Synthesis and luminescence properties of (Z)-2-(difluoroboryl)-3-(quinolin-2-ylmethylidene)-2,3-dihydro-1H-benzo[5,6][1,4]dioxino[2,3-f]isoindol-1-one, a new unsymmetrical BODIPY analogue
- Autores: Nabasov A.A.1, Rumyantseva T.A.1, Galanin N.E.1, Baklagin V.L.2, Abramova M.B.2, Abramov I.G.2
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Afiliações:
- Ivanovo State University of Chemistry and Technology
- Yaroslavl State Technical University
- Edição: Volume 60, Nº 4 (2024)
- Páginas: 502-509
- Seção: Articles
- URL: https://aspvestnik.ru/0514-7492/article/view/672174
- DOI: https://doi.org/10.31857/S0514749224040111
- EDN: https://elibrary.ru/RYSUED
- ID: 672174
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Resumo
The reaction of dibenzo[b, e][1,4]dioxin-2,3-dicarbonitrile with sodium butoxide in butanol followed by treatment with nitric acid gave 1H-benzo[5,6][1,4]dioxino[2,3-f]isoindole-1,3(2H)-dione. Its condensation with quinaldine leads to the formation of (E, Z)-3-(quinolin-2-ylmethylene)-2,3-dihydro-1H-benzo[5,6][1,4]dioxino[2,3-f]isoindol-1-one, which was treated with BF3‧Et2O in the presence of triethylamine in toluene to obtain a new unsymmetrical analog of BODIPY, (Z)-2-(difluoroboryl)-3-(quinolin-2-ylmethylene)-2,3-dihydro-1H-benzo[5,6][1,4]dioxino[2,3-f]isoindol-1-one. The complex exhibits a Stokes shift of 36 nm and a high relative fluorescence quantum yield (0.72). To support the experimental data, the results of DFT and TDDFT calculations are presented.
Sobre autores
A. Nabasov
Ivanovo State University of Chemistry and Technology
Email: nik-galanin@yandex.ru
ORCID ID: 0009-0006-2775-9289
Rússia, prosp. Sheremetevskii, 7, Ivanovo, 153000
T. Rumyantseva
Ivanovo State University of Chemistry and Technology
Email: nik-galanin@yandex.ru
ORCID ID: 0000-0002-4110-0572
Rússia, prosp. Sheremetevskii, 7, Ivanovo, 153000
N. Galanin
Ivanovo State University of Chemistry and Technology
Autor responsável pela correspondência
Email: nik-galanin@yandex.ru
ORCID ID: 0000-0001-6117-167X
Rússia, prosp. Sheremetevskii, 7, Ivanovo, 153000
V. Baklagin
Yaroslavl State Technical University
Email: nik-galanin@yandex.ru
ORCID ID: 0000-0002-0060-1653
Rússia, prosp. Moskovskii, 88, Yaroslavl, 150023
M. Abramova
Yaroslavl State Technical University
Email: nik-galanin@yandex.ru
ORCID ID: 0000-0003-1721-3646
Rússia, prosp. Moskovskii, 88, Yaroslavl, 150023
I. Abramov
Yaroslavl State Technical University
Email: nik-galanin@yandex.ru
ORCID ID: 0000-0002-8204-1660
Rússia, prosp. Moskovskii, 88, Yaroslavl, 150023
Bibliografia
- Treibs A., Kreuzer F.-H. Lieb. Ann. Chem. 1968, 718, 208–223. doi: 10.1002/jlac.19687180119
- Loudet A., Burgess, K. Chem. Rev. 2007, 107, 4891–4932. doi: 10.1021/cr078381n
- Schmitt A., Hinkeldey B., Wild M., Jung G. J. Fluoresc. 2009, 19, 755–759. doi: 10.1007/s10895–008–0446–7
