Electrochemical Studies of TEMPO Substituted α, β-Unsaturated Esters

Yıl 2022, Cilt: 1 Sayı: 2, 1 - 12, 29.12.2022

Merve Gençtürk Atilla Öktemer Emre Biçer

Öz

Electrochemical properties of novel α,β -unsaturated ester compounds bearing 2,2,6,6-
tetramethylpiperidine-N-oxyl were studied. Synthesis of the compounds were realized with
basic aldehydes and malonic acid by Knoevenagel-Doebner reaction followed by the
esterification of the compounds with 4-hydroxy-2,2,6,6-tetramethylpiperidine-N-oxy by
Steglich reactions with high yields. Also, poly(2,2,6,6-tetrametylpiperidine-N-oxy-4-yl 3-
(thiophene-3-yl)acrylate) synthesis and characterization are given. Afterwards, electrochemical
properties were studied by cyclic voltammetry in order to determine the diffusion coefficient
(Do) and standard electron-transfer rate coefficients (ko).

Anahtar Kelimeler

Nitroxide , Ester , Diffusion , Rate Coefficient

Kaynakça

• Aydın, M., Esat, B., Kılıç, Ç., Köse, M.E., Ata, A. and Yılmaz, F. 2011. A polythiophene derivative bearing TEMPO as a cathode material for rechargeable batteries. European Polymer Journal, 47:2283-2294.
• Ertürk, E., Demir, A.S. 2008. Iron(III) trifluoroacetate[Fe(O2CCF3)3] catalyzed epoxide opening with amines. Arkivoc, 2008 (2):160-171.