Mechanistic studies of HF/BF3-catalyzed anthracene polymerization to prepare mesophase pitch

Xi Fan; Qiang Ren; Haiping Shen; Chunlu Wang; Qing Ni; Jun Long

doi:10.1007/s00894-023-05819-7

Mechanistic studies of HF/BF₃-catalyzed anthracene polymerization to prepare mesophase pitch

J Mol Model. 2024 Jan 6;30(1):25. doi: 10.1007/s00894-023-05819-7.

Authors

Xi Fan¹, Qiang Ren², Haiping Shen², Chunlu Wang², Qing Ni², Jun Long²

Affiliations

¹ Research Institute of Petroleum Processing, SINOPEC, Beijing, 10083, China. fanxi_fanxi@163.com.
² Research Institute of Petroleum Processing, SINOPEC, Beijing, 10083, China.

PMID: 38183499
DOI: 10.1007/s00894-023-05819-7

Abstract

Context: The mesophase pitch prepared by acid catalytic method typically had the advantages of low softening point and high solubility. To fully understand the mechanism of acid-catalyzed reactions and gain a deeper understanding of the microstructure of mesophase pitch, this article studied the mechanism of hydrofluoride/boron trifluoride (HF/BF₃)-catalyzed anthracene using molecular simulation methods. The results showed that there might be two types of carbocations present in the system: classical and non-classical carbocations, and five reactions might occur, protonation reaction, chain elongation reaction, intramolecular cyclization reaction, deprotonation reaction, and dehydrogenation reaction. Classical carbocations acted as reactive intermediates in the chain elongation reaction and intramolecular cyclization reaction. When anthracene occurred chain elongation reactions with carbocations to form polymers, the generation of the tetramer required lager energy barriers than that of the dimer and trimer. The stiffness and flatness of molecules could be increased via intramolecular cyclization reactions. The polymers of anthracene might also occurred dehydrogenation reactions when the non-classical carbocations played the role of reactive intermediates. The dehydrogenation reactions required large energy barriers, which might be the reason for the product having a high aliphatic hydrogen content.

Method: The Materials Studio (MS) 2020 software was used to complete the simulation. The atomic charge distribution calculation and the structure optimization of molecules were carried out using the B3LYP functional and DNP basis. The DFT-D (TS) dispersion corrections were added to calculate the dispersion interaction between aromatic molecules. The complete LST/QST method was used to search the transition states and calculate the reaction energy barrier.

Keywords: Acid catalyst; Anthracene; Mechanistic; Mesophase pitch; Molecular simulation.