TY - JOUR
T1 - XAS and XES Techniques Shed Light on the Dark Side of Ziegler–Natta Catalysts: Active-Site Generation
AU - Van Silfhout, Roelof
AU - Groppo, Elena
AU - Gallo, Eric
AU - Lamberti, Carlo
AU - Seenivasan, Kalaivani
AU - Lomachenko, Kirill A
AU - Sommazzi, Anna
AU - Bordiga, Silvia
AU - van Silfhout, Roelof G
AU - Kachatkou, Anton
AU - Bras, Wim
PY - 2015/2/24
Y1 - 2015/2/24
N2 - The local structure and the electronic properties of the active Ti sites in heterogeneous Ziegler–Natta catalysts, generated in situ by interaction of the precatalyst with different Al-alkyl activators, were investigated by combining X-ray absorption and valence-to-core X-ray emission spectroscopy (XAS and vtc- XES), coupled with UV/Vis, FTIR, and DFT theoretical calculations. Irrespective of the activator used, the active system was found to be a highly dispersed TiCl3-like phase in which the Ti sites are surrounded, not only by bridged chlorine ligands (with the same bond length of bulk TiCl3), but also by terminal chlorine ligands, at a much shorter distance. These results set Ziegler–Natta catalysts in the category of complex nanomaterials. Despite the observation that the investigated catalysts polymerize ethylene, cutting-edge XAS and XES techniques do not yet offer unequivocal proof for the presence of any alkyl chain attached to the Ti sites, as a consequence of the small fraction of the active sites.
AB - The local structure and the electronic properties of the active Ti sites in heterogeneous Ziegler–Natta catalysts, generated in situ by interaction of the precatalyst with different Al-alkyl activators, were investigated by combining X-ray absorption and valence-to-core X-ray emission spectroscopy (XAS and vtc- XES), coupled with UV/Vis, FTIR, and DFT theoretical calculations. Irrespective of the activator used, the active system was found to be a highly dispersed TiCl3-like phase in which the Ti sites are surrounded, not only by bridged chlorine ligands (with the same bond length of bulk TiCl3), but also by terminal chlorine ligands, at a much shorter distance. These results set Ziegler–Natta catalysts in the category of complex nanomaterials. Despite the observation that the investigated catalysts polymerize ethylene, cutting-edge XAS and XES techniques do not yet offer unequivocal proof for the presence of any alkyl chain attached to the Ti sites, as a consequence of the small fraction of the active sites.
KW - EXAFS spectroscopy · heterogeneous catalysis · titanium · X-ray absorption spectroscopy · Ziegler–Natta catalysts
U2 - 10.1002/cctc.201402989
DO - 10.1002/cctc.201402989
M3 - Article
VL - 7
SP - 1432
EP - 1437
JO - ChemCatChem
JF - ChemCatChem
SN - 1867-3880
ER -