Palladium Complexes of Pyrimidine-2-thiones: Synthesis, Structures, and Properties
- Авторлар: Kuzovlev A.S.1,2, Gordeeva N.A.3, Pastukhova Z.Y.3, Chernyshev V.V.1,4, Buzanov G.A.5, Dunaev S.F.1, Bruk L.G.3
- 
							Мекемелер: 
							- Moscow State University
- Tyumen State University
- Russian Technological University (MIREA)
- Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences
- Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
 
- Шығарылым: Том 50, № 1 (2024)
- Беттер: 53-61
- Бөлім: Articles
- URL: https://cardiosomatics.ru/0132-344X/article/view/667628
- DOI: https://doi.org/10.31857/S0132344X24010063
- EDN: https://elibrary.ru/OSLSPO
- ID: 667628
Дәйексөз келтіру
Аннотация
Complexes [PdL2Cl2] (I) and [PdL2Вr2] (II) (L is 5-acetyl-6-methyl-4-(3-nitrophenyl)-1,2,3,4-tetrahydropyrimidine-2-thione) are synthesized and characterized by spectral methods (1Н, 13С NMR and IR spectroscopy). The crystal structure of complex I is determined (CIF file ССDС no. 2233053) in which the palladium atom is coordinated by two halide ions and two sulfur atoms of two ligands L in a distorted square planar geometry. The catalytic activity of the synthesized palladium(II) complexes in the model epoxidation of allyl alcohol is estimated in comparison with the catalytic activity of the corresponding palladium halides and titanium-containing zeolite TS-1.
Негізгі сөздер
Толық мәтін
 
