Abstract

In this article, the combination of guanidine hydrochloride with co-catalyst ZnI2 proved to be a highly efficient heterogeneous catalyst for the environmentally benign, solvent-free synthesis of cyclic carbonates under mild reaction conditions. The effects of different co-catalysts as well as reaction parameters including catalyst loadings, CO2 pressure, reaction temperature, and reaction time on the coupling reaction of CO2 to propylene oxide were thoroughly investigated. With the molar ratio of guanidine hydrochloride to ZnI2 at 5:1, excellent yield (94%) and selectivity (≥99%) of propylene carbonate were obtained under 100 °C and at 1 MPa for 1.5 h. Additionally, ZnI2 could be recycled, but because of the washing loss of guanidine hydrochloride, there was a slight decrease in the yield of propylene carbonate. Gratifyingly, the activity of the catalytic system could be restored by adding additional 20 mol% of fresh guanidine hydrochloride, thus exhibiting excellent recyclability of the ZnI2 catalyst. Moreover, the binary catalysts were also versatile when using other epoxides for CO2 cycloaddition. A possible reaction mechanism was proposed wherein guanidine hydrochloride plays a dual role in activating CO2 and epoxide, and ZnI2 activated epoxide, simultaneously. The synergistic effect of guanidine hydrochloride and ZnI2 ensure the reaction proceeds effectively.

Highlights

  • Carbon dioxide can be specially spotlighted as an abundant, inexpensive, and renewable C1 resource, which can replace commonly used toxic C1 building blocks such as phosgene [1]; at the same time CO2 is the main greenhouse gas contributor [2]

  • Almost no activity in forming the product propylene carbonate (PC) was observed with Guanidine hydrochloride (GndCl) or ZnI2 alone (Entries 1 and 2) and only 27% yield of PC was obtained when GndCl was employed under 130 °C

  • It was noted that the selectivity to PC was always above 99%, the rest was due to the trace amounts of propylene oxide (PO) polymerization in side reactions

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Summary

Introduction

Carbon dioxide can be specially spotlighted as an abundant, inexpensive, and renewable C1 resource, which can replace commonly used toxic C1 building blocks such as phosgene [1]; at the same time CO2 is the main greenhouse gas contributor [2]. Chemical fixation of CO2 has been a hot topic from the viewpoint of sustainable development and green chemistry. In this regard, one of the most promising strategies is the transformation of CO2 with epoxides to yield the corresponding cyclic carbonates (Scheme 1) [3], which is considered green because of 100% atom efficiency. Cyclic carbonates can be widely applied in proton inert solvents, as precursors for polycarbonates and polyurethanes synthesis, as electrolytes in lithium secondary batteries, and as intermediates for production of pharmaceuticals, fine chemicals and agricultural chemicals [4,5].

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