One-pot synthesis of 3D-ZIF-7 supported on 2D-Zn-Benzimidazole-Acetate and its catalytic activity in the methoxycarbonylation of aniline with dimethyl carbonate

被引:6
作者
Dahnum, Deliana [1 ,2 ,3 ]
Dang, Huyen Tran [1 ,2 ]
Tran, Ngoc Tuan [1 ,2 ]
Ha, Jeong-Myeong [1 ,2 ]
Lee, Hyunjoo [1 ,2 ]
机构
[1] Korea Inst Sci & Technol, Clean Energy Res Ctr, 5,Hwarang Ro,14 Gil, Seoul 02792, South Korea
[2] Korea Univ Sci & Technol, KIST Sch, Div Energy & Environm Technol, Seoul 02792, South Korea
[3] Indonesian Inst Sci, Res Ctr Chem, LIPI Lembaga Ilmu Pengetahuan Indonesia, Serpong 15314, Tangerang Selat, Indonesia
基金
新加坡国家研究基金会;
关键词
ZIF-7; Zn(BeIM)OAc; One-pot synthesis; Methoxycarbonylation; N-PHENYL CARBAMATE; ZEOLITIC IMIDAZOLATE FRAMEWORK; EFFICIENT HETEROGENEOUS CATALYST; ZIF-8; SEPARATION; STABILITY; SOLVENT; DIAMINE;
D O I
10.1016/j.jiec.2021.04.049
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For the first time, three-dimensional Zeolitic Imidazole Framework (3D) ZIF-7 (Zn(BeIM)(2), BeIM = benzimidazole) supported on two-dimensional (2D) Zn(BeIM)OAc (Zinc-Benzimidazole-Acetate) was synthesized by reacting Zn(OAc)(2) and benzimidazole in a one-pot reaction. By modulating the amount of diethylamine during the reaction, the ZIF-7/Zn(BeIM)OAc with a 1 to 1 molar ratio was obtained when the reactant molar ratio of Zn(OAc)(2) and benzimidazole was 1 to 1.5. It was found that 3D-ZIF-7 was synthesized first and then transformed into 2D-Zn(BeIM)OAc by the reaction with remaining Zn(OAc)(2). The synthesized ZIF-7 (Zn(BeIM)(2)) supported on Zn(BeIM)OAc (1/1) showed enhanced catalytic performance in the methoxycarbonylation of aniline with dimethyl carbonate. The yield of methyl N-phenyl carbamate reached 92.0% in 2 h at 190 degrees C, which was higher than yields obtained using the single component catalysts ZIF-7 (69.9%) and Zn(BeIM)OAc (35.4%). Furthermore, this catalyst was successfully reused four times, maintaining an MPC yield of 92.0%-95.8%. (C) 2021 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:380 / 387
页数:8
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