Elucidating the Key Role of Phosphine-Sulfonate Ligands in Palladium-Catalyzed Ethylene Polymerization: Effect of Ligand Structure on the Molecular Weight and Linearity of Polyethylene

被引:77
作者
Nakano, Ryo [1 ]
Chung, Lung Wa [2 ]
Watanabe, Yumiko [3 ]
Okuno, Yoshishige [3 ]
Okumura, Yoshikuni [4 ]
Ito, Shingo [1 ]
Morokuma, Keiji [5 ]
Nozaki, Kyoko [1 ]
机构
[1] Univ Tokyo, Grad Sch Engn, Dept Chem & Biotechnol, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
[2] South Univ Sci & Technol China, Dept Chem, Shenzhen 518055, Peoples R China
[3] Computat Sci & Technol Informat Ctr, Showa Denko KK, Midori Ku, 1-1-1 Ohnodai, Chiba, Chiba 2670056, Japan
[4] Inst Adv & Core Technol, Showa Denko KK, 2 Nakanosu, Oita, Oita 8701809, Japan
[5] Kyoto Univ, Fukui Inst Fundamental Chem, Sakyo Ku, 34-4 Takano Nishihiraki Cho, Kyoto 6068103, Japan
来源
ACS CATALYSIS | 2016年 / 6卷 / 09期
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
phosphine sulfonate; palladium catalysts; ethylene polymerization; linearity; molecular weight; suppression of beta-hydride elimination; COORDINATION-INSERTION COPOLYMERIZATION; POLAR VINYL MONOMERS; OLEFIN POLYMERIZATION; MECHANISTIC INSIGHTS; CIS/TRANS ISOMERIZATION; METAL CATALYSTS; CHAIN-WALKING; COMPLEXES; NICKEL(II); PROPYLENE;
D O I
10.1021/acscatal.6b00911
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The mechanism of linear polyethylene formation catalyzed by palladium/phosphine sulfonate and the effect of the ligand structure on the catalytic performance, such as linearity and molecular weight of the polyethylene, were reinvestigated theoretically and experimentally. We used dispersion-corrected density functional theory (DFT-D3) to study the entire mechanism of polyethylene formation from (R2PC6H4SO3)PdMe(2,6-lutidine) (R = Me, t-Bu) and elucidated the key steps that determine the molecular weight and linearity of the polyethylene. The alkylpalladium ethylene complex is the key intermediate for both linear propagation and fi-hydride elimination from the growing polymer chain. On the basis of the key species, the effects of substituents on the phosphorus atom (R = t-Bu, i-Pr, Cy, Men, Ph, 2-MeOC6H4, biAr) were further investigated theoretically to explain the experimental results in a comprehensive manner. Thus, the experimental trend of molecular weights of polyethylene could be correlated to the AA G* value between (i) the transition state of linear propagation and (ii) the transition state of the path for ethylene dissociation leading to fi-hydride elimination. Moreover, the experimental behavior of the catalysts under varied ethylene pressure was well explained by our computation on the small set of key species elucidated from the entire mechanism. In our additional experimental investigations, [o-Ani(2)PC(6)H(4)SO(3)]PdH[P(t-Bu)(3)] catalyzed a hydrogen/ deuterium exchange reaction between ethylene and Me0D. The deuterium incorporation from Me0D into the main chain of polyethylene, therefore, can be explained by the incorporation of deuterated ethylene formed by a small amount of Pd H species. These insights into the palladium/phosphine sulfonate system provide a comprehensive understanding of how the phosphine sulfonate ligands function to produce linear polyethylene.
引用
收藏
页码:6101 / 6113
页数:13
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