- Молчанов Е.Е., Марфин Ю.С., Ксенофонтов А.А., Румянцев Е.В. Изв. высш. учебн. завед. Хим. и хим. технол. 2019, 62, 13–18. doi: 10.6060/ivkkt.20196212.6017
- Parhi A.K., Kung M.-P., Ploessl K., Kung H.F. Tetrahedron Lett. 2008, 49, 3395–3399. doi: 10.1016/j.tetlet.2008.03.130
- Liu H., Lu H., Zhou Z., Shimizu S., Li Z., Kobayashi N., Shen Z. Chem. Commun. 2015, 51, 1713–1716. doi: 10.1039/C4CC06704E
- Wu Y., Lu H., Wang S., Li Z., Shen Z. J. Mater. Chem. C. 2015, 3, 12281–12289. doi: 10.1039/c5tc03084f
- Yu C., Fang X., Wu Q., Jiao L., Sun L., Li Z., So P.-K., Wong W.-Y., Hao E. Org. Lett. 2020, 22, 4588–4592. doi: 10.1021/acs.orglett.0c00940
- Zhang X.F., Zhang G.Q., Zhu J. J. Fluoresc. 2019, 29, 407–416. doi: 10.1007/s10895–019–02349–5
- Yue J., Wang N., Wang J., Tao Y., Wang H., Liu J., Zhang J., Jiao J., Zhao W. Anal. Methods. 2021, 13, 2908–2914. doi: 10.1039/D1AY00740H
- Cao T., Gong D., Zheng L., Wang J., Qian J., Liu W., Cao Y., Iqbal K., Qin W., Iqbal A. Anal. Chim. Acta. 2019, 1078, 168–175. doi: 10.1016/j.aca.2019.06.033
- He H., Lo P.-C., Yeung S.-L., Fong W.-P., Ng D.K.P. Chem. Commun. 2011, 47, 4748–4750. doi: 10.1039/C1CC10727E
- Gut A., Ciejka J., Makuszewski J., Majewska I., Brela M., Lapok L. Spectrochim. Acta. A: Mol. Biomol. Spec. 2022, 271, 120898. doi: 10.1016/j.saa.2022.120898
- Duran-Sampedro G., Agarrabeitia A.R., Garcia-Moreno I., Gartzia-Rivero L., de la Moya S., Banuelos J., Lopez-Arbeloa I., Ortiz M.J. Chem. Commun. 2015, 51, 11382–11385. doi: 10.1039/C5CC03408F
- Zhou Y., Xiao Y., Li D., Fu M., Qian X. J. Org. Chem. 2008, 73, 1571–1574. doi: 10.1021/jo702265x
- Nabasov A.A., Koptyaev A.I., Usoltsev S.D., Rumyantseva T.A., Galanin N.E. Macroheterocycles. 2022, 15, 128–132. doi: 10.6060/mhc224262g
- Abramov I.G., Smirnov A.V., Abramova M.B., Plakhtinsky V.V. Chem. Heterocycl. Compd. 2000, 36, 1062–1065. doi: 10.1023/A:1002786015976
- Oliver S.W., Smith T.D. J. Chem. Soc. Perkin Trans. II. 1987, 1579–1582. doi: 10.1039/P29870001579
- Brouwer A.M. Pure Appl. Chem. 2011, 83, 2213–2228. doi: 10.1351/PAC-REP-10–09–31
- Suzuki K., Kobayashi A., Kaneko S., Takehira K., Yoshihara T., Ishida H., Shiina Y., Oishi S., Tobita S. Phys. Chem. Chem. Phys. 2009, 11, 9850–9860. doi: 10.1039/B912178A
- Becke A.D. J. Chem. Phys. 1993, 98, 5648–5652. doi: 10.1063/1.464913
- Slater J.C. Phys. Rev. 1951, 81, 385–390. doi: 10.1103/PhysRev.81.385
- Perdew J.P., Wang Y. Phys. Rev. B. 1992, 45, 13244–13249. doi: 10.1103/PhysRevB.45.13244
- Rappoport D., Furche F. J. Chem. Phys. 2010, 133, 134105. doi: 10.1063/1.3484283
- Granovsky A.A. Firefly, V. 8.2.0 http://classic.chem.msu.su/gran/gamess/index.html
- Andrienko G.A. Chemcraft, V.1.8. http://www.chemcraftprog.com
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