A study of reactions among CrCl2, CrCl3(THF)3, and iminopyridine ligands differing in the nature of the substituents at the iminic carbon and at the ortho positions of the aryl ring (2,6-R12C6H3N=CR2(C5H3N) (R1 = R2 = H (L1); R1 = iPr, R2 = H (L2); R1 = H, R2 = CH3 (L3)) but featuring close electron-accepting properties has provided a new example of the redox chemistry of chromium complexes. The reactions of unsubstituted aniline L1 and of L3 with CrCl2 give rise to [(L1•)CrIIICl2(THF)]- (Cr1) and [(L3•)CrIIICl2(THF)]- (Cr3) complexes, respectively, containing chromium in the physical trivalent oxidation state and the ligand in the monoanionic radical state (L•)- as a result of a one-electron transfer from the metal to the ligand. In contrast, the reactions of CrCl2 with the ortho-substituted L2 and of CrCl3(THF)3 with the unsubstituted L1 give rise to [(L2)CrIICl2(THF)]0 (Cr2) and [(L1)CrIIICl3(THF)]0 (Cr4) having the chromium in the divalent and trivalent oxidation states, respectively, and the unperturbed ligand in the neutral state. All four complexes were used, in combination with methylaluminoxane (MAO), as catalyst precursors for the polymerization of ethylene, cyclic olefins (i.e., norbornene and dicyclopentadiene), and 1,3-butadiene. A chromium to ligand synergy, coupled with a good stability of the active intermediate in the presence of the Al activator, proven particularly effective in the polymerization of ethylene, especially for Cr1, giving high molecular weight linear poly(ethylene)s. The formalism in the metal oxidation state does not affect the reactivity toward the cyclic olefins and 1,3-butadiene, while ligand steric effects emerge clearly. The use of bulky ortho substituents shuts down the activity in the polymerization of cyclic olefins, particularly for the bulkier dicyclopentadiene, and reverses the catalyst chemoselectivity in the polymerization of 1,3-butadiene.

Concerted Electron Transfer in Iminopyridine Chromium Complexes: Ligand Effects on the Polymerization of Various (Di)olefins

Leone G.;Bertini F.;Parisini E.;
2018

Abstract

A study of reactions among CrCl2, CrCl3(THF)3, and iminopyridine ligands differing in the nature of the substituents at the iminic carbon and at the ortho positions of the aryl ring (2,6-R12C6H3N=CR2(C5H3N) (R1 = R2 = H (L1); R1 = iPr, R2 = H (L2); R1 = H, R2 = CH3 (L3)) but featuring close electron-accepting properties has provided a new example of the redox chemistry of chromium complexes. The reactions of unsubstituted aniline L1 and of L3 with CrCl2 give rise to [(L1•)CrIIICl2(THF)]- (Cr1) and [(L3•)CrIIICl2(THF)]- (Cr3) complexes, respectively, containing chromium in the physical trivalent oxidation state and the ligand in the monoanionic radical state (L•)- as a result of a one-electron transfer from the metal to the ligand. In contrast, the reactions of CrCl2 with the ortho-substituted L2 and of CrCl3(THF)3 with the unsubstituted L1 give rise to [(L2)CrIICl2(THF)]0 (Cr2) and [(L1)CrIIICl3(THF)]0 (Cr4) having the chromium in the divalent and trivalent oxidation states, respectively, and the unperturbed ligand in the neutral state. All four complexes were used, in combination with methylaluminoxane (MAO), as catalyst precursors for the polymerization of ethylene, cyclic olefins (i.e., norbornene and dicyclopentadiene), and 1,3-butadiene. A chromium to ligand synergy, coupled with a good stability of the active intermediate in the presence of the Al activator, proven particularly effective in the polymerization of ethylene, especially for Cr1, giving high molecular weight linear poly(ethylene)s. The formalism in the metal oxidation state does not affect the reactivity toward the cyclic olefins and 1,3-butadiene, while ligand steric effects emerge clearly. The use of bulky ortho substituents shuts down the activity in the polymerization of cyclic olefins, particularly for the bulkier dicyclopentadiene, and reverses the catalyst chemoselectivity in the polymerization of 1,3-butadiene.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/1146644
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