2019
DOI: 10.1016/j.jphotochem.2019.111975
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A very fast photodegradation of dyes in the presence of new Schiff’s base N4-macrocyclic Ag-doped Pd(II) complexes under visible-light irradiation

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Cited by 8 publications
(3 citation statements)
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“…The XPS spectrum of the C-1 complex displays peaks at 965.09, 955.76, 945.9, and 935.99 eV for the 2p 1/2 and 2p 3/2 states of Cu of Cu-O and Cu-N bonds, respectively [26,27]. The remaining peaks, such as 203.24 eV for Cl (2p); 534.09 and 531.91 eV for O (1s); and 399.13 and 400.33 eV for Cu-N and Ar-C=N-Ar N (1s) states [21,28], are also displayed. In the case of the C-2 complex, 965.13, 955.55, 945.09 and 935.71 eV are indicated for the Cu-N and Cu-O (2p 1/2 and 2p 3/2 ) bonds.…”
Section: Resultsmentioning
confidence: 99%
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“…The XPS spectrum of the C-1 complex displays peaks at 965.09, 955.76, 945.9, and 935.99 eV for the 2p 1/2 and 2p 3/2 states of Cu of Cu-O and Cu-N bonds, respectively [26,27]. The remaining peaks, such as 203.24 eV for Cl (2p); 534.09 and 531.91 eV for O (1s); and 399.13 and 400.33 eV for Cu-N and Ar-C=N-Ar N (1s) states [21,28], are also displayed. In the case of the C-2 complex, 965.13, 955.55, 945.09 and 935.71 eV are indicated for the Cu-N and Cu-O (2p 1/2 and 2p 3/2 ) bonds.…”
Section: Resultsmentioning
confidence: 99%
“…Photooxidation of aromatic hydrocarbons and methylstyrenes have also been accomplished using Ru (II) and Zn (II) complexes with Schiff base ligands [19]. Other studies have investigated the potential of Pd (II) Schiff base complexes for the synthesis of fused heterocyclic aromatic hydrocarbons and the activation of allylic C-H bonds and Ag-doped Pd (II) complexes under visible-light irradiation for the degradation of dyes [20,21]. Zn (II) complexes have also been investigated for their possible use in the photooxidation of 2,2'-(Ethyne-1,2-diyl) dianilines [22], the photodecomposition of organic dye pollutants [23], and the piezo-photomineralization of dyes and industrial waste [24].…”
Section: Introductionmentioning
confidence: 99%
“…One distinguishing feature that distinguishes acetonitrile from other solvents is its oxygen solubility. Oxygen is highly soluble in acetonitrile (8.1 mM) than in other usually used organic solvents [46], such as DMSO (2.1 mM) and DMF (2.1 mM). Dioxygen plays a crucial role in this conversion.…”
Section: Effect Of Solventmentioning
confidence: 99%