2019
DOI: 10.3390/app9204447
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Light-Activated Zirconium(IV) Phthalocyanine Derivatives Linked to Graphite Oxide Flakes and Discussion on Their Antibacterial Activity

Abstract: In search of an effective antibacterial agent that is useful in photodynamic therapy, new derivatives of zirconium(IV) phthalocyanine (ZrPc) complexes were obtained and linked to graphite oxide flakes. In the syntheses of ZrPc derivatives, two bis-axially substituted ligands with terminal amino group and different lengths of linear carbon chain (C4 in 4-aminobutyric acid or C11 in 11-aminoundecanoic acid) were used. The optical properties (absorption and photoluminescence spectra) of ZrPcs and the composites w… Show more

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Cited by 7 publications
(7 citation statements)
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References 23 publications
(29 reference statements)
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“…In this study, synthesis of composites was already performed in a way to ensure relatively high concentration of ZrPc and it would be difficult to obtain higher phthalocyanine content. But it must be noted that structure of complexes with different functionalities absolutely affects the attachment process that further influence on the 1 O 2 generation as reported in our previous studies of other ligands bonded to ZrPc [38,47].…”
Section: Discussionmentioning
confidence: 73%
“…In this study, synthesis of composites was already performed in a way to ensure relatively high concentration of ZrPc and it would be difficult to obtain higher phthalocyanine content. But it must be noted that structure of complexes with different functionalities absolutely affects the attachment process that further influence on the 1 O 2 generation as reported in our previous studies of other ligands bonded to ZrPc [38,47].…”
Section: Discussionmentioning
confidence: 73%
“…The following samples described in detail previously [ 9 , 29 , 44 , 45 ] were tested in this study: pure graphite oxide (GO), GO-PcZr(Lys) 2 -Ag (0.5 g/10 mL) (IV), GO-Ag (0.5 g/10 mL) (V), and GO-PcZr(Lys) 2 (VI). A brief scheme of composites preparation is shown in Figure 9 .…”
Section: Methodsmentioning
confidence: 99%
“…Due to transesterification, ethyl groups were replaced with pentyl ones during the cyclotetramerization of compound 1 in n-pentanol. 51 The content was cooled to room temperature, treated with a mixture of methanol:water (2:1) and stirred for 1 h. The crude product was centrifuged and dried. The newly synthesized compound was purified by performing a column chromatographic technique.…”
Section: ■ Introductionmentioning
confidence: 99%