Bromide promoted hydrogenation of CO2 to higher alcohols using Ru-Co homogeneous catalyst
文献类型：期刊论文
| 作者 | Cui, Meng1,2; Qian, Qingli1; He, Zhenhong1; Zhang, Zhaofu1; Ma, Jun1; Wu, Tianbin1; Yang, Guanying1; Han, Buxing1 |
| 刊名 | CHEMICAL SCIENCE
 |
| 出版日期 | 2016 |
| 卷号 | 7期号:8页码:5200-5205 |
| 英文摘要 | Iodides are commonly used promoters in C2+ OH synthesis from CO2/CO hydrogenation. Here we report the highly efficient synthesis of C2+OH from CO2 hydrogenation over a Ru-3(CO)(12)-Co-4(CO)(12) bimetallic catalyst with bis(triphenylphosphoranylidene) ammonium chloride (PPNCl) as the cocatalyst and LiBr as the promoter. Methanol, ethanol, propanol and isobutanol were formed at milder conditions. The catalytic system had a much better overall performance than those of reported iodide promoted systems because PPNCl and LiBr cooperated very well in accelerating the reaction. LiBr enhanced the activity and PPNCl improved the selectivity, and thus both the activity and selectivity were very high when both of them were used simultaneously. In addition, the catalyst could be reused for at least five cycles without an obvious change of catalytic performance. |
| 收录类别 | SCI |
| 语种 | 英语 |
| 源URL | [http://ir.iccas.ac.cn/handle/121111/35351]  |
| 专题 | 化学研究所_胶体、界面与化学热力学实验室 |
| 作者单位 | 1.Chinese Acad Sci, Inst Chem, CAS Key Lab Colloid Interface & Chem Thermodynam, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China 2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China |
| 推荐引用方式 GB/T 7714 | Cui, Meng,Qian, Qingli,He, Zhenhong,et al. Bromide promoted hydrogenation of CO2 to higher alcohols using Ru-Co homogeneous catalyst[J]. CHEMICAL SCIENCE,2016,7(8):5200-5205. |
| APA | Cui, Meng.,Qian, Qingli.,He, Zhenhong.,Zhang, Zhaofu.,Ma, Jun.,...&Han, Buxing.(2016).Bromide promoted hydrogenation of CO2 to higher alcohols using Ru-Co homogeneous catalyst.CHEMICAL SCIENCE,7(8),5200-5205. |
| MLA | Cui, Meng,et al."Bromide promoted hydrogenation of CO2 to higher alcohols using Ru-Co homogeneous catalyst".CHEMICAL SCIENCE 7.8(2016):5200-5205. |
入库方式： OAI收割
来源：化学研究所
浏览0
下载0
收藏0
其他版本
除非特别说明，本系统中所有内容都受版权保护，并保留所有权利。