摘要
Chemical fixation of CO2 as C1 source at ambient temperature and low pressure is an energy-saving way to make use of the green-house gas, but it still remains a challenge since efficient catalyst with high catalytic active sites is required. Here, a novel monoclinic azo-functionalized Zr-based metal−organic polyhedron (Zr-AZDA) has been prepared and applied in CO2 fixation with epoxides. The inherent azo groups not only endow Zr-AZDA with good solubilization, but also act as basic sites to enrich CO2 showing efficient synergistic catalysis as confirmed by TPD-CO2 analysis. XPS results demonstrate that the Zr active sites in Zr-AZDA possess suitable Lewis acidity, which satisfies both substrates activation and products desorption. DFT calculation indicates the energy barrier of the rate-determining step in CO2 cycloaddition could be reduced remarkably (by ca. 60.9 %) in the presence of Zr-AZDA, which may rationalize the mild and efficient reaction condition employed (80 °C and 1 atm of CO2). The work provides an effective multi-functional cooperative method for improvement of CO2 cycloaddition.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 12890-12899 |
| 页数 | 10 |
| 期刊 | Chemistry - A European Journal |
| 卷 | 27 |
| 期 | 50 |
| DOI | |
| 出版状态 | 已出版 - 6 9月 2021 |
学术指纹
探究 'Azo-Functionalized Zirconium-Based Metal−Organic Polyhedron as an Efficient Catalyst for CO2 Fixation with Epoxides' 的科研主题。它们共同构成独一无二的指纹。引用此
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver