Crista Diana M A, Esteves da Silva Joaquim C G, Pinto da Silva Luís
Chemistry Research Unit (CIQUP), Institute of Molecular Sciences (IMS), Department of Geosciences, Environment and Territorial Planning, Faculty of Sciences, University of Porto, R. Campo Alegre s/n, 4169-007 Porto, Portugal.
LACOMEPHI, GreenUPorto, Department of Geosciences, Environment and Territorial Planning, Faculty of Sciences, University of Porto, R. Campo Alegre s/n, 4169-007 Porto, Portugal.
Materials (Basel). 2023 Dec 13;16(24):7620. doi: 10.3390/ma16247620.
Considering the increased anthropogenic emissions of CO into the atmosphere, it is important to develop economic incentives for the use of CO capture methodologies. The conversion of CO into heterocyclic carbonates shows significant potential. However, there is a need for suitable organocatalysts to reach the required efficiency for these reactions. Given this, there has been an increasing focus on the development of organocatalytic systems consisting of a nucleophile and a hydrogen bond donor (HBD) so that CO conversion can occur in ambient conditions. In this work, we evaluated the potential of fluorescent carbon dots (CDs) as catalytic HBDs in the ring-opening reaction of epoxides, which is typically the rate-limiting step of CO conversion reactions into heterocyclic carbonates. The obtained results demonstrated that the CDs had a relevant catalytic effect on the studied model reaction, with a rate constant of 0.2361 ± 0.008 h, a percentage of reactant conversion of 70.8%, and a rate constant enhancement of 32.2%. These results were better than the studied alternative molecular HBDs. Thus, this study demonstrated that CDs have the potential to be used as HBDs and employed in organocatalyzed CO conversion into value-added products.
考虑到人为向大气中排放的一氧化碳增加,开发使用一氧化碳捕获方法的经济激励措施很重要。将一氧化碳转化为杂环碳酸酯显示出巨大潜力。然而,需要合适的有机催化剂来达到这些反应所需的效率。鉴于此,人们越来越关注由亲核试剂和氢键供体(HBD)组成的有机催化体系的开发,以便一氧化碳转化能够在环境条件下发生。在这项工作中,我们评估了荧光碳点(CDs)作为环氧化物开环反应中催化性氢键供体的潜力,环氧化物开环反应通常是一氧化碳转化为杂环碳酸酯反应的限速步骤。所得结果表明,碳点对所研究的模型反应具有显著的催化作用,速率常数为0.2361±0.008 h,反应物转化率为70.8%,速率常数提高了32.2%。这些结果优于所研究的其他分子氢键供体。因此,本研究表明碳点有潜力用作氢键供体,并用于有机催化一氧化碳转化为增值产品。