Synthesis and electrochemical properties of copper(II), manganese(III) phthalocyanines bearing chalcone groups at peripheral or nonperipheral positions

In this study, new chalcone compound 1, new phthalonitrile derivatives 2 and 3, new copper(II), manganese(III) phthalocyanines bearing chalcone groups at peripheral or nonperipheral positions were synthesized. Electrochemistry of tetra-(4-{(2E)-3-[2-fluoro-4-(trifluoromethyl)phenyl]prop-2-enoyl}phenoxy) substituted Co(II)Pc and Mn(III)Pcs were studied with cyclic voltammetry (CV) to determine the redox properties of the phthalocyanines. According to the results, while the CuPcs 2a and 3a showed two Pc based reduction reactions and one Pc based oxidation reaction, MnPcs 2b and 3b gave two metal-based reduction reactions. All the redox processes are shifted toward positive potentials as a result of the increased electron-withdrawing ability of the trifluoromethyl substituents.

___

  • Akyuz D, 2017, J ELECTROANAL CHEM, V804, P53, DOI 10.1016/j.jelechem.2017.09.044
  • Biyiklioglu Z, 2020, J MOL STRUCT, V1212, DOI 10.1016/j.molstruc.2020.128144
  • Biyiklioglu Z, 2019, INORG CHIM ACTA, V486, P345, DOI 10.1016/j.ica.2018.10.061
  • Cakir D, 2015, DALTON T, V44, P9646, DOI 10.1039/c5dt00747j
  • Canlica M, 2011, POLYHEDRON, V30, P508, DOI 10.1016/j.poly.2010.11.017
  • Demir F, 2014, J ELECTROCHEM SOC, V161, pG1, DOI 10.1149/2.002403jes
  • Farajzadeh N, 2020, POLYHEDRON, V177, DOI 10.1016/j.poly.2019.114264
  • Ghazal B, 2020, MOLECULES, V25, DOI 10.3390/molecules25071692
  • Gulmez AD, 2017, SENSOR ACTUAT B-CHEM, V241, P364, DOI 10.1016/j.snb.2016.10.073
  • Guo ZJ, 2019, RSC ADV, V9, P37518, DOI 10.1039/c9ra08065a
  • Kahriman N, 2020, BIOORG CHEM, V99, DOI 10.1016/j.bioorg.2020.103805
  • Kahriman N, 2020, J MOL STRUCT, V1200, DOI 10.1016/j.molstruc.2019.127132
  • Karaca H., 2018, J TURKISH CHEM SOC, V5, P701
  • Karaca H, 2018, J COORD CHEM, V71, P1606, DOI 10.1080/00958972.2018.1468027
  • Kong SW, 2019, J MOL LIQ, V288, DOI 10.1016/j.molliq.2019.111012
  • Kose GG, 2020, SYNTHETIC MET, V264, DOI 10.1016/j.synthmet.2020.116386
  • Li D, 2020, BIOORG MED CHEM LETT, V30, DOI 10.1016/j.bmcl.2020.127164
  • Lima LF, 2020, SENSOR ACTUAT B-CHEM, V310, P127893
  • Nas A, 2017, INORG CHIM ACTA, V466, P86, DOI 10.1016/j.ica.2017.05.050
  • Nas A, 2013, DYES PIGMENTS, V99, P90, DOI 10.1016/j.dyepig.2013.04.014
  • Praats R, 2020, ELECTROCHIM ACTA, V334, DOI 10.1016/j.electacta.2019.135575
  • Sahin S, 2020, SPECTROCHIM ACTA A, V227 .
  • Sarki G, 2019, J MOL STRUCT, V1196, P592, DOI 10.1016/j.molstruc.2019.05.123
  • Sekhosana KE, 2017, POLYHEDRON, V138, P154, DOI 10.1016/j.poly.2017.09.033
  • Senoglu S, 2020, SENSOR ACTUAT B-CHEM, V310, DOI 10.1016/j.snb.2020.127860
  • Sezer B, 2010, SYNTHETIC MET, V160, P2155, DOI 10.1016/j.synthmet.2010.08.002
  • Soganci T, 2018, ACS APPL MATER INTER, V10, P21654, DOI 10.1021/acsami.8b06206
  • Song C, 2020, MATER LETT, V270, DOI 10.1016/j.matlet.2020.127666
  • Tuncel S, 2012, ORG BIOMOL CHEM, V10, P1154, DOI 10.1039/c2ob06809e
  • Unver Y, 2019, J MOL STRUCT, V1178, P508, DOI 10.1016/j.molstruc.2018.10.072
  • Usta A, 2007, HELV CHIM ACTA, V90, P1482, DOI 10.1002/hlca.200790154
  • Xu JL, 2020, OPTIK, V200, DOI 10.1016/j.ijleo.2019.163413
  • Yabas E, 2018, POLYHEDRON, V153, P51, DOI 10.1016/j.poly.2018.06.044
  • Yalazan H, 2020, INORG CHEM COMMUN, V118, DOI 10.1016/j.inoche.2020.107998
  • Yalazan H, 2020, POLYHEDRON, V180, DOI 10.1016/j.poly.2020.114419
  • Yalazan H, 2020, J ORGANOMET CHEM, V912, DOI 10.1016/j.jorganchem.2020.121181
  • Yayli N, 2007, J PHOTOCH PHOTOBIO A, V188, P161, DOI 10.1016/j.jphotochem.2006.12.004
  • Yildiz B, 2019, SOL ENERGY, V191, P654, DOI 10.1016/j.solener.2019.09.043
Turkish Journal of Chemistry-Cover
  • ISSN: 1300-0527
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Nasrin ALİASGHARLOU, Farzin ASGHARİ SANA, Saba KHOSHBAKHT, Pezhman ZOLFAGHARİ, Hamed CHARKHİAN

