Abstract
The addition of internal donors (IDs) to the heterogeneous Ziegler-Natta catalyst for propylene polymerization is fundamental to obtain highly isotactic polypropylene, but its role in shaping the stereospecific structure of the catalyst is still not comprehended. In this work, we apply non-empirical structure determination, based on a genetic algorithm and density functional theory calculations, to ternary systems composing MgCl2, TiCl4, and ID. We found that the co-presence of TiCl4 and ID led to the preferential formation of specific surface motifs, involving sharp edges and concavities. This was achieved by concerted adsorption of chelating ID and octahedral TiCl4, and significantly promoted TiCl4 situated in stereospecific environments. The multiplicity of adsorption modes of IDs was found to have a direct consequence in the structural diversity, where phthalate exhibited far greater diversity than 1,3-diether. In conclusion, this study revealed the essentiality of ID-driven reconstruction of MgCl2 in understanding the structure and function of this catalyst.
Supplementary materials
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Supporting Information
Description
Evolutionary progress of supplementary GA run, images of donor templates, detailed GA parameters, discussion on the 7MgCl2/1TiCl4/1DEP composition, most common edges found in the compositions, list of stable structures, classification of stereo-controlling ligands, and simulated vibrational spectrum (PDF)
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Coordinate files
Description
Coordinate files (.mol) of all the energetically accessible structures
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