Solvent free utilization and selective coupling of epichlorohydrin with carbon dioxide over zirconium metal-organic frameworks

被引:34
作者
Demir, Selcuk [1 ]
Usta, Sinem [1 ]
Tamar, Hasan [2 ]
Ulusoy, Mahmut [2 ,3 ]
机构
[1] Recep Tayyip Erdogan Univ, Fac Arts & Sci, Dept Chem, TR-53100 Rize, Turkey
[2] Harran Univ, Fac Arts & Sci, Dept Chem, TR-63190 Sanliurfa, Turkey
[3] Mersin Univ, Dept Met & Mat Engn, Fac Engn, Ciftlikkoy Campus, TR-33343 Mersin, Turkey
关键词
Metal-organic frameworks; Cycloaddition; Carbon dioxide; Epoxide; Ui0-67; CYCLIC CARBONATES; CATALYTIC-ACTIVITY; GAS-STORAGE; CO2; CONVERSION; COMPLEXES; FIXATION; VANADIUM; MOF; CONSTRUCTION;
D O I
10.1016/j.micromeso.2016.10.043
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Ui0 type zirconium metal-organic frameworks (MOFs) have been successfully applied to the synthesis of cyclic carbonates from CO2 and epoxides without using any solvent. All prepared MOFs are good catalysts for the cycloaddition of CO2 to epoxide of epichlorohyrine in the presence of 4-(dimethylamino)pyridine as a co-catalyst. The catalyst system is heterogeneous, easy to separate after completion of reaction and reusable for many runs. After determining the best active catalyst, the effect of the amount of catalysts and variety of base (as co-catalyst) were studied, indicating that the catalytic activity depends strongly on the ratio of catalyst/base/epoxide. (C) 2016 Elsevier inc. All rights reserved.
引用
收藏
页码:251 / 257
页数:7
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