Catalytic Synthesis of Butene-1 and Hexene-1 in the Homogeneous Oligomerization of Ethylene in the Presence of Nickel Complexes Based on N-Heteroaryl-Substituted α-Diphenylphosphinoglycines

封面

如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

It has been experimentally shown that N-heteroaryl-substituted α-diphenylphosphinoglycines N-(pyrazin-2-yl)-α-diphenylphosphinoglycine, N-(pyridin-2-yl)-α-diphenylphosphinoglycine and N-(pyrimidin-2-yl)-α-diphenylphosphinoglycine obtained by the reaction of three-component condensation of diphenylphosphine, the corresponding primary amine and glyoxylic acid monohydrate are capable in combination with Ni(COD)₂, where COD is cyclooctadiene-1,5, to form active forms of catalysts for selective homogeneous dimerization and trimerization of ethylene with the formation of butene-1 and hexene-1 as the main products. It has been established that the obtained organo-nickel catalytic systems provide a yield of short-chain (C₄–C₆) olefins at the level of 90% with a selectivity for linear α-olefins of 97%. The study of the influence of temperature on the process of homogeneous ethylene oligomerization using the obtained compounds made it possible to establish that the optimal temperature for ethylene oligomerization, providing the highest selectivity to butene-1 and hexene-1, is 80–105°C at the optimum pressure of ethylene is 20–35 atm. Under these conditions, the selectivity for butenes is 71.4–72.6% (selectivity for butene-1 – 69.3–71.1%), for hexenes 20.6–21.2% (selectivity for hexene-1 – 19.2–19.5%), and the optimal duration of the oligomerization process at a temperature 105°C is 1.5 h, which provides the rate of formation of butene-1 equal to 168.1 golig gNi⁻¹h⁻¹) and the rate of formation of hexene-1 – 47.3 golig gNi⁻¹h⁻¹).

全文:

