TY - JOUR
T1 - Reaction Mechanism of CO2and Styrene Oxide Catalyzed by Ionic Liquids
T2 - A Combined DFT Calculation and Experimental Study
AU - Zha, Jinyin
AU - Ding, Tong
AU - Chen, Jian
AU - Wang, Rong
AU - Gao, Guohua
AU - Xia, Fei
N1 - Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Bioactive compound 3-aryl-2-oxazolidinone could be synthesized by a green method mixing carbon dioxide, aniline, and ethylene oxide. Our group previously proposed a parallel mechanism for this conversion catalyzed by ionic liquids. Recently, a new study on a similar reaction system of styrene oxide, carbon dioxide, and aniline under the catalysis of K3PO4 gave a different serial mechanism. In order to explore the mechanism of reaction, we conducted a combined theoretical and experimental study on a one-pot conversion of styrene oxide, carbon dioxide, and aniline. In experiments, two isomer products, 3,5-diphenyl-l,3-oxazolidin-2-one and 3,4-diphenyl-l,3-oxazolidin-2-one, were observed. The computational results show that the parallel mechanism is more favored in thermodynamics and in kinetics due to the instability of isocyanate and hardness of its generation. Hence, we believe the previous parallel mechanism is more reasonable under our catalysts and conditions.
AB - Bioactive compound 3-aryl-2-oxazolidinone could be synthesized by a green method mixing carbon dioxide, aniline, and ethylene oxide. Our group previously proposed a parallel mechanism for this conversion catalyzed by ionic liquids. Recently, a new study on a similar reaction system of styrene oxide, carbon dioxide, and aniline under the catalysis of K3PO4 gave a different serial mechanism. In order to explore the mechanism of reaction, we conducted a combined theoretical and experimental study on a one-pot conversion of styrene oxide, carbon dioxide, and aniline. In experiments, two isomer products, 3,5-diphenyl-l,3-oxazolidin-2-one and 3,4-diphenyl-l,3-oxazolidin-2-one, were observed. The computational results show that the parallel mechanism is more favored in thermodynamics and in kinetics due to the instability of isocyanate and hardness of its generation. Hence, we believe the previous parallel mechanism is more reasonable under our catalysts and conditions.
UR - https://www.scopus.com/pages/publications/85092681024
U2 - 10.1021/acs.jpca.0c04662
DO - 10.1021/acs.jpca.0c04662
M3 - 文章
C2 - 32900202
AN - SCOPUS:85092681024
SN - 1089-5639
VL - 124
SP - 7991
EP - 7998
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 39
ER -