| Electron-rich platinum single sites anchored on sulfur-doped covalent organic frameworks for boosting anti-Markovnikov hydrosilylation of alkenes | |
Kou, Jinfang1; Fang, J(方建)1 ; Li, Jianfeng1; Zhao, Huacheng1; Gao, Mengmeng1; Zeng, Gong1; David Wang, Wei1; Zhang, Fengwei2; Ma, JT(马建泰)1; Dong, ZP(董正平)1 | |
| 2023-05-01 | |
| Source Publication | CHEMICAL ENGINEERING JOURNAL Impact Factor & Quartile |
| ISSN | 1385-8947 |
| Volume | 463 |
| Abstract | Selective catalytic hydrosilylation of alkenes for the synthesis of organosilicon products is very important in the fine chemical industry. Nevertheless, conventional Pt-based homogeneous catalysts are hindered by their low reaction selectivity, catalyst residues, and Pt leaching. In this study, a series of covalent organic frameworks (COFs)-anchored single-site Pt catalysts for achieving high-performance alkene hydrosilylation were prepared, and comprehensive characterizations confirmed that the actual coordination environment of Pt active sites is NS-Pt-Cl2. The resulting Pt(0.75%)@BTT-BPh-COF catalyst exhibited superior activity for the anti-Markovnikov hydrosilylation of alkenes with an excellent selectivity (>99%) under solvent-free conditions. Experimental and theoretical analysis revealed that the excellent catalytic performance is attributed to the effective charge transfer and strong coordination effect between Pt and S, N-co-doped COFs, which is conducive to the generation of electron-rich and highly active Pt single sites. High catalyst stability was maintained during recycling experiments due to the strong anchoring effect of the COFs support on atomically dispersed Pt single sites as well as the pore confinement effect. This study not only describes the precise design for the state-of-the-art catalysts with accurate active sites but also affords in-depth insights into alkene hydrosilylation. © 2023 Elsevier B.V. |
| Keyword | Catalyst activity Catalyst selectivity Charge transfer Chemical industry Hydrosilylation Olefins Sulfur Active site Anti-markovnikov hydrosilylation Catalytic hydrosilylation Covalent organic frameworks Electron-rich Hydrosilylations Platinum single site catalyst Single sites Single-site catalysts ]+ catalyst |
| Publisher | Elsevier B.V. |
| DOI | 10.1016/j.cej.2023.142255 |
| Indexed By | EI |
| Language | 英语 |
| EI Accession Number | 20231213745488 |
| EI Keywords | Platinum |
| EI Classification Number | 547.1 Precious Metals ; 802.2 Chemical Reactions ; 803 Chemical Agents and Basic Industrial Chemicals ; 804 Chemical Products Generally ; 804.1 Organic Compounds ; 805 Chemical Engineering, General |
| Original Document Type | Journal article (JA) |
| Citation statistics | |
| Document Type | 期刊论文 |
| Identifier | https://ir.lzu.edu.cn/handle/262010/500476 |
| Collection | 化学化工学院 |
| Corresponding Author | Zhang, Fengwei |
| Affiliation | 1.State Key Laboratory of Applied Organic Chemistry, Laboratory of Special Function Materials and Structure Design of the Ministry of Education, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou; 730000, China; 2.Institute of Crystalline Materials, Institute of Molecular Science, Shanxi University, Taiyuan; 030006, China |
| First Author Affilication | College of Chemistry and Chemical Engineering |
| Recommended Citation GB/T 7714 | Kou, Jinfang,Fang, Jian,Li, Jianfeng,et al. Electron-rich platinum single sites anchored on sulfur-doped covalent organic frameworks for boosting anti-Markovnikov hydrosilylation of alkenes[J]. CHEMICAL ENGINEERING JOURNAL,2023,463. |
| APA | Kou, Jinfang.,Fang, Jian.,Li, Jianfeng.,Zhao, Huacheng.,Gao, Mengmeng.,...&Dong, Zhengping.(2023).Electron-rich platinum single sites anchored on sulfur-doped covalent organic frameworks for boosting anti-Markovnikov hydrosilylation of alkenes.CHEMICAL ENGINEERING JOURNAL,463. |
| MLA | Kou, Jinfang,et al."Electron-rich platinum single sites anchored on sulfur-doped covalent organic frameworks for boosting anti-Markovnikov hydrosilylation of alkenes".CHEMICAL ENGINEERING JOURNAL 463(2023). |
| Files in This Item: | There are no files associated with this item. | ||||
