2019
DOI: 10.1007/s10847-019-00949-z
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Substituted Co(II) and Cu(II) metallophthalocyanines from new Schiff base containing pyrrole units: Synthesis, characterization and investigation of photocatalytic activity on 2,3-dichlorophenol oxidation

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Cited by 11 publications
(4 citation statements)
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“…17 Schiff bases attached to phthalocyanine complexes have found application in different research fields because of their excellent physicochemical, biological, catalytic, and electrochemical properties. [18][19][20][21][22][23] This study focuses on the design, synthesis, and characterization of six phthalocyanine complexes for biochemical assays. The peripheral aldehyde-substituted metallophthalocyanines in this study were synthesized from aldehyde-bearing phthalonitrile (a).…”
Section: Introductionmentioning
confidence: 99%
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“…17 Schiff bases attached to phthalocyanine complexes have found application in different research fields because of their excellent physicochemical, biological, catalytic, and electrochemical properties. [18][19][20][21][22][23] This study focuses on the design, synthesis, and characterization of six phthalocyanine complexes for biochemical assays. The peripheral aldehyde-substituted metallophthalocyanines in this study were synthesized from aldehyde-bearing phthalonitrile (a).…”
Section: Introductionmentioning
confidence: 99%
“…The chemical properties of the side groups in substituted phthalocyanines significantly influence the properties of Pcs, such as electronic absorption, solubility, aggregation, and usability in application areas 17 . Schiff bases attached to phthalocyanine complexes have found application in different research fields because of their excellent physicochemical, biological, catalytic, and electrochemical properties 18–23 …”
Section: Introductionmentioning
confidence: 99%
“…[9][10][11][12][13][14][15][16] In addition, these compounds are used in many modern application areas, such as electrochemistry, photocatalysis, anticancer drugs, and solar cells. [17][18][19][20] The nature of the metal ion in the center of the phthalocyanine ring, the substituents attached to the ring, and the binding positions of the substituents significantly affect the photophysical and photochemical properties of the compounds (Fig. 1).…”
Section: Introductionmentioning
confidence: 99%
“…e strong electron delocalization property of metallophthalocyanines (MPcs) allow them to be used in many applications such as in nonlinear optics, dye-sensitized solar cells (DSSC), and photocatalysis and as gas sensors [1][2][3][4]. Aggregation limits the technological applications of MPcs, but this setback can be improved on (or prevented) by modifying them structurally, such as by changing the position and type of substituents [5].…”
Section: Introductionmentioning
confidence: 99%