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Catalytic Strategies for the Cycloaddition of COsub.2 to Epoxides in Aqueous Media to Enhance the Activity and Recyclability of Molecular Organocatalysts
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Catalytic Strategies for the Cycloaddition of COsub.2 to Epoxides in Aqueous Media to Enhance the Activity and Recyclability of Molecular Organocatalysts
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Journal Article
Catalytic Strategies for the Cycloaddition of COsub.2 to Epoxides in Aqueous Media to Enhance the Activity and Recyclability of Molecular Organocatalysts
2024
Overview
The cycloaddition of CO[sub.2] to epoxides to afford versatile and useful cyclic carbonate compounds is a highly investigated method for the nonreductive upcycling of CO[sub.2]. One of the main focuses of the current research in this area is the discovery of readily available, sustainable, and inexpensive catalysts, and of catalytic methodologies that allow their seamless solvent-free recycling. Water, often regarded as an undesirable pollutant in the cycloaddition process, is progressively emerging as a helpful reaction component. On the one hand, it serves as an inexpensive hydrogen bond donor (HBD) to enhance the performance of ionic compounds; on the other hand, aqueous media allow the development of diverse catalytic protocols that can boost catalytic performance or ease the recycling of molecular catalysts. An overview of the advances in the use of aqueous and biphasic aqueous systems for the cycloaddition of CO[sub.2] to epoxides is provided in this work along with recommendations for possible future developments.
Publisher
MDPI AG
Subject
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