Zinc 2-N-methyl N-confused porphyrin: an efficient catalyst for the conversion of CO2 into cyclic carbonates

被引:27
作者
Ge, Yuansheng [1 ]
Cheng, Guoe [1 ]
Xu, Nanfeng [1 ]
Wang, Weizhou [2 ,3 ]
Ke, Hanzhong [1 ]
机构
[1] China Univ Geosci Wuhan, Fac Mat Sci & Chem, Wuhan 430074, Hubei, Peoples R China
[2] Luoyang Normal Univ, Coll Chem & Chem Engn, Luoyang 471934, Peoples R China
[3] Luoyang Normal Univ, Henan Key Lab Funct Oriented Porous Mat, Luoyang 471934, Peoples R China
基金
美国国家科学基金会;
关键词
METALLOPORPHYRIN CATALYSTS; COUPLING REACTION; DIOXIDE FIXATION; HIGHLY EFFICIENT; EPOXIDES; METAL; COMPLEXES; CAPTURE; ORGANOCATALYSTS; TRANSFORMATION;
D O I
10.1039/c9cy00739c
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
A zinc 2-N-methyl N-confused porphyrin (Zn(NCP)Cl) catalyst was developed for the solvent-free synthesis of cyclic carbonates from epoxides and CO2. Zn(NCP)Cl exhibited very high catalytic activity. Using this catalyst, a series of epoxides have been converted into the corresponding cyclic carbonates in high yields and selectivity (>99%). The turnover frequency (TOF) value reached 266 667 h(-1) for the conversion of CO2 with epichlorohydrin into cyclic carbonate at 120 degrees C and an initial CO2 pressure of 1.7 MPa within 3 h. Furthermore, an almost quantitative cyclic carbonate product was achieved under atmospheric CO2 within 24 h. X-ray structural analysis of Zn(NCP)Cl reveals that the Zn2+ ion is four-coordinate, surrounded by three nitrogen atoms from the N-confused porphyrin and a chlorine atom. Due to the strong electron-withdrawing ability of chloride, zinc shows strong acidity, thereby enhancing its ability to activate epoxide. Density functional theory calculations (DFT) suggest that the ring-opening of epoxide is the rate-determining step of the catalytic cycle.
引用
收藏
页码:4255 / 4261
页数:7
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