Fluorine-Containing Polydentate Bis(heterocycles) Based on Di- And Triketone Analogs in the Synthesis of Zinc(II) Complexes
- Autores: Edilova Y.O.1, Kudyakova Y.S.1, Valova M.S.1, Loseva N.V.2, Slepukhin P.A.1,2, Saloutin V.I.1, Bazhin D.N.1,2
- 
							Afiliações: 
							- Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences
- Ural Federal University named after the first President of Russia B. N. Yeltsin
 
- Edição: Volume 51, Nº 1 (2025)
- Páginas: 41-50
- Seção: Articles
- URL: https://rjeid.com/0132-344X/article/view/691615
- DOI: https://doi.org/10.31857/S0132344X25010054
- EDN: https://elibrary.ru/MHJTLT
- ID: 691615
Citar
Texto integral
 Acesso aberto
		                                Acesso aberto Acesso está concedido
						Acesso está concedido Acesso é pago ou somente para assinantes
		                                							Acesso é pago ou somente para assinantes
		                                					Resumo
Palavras-chave
Sobre autores
Yu. Edilova
Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of SciencesYekaterinburg, Russia
Yu. Kudyakova
Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of SciencesYekaterinburg, Russia
M. Valova
Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of SciencesYekaterinburg, Russia
N. Loseva
Ural Federal University named after the first President of Russia B. N. Yeltsin
														Email: email@example.com
				                					                																			                												                								Yekaterinburg, Russia						
P. Slepukhin
Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences; Ural Federal University named after the first President of Russia B. N. YeltsinYekaterinburg, Russia; Yekaterinburg, Russia
V. Saloutin
Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of SciencesYekaterinburg, Russia
D. Bazhin
Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences; Ural Federal University named after the first President of Russia B. N. Yeltsin
														Email: dnbazhin@gmail.com
				                					                																			                												                								Yekaterinburg, Russia; Yekaterinburg, Russia						
Bibliografia
- He L., Duan L., Qiao J. et al. // Adv. Funct. Mater. 2008. V. 18. P. 2123. https://doi.org/10.1002/adfm.200701505
- Dolinar B.S., Alexandropoulos D.I., Vignesh K.R. // J. Am. Chem. Soc. 2018. V. 140. P. 908. https://doi.org/10.1021/jacs.7b12495
- Bryleva Yu.A., Glinskaya L.A., Agafontsev A.M. et al. // J. Struct. Chem. 2020. V. 61. P. 1810. https://doi.org/10.1134/S0022476619080110
- Bazhina E.S., Bovkunova A.A., Shmelev M.A. et al. // Inorg. Chim. Acta. 2023. V. 547. P. 121359. https://doi.org/10.1016/j.ica.2022.121359
- Zhu Z.-L., Gnanasekaran P., Yan J., Zheng Z. et al. // Inorg. Chem. 2022. V. 61. P. 8898. https://doi.org/10.1021/acs.inorgchem.2c01026
- Yeh H.-H., Ho S.-T., Chi Y.P. et al. // J. Mater. Chem. A. 2013. V. 1. P. 7681. https://doi.org/10.1039/C3TA10988G
- Lu C.-W., Wang Y., Chi Y. // Chem. Eur. J. 2016. V. 22. P. 17892. https://doi.org/:10.1002/chem.201601216
- Hirahara M., Iwamoto A., Teraoka Y.P. et al. // Inorg. Chem. 2024. V. 63. P. 1988. https://doi.org/10.1021/acs.inorgchem.3c03716
- Berkbigler G., Liu Q., Hoefer N. et al. // Eur. J. Inorg. Chem. 2024. P. e202300548. https://doi.org/10.1002/ejic.202300548
- Parshad M., Kumar D., Verma V. // Inorg. Chim. Acta. 2024. V. 560. P. 121789. https://doi.org/10.1016/j.ica.2023.121789
- Kapustina A., Tupolova Y.P., Popov L.D. et al. // Dalton Trans. 2024. V. 53. P. 3330. https://doi.org/10.1039/D3DT03750A
