Journals / Turkish Journal of Chemistry / 2021 / Cilt: 45 - Sayı: 1

Synthesis of nonperipherally tetra-[5-(diethylamino)-2-formylphenoxy] substituted metallophthalocyanines and their electrochemistry

Pages
17–25
Publication Date
2021-02-17
DOI
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

Voltammetric characterizations of n-TY-Co, n-TY-Cu, and n-TY-Mn revealed that while n-TY-Co, n-TY-Cu, and n-TY-Mn showed characteristic Pc ring and/or metal-based reduction reaction, n-TY-Co, n-TY-Cu, and n-TY-Mn were coated on the working electrode during the oxidation processes owing to the cationic electropolymerizations of the [5-(diethylamino)-2-formylphenoxy] substituents.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:3-[5-(diethylamino)-2-formylphenoxy]phthalonitrile (n-TY-CN), metallophthalocyanines n-TY-Co, n-TY-Cu, and n-TY-Mn bearing [5-(diethylamino)-2-formylphenoxy] groups at nonperipheral positions were prepared for the first time.
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Key Findings & Data:These compounds were characterized with IR, NMR (only for n-TY-CN), mass and UV-vis (except n-TY-CN) spectroscopy.
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Conclusion & Impact:Voltammetric characterizations of n-TY-Co, n-TY-Cu, and n-TY-Mn revealed that while n-TY-Co, n-TY-Cu, and n-TY-Mn showed characteristic Pc ring and/or metal-based reduction reaction, n-TY-Co, n-TY-Cu, and n-TY-Mn were coated on the working electrode during the oxidation processes owing to the cationic electropolymerizations of the [5-(diethylamino)-2-formylphenoxy] substituents.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Synthesis · diethylamino · phthalocyanine

Abstract

3-[5-(diethylamino)-2-formylphenoxy]phthalonitrile (n-TY-CN), metallophthalocyanines n-TY-Co, n-TY-Cu, and n-TY-Mn bearing [5-(diethylamino)-2-formylphenoxy] groups at nonperipheral positions were prepared for the first time. These compounds were characterized with IR, NMR (only for n-TY-CN), mass and UV-vis (except n-TY-CN) spectroscopy. Voltammetric characterizations of n-TY-Co, n-TY-Cu, and n-TY-Mn revealed that while n-TY-Co, n-TY-Cu, and n-TY-Mn showed characteristic Pc ring and/or metal-based reduction reaction, n-TY-Co, n-TY-Cu, and n-TY-Mn were coated on the working electrode during the oxidation processes owing to the cationic electropolymerizations of the [5-(diethylamino)-2-formylphenoxy] substituents.

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Cite This Article

KELES, T., UNLUER, D., BİYİKLİOGLU, Z., UNVER, Y. (2021). Synthesis of nonperipherally tetra-[5-(diethylamino)-2-formylphenoxy] substituted metallophthalocyanines and their electrochemistry. Turkish Journal of Chemistry, Cilt: 45 - Sayı: 1, 17–25. https://ajindex.com/articles/201328

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References (8)

  1. Akyuz D, 2020, J MOL STRUCT, V1206, DOI 10.1016/j.molstruc.2019.127674 Akyuz D, 2017,
  2. ELECTROANAL, V29, P2913, DOI 10.1002/elan.201700366 Attia MS, 2019,
  3. TALANTA, V201, P185, DOI 10.1016/j.talanta.2019.03.119 Barut B, 2020, DYES PIGMENTS, V172, DOI 10.1016/j.dyepig.2019.107794 Barut B, 2016, DALTON T, V45, P14301, DOI 10.1039/c6dt02720b Bas H, 2017, INORG CHIM ACTA, V467, P56, DOI 10.1016/j.ica.2017.07.042 Biyiklioglu Z, 2020, TURK J CHEM, V44, P687, DOI 10.3906/kim-2001-54 Biyiklioglu Z, 2020, J MOL STRUCT, V1212, DOI 10.1016/j.molstruc.2020.128144 Biyiklioglu Z, 2018, DYES PIGMENTS, V148, P417, DOI 10.1016/j.dyepig.2017.09.051 Biyiklioglu Z, 2017, J MOL STRUCT, V1148, P15, DOI 10.1016/j.molstruc.2017.07.021 Biyiklioglu Z, 2015, DALTON T, V44, P18993, DOI 10.1039/c5dt03421c Biyiklioglu Z, 2014, SYNTHETIC MET, V196, P166, DOI 10.1016/j.synthmet.2014.07.023 Biyiklioglu Z, 2014, J ORGANOMET CHEM, V752, P59, DOI 10.1016/j.jorganchem.2013.12.004 Biyiklioglu Z, 2014, DYES PIGMENTS, V100, P150, DOI 10.1016/j.dyepig.2013.09.023 Cakir D, 2015, DALTON T, V44, P9646, DOI 10.1039/c5dt00747j Cakir V, 2014, J ORGANOMET CHEM, V768, P28, DOI 10.1016/j.jorganchem.2014.06.006 Filippova A, 2017, J MOL STRUCT, V1149, P17, DOI 10.1016/j.molstruc.2017.07.086 Goktug O, 2017, NEW J CHEM, V41, P14080, DOI 10.1039/c7nj03250a Gungor O, 2016, DALTON T, V45, P7634, DOI 10.1039/c6dt00874g Hohnholz D, 2000, J MOL STRUCT, V521, P231, DOI 10.1016/S0022-2860(99)00438-X Keles T, 2017,
  4. ELECTROANAL, V29, P2125, DOI 10.1002/elan.201700249 Keles T, 2017, DYES PIGMENTS, V139, P575, DOI 10.1016/j.dyepig.2016.12.045 Li Y, 2020, CHEM-ASIAN J, V15, P1970, DOI 10.1002/asia.202000438 Majeed SA, 2019, J LUMIN, V213, P88, DOI 10.1016/j.jlumin.2019.04.034 Ogbodu RO, 2020, J PHOTOCH PHOTOBIO B, V208, DOI 10.1016/j.jphotobiol.2020.111915 Olgac R, 2017, BIOSENS BIOELECTRON, V98, P202, DOI 10.1016/j.bios.2017.06.028 Omeroglu I, 2019,
  5. MACROHETEROCYCLES, V12, P255, DOI 10.6060/mhc190763m Ozmen OT, 2012, SYNTHETIC MET, V162, P2188, DOI 10.1016/j.synthmet.2012.10.013 Porto LS, 2019,
  6. ELECTROANAL, V31, P820, DOI 10.1002/elan.201800789 Sari FA, 2018,
  7. CHEMISTRYSELECT, V3, P13692, DOI 10.1002/slct.201802991 Sekhosana KE, 2017,
  8. POLYHEDRON, V138, P154, DOI 10.1016/j.poly.2017.09.033 Sen P, 2019, SYNTHETIC MET, V258, DOI 10.1016/j.synthmet.2019.116203 Sen P, 2019, RES CHEM INTERMEDIAT, V45, P687, DOI 10.1007/s11164-018-3637-0 Tejerina L, 2016, J PORPHYR PHTHALOCYA, V20, P1361, DOI 10.1142/S1088424616501121 Yildiz B, 20