Synthesis and properties of metal complexes with halogen-substituted octaphenyltetraazaporphyrins

Мұқаба

Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Аннотация

Mg(II)-octa-(4-chlorophenyl)tetraazaporphyrin, Mg(II)-octa-(4-fluorophenyl)tetraazaporphyrin, Zn(II)octa-(4-chlorophenyl)tetraazaporphyrin and Zn(II)-octa-(4-fluorophenyl)tetraazaporphyrin were synthesized by cyclization of di-(4-halophenyl)maleinonitriles with magnesium and zinc(II) acetates in refluxing ethylene glycol. Zn(II)-Octaphenyltetraazaporphyrin was obtained by cyclization of diphenylmaleininitrile with zinc acetate in ethylene glycol. Using the metal exchange reaction of halogen-substituted magnesium complexes with copper(II) and manganese(II) chlorides in dimethylformamide, the corresponding Cu(II) and Mn(III)octaphenyltetraazaporphyrins were synthesized. Structure of the obtained compounds were identified by UV-Vis, IR, 1H NMR spectroscopy and mass spectrometry methods. The photochemical stability of the synthesized complexes was studied.

Авторлар туралы

N. Chizhova

G.A. Krestov Institute of Solutions Chemistry, Russian Academy of Sciences

Email: nvc@isc-ras.ru

A. Likhonina

G.A. Krestov Institute of Solutions Chemistry, Russian Academy of Sciences

N. Mamardashvili

G.A. Krestov Institute of Solutions Chemistry, Russian Academy of Sciences

Әдебиет тізімі

  1. Bajju G.D., Singh N., Deepmala // Chem. Sci. Trans. 2014. Vol. 3. N 1. P. 314. doi: 10.7598/cst2014.583
  2. Katoh K., Yoshida Y., Yamashita M., Miyasaka H., Breedlove B.K., Kajiwara T., Takaishi S., Ishikawa N., Isshiki H., Zhang Y.F., Komeda T., Yamagishi M., Takeya J. // J. Am. Chem. Soc. 2009. Vol. 131. N 29. P. 9967. doi: 10.1021/ja902349t
  3. Chen L., Zhang Z., Wang Y., Guan, Y., Deng K., Lv K., Sun J., Li Z., Li M. // J. Mol. Catal. 2013. Vol. 372. P. 114. doi: 10.1016/j.molcata.2013.02.013
  4. Goslinski T., Tykarska E., Kryjewski M., Osmalek T., Sobiak S., Gdanies M., Dutkiewicz Z., Mielcarek J. // Anal Sci. 2011. Vol. 27. N 5. P. 511. doi: 10.2116/analsci.27.511.
  5. Лермонтова С.А., Григорьев И.С., Шилягина Н.Ю., Пескова Н.Н., Балалаева И.В., Ширманова М.В., Клапшина Л.Г. // ЖОХ. 2016. Т. 86. Вып. 6. C. 1000
  6. Lermontova S.A., Grigoryev I.S., Shilyagina N.Y., Peskova N.N., Balalaeva I.V., Shirmanova M.V., Klapshina L.G. // Russ J Gen. Chem. 2016. Vol 86. N 6. P. 1330. doi: 10.1134/S1070363216060189
  7. Порфирины: спектроскопия, электрохимия, применение / Под ред. Н.С. Ениколопяна. М.: Наука, 1987, 384 с.
  8. Chino M., Leone L., Zambrano G., Pirro F., D'Alonzo D., Firpo V., Aref D., Lista L., Maglio O., Nastri F., Lombardi A. // Biopolymers. 2018. Vol. 109. P. 23107. doi: 10.1002/bip.23107
  9. Lieb D., Zahl A., Shubina T.E., Ivanović-Burmazović I. // J. Am. Chem. Soc. 2010. Vol. 132. N 21. P. 7282. doi: 10.1021/ja1014585
  10. Budimir А., Kalmár J., Fábián I., Lente G., Bányai I., Batinić-Haberle I., Biruš M. // Dalton Trans. 2010. Vol. 39. P. 4405. doi: 10.1039/b926522h
  11. Cook A.H., Linstead R.P. // J. Chem. Soc. 1937. P. 929.
  12. Stuzhin P.A.,Ivanova S.S., Koifman O.I., Petrov O.A., Nazarova A. // Inorg. Chem. Commun. 2014. Vol. 49. P. 72. doi: 10.1016/j.inoche.2014.09.002
  13. Stuzhin P.A., Goryachev M.Y., Ivanova S.S., Nazarova A., Pimkov I., Koifman O.I. // J. Porph. Phthalocyan. 2013. Vol. 17. P. 905. doi: 10.1142/S1088424613500892
  14. Lebedeva I.A. (Yablokova), Ivanova S.S., Novakova V., Zhabanov Yu.A., Stuzin P.A. // J. Fluorine Chem. 2018. Vol. 214. P. 86. doi: 10.1016/j.jfluchem.2018.08.006
  15. Чижова Н.В., Иванова Ю.Б., Русанов А.И., Хрушкова Ю.В., Мамардашвили Н.Ж. // ЖОрХ. 2019. Т. 55. № 5. С. 754
  16. Chizhova N.V., Ivanova Yu.B., Rusanov A.I., Khrushkova Yu.V., Mamardashvili N.Z. // Russ J. Org. Chem. 2019. Vol. 55. N 5. P. 655. doi: 10.1134/S1070428019050129
  17. Dmitrieva O.A., Chizhova N.V., Rusanov A.I., Koifman M.O., Mamardashvili N.Z. // J. Fluoresc. 2020. Vol. 30. P. 657. doi: 10.1007/s10895-020-02530-1
  18. Rusanov A.I., Chizhova N.V., Mamardashvili N.Z. // Molecules. 2022. Vol. 27. N 23. P. 8619. doi: 10.3390/molecules27238619
  19. Хембрайт П. // Усп. хим. 1977. Т. 46. № 7. С. 1207
  20. Hambright P. // Russ. Chem. Rev. 1977. Vol. 46. N 7. P 1207.
  21. Boucher L.J. // Coord. Chem. Rev. 1972. Vol. 7. N 3. P. 289. doi: 10.1016/S0010-8545(00)80024-7
  22. Doro F.G., Lindsay Smith J.R., Ferreira A.G., Assis M.D. // J. Mol. Catal. (A). 2000. Vol. 164. P. 97. doi: 10.1016/S1381-1169(00)00352-6

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML
Жүктеу

© Russian Academy of Sciences, 2023