Dergiler / Manas Journal of Engineering / 2021 / Cilt: 9 - Sayı: 0

Synthesis, spectroscopy, and photophysical properties of newly magnesium (II) phthalocyanine

Sayfa
58–64
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

It can be a good nominee for various technological applications in that it does not aggregate and has good solubility in polar and non-polar solvents, as well as better and favorable fluorescence properties than its analog in the previous study.

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Amaç & Hipotez:2(3),9(10),16(17),23(24)-tetrakis-2,6-dimethoxyphenoxy substituted magnesium (II) phthalocyanine, which has very good solubility in polar and non-polar solvents and does not aggregate, was synthesized.
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Temel Bulgular & Veri:Its structure was characterized by spectroscopic methods such as elemental analysis, UV-vis, FT-IR, MALDI-TOF mass and 1H NMR.
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Sonuç & Katkı:It can be a good nominee for various technological applications in that it does not aggregate and has good solubility in polar and non-polar solvents, as well as better and favorable fluorescence properties than its analog in the previous study.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Phthalocyanine · magnesium (II) · 3-dimethoxyphenol

Abstract

2(3),9(10),16(17),23(24)-tetrakis-2,6-dimethoxyphenoxy substituted magnesium (II) phthalocyanine, which has very good solubility in polar and non-polar solvents and does not aggregate, was synthesized. Its structure was characterized by spectroscopic methods such as elemental analysis, UV-vis, FT-IR, MALDI-TOF mass and 1H NMR. It has very good solubility in polar aprotic solvents such as dimethyl sulfoxide, N, N- Dimethylformamide, tetrahydrofuran, dichloromethane, and non-polar solvents such as toluene, chloroform. Its aggregation properties have been studied both in the solvents mentioned above and in N, N- Dimethylformamide at different concentrations. Its photophysical properties were determined in N, N-dimethyl formamide. The effects of the nature and presence of 2,6-dimethoxyphenoxy group, which is an antioxidant derivative, on the phthalocyanine skeleton on the spectroscopic and photophysical properties were investigated by comparing it with unsubstituted magnesium (II) phthalocyanine. It can be a good nominee for various technological applications in that it does not aggregate and has good solubility in polar and non-polar solvents, as well as better and favorable fluorescence properties than its analog in the previous study.

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Bu Makaleye Atıf Yap

PİŞKİN, M. B., ÖZTÜRK, Ö., ODABAŞ, Z. (2021). Synthesis, spectroscopy, and photophysical properties of newly magnesium (II) phthalocyanine. Manas Journal of Engineering, Cilt: 9 - Sayı: 0, 58–64. https://ajindex.com/articles/415216

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