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Synthesis and TD-DFT investigation of arylhydrazonocyclopentadiene dyes Научная публикация

Журнал Dyes and Pigments
ISSN: 1873-3743 , E-ISSN: 0143-7208
Вых. Данные Год: 2019, Том: 161, Страницы: 500-509 Страниц : 10 DOI: 10.1016/j.dyepig.2018.09.040
Авторы Salikov Rinat F. 1 , Trainov Konstantin P. 2,1 , Platonov Dmitry N. 1 , Davydov Dmitry A. 3,1 , Lee Sangjun 5 , Gerasimov Igor S. 4,3,1,6 , Medvedev Michael G. 6,1 , Levina Anastasia A. 2,1 , Belyy Aleksandr Yu 1 , Tomilov Yury V. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Prospect, 119991, Moscow, Russian Federation
2 Higher Chemical College, Russian Academy of Sciences, Moscow, Russian Federation
3 Moscow Chemical Lyceum, 4 Tamozhennyj Proezd, 111033, Moscow, Russian Federation
4 NUST MISiS, 119490, Moscow, Russian Federation
5 Korea Science Academy of KAIST, Busan, 614-822, Republic of Korea
6 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119991, Moscow, Russian Federation

Реферат: Two approaches for the synthesis of D-A chromophores containing arylhydrazonocyclopentadiene acceptor moieties were developed. The first approach includes the decarboxylative azo coupling reaction between penta(methoxycarbonyl)cyclopentadienyl potassium or sodium and aryldiazonium salts to give products containing four ester groups at the acceptor moiety. The second one includes the reaction of 1,3-dimethoxycarbonyl-4,5-diphenylcyclopentadienone with arylhydrazine hydrochlorides into arylhydrazonocyclopentadienes with two ester and two phenyl groups. Both series of compounds were investigated by means of absorption spectroscopy and the solvatochromic behavior of two representatives of each series was investigated in various dielectric environments. Both compounds demonstrated relative independence on the environment although the product with the stronger acceptor part was less stable and exhibited a slight hypsochromic shift in polar media. However, the optical properties of this product were strongly affected by the basicity of the medium due to the deprotonation of the NH-group. Quantum chemical modeling of the synthesized products adsorption spectra using different density functionals has shown that PBE0-D3/def2TZVP is an optimal method (out of three tested) for all compounds both in non-vibrationally-resolved and vibrationally-resolved TD-DFT calculations. Accounting for vibronic coupling in TD-DFT calculations is necessary to achieve good agreement with the experiment for compounds synthesized herein.
Библиографическая ссылка: Salikov R.F. , Trainov K.P. , Platonov D.N. , Davydov D.A. , Lee S. , Gerasimov I.S. , Medvedev M.G. , Levina A.A. , Belyy A.Y. , Tomilov Y.V.
Synthesis and TD-DFT investigation of arylhydrazonocyclopentadiene dyes
Dyes and Pigments. 2019. V.161. P.500-509. DOI: 10.1016/j.dyepig.2018.09.040 WOS Scopus OpenAlex
Идентификаторы БД:
≡ Web of science: WOS:000449241200060
≡ Scopus: 2-s2.0-85054463707
≡ OpenAlex: W2891145536
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