Recent Progress on Conversion of Carbon Dioxide into Carbamates

IF 13.5 2区 化学 Q1 CHEMISTRY, PHYSICAL 物理化学学报 Pub Date : 2024-04-01 DOI:10.3866/PKU.WHXB202307004
Yanhui Guo, Li Wei, Zhonglin Wen, Chaorong Qi, Huanfeng Jiang
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Abstract

Carbon dioxide (CO2) serves as one of the major greenhouse gases in the atmosphere. However, it is also abundant, non-toxic, and renewable, making it a valuable one-carbon source. Therefore, converting CO2 into valuable chemicals holds immense significance as an effective approach towards achieving carbon neutrality. Nevertheless, due to CO2's thermodynamic stability and kinetic inertness, its activation and conversion present considerable challenges. Organic carbamates, both cyclic and acyclic, represent a crucial class of bioactive compounds found in various natural products, agricultural chemicals, and pharmaceutically relevant molecules. They are also widely used as essential intermediates in organic synthesis. Unfortunately, traditional methods for preparing organic carbamates often rely on highly toxic phosgene and its derivatives as raw materials, posing serious environmental and safety concerns and limiting practical applications. From a cost-effective and sustainable standpoint, substituting CO2 for phosgene in the synthesis of organic carbamates is highly appealing. In recent decades, numerous new reactions, particularly multicomponent reactions involving CO2 and amines, have emerged, providing efficient methods for constructing diverse and valuable carbamates. Some of these reactions can be conducted under transition-metal-free conditions, utilizing organic and inorganic bases, ionic liquids, or small organic molecules as catalysts or promoters. However, in certain cases, transition-metal catalysts, such as those based on copper, palladium, or silver, are required, especially when the reactions involve activating unsaturated hydrocarbons like alkenes and alkynes. Mechanistically, most of these methods involve in situ generation of nucleophilic CO2-amine adducts, such as carbamate salts or carbamic acids, which then react with other electrophiles or coupling partners to yield the desired carbamates. Notably, recent advancements have led to the successful development of several elegant methods for synthesizing specific types of carbamates using electrocatalysis or photocatalysis, which are not achievable through conventional thermal catalysis. This review comprehensively summarizes the recent progress in the synthesis of organic carbamates using CO2 and amines under various catalytic conditions, including transition metal-free conditions, transition metal-catalysis, electrocatalysis, and photocatalysis. Additionally, the review discusses the challenges and future prospects associated with converting CO2 into organic carbamates.
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二氧化碳转化为氨基甲酸酯的研究进展
二氧化碳(CO2)是大气中的主要温室气体之一。然而,它也是丰富的,无毒的,可再生的,使它成为一个有价值的单碳源。因此,将二氧化碳转化为有价值的化学物质作为实现碳中和的有效途径具有巨大的意义。然而,由于CO2的热力学稳定性和动力学惰性,其活化和转化面临着相当大的挑战。有机氨基甲酸酯,无论是环的还是非环的,都是一类重要的生物活性化合物,存在于各种天然产物、农业化学品和药学相关分子中。它们也被广泛用作有机合成的必需中间体。遗憾的是,传统的有机氨基甲酸酯制备方法往往依赖于剧毒的光气及其衍生物作为原料,存在严重的环境和安全问题,限制了实际应用。从成本效益和可持续的角度来看,用二氧化碳代替光气合成有机氨基甲酸酯是非常有吸引力的。近几十年来,出现了许多新的反应,特别是涉及二氧化碳和胺的多组分反应,为构建多样化和有价值的氨基甲酸酯提供了有效的方法。其中一些反应可以在无过渡金属的条件下进行,利用有机和无机碱、离子液体或小有机分子作为催化剂或促进剂。然而,在某些情况下,过渡金属催化剂,如那些基于铜,钯,或银,是必需的,特别是当反应涉及活化不饱和碳氢化合物,如烯烃和炔烃。从机理上讲,这些方法大多涉及原位生成亲核co2 -胺加合物,如氨基甲酸盐或氨基甲酸,然后与其他亲电试剂或偶联伙伴反应以产生所需的氨基甲酸酯。值得注意的是,最近的进展已经成功地开发了几种优雅的方法,用于使用电催化或光催化合成特定类型的氨基甲酸酯,这是通过传统的热催化无法实现的。本文综述了近年来利用CO2和胺在各种催化条件下合成有机氨基甲酸酯的研究进展,包括无过渡金属催化、过渡金属催化、电催化和光催化。此外,本文还讨论了将二氧化碳转化为有机氨基甲酸酯的挑战和未来前景。下载:下载高分辨率图片(117KB)下载:下载全尺寸图片
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来源期刊
物理化学学报
物理化学学报 化学-物理化学
CiteScore
16.60
自引率
5.50%
发文量
9754
审稿时长
1.2 months
期刊介绍:
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