TY - JOUR
T1 - Preparation and structure of [C10H9N]2CuBr2 and its catalytic activity in oxidative carbonylation of ethanol
AU - Xu, Kai
AU - Wang, Xin
AU - Liu, Dinghua
AU - Liu, Xiaoqin
AU - Sun, Linbing
N1 - Publisher Copyright:
©All Right Reserved
PY - 2015/6/1
Y1 - 2015/6/1
N2 - The copper coordination compound [C10H9N]2CuBr2 was prepared by the reaction of 4-methylchinolin with copper bromide in ethanol solution. The compound was characterized with FTIR, EA, ICP-AES and XRD, and its catalytic performance in oxidative carbonylation of ethanol was investigated. The density functional theory (DFT) calculations were performed to analyze its structure, natural atomic charges and frontier orbital energy levels. The introduction of ligand could improve catalytic activity to prepare diethyl carbonate. The per pass conversion of ethanol could reach 21.5% under the reaction conditions of temperature 373 K, pressure 3.5 MPa, time 4 h and mass concentration of catalyst in ethanol 0.075 g·ml-1. Reaction mechanism study showed that the compound had moderate stability, which benefited insertion of CO (the rate-controlling step) and formation of intermediate. Therefore, reaction activity was enhanced.
AB - The copper coordination compound [C10H9N]2CuBr2 was prepared by the reaction of 4-methylchinolin with copper bromide in ethanol solution. The compound was characterized with FTIR, EA, ICP-AES and XRD, and its catalytic performance in oxidative carbonylation of ethanol was investigated. The density functional theory (DFT) calculations were performed to analyze its structure, natural atomic charges and frontier orbital energy levels. The introduction of ligand could improve catalytic activity to prepare diethyl carbonate. The per pass conversion of ethanol could reach 21.5% under the reaction conditions of temperature 373 K, pressure 3.5 MPa, time 4 h and mass concentration of catalyst in ethanol 0.075 g·ml-1. Reaction mechanism study showed that the compound had moderate stability, which benefited insertion of CO (the rate-controlling step) and formation of intermediate. Therefore, reaction activity was enhanced.
KW - Catalyst
KW - Compound
KW - Conversion
KW - Density functional theory
KW - Oxidative carbonylation
UR - http://www.scopus.com/inward/record.url?scp=85050577027&partnerID=8YFLogxK
U2 - 10.11949/j.issn.0438-1157.20150013
DO - 10.11949/j.issn.0438-1157.20150013
M3 - 文章
AN - SCOPUS:85050577027
SN - 0438-1157
VL - 66
SP - 2089
EP - 2097
JO - Huagong Xuebao/CIESC Journal
JF - Huagong Xuebao/CIESC Journal
IS - 6
ER -