SCI和EI收录∣中国化工学会会刊

中国化学工程学报 ›› 2024, Vol. 74 ›› Issue (10): 92-99.DOI: 10.1016/j.cjche.2024.06.019

• Full Length Article • 上一篇    下一篇

Palladium-catalyzed dicarbonylation of 1,3-butadiene with bidentate phosphine ligands: A density functional theory study

Zhongxian Yu, Jianhua Song, Dianhua Liu   

  1. East China University of Science and Technology, Shanghai 200237, China
  • 收稿日期:2024-03-02 修回日期:2024-06-12 接受日期:2024-06-19 出版日期:2024-10-28 发布日期:2024-07-30
  • 通讯作者: Dianhua Liu,Tel:+86 21 64252151.E-mail:dhliu@ecust.edu.cn

Palladium-catalyzed dicarbonylation of 1,3-butadiene with bidentate phosphine ligands: A density functional theory study

Zhongxian Yu, Jianhua Song, Dianhua Liu   

  1. East China University of Science and Technology, Shanghai 200237, China
  • Received:2024-03-02 Revised:2024-06-12 Accepted:2024-06-19 Online:2024-10-28 Published:2024-07-30
  • Contact: Dianhua Liu,Tel:+86 21 64252151.E-mail:dhliu@ecust.edu.cn

摘要: DFT calculations have been performed to discover the mechanism for the synthesis of dimethyl adipate (DMA) by 1,3-butadiene (BD) dicarbonylation catalyzed by a complex consisting of palladium and a bidentate diphosphine ligand. The computational results indicate that BD dicarbonylation involves two catalytic stages with the same reaction mechanism including terminal alkenyl insertion, CO migratory insertion, and methanolysis. Four different reaction routes have been explored, the pathway yielding linear DMA has the lowest alkenyl C-H insertion barrier with an overall barrier of 13.4 kcal·mol-1 (1 kcal·mol-1 = 4.184 kJ·mol-1). The regioselectivity of the BD dicarbonylation depends mainly on the barrier of the alkenyl insertion into the palladium-hydrogen complex site. The computations well reproduced the experimentally observed linear selectivity.

关键词: 1,3-Butadiene, Dicarbonylation, DTBPX, DFT, Catalytic cycle

Abstract: DFT calculations have been performed to discover the mechanism for the synthesis of dimethyl adipate (DMA) by 1,3-butadiene (BD) dicarbonylation catalyzed by a complex consisting of palladium and a bidentate diphosphine ligand. The computational results indicate that BD dicarbonylation involves two catalytic stages with the same reaction mechanism including terminal alkenyl insertion, CO migratory insertion, and methanolysis. Four different reaction routes have been explored, the pathway yielding linear DMA has the lowest alkenyl C-H insertion barrier with an overall barrier of 13.4 kcal·mol-1 (1 kcal·mol-1 = 4.184 kJ·mol-1). The regioselectivity of the BD dicarbonylation depends mainly on the barrier of the alkenyl insertion into the palladium-hydrogen complex site. The computations well reproduced the experimentally observed linear selectivity.

Key words: 1,3-Butadiene, Dicarbonylation, DTBPX, DFT, Catalytic cycle