- Saloutin V.I., Edilova Y.O., Kudyakova Y.S. et al. // Molecules. 2022. V. 27. 7894. https://doi.org/10.3390/molecules27227894
- Yan Y.-B., Yang R.-W., Zhang H.-W. et al. // J. Mol. Struct. 2024. V. 1299. P. 137148. https://doi.org/10.1016/j.molstruc.2023.137148
- Barbieri A., Accorsi G., Armaroli N. // Chem. Commun. 2008. P. 2185. https://doi.org/10.1039/b716650h
- Alam P., Climent C., Alemany P., Laskar I.R. // J. Photochem. Photobiol. C. 2019. V. 41. P. 100317. https://doi.org/10.1016/j.jphotochemrev.2019.100317
- Tong X.-L., Xiong C., Lin J.-Q. et al. // J. Mol. Struct. 2018. V. 1152. P. 344. https://doi.org/10.1016/j.molstruc.2017.09.054
- Zhang X., Chi Z., Zhang Y. et al. // J. Mater. Chem. C. 2013. V. 1. P. 3376. https://doi.org/10.1039/c3tc30316k
- Ali A., Pervaiz M., Saeed Z. et al. // Inorg. Chem. Commun. 2022. V. 145. P. 109903. https://doi.org/10.1016/j.inoche.2022.109903
- Farfán R.A., Britos M.L., Gómez M.I. et al. // J. Mol. Struct. 2022. V. 1258. P. 132654. https://doi.org/10.1016/j.molstruc.2022.132654
- Pervaiz M., Sadiq A., Sadiq S. et al. // Inorg. Chem. Commun. 2022. V. 137. P. 109206. https://doi.org/10.1016/j.inoche.2022.109206
- Pellei M., Bello F.D., Porchia M., Santini C. // Coord. Chem. Rev. 2021. V. 445. P. 214088. https://doi.org/10.1016/j.ccr.2021.214088
- Kumar N., Roopa, Bhalla V., Kumar M. // Coord. Chem. Rev. 2021. V. 427. P. 213550. https://doi.org/10.1016/j.ccr.2020.213550
- Tarushi A., Totta X., Papadopoulos A. et al. // Eur. J. Med. Chem. 2014. V. 74. P. 187. https://doi.org/10.1016/j.ejmech.2013.12.019
- Bazhin D.N., Chizhov D.L., Röschenthaler G.-V. et al. // Tetrahedron Lett. 2014. V. 55. № 42. P. 5714. https://doi.org/10.1016/j.tetlet.2014.08.046
- Edilova Y.O., Kudyakova Y.S., Kiskin M.A et al. // J. Fluor. Chem. 2022. V. 253. P. 109932. https://doi.org/10.1016/j.jfluchem.2021.109932
- Bazhin D.N., Kudyakova Y.S., Röschenthaler G.-V et al. // Eur. J. Org. Chem. 2015. P. 5236. https://doi.org/10.1002/ejoc.201500737
- Кудякова Ю.С., Оноприенко А.Я., Слепухин П.А. и др. // Химия гетероцикл. соед. 2019. Т. 55. С. 517.
- Kudyakova Y.S., Onoprienko A.Y., Slepukhin P.A. et al. // Chem. Heterocycl. Comp. 2019. V. 55. P. 517.https://doi.org/10.1007/s10593-019-02488-4
- Bazhin D.N., Kudyakova Y.S., Slepukhin P.A. et al. // Mendeleev Commun. 2018. V. 26. P. 54. https://doi.org/10.1016/j.mencom.2018.03.032
- Бажин Д.Н., Кудякова Ю.С., Эдилова Ю.О. и др. // Изв. АН. Сер. хим. 2022. Т. 71. № 7. С. 1321.
- Bazhin D.N., Kudyakova Y.S., Edilova Y.O et al. // Russ. Chem. Bull. 2022. V. 71. P. 1321. https://doi.org/10.1007/s11172-022-3539-6
- Gorbunova M.G., Gerus I.I., Kukhar V.P. // Synthesis. 2000. P. 738. https://doi.org/10.1055/s-2000-6386
- Dolomanov O.V., Bourhis L.J., Gildea R.J et al. // J. Appl. Cryst. 2009. V. 42. P. 339. https://doi.org/10.1107/S0021889808042726
- Sheldrick G.M. // Acta Crystallogr. A. 2008. V. 64. P. 112. https://doi.org/10.1107/S0108767307043930
- Mittersteiner M., Bonacorso H.G., Martins M.A.P., Zanatta N. // Eur. J. Org. Chem. 2021. P. 3886. https://doi.org/10.1002/ejoc.202100495
- Kudyakova Y.S., Bazhin D.N, Goryaeva M.V. et al. // Russ. Chem. Rev. 2014. V. 83. P. 120. https://doi.org/10.1070/RC2014v083n02ABEH004388
- Llunell M., Casanova D., Cirera J., et al. SHAPE. Program for the Stereochemical Analysis of Molecular Fragments by Means of Continuous Shape Measures and Associated Tools. V. 2.1. Barcelona, 2013.
Arquivos suplementares
 
				
			 
						 
						 
					 
						 
						 
									

 
  
  
  Enviar artigo por via de e-mail
			Enviar artigo por via de e-mail 
