Zwitterion π-conjugated network polymer based on guanidinium and β-ketoenol as a heterogeneous organo-catalyst for chemical fixation of CO2 into cyclic carbonates

被引:9
|
作者
Garai, Mousumi [1 ]
Rozyyev, Vepa [1 ]
Ullah, Zakir [2 ]
Jamal, Aqil [3 ]
Yavuz, Cafer T. [1 ,2 ,4 ]
机构
[1] Korea Adv Inst Sci & Technol, Grad Sch Energy Environm Water & Sustainabil EEWS, 291 Daehak Ro, Daejeon 34141, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Chem, 291 Daehak Ro, Daejeon 34141, South Korea
[3] Saudi Aramco, Res & Dev Ctr, Dhahran 31311, Saudi Arabia
[4] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, 291 Daehak Ro, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
COVALENT TRIAZINE FRAMEWORKS; POROUS CATIONIC POLYMERS; COOPERATIVE CONVERSION; CLIMATE-CHANGE; IONIC LIQUIDS; METAL; DIOXIDE; CAPTURE; IMIDAZOLIUM; EPOXIDES;
D O I
10.1063/1.5122017
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The chemical fixation of CO2 with epoxides to cyclic carbonate is an attractive 100% atom economic reaction. It is a safe and green alternative to the route from diols and toxic phosgene. In this manuscript, we present a new zwitterionic pi-conjugated catalyst (Covalent Organic Polymer, COP-213) based on guanidinium and beta-ketoenol functionality, which is synthesized from triaminoguanidinium halide and beta-ketoenols via the ampoule method at 120 degrees C. The catalyst is characterized by FTIR-attenuated total reflection (ATR), Powder X-Ray diffraction, thermogravimetric analysis, XPS, and for surface area Brunauer-Emmett-Teller and CO2 uptake. It shows quantitative conversion and selectivity in chemical fixation of CO2 to epoxides under ambient conditions and without the need for cocatalysts, metals, solvent, or pressure. The catalyst can be recycled at least three times without the loss of reactivity. (C) 2019 Author(s).
引用
收藏
页数:7
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