2020
DOI: 10.1016/j.poly.2020.114621
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Synthesis and photophysical characterization of novel Ir(III) complexes with a dipyridophenazine analogue (ppdh) as ancillary ligand

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Cited by 9 publications
(8 citation statements)
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“…In this work, we tested a coordination compound characterized by a positive charge in the first coordination sphere (Figure 4B). The photophysical evaluation of the PSIR-3 performed in acetonitrile solution [40] revealed absorption processes at 375 and 392 nm attributable at the first instance of charge-transfer transitions (Figure 4C,D) [32]. When the We have previously shown that Ir(III)-based compounds, such as PSIR-3, have photodynamic antimicrobial activity against imipenem-resistant Klebsiella pneumoniae [32,33].…”
Section: Photophysical Properties Of the Psir-3 Compoundmentioning
confidence: 88%
See 1 more Smart Citation
“…In this work, we tested a coordination compound characterized by a positive charge in the first coordination sphere (Figure 4B). The photophysical evaluation of the PSIR-3 performed in acetonitrile solution [40] revealed absorption processes at 375 and 392 nm attributable at the first instance of charge-transfer transitions (Figure 4C,D) [32]. When the We have previously shown that Ir(III)-based compounds, such as PSIR-3, have photodynamic antimicrobial activity against imipenem-resistant Klebsiella pneumoniae [32,33].…”
Section: Photophysical Properties Of the Psir-3 Compoundmentioning
confidence: 88%
“…Pharmaceutics 2021, 13, x FOR PEER REVIEW 12 of 18 PSIR-3 compound was excited with a wavelength corresponding to the lowest chargetransfer absorption energy, 375 nm, it showed maximum emission at 598 nm (Figure 4C,D). Figure 4C shows the recorded lifetimes of excited states in 0.32 µs and the calculated quantum yield (Φem) in 0.011 [40]. The aPDI activity of the PSIR-3 compound was compared with the positive PS control [Ru(bpy)3](PF6)2 (bpy = 2,2′-bipyridine) called PS-Ru.…”
Section: Photophysical Properties Of the Psir-3 Compoundmentioning
confidence: 99%
“…In this work, we tested a coordination compound characterized by a positive charge in the first coordination sphere (Figures 4B). The photophysical evaluation of the PSIR-3 performed in acetonitrile solution [40], revealed absorption processes at 375 and 392 nm attributable at the first instance to charge-transfer transitions (Figure 4C and D) [32]. When the PSIR-3 compound was excited with a wavelength corresponding to the lowest charge-transfer absorption energy, 375 nm, it showed maximum emission at 598 nm (Figure 4C and D).…”
Section: Correlation Of Virulence Factors With Antibiotic Resistancementioning
confidence: 99%
“…The structural and photophysical characterization of the PSIR-3 compound was described previously [40]. The complex synthesized can be described using the following general formula: [Ir(C^N)2(N^N)](PF6), where N^N is the ancillary ligand; and C^N corresponds to a cyclometalating ligand.…”
Section: Synthesis Of the Psir-3 Compoundmentioning
confidence: 99%
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