Probing the Interaction of Diester Internal Donors (ID) with AlEt<sub>3</sub> on Ziegler-Natta Surfaces: A Comparison Between Binary (MgCl<sub>2</sub>/ID) and Ternary (MgCl<sub>2</sub>/ID/TiCl<sub>4</sub>) Formulations

Organic electron donors are essential components of Ziegler-Natta (ZN) catalysts to produce isotactic polypropylene. In particular, aromatic or aliphatic diesters are widely used as ‘Internal Donors’ (ID) in MgCl<sub>2</sub>/ID/TiCl<sub>4</sub> precatalyst formulations. Diest...

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Bibliographic Details
Main Authors: Felicia Daniela Cannavacciuolo, Giuseppe Antinucci, Roberta Cipullo, Vincenzo Busico
Format: Article
Language:English
Published: MDPI AG 2025-05-01
Series:Molecules
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Online Access:https://www.mdpi.com/1420-3049/30/10/2176
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Summary:Organic electron donors are essential components of Ziegler-Natta (ZN) catalysts to produce isotactic polypropylene. In particular, aromatic or aliphatic diesters are widely used as ‘Internal Donors’ (ID) in MgCl<sub>2</sub>/ID/TiCl<sub>4</sub> precatalyst formulations. Diesters are reactive with AlEt<sub>3</sub> (by far the most common ZN precatalyst activator) and are partly removed from the solid phase in the early stages of the polymerization process; this is detrimental for catalyst functioning, and a surrogate donor (‘External Donor’ (ED), usually an alkoxysilane) is added to the system to restore performance. Recent studies, however, demonstrated that even in cases where most of the diester is extracted by AlEt<sub>3</sub>, the active sites retain a ‘memory’ of it in several aspects of the catalytic behavior (such as, e.g., the average productivity and the polydispersity index of the polymer produced). Considering that the residual diester is always in molar excess with respect to the active Ti, one may speculate that long-lasting interactions between the latter and diester molecules can occur. In turn, this should imply that the reactivity of AlEt<sub>3</sub> is different with binary MgCl<sub>2</sub>/ID or ternary MgCl<sub>2</sub>/ID/TiCl<sub>4</sub> mixtures. In this work, the latter hypothesis was explored for a library of diester IDs with large structural diversity. In line with the anticipation, the fractional amount of ID extracted by AlEt<sub>3</sub> was generally lower for ternary mixtures, although to an extent exquisitely dependent on diester structure.
ISSN:1420-3049