Molecular simulation of selective coordination for various silyl ester Lewis base donors with MgCl2 in Ziegler–Natta catalysis

Abstract

ABSTRACT In this article, we present the influence of substituents with different electron-donating (ED) powers on the coordination properties of bis(benzoyloxy)dimethylsilane (BDMS) on the MgCl2 support of Ziegler–Natta (ZN) catalysts through molecular simulation of different adsorption adducts. Thermodynamically, the most favourable adsorption structure was found with the diaminoborane substituent in a bridging mode on the (110) crystalline facet, representing a 37.63% increase at PBEh/TZVP in the adsorption strength of the original silyl ester. Generally, the higher the ED strength of the substituent, the higher the exergonicity of donor coordination. All of the new donors except those containing the nitro and formyl groups are preferably chemisorbed on the (110) surface. While the nitro, formyl, vinyl, and hydroxyl substitutions deteriorated the isotacticity of the polymer, a diaminoborane group was predicted to enhance the isotactic index by 306% relative to the original donor. Particularly, nitrophenyl could improve the isotactic index by 69% while its complexation remained in the thermodynamically controlled regime. Overall, the present DFT study demonstrated how a systematic exploration of substituents over a wide range of ED power can help in the design of new Lewis base donors for ZN catalysis.