Abstract
The OSSO-type diol ligand and the TiIV dichloride and bis-isopropoxide complexes with this ligand were synthesized. The structure of the latter complex was determined by single-crystal X-ray diffraction analysis. The catalytic activity of the systems based on the complexes (OSSO)TiCl2 and (OSSO)Ti(OPri)2, which were activated with mixtures of alkylaluminum chlorides (Et2AlCl, Et3Al2Cl3) and dibutylmagnesium, was studied in the polymerization of ethylene and its copolymerization with propylene. It was found that the homopolymerization affords ultra-high-molecular-weight polyethylene (UHMWPE) with a molecular weight up to 10.6·106, and the copolymerization gives copolymers containing up to 43 mol.% propylene units.
References
S. M. Kurtz, in The UHMWPE Handbook: Ultra-high Molecular Weight Polyethylene in Total Joint Replacement, Elsevier Academic Press, 2004.
A. J. Peacock, Handbook of Polyethylene: Structures, Properties and Applications, Marcel Dekker, New York, NY, USA, 2000.
A. N. Ozerin, S. S. Ivanchev, S. N. Chvalun, V. A. Aulov, N. I. Ivancheva, N. F. Bakeev, Catalyst. Polym. Sci., Ser. A, 2012, 54, 950; DOI: https://doi.org/10.1134/S0965545X12100033.
B. P. Rotzinger, H. D. Chanzy, P. Smith, Polymer, 1989, 30, 1814–1819; DOI: https://doi.org/10.1016/0032-3861(89)90350-9.
S. Ronca, G. Forte, H. Tjaden, S. Rastogi, Ind. Eng. Chem. Res., 2015, 54, 7373–7381; DOI: https://doi.org/10.1021/acs.iecr.5b01469.
A. A. Antonov, K. P. Bryliakov, Eur. Polym. J., 2021, 142, 110162; DOI: https://doi.org/10.1016/j.eurpolymj.2020.110162.
S. Ch. Gagieva, V. A. Tuskaev, I. V. Fedyanin, M. I. Buzin, V. G. Vasil’ev, G. G. Nikiforova, E. S. Afanas’ev, S. V. Zubkevich, D. A. Kurmaev, N. A. Kolosov, E. S. Mikhaylik, E. K. Golubev, A. I. Sizov, B. M. Bulychev, J. Organomet. Chem., 2017, 828, 89–95; DOI: https://doi.org/10.1016/j.jorganchem.2016.11.026.
V. A. Tuskaev, S. Ch. Gagieva, D. A. Kurmaev, V. N. Khrustalev, P. V. Dorovatovskii, E. S. Mikhaylik, E. K. Golubev, M. I. Buzin, S. V. Zubkevich, G. G. Nikiforova, V. G. Vasil’ev, B. M. Bulychev, K. F. Magomedov, J. Organomet. Chem., 2018, 877, 85–91; DOI: https://doi.org/10.1016/j.jorganchem.2018.09.014.
V. A. Tuskaev, S. Ch. Gagieva, D. A. Kurmaev, E. K. Melnikova, S. V. Zubkevich, M. I. Buzin, G. G. Nikiforova, V. G. Vasil’ev, D. Saracheno, V. S. Bogdanov, V. I. Privalov, B. M. Bulychev, Appl. Organomet. Chem., 2020, 34, e5933, DOI: https://doi.org/10.1002/aoc.5933.
Z. Janas, Coord. Chem. Rev., 2010, 254, 2227–2233; DOI: https://doi.org/10.1016/j.ccr.2010.05.008.
N. Nakata, T. Toda, A. Ishii, Polym. Chem., 2011, 2, 1597–1610; DOI: https://doi.org/10.1039/c1py00058f.
V. Paradiso, V. Capaccio, D. H. Lamparelli, C. Capacchione, Coord. Chem. Rev., 2021, 429, 213644; DOI: https://doi.org/10.1016/j.ccr.2020.213644.
