Luk James, Goodfellow Alister S, More Nachiket Deepak, Bühl Michael, Kumar Amit
EaStCHEM, School of Chemistry, University of St. Andrews North Haugh, St. Andrews KY16 9ST UK
Chem Sci. 2024 Sep 5;15(40):16594-604. doi: 10.1039/d4sc03948c.
Urea derivatives, polyureas, and poly(urea-urethanes) are materials of great interest. However, their current methods of synthesis involve toxic feedstocks - isocyanate and phosgene gas. There is significant interest in developing alternative methodologies for their synthesis from safer feedstocks. We report here new methods for the synthesis of urea derivatives, polyureas, and poly(urea-urethane) using a ruthenium pincer catalyst. In this approach, urea derivatives and polyureas are synthesized from the self-coupling of formamides and diformamides, respectively, whereas poly(urea-urethanes) are synthesized from the coupling of diformamides and diols. CO and H gases are eliminated in all these processes. Decarbonylation of formamides using such organometallic catalysts has not been reported before and therefore mechanistic insights have been provided using experiments and DFT computation to shed light on pathways of these processes.
尿素衍生物、聚脲和聚(脲-氨酯)是备受关注的材料。然而,它们目前的合成方法涉及有毒原料——异氰酸酯和光气。人们对开发从更安全的原料合成它们的替代方法有着浓厚的兴趣。我们在此报告了使用钌钳形催化剂合成尿素衍生物、聚脲和聚(脲-氨酯)的新方法。在这种方法中,尿素衍生物和聚脲分别由甲酰胺和二甲酰胺的自偶联反应合成,而聚(脲-氨酯)则由二甲酰胺和二醇的偶联反应合成。在所有这些过程中都会消除一氧化碳和氢气。此前尚未有使用此类有机金属催化剂使甲酰胺脱羰的报道,因此我们通过实验和密度泛函理论计算提供了机理见解,以阐明这些过程的途径。