2023
DOI: 10.1016/j.jorganchem.2022.122553
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Synthesis of water soluble copper(II), manganese(III) phthalocyanines and their photocatalytic performances in benzyl alcohol photoxidation

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Cited by 9 publications
(3 citation statements)
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“…[26] Specifically, Au-CuS-TiO 2 NBs degraded 96% of the antibiotic oxytetracycline molecules in an aqueous solution in 1 h sunlight, while the degradation rate of Au-TiO 2 NBs, CuS-TiO 2 NBs, and TiO 2 NBs is 85%, 76%, and 66% respectively. Metal-organic complexes used as photocatalysts include UiOs, [27] MILs, [28] Zn, [29] Cu, [30] phthalocyanines, [31] etc. Li et al designed porous (0.25-0.52 cm 3 g −1 ) Zn-In-S photocatalysts which improved photocatalytic efficiency to tetracycline in 120 min(>85%).…”
Section: Design Objectives Of the Photocatalytic Membranementioning
confidence: 99%
“…[26] Specifically, Au-CuS-TiO 2 NBs degraded 96% of the antibiotic oxytetracycline molecules in an aqueous solution in 1 h sunlight, while the degradation rate of Au-TiO 2 NBs, CuS-TiO 2 NBs, and TiO 2 NBs is 85%, 76%, and 66% respectively. Metal-organic complexes used as photocatalysts include UiOs, [27] MILs, [28] Zn, [29] Cu, [30] phthalocyanines, [31] etc. Li et al designed porous (0.25-0.52 cm 3 g −1 ) Zn-In-S photocatalysts which improved photocatalytic efficiency to tetracycline in 120 min(>85%).…”
Section: Design Objectives Of the Photocatalytic Membranementioning
confidence: 99%
“…The disappearance of the -C≡N vibration (2232 cm -1 ) in the IR spectrum of NP2-Cu and NP2-Mn indicated the conversion of NP2-CN to the phthalocyanine ring. Owing to the paramagnetic nature of Cu(II) and Mn(III) ion, 1 H-NMR and 13 C-NMR measurements of NP2-Cu and NP2-Mn could not be measured [32]. In MALDI-TOF MS spectra of NP2-Cu and NP2-Mn the molecular ion peaks were found at m/z 1476.…”
Section: Synthesis and Characterizationmentioning
confidence: 99%
“…Metal phthalocyanines (MPcs) are highly conjugated cyclic molecules that consist of four isoindole units linked by nitrogen atoms to a central metal. Since the discovery of phthalocyanines as dyes in 1907, 1 their popularity has increased due to their semiconducting, optical and electrochemical properties, thermal stability and chemical inertness, as well as non-toxicity, which led to their use in medicine, [2][3][4] photocatalysis, [5][6][7] catalysis, 8,9 in solar cells, 10,11 and other fields. Another important area of application of phthalocyanines is chemical sensing.…”
Section: Introductionmentioning
confidence: 99%