R. D. J. Froese, D. G. Musaev, T. Matsubara, K. Morokuma, J. Am. Chem. Soc., 1997, 119, 7190–7196; DOI: https://doi.org/10.1021/ja970861g.
R. D. J. Froese, D. G. Musaev, T. Matsubara, K. Morokuma, Organometallics, 1999, 18, 373–379; DOI: https://doi.org/10.1021/om9809466.
L. Lavanant, A. Silvestru, A. Faucheux, L. Toupet, R. F. Jordan, J.-F. Carpentier, Organometallics, 2005, 24, 5604–5619; DOI: https://doi.org/10.1021/om050560c.
V. A. Tuskaev, S. Ch. Gagieva, A. S. Lyadov, D. A. Kurmaev, S. V. Zubkevich, S. S. Shatokhin, V. E. Simikin, E. S. Mikhailik, E. K. Golubev, G. G. Nikiforova, M. I. Buzin, V. G. Vasil’ev, B. M. Bulychev, Petrol. Chem., 2020, 60, 329–333; DOI: https://doi.org/10.1134/S0965544120030226.
V. A. Tuskaev, S. Ch. Gagieva, A. V. Churakov, D. A. Kurmaev, K. F. Magomedov, M. D. Evseeva, E. K. Golubev, M. I. Buzin, G. G. Nikiforova, D. Saracheno, S. S. Shatokhin, B. M. Bulychev, J. Organomet. Chem., 2022, 977, 122457; DOI: https://doi.org/10.1016/j.jorganchem.2022.122457.
S. Alvarez, Chem. Rev., 2015, 115, 13447–13483; DOI: https://doi.org/10.1021/acs.chemrev.5b00537.
K. Mikami, M. Terada, T. Nakai, J. Am. Chem. Soc., 1990, 112, 3949–3954; DOI: https://doi.org/10.1021/ja00166a035.
Sintezy organicheskikh preparatov [Synthesis of Organic Products], Ed. B A Kazanski, Izd-vo Inostran. Lit., Moscow, 1949, 2, 116–118 (in Russian).
O. V. Dolomanov, L. J. Bourhis, R. J. Gildea, J. A. K. Howard, H. Puschmann, J. Appl. Cryst., 2009, 42, 339. DOI: https://doi.org/10.1107/S0021889808042726.
Author information
Authors and Affiliations
Corresponding author
Additional information
Dedicated to Academician of the Russian Academy of Sciences I. P. Beletskaya on the occasion of her anniversary.
The study was financially supported by the Russian Science Foundation (Project No. 23-23-00308). The NMR spectroscopic studies of copolymers were performed within the framework of the state assignment “Substances and materials for safety, reliability, and energy efficiency” (No. AAAA-A21-121011590086-0). The DSC and X-ray diffraction studies were carried out using the equipment of the Center for Molecular Structure Studies of the A. N. Nesmeyanov Institute of Organoelement Compounds of the Russian Academy of Sciences with the financial support from the Ministry of Science and Higher Education of the Russian Federation (state assignment No. 075-00697-22-00). The investigation of the catalytic activity of titanium alkoxides using the model ethylene polymerization reaction and the studies of the properties of the synthesized polyethylene samples were performed within the framework of the Program of the Interdisciplinary Research and Educational School of the Lomonosov Moscow State University “The Future of the Planet and Global Environmental Changes”.
No human or animal subjects were used in this research.
The authors declare no competing interests.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, Vol. 72, No. 4, pp. 1093–1098, April, 2023.
Rights and permissions
About this article
Cite this article
Tuskaev, V.A., Gagieva, S.C., Evseeva, M.D. et al. TiIV complexes with an OSSO-type diol ligand in the catalysis of olefin polymerization. Russ Chem Bull 72, 1093–1098 (2023). https://doi.org/10.1007/s11172-023-3876-4
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11172-023-3876-4