Synthesis, photophysical and electrochemical properties of conjugated d-a-d systems based on 1,3,4-thiadiazoles and fused naphtho[2,1-b]thiophene derivatives

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Дәйексөз келтіру

Толық мәтін

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Аннотация

A series of 2,5-diaryl substituted 1,3,4-thiadiazoles was obtained based on fused benzothiophene-2-carboxylates and alkyl substituted 2,2’-bithiophene-5-carboxylates. The photophysical and electrochemical properties of these compounds were studied and it was determined that an increase in the conjunction chain in the donor fragment of the substituted 1,3,4-thiadiazole leads to narrowing of the band gap mainly due to an increase in the HOMO level.

Толық мәтін

Рұқсат жабық

Авторлар туралы

Evgenii Uliankin

Dostoevsky Omsk State University; Omsk State Technical University

Email: fisyuk@chemomsu.ru
ORCID iD: 0000-0002-2898-5003
Ресей, prosp. Mira, 55a, Omsk, 644077; prosp. Mira, 11, Omsk, 644050

Anastasia Kostyuchenko

Dostoevsky Omsk State University; Omsk State Technical University

Email: fisyuk@chemomsu.ru
ORCID iD: 0000-0002-4331-2560
Ресей, prosp. Mira, 55a, Omsk, 644077; prosp. Mira, 11, Omsk, 644050

Alexander Fisyuk

Dostoevsky Omsk State University; Omsk State Technical University

Хат алмасуға жауапты Автор.
Email: fisyuk@chemomsu.ru
ORCID iD: 0000-0001-6191-9297
Ресей, prosp. Mira, 55a, Omsk, 644077; prosp. Mira, 11, Omsk, 644050

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Әрекет
1. JATS XML
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2. Scheme

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3. Fig. 1. Starting thiophene-2-carboxylates 1a–d.

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4. Fig. 2. Normalized absorption (a) and emission (б) spectra of dilute solutions of compounds 5a (1), 5b (2), 5c (3) and 5d (4) in THF (C = 1.6 ‧ 10–6 M).

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5. Fig. 3. Cyclic voltammograms of 10–3 M solutions of compounds 5a (1), 5b (2), 5c (3), and 5d (4), recorded in 0.1 M Bu4NPF6 solution in CH2Cl2 for the anodic potential range and in THF for the cathodic potential range. Scan rate is 100 mV/s.

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6. Fig. 4. Absolute values ​​of ionization potential (IP) and electron affinity (EA) of compounds 5a–d.

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