2012
DOI: 10.1016/j.jorganchem.2012.04.010
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Synthesis, characterization, spectral and electrical properties of peripherally tetratriazole-substituted phthalocyanines and its metal complexes

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Cited by 20 publications
(9 citation statements)
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“…[17][18][19][20][21][22][23][24][25][26][27] These substituted phthalocyanines can be highly efficient photosensitizers of singlet oxygen due to dual or synergistic therapeutic effect. [28,29] However, only a few works devoted to phthalocyanines [30][31][32] and porphyrin [33] containing pyrazole substituents are known.…”
Section: Introductionmentioning
confidence: 99%
“…[17][18][19][20][21][22][23][24][25][26][27] These substituted phthalocyanines can be highly efficient photosensitizers of singlet oxygen due to dual or synergistic therapeutic effect. [28,29] However, only a few works devoted to phthalocyanines [30][31][32] and porphyrin [33] containing pyrazole substituents are known.…”
Section: Introductionmentioning
confidence: 99%
“…Aggregation of MPcs in aqueous and non-aqueous solution is well known phenomena of phthalocyanine chemistry [35][36][37][38][39][40][41]. Aggregation is usually described as a co-planar association of macrocyclic ring and progressing the formation of monomer to dimmers and higher order aggregates.…”
Section: Aggregation Propertiesmentioning
confidence: 99%
“…However, the aggregates of MPcs in organic solvents also reported [35][36][37][38]. The aggregation of MPcs has been controlled by different methods such as introduction of substituents at peripheral and non-peripheral positions and octahedral co-ordination of the central metal ion [39][40][41]. The aggregate formation of MPcs depends on the concentration and nature of solvent, metal ion and substituents [35][36][37][38][39][40][41].…”
Section: Introductionmentioning
confidence: 99%
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“…In the last decade intensive increase of number of the papers devoted to phthalocyanines, containing various nitrogen heterocycles is observed. [12][13][14][15] A number of the works devoted to synthesis of phthalocyanines containing the pyrazole fragments are known. These substituents are attached to a linked phthalocyanine macroheterocycle directly, [16] through the methoxy spacer moiety [17] or through oxygen atom spacer moiety.…”
Section: Introductionmentioning
confidence: 99%