受限制的访问

作者简介

О. Soficheva

Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences

编辑信件的主要联系方式.
Email: olga.soficheva@iopc.ru
俄罗斯联邦, Arbuzov str., 8, Kazan, 420088

G. Bekmukhamedov

Kazan Federal University

Email: olga.soficheva@iopc.ru
俄罗斯联邦, Kremlyovskaya str., 18, Kazan, 420008

D. Yakhvarov

Kazan Federal University

Email: olga.soficheva@iopc.ru
俄罗斯联邦, Kremlyovskaya str., 18, Kazan, 420008

参考

  1. Fischer K., Jonas K., Misbach P., Stabba R., Wilke G. // Angew. Chem. Int. Ed. Engl. 1973. V. 12. P. 943.
  2. Wilke G. // J. Organomet. Chem. 1980. V. 200. P. 349.
  3. Peuckert M., Keim W. // Organometallics. 1983. V. 2. P. 594.
  4. Breuil P.-A.R., Magna L., Olivier-Bourbigou H. // Catal. Lett. 2015. V. 145. № 1. P. 173.
  5. Keim W., Kowaldt F. H., Goddard R., Krüger C. // Angew. Chem. Int. Ed. Engl. 1978. V.17. P. 466.
  6. Peuckert M., Keim W., Storp S., Weber R. S. // J. Mol. Catal. 1983. V. 20. P. 115.
  7. Keim W., Behr A., Gruber B., Hoffmann B., Kowaldt F., Kürschner U., Limbäcker B., Sistig F. // Organometallics. 1986. V. 5. P. 2356.
  8. Keim W., Schulz R. // J. Mol. Catal. 1994. V. 92. P. 21.
  9. Keim W. // Vysokomol. Soedin. Ser. A. 1994. V. 36. P. 1644.
  10. Pietsch J., Braunstein P., Chauvin Y. // New J. Chem. 1998. P. 467.
  11. Heinicke J., Köhler M., Peulecke N., Keim W. // J. Catal. 2004. V. 225. P. 16.
  12. Keim W. // Angew. Chem. Int. Ed. 2013. V. 52. P. 12492.
  13. Britovsek G. J.P., Malinowski R., McGuinness D.S., Nobbs J. D., Tomov A. K., Wadsley A. W., Young C. T. // ACS Catal. 2015. V. 5. P. 6922.
  14. Herrmann W. A., Beller M., Paciello R. Applied Homogeneous Catalysis with Organometallic Compounds. Wiley, 2017.
  15. Olivier-Bourbigou H., Breuil P. A.R., Magna L., Michel T., Fernandez Espada Pastor M., Delcroix D. // Chem. Rev. 2020. V. 120. № 15. P. 7919.
  16. Bekmukhamedov G. E., Sukhov A. V., Kuchkaev A. M., Yakhvarov D. G. // Catalysts. 2020. V. 10. № 5. P. 498.
  17. Petit J., Magna L., Mézailles N. // Coord. Chem. Rev. 2022. V. 50. № 214227.
  18. Mecking S. // Angew. Chem., Int. Ed. 40. 2001. V. 3. P. 534.
  19. McGuinness D.S., Wasserscheid P., Keim W., Morgan D., Dixon J. T., Bollmann A., Maumela H., Hess F., Englert U. // J. Am. Chem. Soc. 2003. V. 125. P. 5272.
  20. Speiser F., Braunstein P., Saussine L. // Acc. Chem. Res. 2005. V. 38. P. 784.
  21. McGuinness D.S. // Chem. Rev. 2011. V. 111. P. 2321.
  22. Hao P., Song S., Xiao T., Li Y., Redshaw C., Sun W. H. // Polyhedron. 2013. V. 52. P. 1138.
  23. Kuhn P., Sémeril D., Jeunesse C., Matt D., Lutz P., Welter R. // Eur. J. Inorg. Chem. 2005. P. 1477.
  24. Kuhn P., Semeril D., Jeunesse C., Matt D., Neuburger M., Mota A. // Chem. Eur. J. 2006. V. 12. P. 5210.
  25. Braunstein P., Chauvin Y., Mercier S., Saussine L. // Chimie. 2005. V. 8. P. 31.
  26. Heinicke J., He M., Dal A., Klein H., Hetche O., Keim W., Flörke U., Haupt H. // Eur. J. Inorg. Chem. 2000. P. 431.
  27. Wasserscheid P., Hilgers C., Keim W. // J. Mol. Catal. A: Chem. 2004. V. 214. P. 83.
  28. Heinicke J., Köhler M., Peulecke N., Kindermann M. K., Keim W., Köckerling M. // Organometallics. 2005. V. 24. P. 344.
  29. Kuhn P., Semeril D., Jeunesse C., Matt D., Lutz P. J., Louis R., Neuburger M. // Dalton Trans. 2006. P. 3647.
  30. Scholz J., Hager V., Wang X., Kohler F. T.U., Sternberg M., Haumann M., Szesni N., Meyer K., Wasserscheid P. // ChemCatChem. 2014. V. 6. P. 162.
  31. Kohler F. T.U., Gärtner K., Hager V., Haumann M., Sternberg M., Wang X., Szesni N., Meyer K., Wasserscheid P. // Catal. Sci. Technol. 2014. V. 4. P. 936.
  32. Heinicke J., Lach J., Basvani K. R., Peulecke N., Jones P. G., Köckerling M. // Phosphorus Sulfur Silicon Relat. Elem. 2011. V. 186. P. 666.
  33. Фомина (Софьичева) О.С., Синяшин О. Г., Хайнике И., Яхваров. Д.Г. // Бутлеровские сообщения. 2012. Т. 10. С. 63.
  34. Ghalib M., Lach J., Fomina O. S., Yakhvarov D. G., Jones P. G., Heinicke J. // Polyhedron. 2014. V. 77. P. 10.
  35. Lach J., Peulecke N., Kindermann M. K., Palm G. J., Köckerling M., Heinicke J. W. // Tetrahedron. 2015. V.71. P. 4933.
  36. Fomina O. S., Heinicke J. W., Sinyashin O. G., Yakhvarov D. G. // Phosphorus Sulfur Silicon Relat. Elem. 2016. V. 191. P. 1478.
  37. Peulecke N., Yakhvarov D. G., Heinicke J. W. // Eur J. Inorg. Chem. 2019. P. 1507.
  38. Soficheva O. S., Bekmukhamedov G. E., Dobrynin A.B, Heinicke J. W., Sinyashin O. G., Yakhvarov D. G. // Mendeleev Commun. 2019. V. 29. P. 575.
  39. Soficheva O. S., Nesterova A. A., Dobrynin A. B., Zueva E. M., Heinicke J. W., Sinyashin O. G., Yakhvarov D. G. // Mendeleev Commun. 2020. V. 30. P. 516.
  40. Kagileva A. A., Kagilev A. A., Kantyukov A. O., Gafurov Z. N., Sakhapov I. F., Bekmukhamedov G. E., Khayarov K. R., Zueva E. M., Soficheva O. S., Yakhvarov D. G. // New J. Chem. 2022. V. 46. P. 17303.

补充文件

附件文件
动作
1. JATS XML
2. Schema 1.

下载 (96KB)
3. Fig.1

下载 (138KB)
4. Fig.2

下载 (182KB)
5. Fig.3

下载 (66KB)
6. Fig.4

下载 (138KB)
7. Fig.5

下载 (136KB)
8. Fig.6

下载 (69KB)