Design, synthesis, cytotoxic activity, and apoptosis inducing effects of 4- and N-substituted benzoyltaurinamide derivatives

Cumhur GÜNDÜZ, Çağla KAYABAŞI, Özlem AKGÜL, Mümin Alper ERDOĞAN, Güliz ARMAĞAN, Derviş BİRİM

Tokuma GETAHUN, Vinit SHARMA, Deepak KUMAR, Neeraj GUPTA

Processing impact on tocopherols and triglycerides composition of soybean oil and its deodorizer distillate evaluated by high-performance liquid chromatography

Mustafa TOPKAFA, Hüseyin KARA, Hamide Filiz AYYILDIZ, Syed Tufail Hussain SHERAZI, Sarfaraz Ahmed MAHESAR, Siraj Uddin, Zahid Hussain LAGHARI

Chemical composition, antimicrobial, and lipase enzyme activity of essential oil and solvent extracts from Serapias orientalis subsp. orientalis

Şengül Alpay KARAOĞLU, Gözde KILIÇ, Elif ÖZTÜRK, Nurettin YAYLI, İshak ERİK

Huseyin BAS, Nuran KAHRİMAN, Zekeriya BİYİKLİOGLU

Senem GUNER, Yavuz YAGİZ, Zeynal TOPALCENGİZ, Hordur G. KRİSTİNSSON, George BAKER, Paul SARNOSKİ, Bruce A. WELT, Amarat SİMONNE, Maurice R. MARSHALL

Fabrication and characterization of boric acid-crosslinked ethyl cellulose and polyvinyl alcohol films as potential drug release systems for topical drug delivery

Pezhman ZOLFAGHARI, Nasrin ALIASGHARLOU, Saba KHOSHBAKHT, Farzin ASGHARI SANA, Hamed CHARKHIAN

Synthesis and electrochemical properties of copper(II), manganese(III) phthalocyanines bearing chalcone groups at peripheral or nonperipheral positions

Zekeriya BIYIKLIOĞLU, Hüseyin BAŞ, Nuran KAHRİMAN

Nivedita BHARDWAJ, Diksha CHOUDHARY, Akashdeep PATHANİA, Somesh BARANWAL, Pradeep KUMAR