluoroalkanoyloxy and polyfluoroalkyloxy groups have been reported to show improved solubility .…”
Section: Introductionmentioning
confidence: 99%