Agirtas, Mehmet SalihSolgun, Derya Gungordu2025-12-302025-12-3020251042-65071563-532510.1080/10426507.2025.25968122-s2.0-105024092679https://doi.org/10.1080/10426507.2025.2596812https://hdl.handle.net/20.500.14720/29357In this study, first 3-(1,1-diphenylethoxy) propionic acid was obtained from the reaction of 1,1-diphenylethanol and 3-chloropropionic acid. Bis(3-(1,1-diphenylethoxy) propanoate) silicon phthalocyanine was obtained from the reaction of 3-(1,1-diphenylethoxy) propionic acid with SiPcCl2. The newly prepared compounds were characterized by H-1 NMR, FT-IR, mass spectrometry and UV-vis spectroscopy. The singlet oxygen quantum yield for silicon phthalocyanine, which has the potential to be a photosensitizer, was determined as 0.13 by chemical method. Finally, metal ion selectivity of bis(3-(1,1-diphenylethoxy) propanoate) silicon phthalocyanine was determined by UV absorption spectroscopy. A total of 11 metal ions (Mg2+, Mn2+, Na+, Ni2+, Zn2+, Fe3+, Ba2+, Cd2+, Cu2+, Co2+, and Ag+) were used for testing. Of these metal ions, only the Fe3+ ion was selectively determined. [GRAPHICS] .eninfo:eu-repo/semantics/closedAccessSynthesisSelectivePhthalocyanineFe3(+)UV-VisibleMetal Ion Selectivity Feature and Synthesis of Axially bis(3-(1,1-diphenylethoxy)propanoate) Substitute Silicon PhthalocyanineArticleQ3Q4WOS:001632913800001