												
	                        Авторлар туралы
A. Kuzovlev
Moscow State University; Tyumen State University
							Хат алмасуға жауапты Автор.
							Email: a.s.kuzovlev@gmail.com
				                					                																			                												                	Ресей, 							Moscow; Tyumen						
N. Gordeeva
Russian Technological University (MIREA)
														Email: a.s.kuzovlev@gmail.com
				                					                																			                												                	Ресей, 							Moscow						
Zh. Pastukhova
Russian Technological University (MIREA)
														Email: a.s.kuzovlev@gmail.com
				                					                																			                												                	Ресей, 							Moscow						
V. Chernyshev
Moscow State University; Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences
														Email: a.s.kuzovlev@gmail.com
				                					                																			                												                	Ресей, 							Moscow; Moscow						
G. Buzanov
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
														Email: a.s.kuzovlev@gmail.com
				                					                																			                												                	Ресей, 							Moscow						
S. Dunaev
Moscow State University
														Email: a.s.kuzovlev@gmail.com
				                					                																			                												                	Ресей, 							Moscow						
L. Bruk
Russian Technological University (MIREA)
														Email: a.s.kuzovlev@gmail.com
				                					                																			                												                	Ресей, 							Moscow						
Әдебиет тізімі
- Kokina T.E., Glinskaya L. A., Sheludyakova L. A. et al. // Polyhedron. 2019. V. 163. P. 121.
- Moro A.C., Mauro A. E., Netto A. V.G. et al. // Eur. J. Med. Chem. 2009. V. 44. № 11. P. 4611.
- Nadeem S., Bolte M., Ahmad S. et al. // Inorg. Chim. Acta. 2010. V. 363. № 13. P. 3261.
- Rohini G., Ramaiah K., Aneesrahman K. N. et al. // Appl. Organomet. Chem. 2018. V. 32. № 12. P. 4567.
- Da Silva D. L., Reis F. S., Muniz D. R. et al. // Bioorg. Med. Chem. 2012. V. 20. № 8. P. 2645.
- Sashidhara K.V., Avula S. R., Sharma K. et al. // Eur. J. Med. Chem. 2013. V. 60. P. 120.
- Kuzovlev A.S., Volkova D. A., Parfenova I. V. et al. // New J. Chem. 2020. V. 44. P. 7865.
- Kappe C.O. // Eur. J. Med. Chem. 2000. V. 35. P. 1043.
- Sati B. E., Sati H., Nargund L. V.G et al. // Orient. J. Chem. 2012. V. 28. № 2. P. 1055.
- Chikhale R., Thorat S., Pant A. et al. // Bioorg. Med. Chem. 2015. V. 23. № 20. P. 6689.
- Sawant R.L., Sarode V. I., Jadha G. D. et al. // Med. Chem. Res. 2011. V. 21. № 8. P. 1825.
- Kwon O.W., Moon E., Chari M. A. et al. // Bioorg. Med. Chem. Lett. 2012. V. 22. № 16. Р. 5199.
- Shkurko O.P., Tolstikova T. G., Sedova V. F. // Rus. Chem. Rev. 2016. V. 85. № 10. P. 1056.
- Lauro G., Strocchia M., Terracciano S. et al. // Eur. J. Med. Chem. 2014. V. 80. P. 407.
- Crespo A., El Maatougui A., Biagini P. et al. // ACS Med. Chem. Lett. 2013. V. 4. № 11. P. 1031.
- Cepeda V., Fuertes M., Castilla J. et al. // Anti-Cancer Agents Med. Chem. 2007. V. 7. № 1. P. 3.
- Alderden R.A., Hall M. D., Hambley T. W. // J. Chem. Ed. 2006. V. 83. № 5. P. 728.
- Kartalou, M. Essigmann, J.M. // Mut. Res. 2001. V. 478. № 1–2. Р. 23.
- De Moura T. R., Cavalcanti S. L., Sakamoto-Hojo E.T. et al. // Transition Met. Chem. 2017. V. 42. № 6. P. 565.
- Dorairaj D.P., Haribabu J., Hsu S. C.N. et al. // Inorg. Chem. Commun. 2021. V. 134. P. 109018.
- Dorairaj D.P., Haribabu J., Chithravel V. et al. // Res. Chem. 2021. V. 3. P. 100157.
- Bharati P., Bharti A., Nath P. et al. // Inorg. Chim. Acta. 2016. V. 443. P. 160.
- Pearson R.G. // Phys. Inorg. Chem. 1963. V.85. № 22. P. 3533.
- Ruan J., Xiao J. // Acc. Chem. Res. 2011. V. 44. № 8. Р. 614.
- Sherwood J., Clark J. H., Fairlamb I. J.S. et al. // Green Chem. 2019. V. 21. P. 2164.
- Gadge S.T., Bhanage B. M. // RSC Adv. 2014. V. 4. P. 10367.
- Wang D., Weinstein A. B., White P. B. et al. // Chem. Rev. 2018. V. 118. № 5. P. 2636.
- Engle K.M., Yu J-Q. // J. Org. Chem. 2013. V. 78. P. 8927.
- Zhang L-M., Li H-Y., Li H-X. et al. // Inorg. Chem. 2017. V. 56. P. 11230.
- Jia W-G., Gao L-L, Wang Z-B. et al. // RSC Adv. 2017. V. 7. P. 42792.
- Chernyshev V.V. // Russ. Chem. Bull. Int. Ed. 2001. V. 50. P. 2273.
- Cerny R. // Crystals. 2017. V. 7. P. 142.
- Hughes C.E., Reddy G. N.M., Masiero S. et al. // Chem. Sci. 2017. V. 8. P. 3971.
- Pawley G.S. // J. Appl. Crystallogr. 1981. V. 14. P. 357.
- Zlokazov V.B., Chernyshev V. V. // J. Appl. Crystallogr. 1992. V. 25. P. 447.
- Zhukov S.G., Chernyshev V. V., Babaev E. V. et al. // Z. Kristallogr. 2001. V. 216. P. 5.
- Zlokazov V.B., Chernyshev V. V. // J. Appl. Crystallogr. 1992. V. 25. P. 447.
- Andreev S.V., Zverev S. A., Zamilatskov I. A. et al. // Acta Crystallorg. C. 2017. V. 73. P. 47.
- Erzina D.R., Zamilatskov I.A, Stanetskaya N. M. et al. // Eur. J. Org. Chem. 2019. P. 1508.
- Spek A.L. // Acta Crystallorg. D. 2009. V. 65. P. 148.
- Pastukhova Zh. Yu., Levitin V. V., Katsman E. A. et al. // Kinet. Catal. 2021. V. 62. № 5. P. 551.
- Groom C.R., Allen F. H. // Angew. Chem. 2014. V. 53. P. 662.
- Bordiga S., Bonina F., Damin A. et al. // Phys. Chem. Chem. Phys. 2007. V. 9. № 35. P. 4854.
- Taramasso M., Perego G., Notari B. US Pat. № 4410501. 1983.
- Flaningen E.M., Bennett J. M., Grose R. W. et al. // Nature. 1978. V. 271. P. 512.
- Lane B.S., Burgess K. // Chem. Rev. 2003. V. 103. P. 2457.
Қосымша файлдар
 
				
			 
						 
					 
						 
						 
						

 
  
  
  Мақаланы E-mail арқылы жіберу
			Мақаланы E-mail арқылы жіберу 
 Ашық рұқсат
		                                Ашық рұқсат Рұқсат берілді
						Рұқсат берілді




