Coordination structure dominated performance of single-atomic Pt catalyst for anti-Markovnikov hydroboration of alkenes

• Published in: Science China materials 2020-06, Vol.63 (6), p.972-981
• Main Authors: Xu, Qi, Guo, ChenXi, Tian, Shubo, Zhang, Jian, Chen, Wenxing, Cheong, Weng-Chon, Gu, Lin, Zheng, Lirong, Xiao, Jianping, Liu, Qiang, Li, Bijie, Wang, Dingsheng, Li, Yadong
• Format: Article
• Language: English
• Subjects: Alkenes; Atomic properties; Catalysts; Catalytic activity; Chemistry and Materials Science; Chemistry/Food Science; Coordination; Density functional theory; Esters; Hydroboration; Materials Science; Phase diagrams
• ISSN: 2095-8226; 2199-4501
• DOI: 10.1007/s40843-020-1334-6

The rational design of efficient single-atomic (SA) catalysts is essential and highly desirable but impeded by the lack of sufficient acknowledge between structure and property. To this end, it is critical to clarify the effect of the coordination structure of active metal centers on the catalytic activities for the design of such catalysts. Here, we report that different coordination structures of SA Pt catalysts can dramatically influence their activities for anti-Markovnikov hydroboration of alkenes. Compared with the other two coordination structures (Pt-N 4 and Pt-O 2 ), the SA Pt species coordinated with three O atoms (Pt-O 3 ) display the highest turnover number value of 3288 for the hydroboration reaction to access the important alkylboronic esters. Density functional theory calculations reveal that a superior catalytic activity can be expected for alkene hydroboration over the three O coordinated Pt species due to the lowest reaction energy (Δ G ) limiting step from the reaction phase diagram.